]11[]21[ 135733 שיטת החפיה ]54[ ENCAPSULATION METHOD ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 24.09.1998 9703874-9 ]32[ 23.10.1997 ]33[ SE Int. Cl.7 A61K 009/00, 009/14, 009/50, B01J 013/00 JAGOTEC AG, SWITZERLAND WO/1999/020253 EITAN, PEARL, LATZER AND , לצר וכהן צדק, פרל,איתן COHEN ZEDEK, הרצליה,12688 .ד. ת, 7 רחוב שנקר P.O.B. 12688 HERZLIYA 46733 [57] A method of encapsulating an active substance in a biodegradable polymer, which comprises: (a) dissolving said biodegradable polymer in an organic solvent thereof; (b1) dispersing said active substance in the organic solution obtained in step (a), to provide a dispersion with the active substance as the inner phase thereof, or alternatively (b2) emulsifying said active substance, dissolved in water or other aqueous solvent therefor, in the organic solution obtained in step (a), to provide an emulsion with the active substance as the inner aqueous phase thereof; and (c) subjecting the dispersion obtained in step (b1), or alternatively the emulsion obtained in step (b2), to an encapsulation operation with an aqueous polyethylene glycol solution as a continuous phase, such that micro or nanoparticles having the active substance encapsulated therein are obtained. __________ ]11[]21[ ]54[ HIGH SENSOR RESOLUTION POSITION SENSOR DEVICE AND METHOD ]22[ ]51[ ]71[ 08.05.2000 Int. Cl.7 G01D 005/244 YASKAWA ESHED TECHNOLOGY LTD. YVES VILLARET, SHMUEL PROKOPETS EDWARD LANGER, 44-46 MONTEFIORE STREET TEL AVIV 65201 ]72[ ]74[ November 20, 2005– י"ח בחשון התשס"ו 136016 שיטה והתקן לחיישן מיקום ברזולוציה גבוהה ראש העין,יאסקווה אשד טכנולוגיה בע''מ שמואל פרוקופץ,איב וילרה ,אדוארד לנגר תל אביב,44-46מונטיפיורי 1956 [57] A sensor device (10) for measuring a changing variable of a system and providing output values representing the system variable with increased resolution, said device comprising: means (24) for providing a pulse with each transition of the measured variable over a level of each of a set of regularly spaced apart predetermined levels, means (26) for generating a train of system clock pulses at a first rate and a train of divided system clock pulses at a fraction of said first rate; first means (30) for counting a first number of pulses of said divided system clock pulse train occurring between each occurrence of said transition pulse; means (32) for storing said first counted number of pulses of said divided system clock pulse train; second means (34) for counting a second number of pulses of said divided system clock pulse train, and resetting said second counted number upon each transition pulse; second means for storing said second counted number of pulses of said divided system clock pulse train, in a register at a shifted storage position representing a multiple of said second counted number of pulses; means (40) for repeatedly comparing, at a relatively high rate, said shifted, stored second counted number and said stored first counted number and producing a difference count therebetween if the former exceeds the latter; means (37) for generating a high resolution pulse upon replacing said shifted, stored second counted number with said difference count in said register, thus providing several high resolution pulses between transition pulses; and means for calculating the system variable by counting the number of high resolution pulses in the interval between occurrences of said transition pulses. __________ 1957 November 20, 2005– י"ח בחשון התשס"ו ]11[]21[ ]54[ KIT CONTAINING ESTROGEN FOR POSTMENOPAUSAL USE ]22[ ]31[ ]51[ ]71[ 19.11.1998 975599 ]32[ 21.11.1997 Int. Cl.7 A61K 031/57, A61P 005/24 BERLEX LABORATORIES, INC., U.S.A. THE REGENTS OF THE UNIVERSITY OF CALIFORNIA, U.S.A. THE PERMANENTE MEDICAL GROUP, INC., U.S.A. KAISER FOUNDATION HEALTH PLAN, INC., U.S.A. WO/1999/026631 WOLFF, BREGMAN AND GOLLER, KEREN HAYESOD ST 19B, P.O.B. 1352 JERUSALEM 91013 ]87[ ]74[ [57] A composition for treating a physical condition resulting from postmenopausal estrogen decline in a postmenopausal subject, the composition comprising: an amount of estrogen which is effective to produce a serum estradiol level of between about 5 ph/ml and about 15 pg/ml in the 136175 ערכה המכילה אסטרוגן לשמוש לאחר הפסקת הוסת ]33[ US , ברגמן וגולר,וולף ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד subject, wherein the physical condition comprises at least one of postmenopausal estrogen decline, increased risk of osteoporotic bone fracture due to postmenopausal osteoporosis, and loss of bone mineral density. __________ November 20, 2005– י"ח בחשון התשס"ו 1958 ]11[]21[ ]54[ PARAMAGNETIC CARBOHYDRATE REAGENT FOR TUMOR IMAGING AND /OR TREATMENT ]22[ ]31[ 19.11.1998 60/067081 ]32[ 20.11.1997 09/195341 18.11.1998 Int. Cl.7 A61K 049/08 DAVID PLATT, U.S.A. WO/1999/026535 SANFORD T.COLB & CO.,, P.O.B. 2273, REHOVOT 76122 ]51[ ]71[ ]87[ ]74[ [57] A reagent for magnetic resonance imaging of a cancerous tumor in vivo comprising: a carbohydrate which is capable of binding to or penetrating a cancerous cell, said carbohydrate having a 136210 ריאגנט פחמימתי פאראמגנטי להדמייה או טיפול בגידולים/ו ]33[ US US ,' קולב ושות.סנפורד ט רחובות,2273 .ד. ת, מרמורק,4 שער הגיא paramagnetic atom bonded thereto, said carbohydrate having an average molecular weight equal to or less than 2000 daltons; and a carrier suitable for delivery of said carbohydrate to the cancerous cell. __________ ]11[]21[ 136436 ,תרכובות המעכבות קולטן מזרחן ורכיבים המרכיבים אותם,הכנתן ]54[ PDGF RECEPTOR KINASE INHIBITOR COMPOUNDS, THEIR PREPARATION AND COMPOSITIONS CONTAINING THEM ]22[ ]31[ ]51[ ]71[ 30.11.1998 980596 ]32[ 01.12.1997 ]33[ US Int. Cl.7 A61K 031/495, A61P 035/00, C07D 487/02, C07F 015/02 YISSUM RESEARCH יישום חברה לפיתוח המחקר של DEVELOPMENT COMPANY OF ירושלים,האוניברסיטה העברית בירושלים THE HEBREW UNIVERSITY OF JERUSALEM ALEXANDER LEVITZKI, AVIV , שמואל בנאי, אביב גזית,אלכסנדר לויצקי GAZIT, SHMUEL BANAI, DAVID גרשון גולומב,דוד גרץ GERTZ, GERSHON GOLOMB WO/1999/028304 G.E. EHRLICH (1995) LTD., ,) בע"מ1995( ארליך.אי.ג'י 11 MENACHEM BEGIN STREET רמת גן,11מנחם בגין RAMAT GAN 52521 ]72[ ]87[ ]74[ 1959 November 20, 2005– י"ח בחשון התשס"ו [57] A compound comprising a tyrphostin of the formula: wherein R1 and R2 are each independently selected from the group consisting of alkyl, alkoxy, halogen, nitro and amine group and Ar is selected from the group consisting of phenyl, ferrocene, thiophene, furane, pyrrole, indole, thiazole, imidazole and pyridine. __________ ]11[]21[ ]54[ SURGICAL CLIP ]22[ ]51[ ]71[ 12.06.2000 Int. Cl.7 A61B 017/122 NITI ALLOYS TECHNOLOGIES LTD. LEONID MONASSEVITCH, SHLOMO LELCUK, MICHAEL ARAD JEREMY M. BEN-DAVID & CO. LTD., HAR HOTZVIM HI-TECH PARK, P.O. B0X 45087 JERUSALEM ]72[ ]74[ [57] A surgical clip (10) formed at least partly of a shape memory alloy, said clip including: a first length of a wire (12) defining a closed geometrical shape having a central opening; a second length of a wire (22) defining a closed geometrical shape similar in configuration and magnitude to that of said first length of wire, wherein, when placed in side-by-side registration, said first and second lengths of wire fully overlap; an intermediate portion (13) located between said first length of wire and said second length of wire, said intermediate portion formed of a November 20, 2005– י"ח בחשון התשס"ו 136702 מהדק כירורגי נתניה,טכנולוגיות סגסוגות ניטי בע"מ מיכאל ארד, שלמה ללצ'וק,לאוניד מונסביץ ,דוד ושות' בע"מ- בן.ירמיהו מ ירושלים,45087 .ד. ת, הר חוצבים shape memory alloy; a cutting element (48) associated with said first length of wire; a counter element (26) associated with said second length of wire and arranged for cutting engagement with said cutting element; wherein when at a first temperature or higher, said first and second lengths of wire are positioned in a side-byside closed position and said shape memory alloy is in an elastic state, and further, when at a second temperature or lower, below said first temperature, said shape memory alloy is in a plastic state, thereby enabling said first and second 1960 lengths of wire to be moved into and to retain a spaced apart position, and upon heating of said clip to a temperature at least equal to said first temperature, said first and second lengths of wire return to said side-by-side closed position, thereby to apply a compressive force to tissue located therebetween. __________ ]11[]21[ 136783 תרכובות בנזוקסאזין להגברת תגובה הכנתן ותכשירי רוקחות,סינפטית המכילים אותן ]54[ SYNAPTIC RESPONSE ENHANCING BENZOXAZINE COMPOUNDS, THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM ]22[ ]31[ ]51[ ]71[ 16.12.1998 998300 ]32[ 24.12.1997 ]33[ US Int. Cl.7 A61K 031/395, A61P 025/00, C07D 498/04, 498/14, 513/04, 513/14 THE REGENTS OF THE UNIVERSITY OF CALIFORNIA, U.S.A. WO/1999/033469 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST. תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.BOX 4060, TEL AVIV 61040 ]87[ ]74[ [57] A compound of the formula 1961 November 20, 2005– י"ח בחשון התשס"ו wherein: X1 and X2 are independently selected from H, NR32,-OR4, and –CH2OR4; or X1 and X2 taken together are –OCR52O-, OCR52CR52O-, or –OCR5=CR5O-; or X1 and X2 taken together are – N=CR6CR6=N-; or X1 and X2 taken together are –N=CR3NR3; or X1 and X2 taken together are =N-O-N= or =N-S-N=; or X1 and X2 taken together are –O-CR3=N; Z is O, NR7, and S; R1 is H, C1-C6 alkyl, or C1-C3 fluoroalkyl, each occurrence of R2 is independently H, halogen, cyano, hydroxy, C1-C6 alkoxy, C1-C3 fluoroalkoxy, mercapto, C1-C6 alkyl, C1-C3 fluoroalkyl, C2-C6 alkoxyalkyl, C6C12 aryl C3-C12 heteroaryl, C7-C12 arylalkyl, C4-C12 heteroarylalkyl, C6-C12 aryloxy, C7-C12 aryloxyalkyl, C7-C12 arylalkoxy, or C4-C12 heteroarylalkoxy; each occurrence of R3 and R7 is independently H, C1-C6 alkyl, C1-C3 fluoroalkyl, C7-C12 arylalkyl or C4-C12 heteroarylalkyl; each occurrence of R4 is independently H, C1-C6 alkyl, C1-C3 fluoroalkyl, C2-C6 alkoxyalkyl, C7-C12 arylalkyl, C4-C12 heteroarylalkyl, or C7-C12 aryloxyalkyl; both R5 are identical, at each occurrence being H, halogen, cyano, C1-C6 alkyl, C1C3 fluoroalkyl, C2-6 alkoxyalkyl, C7-C12, arylalkyl, C4-C12 heteroarylalkyl, or C7-C12 aryloxyalkyl; both R6 are identical, at each occurrence being H, cyano, hydroxy, C1C6 alkoxy, C1-C6 alkyl, C1-C3 fluoroalkyl, C2-C6 alkoxyalkyl, C7-C12 aryalkyl, C4-C12 heteroarylalkyl, C6-C12 aryloxy, C7-C12 aryloxyalkyl, C7-C12 arylalkoxy, or C4-C12 heteroarylalkoxy and n is 2, 3 or 4. __________ ]11[]21[ November 20, 2005– י"ח בחשון התשס"ו 137245 1962 ]54[ INTRAOCULAR LENS IMPLANT WITH TELESCOPE SUPPORT ]22[ ]31[ ]51[ ]71[ 05.01.1999 09/007379 ]32[ 15.01.1998 Int. Cl.7 A61F 002/16 VISIONCARE OPHTHALMIC TECHNOLOGIES, INC., U.S.A. YOSEF GROSS, GIDEON DOTAN, ISAAC LIPSHITZ WO/1999/036004 SANFORD T.COLB & CO.,, P.O.B. 2273, REHOVOT 76122 ]72[ ]87[ ]74[ [57] An intraocular lens (IOL) implant (10) for implantation in an eye having a capsular bag, a posterior chamber and an anterior chamber, the implant comprising: a first carrying member (12) adapted to be attached to said capsular bag; and a telescope (16) attached to and extending from said first carrying member; השתלת עדשות אינטראוקולריים בעלי תמיכה טלסקופית ]33[ US יצחק ליפשיץ, גדעון דותן,יוסף גרוס ,' קולב ושות.