AAAAAA

   
Results: 1-25 | 26-45
Results: 1-25/45
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
GEOGRAPHIC-DISTRIBUTION OF THE 20210-G TO 20210-A PROTHROMBIN VARIANT
Authors: ROSENDAAL FR DOGGEN CJM ZIVELIN A ARRUDA VR AIACH M SISCOVICK DS HILLARP A WATZKE HH BERNARDI F CUMMING AM PRESTON FE REITSMA PH
Citation: Fr. Rosendaal et al., GEOGRAPHIC-DISTRIBUTION OF THE 20210-G TO 20210-A PROTHROMBIN VARIANT, Thrombosis and haemostasis, 79(4), 1998, pp. 706-708
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
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
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
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 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
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
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
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
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
Risultati: 1-25 | 26-45