AAAAAA

   
Results: 1-25 | 26-50 | 51-75
Results: 26-50/75
INHERITED THROMBOPHILIA .2. (VOL 76, PG 824, 1996)
Authors: LANE DA MANNUCCI PM BAUER KA BERTINA RM BOCHKOV NP BOULYJENKOV V CHANDY M DAHLBACK B GINTER EK MILETICH JP ROSENDAAL FR SELIGSOHN U
Citation: Da. Lane et al., INHERITED THROMBOPHILIA .2. (VOL 76, PG 824, 1996), Thrombosis and haemostasis, 77(5), 1997, pp. 1047-1047
LINKAGE OF COMBINED FACTOR-V AND FACTOR-VII DEFICIENCY TO CHROMOSOME 18Q BY HOMOZYGOSITY MAPPING
Authors: NICHOLS WC SELIGSOHN U ZIVELIN A TERRY VH ARNOLD ND SIEMIENIAK DR KAUFMAN RJ GINSBURG D
Citation: Wc. Nichols et al., LINKAGE OF COMBINED FACTOR-V AND FACTOR-VII DEFICIENCY TO CHROMOSOME 18Q BY HOMOZYGOSITY MAPPING, The Journal of clinical investigation, 99(4), 1997, pp. 596-601
IMPROVED METHOD FOR GENOTYPING APOLIPOPROTEIN-E POLYMORPHISMS BY A PCR-BASED ASSAY SIMULTANEOUSLY UTILIZING 2 DISTINCT RESTRICTION ENZYMES
Authors: ZIVELIN A ROSENBERG N PERETZ H AMIT Y KORNBROT N SELIGSOHN U
Citation: A. Zivelin et al., IMPROVED METHOD FOR GENOTYPING APOLIPOPROTEIN-E POLYMORPHISMS BY A PCR-BASED ASSAY SIMULTANEOUSLY UTILIZING 2 DISTINCT RESTRICTION ENZYMES, Clinical chemistry, 43(9), 1997, pp. 1657-1659
ACQUIRED VON-WILLEBRAND DISEASE IN A PATIENT WITH ANGIODYSPLASIA RESULTING FROM IMMUNE-MEDIATED CLEARANCE OF VON-WILLEBRAND-FACTOR
Authors: INBAL A BANK I ZIVELIN A VARON D DARDIK R SHAPIRO R ROSENTHAL E SHENKMAN B GITEL S SELIGSOHN U
Citation: A. Inbal et al., ACQUIRED VON-WILLEBRAND DISEASE IN A PATIENT WITH ANGIODYSPLASIA RESULTING FROM IMMUNE-MEDIATED CLEARANCE OF VON-WILLEBRAND-FACTOR, British Journal of Haematology, 96(1), 1997, pp. 179-182
THE 2 COMMON MUTATIONS CAUSING FACTOR-XI DEFICIENCY IN JEWS STEM FROMDISTINCT FOUNDERS - ONE OF ANCIENT MIDDLE-EASTERN ORIGIN AND ANOTHER OF MORE RECENT EUROPEAN ORIGIN
Authors: PERETZ H MULAI A USHER S ZIVELIN A SEGAL A WEISMAN Z MITTELMAN M LUPO H LANIR N BRENNER B SHPILBERG O SELIGSOHN U
Citation: H. Peretz et al., THE 2 COMMON MUTATIONS CAUSING FACTOR-XI DEFICIENCY IN JEWS STEM FROMDISTINCT FOUNDERS - ONE OF ANCIENT MIDDLE-EASTERN ORIGIN AND ANOTHER OF MORE RECENT EUROPEAN ORIGIN, Blood, 90(7), 1997, pp. 2654-2659
COMBINED FACTOR-V AND FACTOR-VII DEFICIENCY IS CAUSED BY MUTATIONS INA RESIDENT PROTEIN OF THE ENDOPLASMIC-RETICULUM GOLGI INTERMEDIATE COMPARTMENT
Authors: NICHOLS WC SELIGSOHN U ZIVELIN A TERRY VH HERTEL CH WHEATLEY MA YANG A SIEMIENIAK DR HAURI HP KAUFMAN RJ GINSBURG D