סנפורד ט רחובות,2273 .ד. ת, מרמורק,4 שער הגיא characterized by said telescope being further attached to at least one second carrying member (18), wherein said at least one second carrying member is adapted to be attached to a portion of the eye. __________ ]11[]21[ 1963 137276 November 20, 2005– י"ח בחשון התשס"ו ]54[ EXTENSIBLE DISTRIBUTED ENTERPRISE APPLICATION INTEGRATION SYSTEM ]22[ ]31[ 18.11.1999 60/108993 ]32[ 18.11.1998 412595 05.10.1999 412633 05.10.1999 Int. Cl.7 G06F 009/54, 015/163 SAGA SOFTWARE, INC., U.S.A. WO/2000/029924 SANFORD T.COLB & CO.,, P.O.B. 2273, REHOVOT 76122 ]51[ ]71[ ]87[ ]74[ [57] A system for integrating a plurality of computer applications, comprising: first means for routing plurality of messages within the system; means for storing a plurality of data transformation configurations and a plurality of business process rules; means for applying said data transformation configurations to said plurality of messages; second means for routing said plurality of messages between said first means for routing messages within the system and a plurality of computer applications, wherein said second means for routing said plurality of מערכת שילוב יישומים מופצים של מפעלים הניתנת להרחבה ]33[ US US US ,' קולב ושות.סנפורד ט רחובות,2273 .ד. ת, מרמורק,4 שער הגיא messages between said first means for routing messages within the system and the plurality of computer applications, includes: an adapter configured for each of the plurality of computer applications; an agent service hosting said adapter; a message definition for each of said plurality of messages said adapter will produce, receive, or reply to; means for connecting said adapter to its respective computer applications; and means for implementing said adapter through said connecting means. __________ ]11[]21[ November 20, 2005– י"ח בחשון התשס"ו 137302 1964 ]54[ APPARATUS FOR USE IN CONNECTION WITH REMOVAL OF ELEMENTS, ESPECIALLY EXOGENOUS ANTIBODIES, FROM BLOOD OR PLASMA ]22[ ]31[ ]51[ ]71[ 14.01.1999 0070/98 ]32[ 20.01.1998 Int. Cl.7 A61M 001/34, B01D 024/16 MITRA MEDICAL TECHNOLOGY AB, SWEDEN WO/1999/036110 LUZZATTO & LUZZATTO, P.O.B. 5352 BEER-SHEVA 84965 ]87[ ]74[ [57] An apparatus for removing elements from blood or plasma or plasma flowing in an extracorporeal blood circulation system of a patient, said apparatus comprising a container (1) comprising, in sequence, an inlet chamber (31), an adsorption chamber for receiving an adsorbent, and an outlet chamber (32), said container also comprising a plurality of filter units (11, 12) for filtering the blood or plasma, including a first filter unit between the outlet chamber and the adsorption chamber and a second filter unit between the adsorption chamber and the inlet chamber, and a container wall portion that, with the first filter unit, defines the outlet chamber, said container wall portion comprising (a) an inlet (15) and an outlet (16) adjacent 1965 בייחוד נוגדנים,מתקן לסילוק גורמים מדם או פלסמה,אקסוגניים ]33[ DK ,לוצאטו את לוצאטו באר שבע,5352 .ד. ת, עומר,גן תעשיה one another, (b) a plurality of passages, including a first passage that communicates with a transfer channel that extends from the first passage to the inlet chamber, and a second passage that communicates with the outlet chamber, (c) a bypass channel having first and second ends, and (d) valve means (21) for connecting the inlet and the outlet with the respective first and second passages in a first arrangement of the valve means and for connecting the inlet and the outlet with the respective first and second ends of the bypass channel in a second arrangement of the valve means, said apparatus further comprising means for controlling movement of the valve means between said first and second arrangements. November 20, 2005– י"ח בחשון התשס"ו __________ ]11[]21[ 137332 בנזותיאדיאזולים ונגזרותיהם הכנתם ותכשירי רוקחות המכילים אותם ]54[ BENZOTHIADIAZOLES AND DERIVATIVES, THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEM ]22[ ]31[ ]51[ 01.02.1999 9802251.0 ]32[ 03.02.1998 ]33[ GB Int. Cl.7 A61K 031/41, 031/433, A61P 043/00, C07D 403/10, 413/10, 417/00, 417/10, 473/10, 495/10 NOVARTIS AG, SWITZERLAND WO/1999/040089 LUZZATTO & LUZZATTO, ,לוצאטו את לוצאטו P.O.B. 5352 BEER-SHEVA 84965 באר שבע,5352 .ד. ת, עומר,גן תעשיה ]71[ ]87[ ]74[ [57] CRFI receptor antagonist compounds of the formula November 20, 2005– י"ח בחשון התשס"ו 1966 wherein X is O, S, N-CH3 CH=CH or Calk = Calk, where the Alk independently are (C1-4) alkyl, R1 and R1 and R2 independently, are hydrogen, halogen, (C1-4) alkyl, (C1-4) alkoxy or trifluoromethyl, and Het is a radical having one of the formulae (a) to (p) below: wherein R3 and R8, independently, are hydrogen or (C1-4) alkyl, R4 is hydrogen, (C1-4) alkyl, cyano, nitro, formyl or (C1-4) alkylcarbonyl, R5 and R6, independently, are hydrogen, (C1-7) alkyl, (C3-7) alkenyl, (C3-7) cycloalkyl, (C3-7) cycloalkyl (C1-4) alkyl, (C1-4) alkoxy (C2-5) alkyl or benzyl, R7 is hydrogen, hydroxy, (C1-4) alkyl or (C1-4) alkoxy, W is N, C-CN, C-NO2, C-COH or C-COAlk where Alk is as defined above, and X is as defined above, in free base or acid addition salt form. __________ 1967 November 20, 2005– י"ח בחשון התשס"ו ]11[]21[ ]54[ ABSORBENT ARTICLE WITH BREATHABLE DUAL LAYER BACKSHEET COMPRISING ONE LAYER WITH SLANTED CAPILLARY APERTURES ]22[ ]31[ ]51[ ]71[ 03.02.1999 98101867.4 ]32[ 04.02.1998 Int. Cl.7 A61F 013/15 THE PROCTER & GAMBLE COMPANY, U.S.A. WO/1999/039673 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST. P.O.BOX 4060, TEL AVIV 61040 ]87[ ]74[ [57] Breathable disposable absorbent article of layered construction, each layer or system of layers having a garment facing surface, which is oriented to face in a direction of a garment (21) during use of the article, and a wearer facing surface, which is oriented to face in the direction of the wearer during use of the article, said article comprising at least an absorbent core (40, 42, 44); a breathable backsheet (50, 52) located on said garment facing surface of said absorbent surface of said core said backsheet comprising at least a first backsheet layer (50) and a second backsheet layer (52), said first backsheet layer being positioned between said garment facing surface of said absorbent core and said wearer facing surface of said second backsheet layer, said first and said November 20, 2005– י"ח בחשון התשס"ו 137399 פריט סופג בעל שיכבה אחורית כפולה ונושמת והמכיל שיכבה אחת בעלת פתחים קפילרים משופעים ]33[ EP ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם second backsheet layers being water vapor permeable, said first backsheet layer comprising a resilient, three dimensional web, said web consists of a liquid impervious polymeric film having apertures, said apertures forming capillaries, said capillaries having walls which extend away from said wearer facing surface of said film, said capillaries having a first opening in said garment facing surface of said film and a second opening at the end of said capillaries spaced apart from said wearer facing surface of said film said article being characterized in that said capillaries extend away from said wearer facing surface of said film at an angle of less than 90o measured from the plane of said film. 1968 __________ ]11[]21[ ]54[ TARGET DETECTION ARRANGEMENT ]22[ ]31[ ]51[ ]71[ 02.02.1999 1008276 ]32[ 11.02.1998 Int. Cl.7 G01S 017/02 THALES NEDERLAND B.V., THE NETHERLANDS WO/1999/041622 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST. P.O.BOX 4060, TEL AVIV 61040 ]87[ ]74[ [57] Detection arrangement for the remote detection of targets, comprising: a radar signal generator, provided with a COHO signal and STALO signal, for generating coded RF radars signals; a transmitter unit controlled by the coded RF signals; a radar receiver unit; and a video processor connected to the radar receiver unit; and a video processor connected to the radar receiver unit; the transmitter unit being designed to transmit optical signals modulated by the coded RF radar signals 1969 137408 מערך של גילוי מטרה ]33[ NL ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם and an optical detector being positioned in front of the radar receiver unit for converting echo signals from the transmitted optical signals into coded RF radar signals, possibly containing target information, characterized in that the RF signals are, using the STALO signal, mixed down to an intermediate frequency, subsequently filtered and, along with the COHO signal serving as reference signal, applied to a quadrature detector to produce quadrature video. November 20, 2005– י"ח בחשון התשס"ו __________ ]11[]21[ 137422 -1-הידרוקסי-3-(ציס-) תהליך להכנת פיפרידין- )טרימתוקסיפניל-2,4,6)-4-מתיל ]54[ METHOD FOR PRODUCING ()CIS-3-HYDROXY-1-METHYL-4(2,4,6-TRIMETHOXYPHENYL)PIPERIDINE ]22[ ]31[ ]51[ ]71[ 18.12.1998 19802449.5 ]32[ 23.01.1998 ]33[ Int. Cl.7 C07D 211/02, 211/42, 211/72, 211/74 AVENTIS PHARMA DEUTSCHLAND GMBH, GERMANY WO/1999/037615 EITAN, PEARL, LATZER AND COHEN ZEDEK, P.O.B. 12688 HERZLIYA 46733 ]87[ ]74[ DE , לצר וכהן צדק, פרל,איתן הרצליה,12688 .