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
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
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
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
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
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
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
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
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
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