Citation: Wc. Nichols et al., COMBINED FACTOR-V AND FACTOR-VII DEFICIENCY IS CAUSED BY MUTATIONS INA RESIDENT PROTEIN OF THE ENDOPLASMIC-RETICULUM GOLGI INTERMEDIATE COMPARTMENT, Blood, 90(10), 1997, pp. 537-537
EXTENSIVE VENOUS AND ARTERIAL THROMBOSIS IN A PATIENT WITH FAMILIAL APC RESISTANCE WITHOUT R506Q FACTOR-V MUTATION
Authors: INBAL A GRIFFIN JH XU X FERNANDEZ JA ZIVELIN A GITEL S MARTINOWITZ U HALKIN H SELIGSOHN U
Citation: A. Inbal et al., EXTENSIVE VENOUS AND ARTERIAL THROMBOSIS IN A PATIENT WITH FAMILIAL APC RESISTANCE WITHOUT R506Q FACTOR-V MUTATION, Blood, 90(10), 1997, pp. 660-660
PROTHROMBOTIC POLYMORPHIC MARKERS IN YOUNG-PATIENTS WITH MYOCARDIAL-INFARCTION
Authors: INBAL A FRAIMARK D MODAN B CHETRIT A HOD H ROSENBERQ N DARDIK R SELIGSOHN U
Citation: A. Inbal et al., PROTHROMBOTIC POLYMORPHIC MARKERS IN YOUNG-PATIENTS WITH MYOCARDIAL-INFARCTION, Blood, 90(10), 1997, pp. 661-661
RISK ASSESSMENT OF SINGLE, DOUBLE AND TRIPLE PROTHROMBOTIC POLYMORPHISMS IN PATIENTS WITH IDIOPATHIC VENOUS THROMBOEMBOLISM
Authors: SALOMON O ZIVELIN A DARDIK R INBAL A VARON D MARTINOWITZ U MANI A LUBETSKY A STEINBERG DM SELIGSOHN U
Citation: O. Salomon et al., RISK ASSESSMENT OF SINGLE, DOUBLE AND TRIPLE PROTHROMBOTIC POLYMORPHISMS IN PATIENTS WITH IDIOPATHIC VENOUS THROMBOEMBOLISM, Blood, 90(10), 1997, pp. 1125-1125
FACTOR-II GENE G20210A POLYMORPHISM ASSOCIATED WITH VENOUS THROMBOSISPROBABLY HAS A COMMON ANCESTRY
Authors: ZIVELIN A ROSENBERG N FAIER S SELIGSOHN U
Citation: A. Zivelin et al., FACTOR-II GENE G20210A POLYMORPHISM ASSOCIATED WITH VENOUS THROMBOSISPROBABLY HAS A COMMON ANCESTRY, Blood, 90(10), 1997, pp. 1127-1127
A SINGLE GENETIC-ORIGIN FOR A COMMON CAUCASIAN RISK FACTOR FOR VENOUSTHROMBOSIS
Authors: ZIVELIN A GRIFFIN JH XU X PABINGER I SAMAMA M CONARD J BRENNER B ELDOR A SELIGSOHN U
Citation: A. Zivelin et al., A SINGLE GENETIC-ORIGIN FOR A COMMON CAUCASIAN RISK FACTOR FOR VENOUSTHROMBOSIS, Blood, 89(2), 1997, pp. 397-402
GLANZMANN THROMBASTHENIA CAUSED BY AN 11.2-KB DELETION IN THE GLYCOPROTEIN IIIA (BETA(3)) IS A 2ND MUTATION IN IRAQI JEWS THAT STEMMED FROMA DISTINCT FOUNDER
Authors: ROSENBERG N YATUV R ORION Y ZIVELIN A DARDIK R PERETZ H SELIGSOHN U
Citation: N. Rosenberg et al., GLANZMANN THROMBASTHENIA CAUSED BY AN 11.2-KB DELETION IN THE GLYCOPROTEIN IIIA (BETA(3)) IS A 2ND MUTATION IN IRAQI JEWS THAT STEMMED FROMA DISTINCT FOUNDER, Blood, 89(10), 1997, pp. 3654-3662