ד. ת, 7 רחוב שנקר [57] A process for the preparation of (-) cis-3-hydroxy-1-methyl-4-(2, 4, 6trimethoxyphenyl) piperidine November 20, 2005– י"ח בחשון התשס"ו 1970 Which comprises (a1) converting 1-methylpiperidin-4-one into the hydrobromide according to known processes, or (a2) converting 1-methylpiperidin-4-one (III) directly into the hydrobromide, prior to the subequent bromination, by introduction of 1-methylpiperidin-4-one into an HBr glacial acetic acid solution, and (b) reacting 1-methylpiperidin-4-one hydrobromide in a suitable solvent in the temperature range from 0oC-30oC with bromine to give 3(R, S)-bromo-1-methyl4-oxopiperidine hydrobromide (c) reacting this intermediate directly by addition of 0.8-1 equivalent of 1, 3,5trimethoxybenzene to the reaction solution at 0o-30oC to give 3(R, S)-bromo-1-methyl-4- (2, 4, 6- 1971 trimethoxyphenyl)-1,2,3,6tetrahydropyridine hydrobromide November 20, 2005– י"ח בחשון התשס"ו and, if appropriate, additionally adding acetic anhydride to remove any water of reaction formed (d1) first isolating the compound (VI) as a solid by stirring the reaction solution into a suitable organic solvent, and subsequently reacting the resulting product with water and by stirring at 50o-100oC to give 3(R,S)-hydroxy-1-methyl-4-(2,4,6)trimethoxyphenyl)-1,2,3,6tetrahydropyridine or (d2) treating the reaction mixture containing the compound (VI) directly with water and reacting by stirring at 50o100oC to give 3(R, S)- hydroxy-1-methyl4-(2, 4,6-trimethoxyphenyl)-1,2,3,6tetrahydropyridine (VII), and (d3) cooling the reaction mixtures obtained according to (d1) or (d2), if appropriate diluting further with water and adjusting to pH>12 at 0o-30oC by addition of aqueous alkali, 3(R, S)-hydroxy-1-methyl-4- (2, 4, 6-trimethoxyphenyl)-1,2,3,6tetrahydropyridine (VII) precipitating, filtering off the resulting crude product with suction and if appropriate, for purification, taking it up again in aqueous hydrochloric acid, filtering and optionally extracting with a water-immiscible solvent, and then adjusting the aqueous phase to pH>12 by addition of aqueous alkali, 3(R,S)-hydroxy-1-methyl-4-(2, 4,6trimethoxyphenyl)-1,2,3,6tetrahydropyridine (VII) precipitating, extracting the precipitated product, if appropriate for further purification, by stirring with one or more suitable organic solvents or alternatively mixtures of these solvents, and (e1) catalytically hydrogenating the resulting product (VII) in a suitable solvent or mixtures of these solvents using a suitable catalyst to give the racemic 3,4-cis alcohol November 20, 2005– י"ח בחשון התשס"ו 1972 where the 3,4-trans alcohol, which possibly results in srnall amounts during the reduction, can be removed by crystalliation from suitable solvents, or (e2) for the hydrogenation, employing easily accessible esters (IXa) or carbonates (IXb) of the compound (VII) in which R is (C1-C16) – alkyl, (C6-C14)aryl-(C1-C16)-alkyl or (C6-C14)-aryl and in the formula (IXa) is further carboxy-(C2C6)- alkyl, compounds (Xa) and (Xb) being obtained, from which the compound (VII) can be liberated by known procedures, (f1) obtaining the enantiomerically pure cis alcohol (II) from the compound (VIII) by a known process by resolution using suitable chiral auxiliary reagents; or (f2) carrying out the resolution using the compounds 1973 November 20, 2005– י"ח בחשון התשס"ו where R is (C1-C16)-alkyl, (C6-C14)-aryl(C1-C16)-alkyl or (C6-C14)-aryl and in the formula (Xa) is further carboxy-(C2-C6)alkyl, and then converting these into the compound (II) by known processes, it also being possible to exchange the sequence of the reaction steps e) and f), i.e. also to carry out the resolution as early as at the stage of the allyl alcohol (VII) or of the compounds (IXa) and (IXb) obtained therefrom. Claimed as novel are the compounds 3(R,S)-bromo-1-methyl-4-(2, 4, 6trimethoxyphenyl)-1,2,3,6tetrahydropyridine hydrobromide (VI) and 3(R,S)-hydroxy-1-methyl-4-(2, 4, 6trimethoxyphenyl)-1,2,3,6tetrahydropyridine (VII). __________ ]11[]21[ 137453 השימוש בתכשירים אבקתיים המכילים הידרוקסיפירידונים להכנת תרופה לטפול בכיבי רגליים ופצעי לחץ ]54[ UTILIZATION OF POWDER PREPARATIONS CONTAINING HYDROXYPYRIDONES FOR THE PRODUCTION OF A MEDICAMENT FOR THE TREATMENT OF LEG ULCERS AND DECUBITUS ULCERS ]22[ ]31[ ]51[ ]71[ 11.01.1999 19802708.7 ]32[ 24.01.1998 ]33[ DE Int. Cl.7 A61K 009/18, 031/44, A61P 031/00, C07D 213/00, 213/89 AVENTIS PHARMA DEUTSCHLAND GMBH, GERMANY WO/1999/037300 EITAN, PEARL, LATZER AND , לצר וכהן צדק, פרל,איתן COHEN ZEDEK, הרצליה,12688 .ד. ת, 7 רחוב שנקר P.O.B. 12688 HERZLIYA 46733 ]87[ ]74[ [57] The use of powder and at least one 1-hydroxy-2-pyridone of the formula or a salt thereof, where R1, R2 and R3, which are identical or different, are a November 20, 2005– י"ח בחשון התשס"ו hydrogen atom or alkyl with 1-4 carbon atoms, and 1974 R4 is a saturated hydrocarbon radical with 6 to 9 carbon atoms or a radical of the formula where X is S or O, Y is a hydrogen atom or up to 2 halogen atoms, Z is a single bond or the divalent radical being O,S,-CR2-, in which R is hydrogen or (C1-C4)-alkyl, or other divalent radical with 2-10 C and, optionally, O and/or S atoms linked in the form of a chain, wherein – if the radicals contain 2 or more O and/or S atoms – the latter are separated from one another by at least 2 C atoms, and it also being possible for 2 adjacent C atoms to be linked together by a double bond, and the free valencies of the C atoms being saturated by a hydrogen atom and/or (C1-C4)- alkyl groups, Ar is an aromatic ring system which has up to two rings and which may be substituted by up to three radicals from the group of fluorine, chlorine, bromine, methoxy, (C1C4)-alkyl, trifluoromethyl and trifluoromethoxy, for the production of a medicament for the treatment of leg ulcers and/or decubitus ulcers, wherein the ulcer is not infected. __________ ]11[]21[ ]54[ METHOD AND APPARATUS FOR INTEGRATING MANUAL INPUT ]22[ ]31[ 25.01.1999 60/072509 ]32[ 26.01.1998 236513 25.01.1999 Int. Cl.7 G09G 005/00 WAYNE WESTERMAN, U.S.A. JOHN G. ELIAS, U.S.A. ]51[ ]71[ ]87[ ]74[ WO/1999/038149 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST. P.O.BOX 4060, TEL AVIV 61040 [57] A sensing device that is sensitive to changes in self-capacitance brought about by changes in proximity of a touch device to the sensing device, the sensing device comprising: two electrical switching means (30, 31) connected together in series 1975 137478 שיטה והתקן לשילוב קלט ידני ]33[ US US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם having a common node (48), an input node (46), and an output node (45); a dielectriccovered sensing electrode (33) connected to the common node between the two switching means; a power supply (34) providing an approximately constant November 20, 2005– י"ח בחשון התשס"ו voltage connected to the input node of the series-connected switching means; an integrating capacitor (37) to accumulate charge transferred during multiple consecutive switching of the series connected switching means; another switching means (36) connected in parallel across the integrating capacitor to deplete its residual charge; and a voltage-tovoltage translation device (35) connected to the output node of the series-connected switching means which produces a voltage representative of the proximity of the touch device (38) to the sensing device. __________ ]11[]21[ ]54[ READOUT SYSTEM FOR SOLID STATE DETECTOR ARRAYS ]22[ ]51[ ]71[ 30.07.2000 Int. Cl.7 G01T 001/00 INTEGRATED DETECTOR & ELECTRONICS (IDE) S.A., NORWAY ORBOTECH MEDICAL SOLUTIONS LTD. SANFORD T.COLB & CO.,, P.O.B. 2273, REHOVOT 76122 ]74[ [57] A signal readout system for a solid state detector array, comprising: a plurality of detection channels (50); and a switching network comprising an arbitrator (54) and a plurality of multiplexer units (56), wherein said arbitrator directs the November 20, 2005– י"ח בחשון התשס"ו 137580 מערכת קריאה למערך גלאי מצב מוצק אורבוטק מדיקל סלושנס בע"מ ,' קולב ושות.סנפורד ט רחובות,2273 .ד. ת, מרמורק,4 שער הגיא outputs of at least two of said plurality of detection channels into at least two of said plurality of multiplexer units according to the content of said at least two detection channels, such that data are output simultaneously from at least two of said plurality of detection channels. 