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Results: 1-25 | 26-50 | 51-75
Results: 1-25/75
COMBINED FACTOR-V AND FACTOR-VIII DEFICIENCY - THE SOLUTION
Authors: GINSBURG D NICHOLS WC ZIVELIN A KAUFMAN RJ SELIGSOHN U
Citation: D. Ginsburg et al., COMBINED FACTOR-V AND FACTOR-VIII DEFICIENCY - THE SOLUTION, Haemophilia, 4(4), 1998, pp. 677-682
ANALYSIS OF GENETIC POLYMORPHISMS RELATED TO THROMBOSIS AND OTHER RISK-FACTORS IN PATIENTS WITH RETINAL VEIN OCCLUSION
Authors: SALOMON O MOISSEIEV J ROSENBERG N VIDNE O YASSUR I ZIVELIN A TREISTER G STEINBERG DM SELIGSOHN U
Citation: O. Salomon et al., ANALYSIS OF GENETIC POLYMORPHISMS RELATED TO THROMBOSIS AND OTHER RISK-FACTORS IN PATIENTS WITH RETINAL VEIN OCCLUSION, Blood coagulation & fibrinolysis, 9(7), 1998, pp. 617-622
GLANZMANN THROMBASTHENIA IN 2 IRAQI-JEWISH SIBLINGS IS CAUSED BY A NOVEL SPLICE JUNCTION MUTATION IN THE GLYCOPROTEIN IIB
Authors: YATUV R ROSENBERG N DARDIK R BRENNER B SELIGSOHN U
Citation: R. Yatuv et al., GLANZMANN THROMBASTHENIA IN 2 IRAQI-JEWISH SIBLINGS IS CAUSED BY A NOVEL SPLICE JUNCTION MUTATION IN THE GLYCOPROTEIN IIB, Blood coagulation & fibrinolysis, 9(3), 1998, pp. 285-288
MUTATIONS IN THE ALPHA(IIB) AND BETA(3) GENES THAT CAUSE GLANZMANN THROMBASTHENIA CAN BE DISTINGUISHED BY A SIMPLE PROCEDURE USING TRANSFORMED B-LYMPHOCYTES
Authors: ROSENBERG N DARDIK R ROSENTHAL E ZIVELIN A SELIGSOHN U
Citation: N. Rosenberg et al., MUTATIONS IN THE ALPHA(IIB) AND BETA(3) GENES THAT CAUSE GLANZMANN THROMBASTHENIA CAN BE DISTINGUISHED BY A SIMPLE PROCEDURE USING TRANSFORMED B-LYMPHOCYTES, Thrombosis and haemostasis, 79(2), 1998, pp. 244-248
MUTATIONS IN THE ER-GOLGI INTERMEDIATE COMPARTMENT PROTEIN ERGIC-53 CAUSE COMBINED DEFICIENCY OF COAGULATION-FACTOR-V AND COAGULATION-FACTOR-VIII
Authors: NICHOLS WC SELIGSOHN U ZIVELIN A TERRY VH HERTEL CE WHEATLEY MA MOUSSALLI MJ HAURI HP CIAVARELLA N KAUFMAN RJ GINSBURG D
Citation: Wc. Nichols et al., MUTATIONS IN THE ER-GOLGI INTERMEDIATE COMPARTMENT PROTEIN ERGIC-53 CAUSE COMBINED DEFICIENCY OF COAGULATION-FACTOR-V AND COAGULATION-FACTOR-VIII, Cell, 93(1), 1998, pp. 61-70
PRENATAL-DIAGNOSIS OF GLANZMANN THROMBASTHENIA USING THE POLYMORPHIC MARKERS BRCA1 AND THRA1 ON CHROMOSOME-17
Authors: FRENCH DL COLLER BS USHER S BERKOWITZ R ENG C SELIGSOHN U PERETZ H