GENETIC-EVIDENCE FOR A COMMON ORIGIN AMONG ROMAN JEWS AND ASHKENAZI JEWS
Authors: ODDOUX C GUILLENNAVARRO E CLAYTON CM NELSON H PERETZ H SELIGSOHN U LUZZATTO L NARDI M KARPATKIN M DITIVOLI C DICAVE E AXELROD F OSTRER H
Citation: C. Oddoux et al., GENETIC-EVIDENCE FOR A COMMON ORIGIN AMONG ROMAN JEWS AND ASHKENAZI JEWS, American journal of human genetics, 61(4), 1997, pp. 1200-1200
CURRENT STRATEGY FOR GENETIC-ANALYSIS OF HEMOPHILIA-A FAMILIES
Authors: DARDIK R PERETZ H USHER S SELIGSOHN U MARTINOWITZ U
Citation: R. Dardik et al., CURRENT STRATEGY FOR GENETIC-ANALYSIS OF HEMOPHILIA-A FAMILIES, Haemophilia, 2(1), 1996, pp. 11-17
A 14-BP DELETION (CODON-554 DEL AAGGTAACAGAGTG) AT EXON-14 INTRON N JUNCTION OF THE COAGULATION-FACTOR-XI GENE DISRUPTS SPLICING AND CAUSESSEVERE FACTOR-XI DEFICIENCY
Authors: PERETZ H ZIVELIN A USHER S SELIGSOHN U
Citation: H. Peretz et al., A 14-BP DELETION (CODON-554 DEL AAGGTAACAGAGTG) AT EXON-14 INTRON N JUNCTION OF THE COAGULATION-FACTOR-XI GENE DISRUPTS SPLICING AND CAUSESSEVERE FACTOR-XI DEFICIENCY, Human mutation, 8(1), 1996, pp. 77-78
INHERITED THROMBOPHILIA .2.
Authors: LANE DA MANNUCCI PM BAUER KA BERTINA RM BOCHKOV NP BOULYJENKOV V CHANDY M DAHLBACK B GINTER EK MILETICH JP ROSENDAAL FR SELIGSOHN U
Citation: Da. Lane et al., INHERITED THROMBOPHILIA .2., Thrombosis and haemostasis, 76(6), 1996, pp. 824-834
INHERITED THROMBOPHILIA .1.
Authors: LANE DA MANNUCCI PM BAUER KA BERTINA RM BOCHKOV NP BOULYJENKOV V CHANDY M DAHLBACK B GINTER EK MILETICH JP ROSENDAAL FR SELIGSOHN U
Citation: Da. Lane et al., INHERITED THROMBOPHILIA .1., Thrombosis and haemostasis, 76(5), 1996, pp. 651-662
ALA244VAL IS A COMMON, PROBABLY ANCIENT MUTATION CAUSING FACTOR-VII DEFICIENCY IN MOROCCAN AND IRANIAN JEWS
Authors: TAMARY H FROMOVICH Y SHALMON L REICH Z DYM O LANIR N BRENNER B PAZ M LUDER AS BLAU O KOROSTISHEVSKY M ZAIZOV R SELIGSOHN U
Citation: H. Tamary et al., ALA244VAL IS A COMMON, PROBABLY ANCIENT MUTATION CAUSING FACTOR-VII DEFICIENCY IN MOROCCAN AND IRANIAN JEWS, Thrombosis and haemostasis, 76(3), 1996, pp. 283-291
CYCLOSPORINE THERAPY FOR ACQUIRED FACTOR-VIII INHIBITOR IN A PATIENT WITH SYSTEMIC LUPUS-ERYTHEMATOSUS
Authors: SCHULMAN S LANGEVITZ P LIVNEH A MARTINOWITZ U SELIGSOHN U VARON D
Citation: S. Schulman et al., CYCLOSPORINE THERAPY FOR ACQUIRED FACTOR-VIII INHIBITOR IN A PATIENT WITH SYSTEMIC LUPUS-ERYTHEMATOSUS, Thrombosis and haemostasis, 76(3), 1996, pp. 344-346