1976 __________ ]11[]21[ ]54[ INTEGRAL CONTAINER FOR TOILET RIM BLOCK ]22[ ]51[ ]71[ 14.08.2000 Int. Cl.7 E03D 009/03 SANO BRUNO'S ENTERPRISES LTD. REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST. P.O.BOX 4060, TEL AVIV 61040 ]74[ [57] An integral mold cast container (10) for a block of chemical adapted for gradual washing out of said chemical by flushing a liquid through the container, said container comprising a first (12) and a second (14) cup-shaped section, each section having a 1977 137841 מיכל חומר חיטוי אינטגרלי לאסלה תל אביב,סנו מפעלי ברונוס בע"מ ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם bottom part (18), side walls (20, 22) with rims (24, 26), and an open part, wherein said sections are connected by a hinge (40) that connects the bottom of the first section to a rim of the second section. November 20, 2005– י"ח בחשון התשס"ו __________ ]11[]21[ ]54[ PROCESS FOR PREPARING 4, 6 DICHLORO- 5 FLUOROPYRIMIDINE ]22[ ]31[ 15.08.2000 19939190.4 ]32[ 18.08.1999 19948933.5 11.10.1999 Int. Cl.7 C07D 239/30 BAYER AKTIENGESELLSCHAFT, GERMANY REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST. P.O.BOX 4060, TEL AVIV 61040 ]51[ ]71[ ]74[ November 20, 2005– י"ח בחשון התשס"ו 137866 - 5 - דיכלורו- 4 ,6 - תהליך להכנת פלואורופירמידין ]33[ DE DE ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם 1978 [57] Process for preparing 4,6-dichloro5-fluoro-pyrimidine of the formula characterized in that (a) compounds of the formula in which R represents methyl or ethyl are reacted with formamide in the presence of alkali metal alkoxides in a diluent at elevated temperature, if appropriate under pressure, and the reaction mixture is acidified with an acid after the reaction, where from 2.5 to 8 mol of formamide are employed per mole of the compound of the formula (II) and the compound of the formula (II) is added by metered addition over a period of from 2 to 4 hours, and (b) the resulting 4,6-dihydroxy-5fluoropyrimidine is reacted with phosphorus oxychloride, and the resulting reaction mixture is subsequently reacted with chlorine in the presence of phosphorus trichloride such that in each case at most 99.9% by weight of the chlorophosphonic acid which is present in the reaction mixture are converted, and the resulting reaction mixture is worked up distillatively, whereby the 4,6-dichloro-5fluoropyrimidine formed is separated off and the phosphorus oxychloride is recovered. __________ 1979 November 20, 2005– י"ח בחשון התשס"ו ]11[]21[ ]54[ DIGITAL ELECTRONIC CONTROL UNIT ]22[ 05.07.1999 ]51[ Int. Cl.7 F24F 011/02, G05D 029/00 ]71[ VASU TECH LIMITED, INDIA ]87[ WO/2001/002924 ]74[ WOLFF, BREGMAN AND GOLLER, KEREN HAYESOD ST 19B, P.O.B. 1352 JERUSALEM 91013 [57] A digital electronic control unit for an appliance, comprising: a plurality of sensor drive circuits (2a-2d) each driving one of a plurality of sensing elements (1a1d) external to said digital electronic control unit, each sensing element converting a sensed parameter to an electrical signal; an analog multiplexer (3) that receives the electrical signal from each external sensing element and selectively routes a selected electrical signal to a multiplexer output; an analog-to-digital converter (4) connected to the output of said analog multiplexer and converting the selected electrical signal to digital values; a linearity, sensitivity and offset correction circuit (5) connected to the output of said analog-to-digital converter for correcting the digital values received from it, using sensor calibration data stored in a nonvolatile memory (17); a central-control unit (6) that receives corrected output from November 20, 2005– י"ח בחשון התשס"ו 137899 יחידת בקרה אלקטרונית ספרתית , ברגמן וגולר,וולף ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד said linearity, sensitivity and offset correction circuit, and generates control signals for operating the appliance, as well as selection signals for controlling said analog multiplexer, using control data supplied by the non-volatile memory; a digital de-multiplexer (8) connected to an output of said central control unit for selecting one of a plurality of demultiplexer outputs to which a demultiplexer input coupled to said central control unit is to be connected; a plurality of control latches (9a-9f) each connected at one of said de-multiplexer outputs, for storing the digital data received from it and actuating a part of the appliance to adjust the sensed parameter; a non-volatile memory (17) that stores data and control parameters for the operation of said central control unit, linearity, sensitivity and offset correction circuit. 1980 __________ ]11[]21[ ]54[ SYSTEM AND METHOD FOR HEAT CONTROL OF A LIVING BODY ]22[ ]31[ 29.01.1999 123573 ]32[ 05.03.1998 126783 27.10.1998 Int. Cl.7 A61F 007/00 M.T.R.E. ADVANCED TECHNOLOGIES LTD. ]51[ ]71[ ]87[ ]74[ WO/1999/044552 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST. P.O.BOX 4060, TEL AVIV 61040 [57] A system for controlling an individual's body core temperature (BCT) comprising: a heat exchanger (20) for transferring heat to or removing heat from portions of the individual's body surface; at least one BCT-sensing device for measuring the individual's actual BCT (aBCT) and emitting an aBCT data signal; at least one sensing device for measuring a parameter indicative of the heat transfer 1981 137948 מערכת ושיטה לבקרת חום של גוף חי ]33[ IL IL , טכנוגלוגיות מתקדמות בע"מ.אי.אר.טי.אמ קיסריה ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם dynamics (HTD) between the body surface and the body's core, and emitting an HTD data signal; and a control module (48) for receiving data signal from measuring devices, comprising the aBCT data signal and the HTD data signal, and for emitting a control signal for controlling heat exchange properties of said heat exchanger as a function of the data signals and a desired body core temperature (dBCT). November 20, 2005– י"ח בחשון התשס"ו __________ ]11[]21[ ]54[ METHOD FOR PRODUCING SPHERICAL PELLETS WITH A POLYMERIC COATING ]22[ ]31[ ]51[ ]71[ 24.02.1999 19808634.2 ]32[ 24.02.1998 Int. Cl.7 A61K 009/00 SCHERING AKTIENGESELLSCHAFT, GERMANY WO/1999/043303 WOLFF, BREGMAN AND GOLLER, KEREN HAYESOD ST 19B, P.O.B. 1352 JERUSALEM 91013 ]87[ ]74[ [57] A process for the production of encased, spherical granular grains comprising: (a) spraying crude grains, which consist of at least one prostane derivative as pharmaceutical active ingredient and cyclodextrin as a vehicle, which form together a prostane-cyclodextrin-clathrate, and optionally pharmaceutically compatible additives and/or vehicles, with an aqueous polymer dispersion and additives which comprise an ethyl cellulose and/or a poly(meth) acrylic acid 137965 תהליך להכנת גלולות עגולות עם צפוי פולומרי ]33[ DE , ברגמן וגולר,וולף ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד ester as a polymer, in a fluidized bed or boiling bed, (b) applying said polymer dispersion to obtain a polymer thickness in the range of 1 to 5% (w/w) of the total mass and wherein the total mass corresponds to the composition of the encased grains, and (c) curing the grains that are encased with said polymer dispersion at a temperature of 45 to 65˚C for at least 24 hours and wherein said grains have a pharmaceutical active ingredient release profile which remains unchanged over the storage time. __________ November 20, 2005– י"ח בחשון התשס"ו 1982 ]11[]21[ 137988 פוליאוריתנים הקשורים בקשר קוולנטי לחומצה היאלורונית המכילה סולפט או תהליך,לנגזרות שלה המכילות סולפט להכנתם וחומרים המוקומפטיביליים המכילים אותם ]54[ POLYURETHANES BOUND COVALENTLY TO SULPHATED HYALURONIC ACID OR SULPHATED HYALURONIC ACID DERIVATIVES, PROCESS FOR THEIR PREPARATION AND HAEMOCOMPATIBLE MATERIALS COMPRISING THE SAME ]22[ ]31[ ]51[ ]71[ 24.02.1999 PD98A000037 ]32[ 25.02.1998 ]33[ IT Int. Cl.7 A61L 027/00, 033/00, 033/06, C08G 002/30, 018/28, 018/83 FIDIA ADVANCED BIOPOLYMERS S.R.L., ITALY WO/1999/043728 LUZZATTO & LUZZATTO, ,לוצאטו את לוצאטו P.O.B. 5352 BEER-SHEVA 84965 באר שבע,5352 .ד. ת, עומר,גן תעשיה ]87[ ]74[ [57] A polyurethane bound covalently to sulphated hyaluronic acid or to a sulphated hyaluronic acid derivative. __________ ]11[]21[ ]54[ ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ [57] METHOD AND APPARATUS FOR DOWNCONVERTING SIGNALS TRANSMITTED USING A PLURALITY OF MODULATION FORMATS TO A COMMON INTERMEDIATE FREQUENCY RANGE 02.03.1999 60/076520 ]32[ 02.03.1998 259242 26.02.1999 Int. Cl.7 H04B 001/40, H04L 027/00 QUALCOMM INCORPORATED, U.S.A. WO/1999/045654 SANFORD T.COLB & CO.,, P.O.B. 2273, REHOVOT 76122 A receiver that downconverts signals 1983 138019 שיטה והתקן להמרת אותות המשודרים באמצעות מגוון תצורות אפנון לטווח תדר תווך משותף ]33[ US US ,' קולב ושות.סנפורד ט רחובות,2273 .ד. ת, מרמורק,4 שער הגיא modulated using a plurality of modulation November 20, 2005– י"ח בחשון התשס"ו formats to a common intermediate frequency range, comprising: a first band selection filter that selects a first frequency range; a second band selection filter that selects a second frequency range; a third band selection filter that selects a third frequency range; a first downconverter, coupled to an output of the first band selection filter, that downconverts signals from the first frequency range to the common intermediate frequency range; a second downconverter, selectively coupled to a switch to either an output of the second band selection filter or an output of the third band selection filter, that downconverts signals from either the second frequency range or the third frequency range to the common intermediate frequency range,wherein the second downconverter has an input coupled to a frequency doubling circuit; switching circuitry that selectively couples one of either a first oscillating signal from a voltage controller oscillator (VCO) having VCO frequency range or a second oscillating signal at a second frequency that is outside the VCO frequency range to an input of the first downconverter and an input of the frequency doubling circuit. __________ ]11[]21[ 138068 תרכובות אמינו ציקליות ותכשריי רוקחות המכילים אותן ]54[ CYCLIC AMINO COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME ]22[ ]31[ ]51[ 26.02.1999 10-46921 ]32[ 27.02.1998 ]33[ JP Int. Cl.7 A61K 031/395, A61P 009/10, 043/00, C07D 205/04, 207/12 , 211/54, 211/72, 471/08 UBE INDUSTRIES LTD., JAPAN SANKYO COMPANY LIMITED, JAPAN WO/1999/043648 WOLFF, BREGMAN AND GOLLER, , ברגמן וגולר,וולף KEREN HAYESOD ST 19B, ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד P.O.B. 1352 JERUSALEM 91013 ]71[ ]87[ ]74[ November 20, 2005– י"ח בחשון התשס"ו 1984 [57] Platelet aggregation inhibiting cyclic amino compounds of the formula wherein: R1 represents a phenyl group which may optionally be substituted by at least one substituent selected from the group consisting of halogen atoms, C1-C4 alkyl groups, fluoro-substituted –( C1-C4 alkoxy) groups, cyano groups and nitro groups; R2 represents a C1-C8 aliphatic acyl group which may optionally be substituted by at least one substituent selected from the group consisting of halogen atoms, C1-C4 alkoxy groups and cyano groups, a benzoyl group which may optionally be substituted by at least one substituent selected from the group consisting of halogen atoms, C1C4 alkyl groups and C1-C4 alkoxy groups, or a (C1-C4 alkoxy) carbonyl group; and R3 represents a saturated cyclic amino group having in total from 2 to 8 carbon atoms in one or more rings, the largest nitrogen-containing ring having from 3 to 7 ring atoms, said saturated cyclic amino group being substituted by a group having the formula –S-X-R4 wherein R4 and X are as defined below, said saturated cyclic amino group being attached via a ring nitrogen atom thereof to the adjacent carbon atom to which substituents R1 and R2 are attached, and said saturated cyclic amino group optionally containing a further ring heteroatom selected from the group consisting of oxygen, nitrogen and sulfur atoms, R4 represents a phenyl group which may optionally be substituted by at least one substituent selected from the group consisting of halogen atoms, C1-C4 alkyl groups, C1-C4 alkoxy groups, nitro groups and cyano groups, a C1-C6 alkyl group which may optionally be substituted by at least one substituent selected from the group consisting of amino groups, hydroxyl groups, carboxyl groups, (C1-C4 alkoxy) carbonyl groups, substituents having the formula –NH-A1 (wherein, A1 represents an α-amino acid residue), or a C3-C8 cycloalkyl group, and X represents a sulfur atom, a sulfinyl group or a sulfonyl group, and said cyclic amino group may optionally be further substituted by a group having the formula =CR5R6, wherein R5 and R6 are the same or different and each independently represents a hydrogen atom, a C1-C4 alkyl group, a carboxyl group, a (C1-C4 alkoxy) carbonyl group, a carbamoyl group, a (C1C4 alkyl) carbamoyl group or a di-( C1-C4 alkyl)carbamoyl group; or a pharmacologically acceptable salt thereof. __________ 1985 November 20, 2005– י"ח בחשון התשס"ו ]11[]21[ ]54[ APPARATUS AND METHOD FOR IMPROVED CONNECTIVITY IN WIRELESS OPTICAL COMMUNICATION SYSTEMS ]22[ ]31[ ]51[ ]71[ 21.04.1999 99100423.5 ]32[ 11.01.1999 Int. Cl.7 H04B 010/10 INTERNATIONAL BUSINESS MACHINES CORPORATION, U.S.A. WO/2000/042719 SANFORD T.COLB & CO.,, P.O.B. 2273, REHOVOT 76122 ]87[ ]74[ [57] Apparatus for receiving an infrared signal (S1, S2, S3) comprising at least two receiving units (1,2,3), each comprising a converter (12, 22, 32)-which converts the received infrared signal (S1, S2, S3) to a digital signal (RxS_1, RxS_2, RxS_3), whereby the digital signals represent data carried in frames comprising at least a data field and a heater field which contains a November 20, 2005– י"ח בחשון התשס"ו 138080 התקן ושיטה לחיבור משופר במערכת תקשורת אופטיות אלחוטיות ]33[ EP ,' קולב ושות.סנפורד ט רחובות,2273 .ד. ת, מרמורק,4 שער הגיא preamble being identical for each of said digital signals, and a selector (Fig 2) for determining for at least part of each of the preambles a measure (A, B, C) related to its signal-to-noise ratio and comparing the measures (A, B, C) in order to select for further processing the one digital signal (RxS_1) with the highest signal-to-noise ratio. 1986 __________ ]11[]21[ 138137 אמידים של חומצה כולנית ותכשיר רוקחות שלהם ]54[ CHOLENIC ACID AMIDES AND PHARMACEUTICAL COMPOSITIONS THEREOF ]22[ ]31[ ]51[ ]71[ 08.03.1999 9804861.4 ]32[ 06.03.1998 ]33[ GB Int. Cl.7 A61K 031/57, 031/58, C07J 041/00, 043/00 RESEARCH INSTITUTE FOR MEDICINE AND CHEMISTRY INC., U.S.A. WO/1999/045024 EITAN, PEARL, LATZER AND , לצר וכהן צדק, פרל,איתן COHEN ZEDEK, הרצליה,12688 .ד. ת, 7 רחוב שנקר P.O.B. 12688 HERZLIYA 46733 ]87[ ]74[ [57] Compounds of the formula 1987 November 20, 2005– י"ח בחשון התשס"ו in which: R1 represents a hydroxyl group or protected hydroxyl group, R2 represents a hydrogen atom and a double bond is present at c, or R1 and R2 together represent an oxo group and a double bond is present at b or double bonds are present at a and b; R3 represents a methyl group having α- or β-configuration; R4 and R5, which may be the same or different, are selected from hydrogen atoms and aliphatic, cycloaliphatic, araliphatic and aryl groups, or together with the nitrogen atom to which they are attached form a heterocyclic group; and X represents a polymethylene group containing 2-5 carbon atoms, an oxa group-containing analogue thereof in which a methylene group other than that attached to the –CO.NR4R5 moiety is replaced by an oxygen atom, or an unsaturated analogue thereof containing up to two double bonds, with the provisos that: (i) when R3 is α-CH3 and X is (CH2)2 then R4R5N- does not represent an amino, dimethylamino, diethylamino, imidazolyl or triazolyl group; (ii) when R3 is α-CH3 and X is (CH2)3 then R4R5N- is not morpholino; and (iii) when R3 is α-CH3 and X is O (CH2)2 then R4R5N is not dimethylamino. __________ ]11[]21[ ]54[ STAPLES FOR BONE FIXATION ]22[ ]51[ ]71[ 07.09.2000 Int. Cl.7 A61B 017/15, 017/84 NITI ALLOYS TECHNOLOGIES LTD. LEONID MONASSEVITCH, ZVI LASTER, MICHAEL ARAD JEREMY M. BEN-DAVID & CO. LTD., HAR HOTZVIM HI-TECH PARK, P.O. B0X 45087 JERUSALEM ]72[ ]74[ [57] Apparatus for increasing a length span of a staple (10), which includes: proximal and distal ends with respect to a user, which define a z-axis of an x; y; z coordinate system between them; and first and second prongs (14, 16), joined by a system which provides a mechanical advantage to selectably bringing said first and second prongs together and pushing them apart, wherein said first prong further includes, at said distal end, a staple receptor, with a channel, for mounting November 20, 2005– י"ח בחשון התשס"ו 138320 מהדקים לחיבור עצם נתניה,טכנולוגיות סגסוגות ניטי בע"מ מיכאל ערד, צבי לסטר,לאוניד מונסביץ ,דוד ושות' בע"מ- בן.ירמיהו מ ירושלים,45087 .ד. ת, הר חוצבים said staple thereon, said channel defining an x-axis of the x; y; z coordinate system, parallel to said staple length span, and perpendicular to the direction of bringing first and second prongs together and pushing them apart, wherein said second prong further includes, at said distal end, a thin, cam-like head, having a width span that increases in the direction of increasing y, operable to increase said staple length span, and wherein, as said first and second prongs are brought together, said thin, 1988 cam-like head is arranged to slide between said staple receptor and said staple, mounted thereon, so as to wedge between said staple receptor and said staple and increase the length span of said staple. __________ ]11[]21[ ]54[ SOFTWARE DRIVEN PROTOCOL FOR MANAGING A VIRTUAL CLINICAL NEUROPSYCHOLOGICAL TESTING PROGRAM AND APPURTENANCES FOR USE THEREWITH ]22[ ]51[ ]71[ 07.09.2000 Int. Cl.7 A61B 005/00 NEUROTRAX CORPORATION, U.S.A. ELY SIMON JEREMY M. BEN-DAVID & CO. LTD., HAR HOTZVIM HI-TECH PARK, P.O. B0X 45087 JERUSALEM ]72[ ]74[ [57] A software driven protocol for managing a virtual clinical neuropsychological testing program, the protocol including for each client of a plurality of clients the steps: (a) evaluating of a prior history of the client; (b) according to the evaluated prior 1989 138322 פרוטוקול תוכנה וירטואלית לניהול תכנית מבחן קלינית בנוירו פסיכולוגי וכלים לשימוש בה ,דוד ושות' בע"מ- בן.ירמיהו מ ירושלים,45087 .ד. ת, הר חוצבים history, forming an appropriate battery of tests for testing the client wherein said battery incorporates pseudo-randomization of at least one representational or organizational parameter; (c) via a data-communications medium, interactively (i) delivering, to the client, the formed November 20, 2005– י"ח בחשון התשס"ו battery of tests, and (ii) accepting, from the client, a substantially completed response to the delivered formed battery of tests; (d) analyzing the accepted response; and (e) into the prior history of the client, integrating (i) the accepted substantially completed response or (ii) at least one analytical metric thereof. __________ ]11[]21[ 138411 מערכת ושיטת מוליך ראשי בעלות מהירות לשימוש במתח ויחסי עיתוי מתנודדים עבור גילוי אותות ]54[ HIGH SPEED BUS SYSTEM AND METHOD FOR USING VOLTAGE AND TIMING OSCILLATING REFERENCES FOR SIGNAL DETECTION ]22[ ]31[ 08.03.1999 057158 ]32[ 07.04.1998 ]33[ US 60/078213 16.03.1998 US 165705 02.10.1998 US Int. Cl.7 H03M 009/00, H04L 025/02, 025/06 JAZIO, INC., U.S.A. WO/1999/048260 REINHOLD COHN AND PARTNERS, ,ריינהולד כהן ושותפיו 21 AHAD HA'AM ST. תל אביב,4060 .