Citation: Dl. French et al., PRENATAL-DIAGNOSIS OF GLANZMANN THROMBASTHENIA USING THE POLYMORPHIC MARKERS BRCA1 AND THRA1 ON CHROMOSOME-17, British Journal of Haematology, 102(2), 1998, pp. 582-587
GLYCOPROTEIN IIIA TRUNCATION RATHER THAN ABSENCE OF CYSTEINE(406)-CYSTEINE(665) BOND CAUSES THROMBASTHENIA IN MOST IRAQI-JEWISH PATIENTS
Authors: YATUV R ROSENBERG N DARDIK R SELIGSOHN U
Citation: R. Yatuv et al., GLYCOPROTEIN IIIA TRUNCATION RATHER THAN ABSENCE OF CYSTEINE(406)-CYSTEINE(665) BOND CAUSES THROMBASTHENIA IN MOST IRAQI-JEWISH PATIENTS, British Journal of Haematology, 102(1), 1998, pp. 285-285
ASSOCIATION BETWEEN HYPERFLEXIBILITY OF THE THUMB AND AN UNEXPLAINED BLEEDING TENDENCY - IS IT A RULE OF THUMB
Authors: KAPLINSKY C KENET G SELIGSOHN U RECHAVI G
Citation: C. Kaplinsky et al., ASSOCIATION BETWEEN HYPERFLEXIBILITY OF THE THUMB AND AN UNEXPLAINED BLEEDING TENDENCY - IS IT A RULE OF THUMB, British Journal of Haematology, 101(2), 1998, pp. 260-263
A SINGLE GENETIC-ORIGIN FOR THE COMMON PROTHROMBOTIC G20210A POLYMORPHISM IN THE PROTHROMBIN GENE
Authors: ZIVELIN A ROSENBERG N FAIER S KORNBROT N PERETZ H MANNHALTER C HORELLOU MH SELIGSOHN U
Citation: A. Zivelin et al., A SINGLE GENETIC-ORIGIN FOR THE COMMON PROTHROMBOTIC G20210A POLYMORPHISM IN THE PROTHROMBIN GENE, Blood, 92(4), 1998, pp. 1119-1124
RECURRENT VASCULAR ACCESS THROMBOSIS (RVAT) IN HEMODIALYSIS-PATIENTS IS ASSOCIATED WITH HOMOZYGOSITY FOR THE 677C-]T MUTATION IN THE METHYLENE TETRAHYDROFOLATE REDUCTASE (MTHFR) GENE
Authors: DINOUR D ROSENBERG N SELIGSOHN U RAPOPORT J
Citation: D. Dinour et al., RECURRENT VASCULAR ACCESS THROMBOSIS (RVAT) IN HEMODIALYSIS-PATIENTS IS ASSOCIATED WITH HOMOZYGOSITY FOR THE 677C-]T MUTATION IN THE METHYLENE TETRAHYDROFOLATE REDUCTASE (MTHFR) GENE, Journal of the American Society of Nephrology, 8, 1997, pp. 740-740
COULD THE 185DELAG BRCA1 MUTATION BE AN ANCIENT JEWISH MUTATION
Authors: BARSADE RB THEODOR L GAK E KRUGLIKOVA A HIRSCHYECHEZKEL G MODAN B KUPERSTEIN G SELIGSOHN U RECHAVI G FRIEDMAN E
Citation: Rb. Barsade et al., COULD THE 185DELAG BRCA1 MUTATION BE AN ANCIENT JEWISH MUTATION, European journal of human genetics, 5(6), 1997, pp. 413-416
BLEEDING PREDICTORS IN FACTOR-XI-DEFICIENT PATIENTS
Authors: BRENNER B LAOR A LUPO H ZIVELIN A LANIR N SELIGSOHN U
Citation: B. Brenner et al., BLEEDING PREDICTORS IN FACTOR-XI-DEFICIENT PATIENTS, Blood coagulation & fibrinolysis, 8(8), 1997, pp. 511-515