COEXISTENCE OF HEREDITARY HOMOCYSTINURIA AND FACTOR-V LEIDEN - EFFECTON THROMBOSIS
Authors: MANDEL H BRENNER B BERANT M ROSENBERG N LANIR N JAKOBS C FOWLER B SELIGSOHN U
Citation: H. Mandel et al., COEXISTENCE OF HEREDITARY HOMOCYSTINURIA AND FACTOR-V LEIDEN - EFFECTON THROMBOSIS, The New England journal of medicine, 334(12), 1996, pp. 763-768
VENOUS THROMBOEMBOLISM ASSOCIATED WITH DOUBLE HETEROZYGOSITY FOR R506Q MUTATION OF FACTOR-V AND FOR T298M MUTATION OF PROTEIN-C IN A LARGE FAMILY OF A PREVIOUSLY DESCRIBED HOMOZYGOUS PROTEIN C-DEFICIENT NEWBORN WITH MASSIVE THROMBOSIS
Authors: BRENNER B ZIVELIN A LANIR N GREENGARD JS GRIFFIN JH SELIGSOHN U
Citation: B. Brenner et al., VENOUS THROMBOEMBOLISM ASSOCIATED WITH DOUBLE HETEROZYGOSITY FOR R506Q MUTATION OF FACTOR-V AND FOR T298M MUTATION OF PROTEIN-C IN A LARGE FAMILY OF A PREVIOUSLY DESCRIBED HOMOZYGOUS PROTEIN C-DEFICIENT NEWBORN WITH MASSIVE THROMBOSIS, Blood, 88(3), 1996, pp. 877-880
PRENATAL-DIAGNOSIS OF GLANZMANN THROMBASTHENIA USING THE POLYMORPHIC MARKERS BRCA1 AND THRA1 ON CHROMOSOME-17
Authors: FRENCH DL COLLER BS SELIGSOHN U PERETZ H
Citation: Dl. French et al., PRENATAL-DIAGNOSIS OF GLANZMANN THROMBASTHENIA USING THE POLYMORPHIC MARKERS BRCA1 AND THRA1 ON CHROMOSOME-17, Blood, 88(10), 1996, pp. 110-110
A SINGLE GENETIC-ORIGIN FOR THE COMMON CAUCASIAN FACTOR-V MUTATION PREDISPOSING TO THROMBOSIS
Authors: ZIVELIN A GRIFFIN JH XU X PABINGER I SAMAMA M CONARD J BRENNER B ELDOR A SELIGSOHN U
Citation: A. Zivelin et al., A SINGLE GENETIC-ORIGIN FOR THE COMMON CAUCASIAN FACTOR-V MUTATION PREDISPOSING TO THROMBOSIS, Blood, 88(10), 1996, pp. 1123-1123
THE GENE FOR COMBINED FACTOR-V AND FACTOR-VIII DEFICIENCY MAPS TO A 2.4 CM REGION ON CHROMOSOME-18
Authors: NICHOLS WC SELIGSOHN U ZIVELIN A TERRY VH ARNOLD ND SIEMIENIAK DR GINSBURG D
Citation: Wc. Nichols et al., THE GENE FOR COMBINED FACTOR-V AND FACTOR-VIII DEFICIENCY MAPS TO A 2.4 CM REGION ON CHROMOSOME-18, Blood, 88(10), 1996, pp. 2612-2612
THE LABORATORY DIAGNOSIS OF HEMOPHILIA - RECOMMENDATIONS BY THE LABORATORY ACTIVITIES COMMITTEE OF THE WORLD FEDERATION OF HEMOPHILIA
Authors: PEAKE I SELIGSOHN U GITEL S KITCHEN S ZIVELIN A
Citation: I. Peake et al., THE LABORATORY DIAGNOSIS OF HEMOPHILIA - RECOMMENDATIONS BY THE LABORATORY ACTIVITIES COMMITTEE OF THE WORLD FEDERATION OF HEMOPHILIA, Haemophilia, 1(3), 1995, pp. 159-164
Risultati: 1-25 | 26-50 | 51-75