ד. ת, 21 רחוב אחד העם P.O.BOX 4060, TEL AVIV 61040 ]51[ ]71[ ]87[ ]74[ [57] A method, comprising: using a master device to transmit a control signal via a control bus to a first slave device; transmitting a first oscillating reference for detecting transitions in the control signal via a first reference bus to the first slave device; using the master device to transmit a first data signal associated with the control signal via a first data bus to the first slave device; and transmitting a second oscillating reference for detecting transitions in the first data signal via a second reference bus to the first slave device. _________ November 20, 2005– י"ח בחשון התשס"ו 1990 ]11[]21[ תווית מרובדת אלסטית ]54[ ELASTIC TAB LAMINATE ]22[ ]31[ ]51[ ]71[ 01.09.1998 09/049727 ]32[ 27.03.1998 Int. Cl.7 A61F 002/00, 013/56, 013/66 MINNESOTA MINING AND MANUFACTURING COMPANY, U.S.A. WO/1999/048455 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST. P.O.BOX 4060, TEL AVIV 61040 ]87[ ]74[ 138450 [57] An extensible elastic tab (10) comprising a coextruded extensible elastic film comprising at least one elastic layer (11) and at least one second layer (15) on at least a first face of the elastic layer, the coextruded elastic film is attached to at least a partially extensible nonwoven layer on at least one face the partially extensible nonwoven layer (7) having a first direction and a second direction the partially extensible nonwoven layer having at least one first portion being extensible in the first direction to an extension limit and at least one second inextensible portion (18) in the first direction, wherein the coextruded elastic and the nonwoven layer when stretched to the extension limit of the ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם nonwoven layer first portion(s) in the first direction will elastically recover at least 1.0 cm, providing an elastic table having a Useful Stretch Ratio (USR) of at least 30 percent, wherein the USR is defined as the ratio of the useful range of elasticity to the initial extension length of the first portion at the upper extension limit, wherein the useful range of elasticity includes the portion of the elastic recovery length having an elastic recovery force of greater than 20 grams/cm force up to the upper extension limit where the upper extension limit is where the extensible elastic tab has an incremental extension force of about 300 grams/cm to 350 grams/cm. __________ 1991 November 20, 2005– י"ח בחשון התשס"ו ]11[]21[ ]54[ SUSTAINED RELEASE FORMULATIONS CONTAINING MACROLIDE COMPOUNDS ]22[ ]31[ 25.03.1999 10-79039 ]32[ 26.03.1998 10-182963 29.06.1998 Int. Cl.7 A61K 031/40 FUJISAWA PHARMACEUTICAL CO., LTD., JAPAN WO/1999/049863 WOLFF, BREGMAN AND GOLLER, KEREN HAYESOD ST 19B, P.O.B. 1352 JERUSALEM 91013 ]51[ ]71[ ]87[ ]74[ 138466 תכשירים לשחרור ממושך המכילים תרכובות מקרולידיות ]33[ JP JP , ברגמן וגולר,וולף ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד [57] A sustained-release formulation of a macrolide compound, wherein the time (T63.2%) required for 63.2% of the maximum amount of macrolide compound to be dissolved is 0.7 to 15 hours, as measured according to the Japanese Pharmacopoeia, the 13-th edition, Dissolution Test, No. 2 (Paddle method 50 rpm) using a test solution which is an aqueous 0.005% hydroxypropyl cellulose solution adjusted to pH 4.5, in which the macrolide compound is a tricyclic compound of the general formula or a pharmaceutically acceptable salt thereof, wherein each of adjacent pairs of R1 and R2, R3 and R4, and R5 and R6 independently (a) is two adjacent hydrogen atoms, but R2 may also be an alkyl group or (b) may form another bond formed between the carbon atoms to which they are attached; R7 is a hydrogen atom, a hydroxyl group, a protected hydroxyl group, or an alkoxy group, or an oxo group together with R1; R8 and R9 are independently a hydrogen atom or a hydroxyl group; R10 is a hydrogen atom, an alkyl group, an alkyl group substituted by one or more hydroxyl groups, an alkenyl group, an alkenyl group substituted by one or more November 20, 2005– י"ח בחשון התשס"ו 1992 hydroxyl groups, or an alkyl group substituted by an oxo group; X is an oxo group, (a hydrogen atom and a hydroxyl group), (a hydrogen atom and a hydrogen atom), or a group represented by the formula –CH2-O-; Y is an oxo group (a hydrogen atom and a hydroxyl group), (a hydrogen atom and a hydrogen atom), or a group represented by the formula N-NR11R12 or N-OR13; R11 and R12 are independently a hydrogen atom, an alkyl group, an aryl group or a tosyl group; R13, R14, R15, R16, R17, R18, R19, R22 and R23 are independently a hydrogen atom or an alkyl group; R24 is an optionally substituted ring system which may contain one or more heteroatoms; n is an integer of 1 or 2; and in addition to the above definitions, Y, R10 and R23, together with the carbon atom to which they are attached, may represent a saturated or unsaturated 5- or 6-membered nitrogen, sulfur- and/or oxygen-containing heterocyclic ring optionally substituted by one or more groups selected from the group consisting of an alkyl, a hydroxyl, an alkoxy, a benzyl, a group of the formula –CH2Se (C6H5), and an alkyl substituted by one or more hydroxyl groups, which comprises a solid dispersion composition, wherein the macrolide compound (I) is present as an amorphous state in a waterinsoluble base, in which the waterinsoluble base comprised in the solid dispersion composition is selected from water-insoluble polymer or wax. __________ ]11[]21[ תכשירים תוססים ]54[ FIZZY FORMULATIONS ]22[ ]31[ ]51[ ]71[ 20.03.1999 19814257.9 ]32[ 31.03.1998 Int. Cl.7 A61K 009/00 VIATRIS GMBH & CO. KG, GERMANY WO/1999/049842 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST. P.O.BOX 4060, TEL AVIV 61040 ]87[ ]74[ 138605 [57] Solid, rapidly disintegrating administration forms for oral administration in the form of effervescent formulations which comprise selegiline or its pharmaceutically acceptable salts as active ingredient and an effervescent base ]33[ DE ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם consisting of one or more alkaline earth metal carbonates, an organic edible acid and/or an alkali metal salt of citric acid and, if appropriate, pharmaceutically acceptable auxiliaries. __________ 1993 November 20, 2005– י"ח בחשון התשס"ו ]11[]21[ ]54[ TRANSDERMAL THERAPEUTIC SYSTEM WHICH CONTAINS A D2 AGONIST AND WHICH IS PROVIDED FOR TREATING PARKINSONISM AND A METHOD FOR THE PRODUCTION THEREOF ]22[ ]31[ ]51[ ]71[ 18.03.1999 19814084.3 ]32[ 30.03.1998 Int. Cl.7 A61K 009/00, 009/70 LTS LOHMANN THERAPIESYSTEME AG, GERMANY ADERIS PHARMACEUTICALS, INC., U.S.A. WO/1999/049852 DR. YITZHAK HESS & PARTNERS, 279 HAYARKON STREET P.O.B. 6451 TEL AVIV 61063 ]87[ ]74[ [57] Transdermal therapeutical system comprising a backing layer which is inert to the ingredients of the matrix, a selfadhering matrix layer containing (-)5,6,7,8-tetrahydro-6-[propyl [2-(2-thienyl) ethyl]amino]-1-naphthol, and a protective layer which is to be removed before application, characterized in that the matrix layer 138722 מערכת רפואית טרנסדרמלית המכילה ואשר מסופקת עבור טיפולD2 אגוניסט במחלת הפרקינסון ושיטה עבור הייצור של הנ"ל ]33[ DE , עו"פ,ד"ר יצחק הס ושותפיו תל אביב,6451 .ד. ת, 279 רחוב הירקון (a) contains as a basis a non-aqueous polymer adhesive based on acrylate or silicone, (b) has a solubility of ≥ 5% (per weight) for the free base (-)-5,6,7,8-tetrahydro-6[propyl [2-(2-thienyl) ethyl]-amino]-1naphthol, and (c) contains the free base (-)-5,6,7,8tetrahydro-6-[propyl [2-(2-thienyl) ethyl]amino]-1-naphthol in an effective amount. __________ ]11[]21[ November 20, 2005– י"ח בחשון התשס"ו 138723 1994 ]54[ COMPOSITION CONTAINING CISPLATIN AND STILBENE FOR TREATMENT OF TUMORS ]22[ ]31[ 29.03.1999 10-108708 ]32[ 03.04.1998 19-229843 14.08.1998 Int. Cl.7 A61K 033/24 AJINOMOTO CO., INC., JAPAN WO/1999/051246 DR. YITZHAK HESS & PARTNERS, 279 HAYARKON STREET P.O.B. 6451 TEL AVIV 61063 ]51[ ]71[ ]87[ ]74[ תכשיר המכיל ציספלטין וסטילבן לטיפול בגידולים ממאירים ]33[ JP JP , עו"פ,ד"ר יצחק הס ושותפיו תל אביב,6451 .ד. ת, 279 רחוב הירקון [57] An antitumor agent comprising a stilbene derivative and a platinum coordination compound, said agent optionally containing one or more of pharmaceutically acceptable carriers or diluents, wherein said stilbene derivative is at least one of compounds represented by the following general formulae (1) and (2) and pharmaceutically acceptable salts thereof; in which the compound may be in the form of salt, hydrate, solvate or ester; in which R1, R2 and R3 are independent from each other and each denotes a lower alkoxy group, R4, R5 and R6 are independent from each other and each denotes any substituent group of a hydrogen atom, a halogen atom, a nitro group, a lower alkoxy group, a phosphoric acid ester, a phosphoric acid amide, an amino lower alkoxy group, a lower alkyl amino lower alkoxy group, a di-lower alkyl amino lower alkoxy group, a mercapto group, a lower alkyl thio group, an amino group, a lower alkyl amino group, a di-lower alkyl amino group, a lower alkyl group, an amino lower alkyl group, a trifluoromethyl group, a lower alkanoyl group, a lower alkanoyl amino group and an amino acid acylamino group, X denotes a hydrogen atom or a nitrile group, and Het denotes a heterocyclic ring. __________ ]11[]21[ 1995 138761 November 20, 2005– י"ח בחשון התשס"ו ]54[ METHOD AND SYSTEM FOR EFFECTIVELY UTILIZING THE SWITCHING CAPACITY OF LOCAL EXCHANGES ]22[ ]51[ ]71[ ]74[ 28.09.2000 Int. Cl.7 H04L 012/56, H04Q 003/60 ECI TELECOM LTD. ECI TELECOM LTD, 30 HASIVIM ST. PETACH TIKVA 49517 [57] A method for supporting a changing volume of a voice-grade traffic in an access network having a local exchange with a limited capacity, the method comprising steps of: providing two or more access networks, each having its subscribers and its associated local exchange with a limited capacity; each of the access networks being capable of dividing traffic, outgoing from its subscribers, into the voice-grade traffic portion and data traffic portion, and capable of directing the data traffic portion to a packet network while directing the voice-grade traffic portion to a PSTN network via said associated local exchange; wherein the PSTN network and the packet network are respectively common for said two or more access networks, defining an overload condition November 20, 2005– י"ח בחשון התשס"ו שיטה ומערכת לניצול אפקטיבי של יכולת המיתוג של מרכזיית טלפון פתח תקוה, טלקום בע"מ.איי.סי.אי , טלקום בע"מ. איי. סי.