VARIABLE POTENTIAL OF THE INTRINSIC COAGULATION PATHWAY FOR INHIBITION OF PLASMA CLOT LYSIS IN NORMAL AND FACTOR-XI DEFICIENT INDIVIDUALS
Authors: VONDEMBORNE PAK MEIJERS JCM SELIGSOHN U BOUMA BN
Citation: Pak. Vondemborne et al., VARIABLE POTENTIAL OF THE INTRINSIC COAGULATION PATHWAY FOR INHIBITION OF PLASMA CLOT LYSIS IN NORMAL AND FACTOR-XI DEFICIENT INDIVIDUALS, Thrombosis and haemostasis, 1997, pp. 858-858
A LOW-FREQUENCY OF 2 GENETIC RISK-FACTORS FOR THROMBOSIS IN YEMENITE-JEWS WHO MANIFEST A DECREASED INCIDENCE OF CORONARY-ARTERY DISEASE
Authors: ZIVELIN A ROSENBERG N DARDIK R AMIT Y KENET G KORNBROT N FRIDMAN A SELIGSOHN U
Citation: A. Zivelin et al., A LOW-FREQUENCY OF 2 GENETIC RISK-FACTORS FOR THROMBOSIS IN YEMENITE-JEWS WHO MANIFEST A DECREASED INCIDENCE OF CORONARY-ARTERY DISEASE, Thrombosis and haemostasis, 1997, pp. 904-904
RAPID DETECTION OF APOLIPOPROTEIN E2, E3 AND E4 POLYMORPHISMS BY A NEW PCR-BASED METHOD
Authors: ZIVELIN A ROSENBERG N PERETZ H AMIT Y KOMBROT N SELIGSOHN U
Citation: A. Zivelin et al., RAPID DETECTION OF APOLIPOPROTEIN E2, E3 AND E4 POLYMORPHISMS BY A NEW PCR-BASED METHOD, Thrombosis and haemostasis, 1997, pp. 1326-1326
A 3RD MUTATION CAUSING THROMBASTHENIA IN IRAQI-JEWS
Authors: YATUV R ROSENBERG N DARDIK R BRENNER B SELIGSOHN U
Citation: R. Yatuv et al., A 3RD MUTATION CAUSING THROMBASTHENIA IN IRAQI-JEWS, Thrombosis and haemostasis, 1997, pp. 1477-1477
A SIMPLE PROCEDURE FOR IDENTIFICATION OF THE MUTATED GENE CAUSING GLANZMANN THROMBASTHENIA USING B-LYMPHOCYTES
Authors: ROSENBERG N DARDIK R ZIVELIN A SELIGSOHN U
Citation: N. Rosenberg et al., A SIMPLE PROCEDURE FOR IDENTIFICATION OF THE MUTATED GENE CAUSING GLANZMANN THROMBASTHENIA USING B-LYMPHOCYTES, Thrombosis and haemostasis, 1997, pp. 1480-1480
LINKAGE OF COMBINED FACTOR-V AND FACTOR-VIII DEFICIENCY TO CHROMOSOME-18Q
Authors: NICHOLS WC SELIGSOHN U ZIVELIN A TERRY VH ARNOLD ND SIEMIENIAK DR GINSBURG D
Citation: Wc. Nichols et al., LINKAGE OF COMBINED FACTOR-V AND FACTOR-VIII DEFICIENCY TO CHROMOSOME-18Q, Thrombosis and haemostasis, 1997, pp. 1551-1551
2 NOVEL MUTATIONS CAUSING FACTOR-VII DEFICIENCY
Authors: TAMARY H FROMOVITCHAMIT Y SHALMON L ZIVELIN A PERETZ H LANIR N BRENNER B ZAIZOV R SELIGSOHN U
Citation: H. Tamary et al., 2 NOVEL MUTATIONS CAUSING FACTOR-VII DEFICIENCY, Thrombosis and haemostasis, 1997, pp. 1686-1686
