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Results: 1-12 |
Results: 12
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
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
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
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
A LEU660PRO MUTATION IN THE GENE ENCODING FOR SUBUNIT-A OF FACTOR-XIII IS THE CAUSE OF FACTOR-XIII DEFICIENCY IN 3 UNRELATED ARAB FAMILIES
Authors: INBAL A ZIVELIN A KORNBROT N BRENNER B SELIGSOHN U
Citation: A. Inbal et al., A LEU660PRO MUTATION IN THE GENE ENCODING FOR SUBUNIT-A OF FACTOR-XIII IS THE CAUSE OF FACTOR-XIII DEFICIENCY IN 3 UNRELATED ARAB FAMILIES, Thrombosis and haemostasis, 73(6), 1995, pp. 1210-1210
CURRENT STRATEGY FOR GENETIC-ANALYSIS OF HEMOPHILIA-A FAMILIES
Authors: DARDIK R PERETZ H USHER S KORNBROT N SHAKI R SELIGSOHN U MARTINOWITZ U
Citation: R. Dardik et al., CURRENT STRATEGY FOR GENETIC-ANALYSIS OF HEMOPHILIA-A FAMILIES, Thrombosis and haemostasis, 73(6), 1995, pp. 1220-1220
VERY-LOW FREQUENCY OF NORMANDY TYPE MUTATIONS AMONG TYPE-1 VON-WILLEBRAND DISEASE FAMILIES
Authors: INBAL A KORNBROT N MANNUCCI PM SADLER JE
Citation: A. Inbal et al., VERY-LOW FREQUENCY OF NORMANDY TYPE MUTATIONS AMONG TYPE-1 VON-WILLEBRAND DISEASE FAMILIES, Thrombosis and haemostasis, 73(2), 1995, pp. 324-324
HOW TO CALCULATE THE MAXIMUM RISK - REPLY
Authors: INBAL A EPSTEIN O BLICKSTEIN D KORNBROT N BRENNER B MARTINOWITZ U
Citation: A. Inbal et al., HOW TO CALCULATE THE MAXIMUM RISK - REPLY, Blood coagulation & fibrinolysis, 5(5), 1994, pp. 851-851
EVALUATION OF SOLVENT DETERGENT-TREATED PLASMA IN THE MANAGEMENT OF PATIENTS WITH HEREDITARY AND ACQUIRED COAGULATION DISORDERS
Authors: INBAL A EPSTEIN O BLICKSTEIN D KORNBROT N BRENNER B MARTINOWITZ U
Citation: A. Inbal et al., EVALUATION OF SOLVENT DETERGENT-TREATED PLASMA IN THE MANAGEMENT OF PATIENTS WITH HEREDITARY AND ACQUIRED COAGULATION DISORDERS, Blood coagulation & fibrinolysis, 4(4), 1993, pp. 599-604
EFFECT OF TYPE IIB VON-WILLEBRAND DISEASE MUTATION ARG(545)CYS ON PLATELET GLYCOPROTEIN IB BINDING-STUDIES WITH RECOMBINANT VON-WILLEBRAND-FACTOR
Authors: INBAL A KORNBROT N HARRISON P RANDI AM SADLER JE
Citation: A. Inbal et al., EFFECT OF TYPE IIB VON-WILLEBRAND DISEASE MUTATION ARG(545)CYS ON PLATELET GLYCOPROTEIN IB BINDING-STUDIES WITH RECOMBINANT VON-WILLEBRAND-FACTOR, Thrombosis and haemostasis, 70(6), 1993, pp. 1058-1062
EFFECT OF TYPE-IIB VON-WILLEBRAND DISEASE MUTATION ARG-(545) CYS ON PLATELET GLYCOPROTEIN-IB BINDING - STUDIES WITH RECOMBINANT VON-WILLEBRAND-FACTOR
Authors: INBAL A KORNBROT N HARRISON P RANDI AM SADLER JE
Citation: A. Inbal et al., EFFECT OF TYPE-IIB VON-WILLEBRAND DISEASE MUTATION ARG-(545) CYS ON PLATELET GLYCOPROTEIN-IB BINDING - STUDIES WITH RECOMBINANT VON-WILLEBRAND-FACTOR, Thrombosis and haemostasis, 69(6), 1993, pp. 1008-1008
IDENTIFICATION OF 3 CANDIDATE MUTATIONS CAUSING TYPE-IIA VON-WILLEBRAND DISEASE USING A RAPID, NONRADIOACTIVE, ALLELE-SPECIFIC HYBRIDIZATION METHOD
Authors: INBAL A ENGLENDER T KORNBROT N RANDI AM CASTAMAN G MANNUCCI PM SADLER JE
Citation: A. Inbal et al., IDENTIFICATION OF 3 CANDIDATE MUTATIONS CAUSING TYPE-IIA VON-WILLEBRAND DISEASE USING A RAPID, NONRADIOACTIVE, ALLELE-SPECIFIC HYBRIDIZATION METHOD, Blood, 82(3), 1993, pp. 830-836
Risultati: 1-12 |