אי פתח תקוה,30רחוב הסיבים of a local exchange as a condition when traffic there-through equals to a predetermined threshold forming at least a portion of the local exchange capacity; defining a normal load condition of the local exchange as a condition when traffic there-through is below said predetermined threshold, detecting the overload condition on one of said local exchanges, the overload local exchange being indicated LE1; finding a remaining one of said local exchanges being in the normal load condition, the non-overload local exchange being called LE2; partially diverting the voice-grade traffic intended for the local exchange LE1 and passing the diverted voice-grade traffic to its destination via said packet network and the local exchange LE2, thereby reducing volume of the voice-grade traffic via the LE1. 1996 __________ ]11[]21[ ]54[ TARGETED ADVERTISEMENT USING TELEVISON DELIVERY SYSTEMS ]22[ ]31[ ]51[ ]71[ 01.04.1999 054419 ]32[ 03.04.1998 Int. Cl.7 H04N 007/173 SEDNA PATENT SERVICES, LLC., U.S.A. WO/1999/052285 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST. P.O.BOX 4060, TEL AVIV 61040 ]87[ ]74[ [57] A method for targeting advertisements to a plurality of television terminals, comprising: assigning at least one primary advertisement to each of a program channel; assigning at least one alternate advertisement to at least one 1997 138805 פרסומות ממוקדות באמצעות מערכות טלויויזיה ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם feeder channel; and generating a switching plan, wherein the switching plan instructs each of the television terminals to select one of the program channel and the at least one feeder channel during a program break occurring in a broadcast of a program on November 20, 2005– י"ח בחשון התשס"ו the program channel, wherein generating the switching plan comprises: assigning each of the television terminals to at least one group, designating a unique group mask for each of the groups, and assigning each of the groups to one of the program channel and the at least one feeder channel, wherein the group mask indicates which of the television terminals tune to the program channel and the at least one feeder channel during the program break. __________ ]11[]21[ ]54[ PROCESSING OF TEXTUAL INFORMATION AND AUTOMATED APPREHENSION OF INFORMATION ]22[ ]31[ ]51[ ]71[ 11.02.1999 98109952.6 ]32[ 02.06.1998 Int. Cl.7 G06F 017/28 INTERNATIONAL BUSINESS MACHINES CORPORATION, U.S.A. WO/1999/063455 SANFORD T.COLB & CO.,, P.O.B. 2273, REHOVOT 76122 ]87[ ]74[ 138861 עיבוד מידע טקסטואלי מידע אוטומטית ]33[ EP ,' קולב ושות.סנפורד ט רחובות,2273 .ד. ת, מרמורק,4 שער הגיא [57] A method of processing textual November 20, 2005– י"ח בחשון התשס"ו 1998 information, comprising the steps of: segmenting an input string which includes textual information into segments; and combining the segments with semantical units from a knowledge database representing a network of hierarchically arranged semantical units which are similar across hierarchies, the combining step generating a resulting semantic network of hierarchically arranged semantical units which are similar across hierarchies. __________ ]11[]21[ ]54[ MULTIPLE WAVEFORM SOFTWARE RADIO ]22[ ]31[ ]51[ ]71[ ]87[ ]74[ 27.05.1999 086804 ]32[ 29.05.1998 Int. Cl.7 H04B 001/38 MOTOROLA, INC., U.S.A. WO/1999/062194 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST. P.O.BOX 4060, TEL AVIV 61040 [57] A transceiver comprising: a transmitter comprising: an information receiving input receiving input digital information; an rf up-converter operatable over a plurality of waveforms; and one or more processor means disposed between said input and said rf up-converter for operating in accordance with a plurality of 1999 138931 תוכנת רדיו בעלת צורת גלים רבות ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם predetermined first waveform software each first waveform software being associated with a corresponding one of a plurality of first waveforms such that said digital information is processed in accordance with selected ones of said plurality of predetermined first waveform software to produce digital output November 20, 2005– י"ח בחשון התשס"ו information representative of said input digital information for said rf up converter whereby one or more first waveforms of said plurality of first waveforms is produced; a receiver comprising: a second waveform receiving input receiving one or more of a plurality of second waveforms; an rf down-converter coupled to said second waveform receiving input and operable over a plurality of second waveforms to produce received digital output information; an output; and said one or more second processor means being operable in accordance with a plurality of predetermined second waveform software; each said second waveform software being associated with a corresponding one second waveform of a plurality of second waveforms such that said received digital information is processed in accordance with selected ones of said plurality of predetermined second waveform software to produce received digital output information at said output; a first memory having stored therein said plurality of predetermined first waveform software; a second memory for receiving one or more first waveform software of said plurality of first waveform software for a corresponding number of selected ones of said plurality of first waveforms; said second memory receiving said one or more first waveform software from said first memory; and said second memory being coupled to said one or more processor means to provide said selected ones of said predetermined first waveform software to said one or more processor means; a third memory having stored therein said plurality of predetermined second waveform software; a fourth memory for receiving one or more second waveform software of said plurality of second waveform software for a corresponding number of selected ones of said plurality of second waveforms, said second memory receiving said one or more second waveform software from said third memory; and said fourth memory being coupled to said one or more processor means to provide said selected ones of said predetermined second waveform software to said one or more processor means. __________ ]11[]21[ November 20, 2005– י"ח בחשון התשס"ו 139003 2000 ]54[ POSITIVE LOCK COUPLING ]22[ ]31[ ]51[ ]71[ 14.04.1999 09/070230 ]32[ 30.04.1998 Int. Cl.7 F16L 019/00 STANLEY AVIATION CORPORATION, U.S.A. WO/1999/057476 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST. P.O.BOX 4060, TEL AVIV 61040 ]87[ ]74[ [57] A threaded coupling apparatus (10) for interconnecting ends of first and second fluid-carrying conduit members (11, 12) in a fixed releasable locking relationship which includes first and second coupling members (34, 25) circumferentially engageable with the ends of the conduit members to hold them in fluid communication, said coupling members each having annular outer surfaces and being rotatable with respect to each other in a locking direction to a locked position and rotatable in an opposite unlocking direction to an unlocked position, said second coupling member having a peripheral groove (46) in said annular outer surface thereof and a first peripheral facing surface (75) located on said first coupling member, the improvement comprising: a lock ring (40) located on said second coupling member , said lock ring having an annular wall forming a second peripheral facing surface (56) which faces said first peripheral facing surface and an internal peripheral retaining groove (54); a complementary locking tab (76) located on said first peripheral facing surface; a complementary locking slot (64) located on said second peripheral facing surface configured for locking engagement with said complementary locking tab; first and second cooperating elements (32, 38) on said first and second coupling members, 2001 מחבר נעילה ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם respectively, for moving said first and second peripheral facing surfaces toward each other when said coupling members are rotated in the locking direction; an annular spring (42) mounted within said internal peripheral retaining groove of said lock ring, said annular spring having an inner peripheral edge with a plurality of peripherally spaced spring tabs extending therefrom and received in said peripheral retaining groove of said second coupling member, said annular spring urging said second peripheral facing surface of said lock ring toward said first peripheral facing surface of said first coupling member so that said complementary locking tab and complementary locking slot become aligned and subsequently engage with each other in a fixed and locked position; a longitudinally extending first keyway, having a first width, formed in said annular outer surface of said second coupling member which intersects said peripheral retaining groove; a spring key (50) of substantially said first width located on said inner peripheral edge of said annular spring which is placed in said first keyway to angularly orient said annular spring with said second coupling member; a first lock ring key (68) of substantially said first width extending from said inner peripheral edge of said annular wall of said lock ring positioned in said first keyway to angularly orient said lock ring with said second coupling November 20, 2005– י"ח בחשון התשס"ו member and said annular spring, a longitudinally extending second keyway (71), having a second width, formed in said annular outer surface of said second coupling member, angularly spaced from said first keyway, and intersecting said peripheral retaining groove; and a second lock ring key (70) of substantially said second width extending from said inner peripheral edge of said annular wall of said lock ring, angularly spaced from said