HOMOZYGOSITY FOR C677T MUTATION IN METHYLENETETRA-HYDROFOLATE REDUCTASE (MTHFR) IS A RISK FACTOR FOR RETINAL VEIN-THROMBOSIS
Authors: SALOMON O MOUSSEIV J ROSENBERG N VIDNE O YASSUR Y SELIGSOHN U
Citation: O. Salomon et al., HOMOZYGOSITY FOR C677T MUTATION IN METHYLENETETRA-HYDROFOLATE REDUCTASE (MTHFR) IS A RISK FACTOR FOR RETINAL VEIN-THROMBOSIS, Thrombosis and haemostasis, 1997, pp. 2162-2162
HOMOZYGOUS METHYLENETETRAHYDROFOLATE REDUCTASE THERMOLABILITY (MTHFR-T) IS AN INDEPENDENT RISK FACTOR FOR IDIOPATHIC DEEP-VEIN THROMBOSIS (DVT)
Authors: SALOMOR O DARDIK R ZIVELIN A INBAL A VARON D MARTINOWITZ U MANI A SELIGSOHN U
Citation: O. Salomor et al., HOMOZYGOUS METHYLENETETRAHYDROFOLATE REDUCTASE THERMOLABILITY (MTHFR-T) IS AN INDEPENDENT RISK FACTOR FOR IDIOPATHIC DEEP-VEIN THROMBOSIS (DVT), Thrombosis and haemostasis, 1997, pp. 2326-2326
GENERATION OF PLATELET PROCOAGULANT ACTIVITY IN CLOTTING PLASMA, ROLEOF FIBRIN AND GPIIB IIIA RECEPTORS/
Authors: KUMAR R BEGUIN S KEULARTS I COLLER BS SELIGSOHN U HEMKER HC
Citation: R. Kumar et al., GENERATION OF PLATELET PROCOAGULANT ACTIVITY IN CLOTTING PLASMA, ROLEOF FIBRIN AND GPIIB IIIA RECEPTORS/, Thrombosis and haemostasis, 1997, pp. 2395-2395
THROMBOPHILIA AS A MULTIGENIC DISORDER
Authors: SELIGSOHN U ZIVELIN A
Citation: U. Seligsohn et A. Zivelin, THROMBOPHILIA AS A MULTIGENIC DISORDER, Thrombosis and haemostasis, 78(1), 1997, pp. 297-301
FACTOR-XIII DEFICIENCY DUE TO A LEU660PRO MUTATION IN THE FACTOR-XIIISUBUNIT-A GENE IN 3 UNRELATED PALESTINIAN ARAB FAMILIES
Authors: INBAL A YEE VC KORNBROT N ZIVELIN A BRENNER B SELIGSOHN U
Citation: A. Inbal et al., FACTOR-XIII DEFICIENCY DUE TO A LEU660PRO MUTATION IN THE FACTOR-XIIISUBUNIT-A GENE IN 3 UNRELATED PALESTINIAN ARAB FAMILIES, Thrombosis and haemostasis, 77(6), 1997, pp. 1062-1067
PURPURA FULMINANS INDUCED BY DISSEMINATED INTRAVASCULAR COAGULATION FOLLOWING INFECTION IN 2 UNRELATED CHILDREN WITH DOUBLE HETEROZYGOSITY FOR FACTOR-V-LEIDEN AND PROTEIN-S DEFICIENCY
Authors: INBAL A KENET G ZIVELIN A YERMIYAHU T BRONSTEIN T SHEINFELD T TAMARI H GITEL S ESHEL G DUCHEMIN J AIACH M SELIGSOHN U
Citation: A. Inbal et al., PURPURA FULMINANS INDUCED BY DISSEMINATED INTRAVASCULAR COAGULATION FOLLOWING INFECTION IN 2 UNRELATED CHILDREN WITH DOUBLE HETEROZYGOSITY FOR FACTOR-V-LEIDEN AND PROTEIN-S DEFICIENCY, Thrombosis and haemostasis, 77(6), 1997, pp. 1086-1089
Risultati: 1-25 | 26-50 | 51-75