first lock ring key a distance equal to the angular spacing of said first and second keyways and positioned in said second keyway. __________ November 20, 2005– י"ח בחשון התשס"ו 2002 ]11[]21[ ]54[ LIGHTWEIGHT POSITIVE LOCK COUPLING ]22[ ]31[ ]51[ ]71[ 14.04.1999 070229 ]32[ 30.04.1998 Int. Cl.7 F16L 019/00 STANLEY AVIATION CORPORATION, U.S.A. WO/1999/057477 REINHOLD COHN AND PARTNERS, 21 AHAD HA'AM ST. P.O.BOX 4060, TEL AVIV 61040 ]87[ ]74[ [57] A threaded coupling apparatus (10) for interconnected ends of first and second fluid-carrying conduit members (11, 12) in a fixed releasable locking relationship which includes first and second coupling members (25, 36), each having a peripheral surface, circumferentially engageable with the ends of the conduit members to hold them in fluid communication, said coupling members being rotatable with respect to each other in a locking direction to a locked position and in an opposite unlocking direction to an unlocked position to unfasten said coupling apparatus, the improvement comprising: a lock ring (43) mounted about said peripheral surface of said first coupling member; at least one complementary locking recess (58) located on said lock ring; at least one complementary locking tab (68) located on said second coupling member; external threads (34) on said first coupling member, said external threads forming alternating ridges and valleys, said ridges having a 2003 139004 מחבר נעילה ]33[ US ,ריינהולד כהן ושותפיו תל אביב,4060 .ד. ת, 21 רחוב אחד העם first larger diameter and said valleys having a second smaller diameter; internal threads (42) on said second coupling member for cooperative engagement with said external threads, said threads being angularly oriented with said at least one locking recess and said at least one locking tab so that they become aligned only when said coupling members are rotated with respect to each other to said locked position; and an annular resilient member (44) having an internal peripheral edge having a diameter which is lesser than said first larger diameter mounted within and supporting said lock ring and positioned on said first coupling member for urging said at least one locking recess toward said at least one locking tab so that they make contact with each other and subsequently interlock during rotation in the locking direction when said at least one locking recess and said at least one locking tab become aligned to hold said first and second coupling members in a fixed rotational and locked position. November 20, 2005– י"ח בחשון התשס"ו __________ ]11[]21[ 139130 )בנזיל-(אמינואתוקסי-2)-4} -1-פניל-2 אינדול בתערובת עם אסטרוגנים ]54[ 2-PHENYL-1 {4-(2AMINOETHOXY)- BENZYL} INDOLE IN COMBINATION WITH ESTROGENS ]22[ ]31[ ]51[ 11.05.1999 079561 ]32[ 15.05.1998 ]33[ US Int. Cl.7 A61K 031/40, 031/565, A61P 005/00, 009/00, C07D 209/08, 209/10, 401/12, 403/12, 405/12 WYETH, U.S.A. WO/1999/059581 REINHOLD COHN AND ,ריינהולד כהן ושותפיו PARTNERS, תל אביב,4060 .ד. ת, 21 רחוב אחד העם 21 AHAD HA'AM ST. P.O.BOX 4060, TEL AVIV 61040 ]71[ ]87[ ]74[ November 20, 2005– י"ח בחשון התשס"ו 2004 [57] A pharmaceutical composition comprising one or more estrogens and a compound having the structure: wherein: R1 is selected from H, OH or the C1-C12 esters (straight chain or branched) or C1-C12 (straight chain or branched or cyclic) alkyl ethers thereof, or halogens; or C1-C4 halogenated ethers including trifluoromethyl ether and trichloromethyl ether, R2, R3, R4, R5, and R6 are independently selected from H, OH or the C1-C12 esters (straight chain or branched) or C1-C12 alkyl ethers (straight chain or branched or cyclic) thereof, halogens, or C1-C4 halogenated ethers including trifluoromethyl ether and trichloromethyl ether, cyano, C1-C6 alkyl (straight chain or branched), or trifluoromethyl, with the proviso that, when R1 is H, R2 is not OH, X is selected from H, C1-C6 alkyl, cyano, nitro, trifluoromethyl, halogen; n is 2 or 3; Y is selected from: (a) the moiety; wherein R7 and R8 are independently selected from H, C1-C6 alkyl, or phenyl optionally substituted by CN, C1-C6 alkyl (straight chain or branched), C1-C6 alkoxy (straight chain or branched), halogen, -OH, -CF3 or –OCF3; or R7 and R8 are concatenated together as –(CH2)p-, wherein p is an integer of from 2 to 6, preferably 4 to 6, the ring so formed is optionally substituted with 1-3 substituents selected from C1-C3 alkyl, trifluoromethyl, halogen, hydrogen, phenyl, nitro and –CN (b) a five-, six- or seven- membered saturated, unsaturated or partially unsaturated heterocycle containing up to two heteroatoms selected from –O-, -NH-, N(C1-C4 alkyl)-, N= and –S(O)m-, wherein m is an integer of from 0-2 optionally substituted with 1-3 substituents independently selected from hydroxyl, halo, C1-C4 alkyl, trihalomethyl, C1-C4 alkoxy, trihalomethoxy, C1-C4 acyloxy, C1C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, hydroxyl (C1-C4) alkyl, CO2H, -CN, -CONHR1-, -NH2 C1-C4 alkylamino, di-( C1-C4) alkylamino, NHSO2R1, -NHCOR1-, -NO2, and phenyl optionally substituted with 1-3 (C1-C4) 2005 November 20, 2005– י"ח בחשון התשס"ו alkyl, wherein R1 is as defined above or C1-C6 alkyl; (c) a bicyclic heterocycle containing from 6-12 carbon atoms either bridged or fused and containing up to two heteroatoms selected from –O-, -NH-, -N(C1-C4 alkyl)-, and –S(O)m-, wherein m is an integer of from 0-2, optionally substituted with 1-3 substituents independently selected hydroxyl, halo, C1-C4 alkyl, trihalomethyl, C1-C4 alkoxy, trihalomethoxy, C1-C4 acyloxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, hydroxyl (C1-C4) alkyl, -CO2H, -CN-, CONHR1-, -NH2 C1-C4 alkylamino, di(C1C4) alkylamino, -NHSO2R1, -NHCOR1, NO2-, and phenyl optionally substituted with 1-3 (C1-C4) alkyl; or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient. __________ ]11[]21[ 139141 B12 1,2,6,7,8 -פתלאימידו--7 ביניים-חומרי -] בנזאזפיןA - 1,2[ ]2[ פיריד-הקסאהידרואון ואנאלוגים שלהם להכנת מעכבים-6 וטטראציקליים לאנקפאלינז ולאנזים-טרי הממיר אנגיוטנזין ]54[ 7-PHTHALIMIDO-1,2,6,7,8,12B HEXAHYDRO-PYRIDO [2,1A]BENZAZEPIN-6- ONE AND ANALOGS THEREOF INTERMEDIATES FOR PREPARING TRI-AND TETRACYCLIC INHIBITORS OF ENKEPHALINASE AND ANGIOTENSIN CONVERTING ENZYME ]22[ ]31[ 18.12.1995 360915 ]32[ 21.12.1994 ]33[ US 535403 24.10.1995 US Int. Cl.7 C07D 401/10, 401/14, 405/14, 409/14, 471/04, 471/14, 491/147, 495/14 DIVISION FROM 116428 AVENTIS PHARMACEUTICALS INC., U.S.A. EITAN, PEARL, LATZER AND , לצר וכהן צדק, פרל,איתן COHEN ZEDEK, הרצליה,12688 .ד. ת, 7 רחוב שנקר P.O.B. 12688 HERZLIYA 46733 ]51[ ]62[ ]71[ ]74[ [57] A compound of the formula November 20, 2005– י"ח בחשון התשס"ו 2006 wherein G completes an aromatic ring selected from the group consisting of wherein X1 is selected from the group consisting of S and NH; X2 is selected from the group consisting of S, O, and NH; and R is selected from the group consisting of hydrogen, hydroxyl, phenyl , and C1-C4 alkoxy. __________ ]11[]21[ ]54[ PHARMACEUTICAL COMPOSITION CONTAINING A MACROLIDE COMPOUND ]22[ ]31[ ]51[ ]71[ 26.04.1999 10-117271 ]32[ 27.04.1998 Int. Cl.7 A61K 031/40, A61P 017/00 FUJISAWA PHARMACEUTICAL CO., LTD., JAPAN WO/1999/055332 WOLFF, BREGMAN AND GOLLER, KEREN HAYESOD ST 19B, P.O.B. 1352 JERUSALEM 91013 ]87[ ]74[ [57] A pharmaceutical composition in a gel form, which consists essentially of a tricyclic compound, a dissolution/absorption promoter, a 2007 139210 תכשיר רוקחות המכיל תרכובות מקרולידית ]33[ JP , ברגמן וגולר,וולף ירושלים,1352 .ד. ת, 'ב19 רחוב קרן היסוד pharmaceutical base, a compatibilizing agent and a thickener, wherein said tricyclic compound is the compound of the formula November 20, 2005– י"ח בחשון התשס"ו (wherein each of adjacent pairs of R1 and R2, R3 and R4, R5 and R6 independently (a) is two adjacent hydrogen atoms, but R2 may also be an alkyl group or, (b) may form another bond formed between the carbon atoms to which they are attached; R7 is a hydrogen atom, a hydroxyl group, a protected hydroxyl group, or an alkoxy group, or an oxo group together with R1; R8 and R9 are independently a hydrogen atom or a hydroxyl group; R10 is a hydrogen atom, an alkyl group, an alkyl group substituted by one or more hydroxyl groups, an alkenyl group, an alkenyl group substituted by one or more hydroxyl groups, or an alkyl group substituted by an oxo group; X is an oxo group, (a hydrogen atom) or a group represented by the formula -CH2O-; Y is an oxo group, (a hydrogen atom, and a hydroxyl group), (a hydrogen atom and a hydrogen atom), or a group represented by the formula -N-NR11R12 or N-OR13; R11 and R12 are independently a hydrogen atom, an alkyl group, an aryl group or a tosyl group; R13, R14, R15, R16, R17, R18, R19, R22 and R23 are independently a hydrogen atom or an alkyl group; R24 is an optionally substituted ring system which may contain one or more heteroatoms; n is an integer of 1 or 2; and in addition to the above definitions, Y, R10 and R23, together with the carbon atoms to which they are attached, may represent a saturated or unsaturated 5- or 6-membered nitrogen, sulfur and/or oxygen containing heterocyclic ring optionally substituted by one or more groups selected from the group consisting of an alkyl, a hydroxyl, an alkoxy, a benzyl, a group of the formula –CH2Se(C6H5), and an alkyl substituted by one or more hydroxyl groups; the dissolution/absorption promoter is diethyl sebacate; the pharmaceutical base is a hydrophilic glycol, the compatibilizing agent is diethylene glycol monoethyl ether; and the thickener is cellulose polymer or carboxyvinyl polymer, in which the amount of the dissolution/absorption promoter and the compatibilizing agent in the total composition is about 1-20% (w/w) and about 5-15% (w/w), respectively. __________ November 20, 2005– י"ח בחשון התשס"ו 2008