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Results: 1-11 |
Results: 11
UNUSUAL ASSOCIATION OF ACQUIRED WILLEBRAND-DISEASE AND THROMBOEMBOLICSYNDROME - EFFICACY OF IMMUNOGLOBULINS
Authors: FUERTES C SALMERON S DUCHEMIN J WEILL B TCHERNIA G DREYFUS M
Citation: C. Fuertes et al., UNUSUAL ASSOCIATION OF ACQUIRED WILLEBRAND-DISEASE AND THROMBOEMBOLICSYNDROME - EFFICACY OF IMMUNOGLOBULINS, Thrombosis and haemostasis, 1997, pp. 879-879
LUPUS ANTICOAGULANT ASSOCIATED WITH ANTI-PROTHROMBIN AUTOANTIBODY
Authors: DUCHEMIN J BADERMEUNIER B DOIRON R BEZEAUD A TCHERNIA G DREYFUS M
Citation: J. Duchemin et al., LUPUS ANTICOAGULANT ASSOCIATED WITH ANTI-PROTHROMBIN AUTOANTIBODY, Thrombosis and haemostasis, 1997, pp. 2197-2197
SYSMEX CA-6000 - A NEW TOOL FOR OLD ASSAYS
Authors: PROULLE V DUCHEMIN J COVILLE E LELEU P TCHERNIA G DREYFUS M
Citation: V. Proulle et al., SYSMEX CA-6000 - A NEW TOOL FOR OLD ASSAYS, Thrombosis and haemostasis, 1997, pp. 2590-2590
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
5 NOVEL MUTATIONS OF THE PROTEIN-S ACTIVE GENE (PROS-1) IN 8 NORMAN FAMILIES
Authors: DUCHEMIN J BORG JY BORGEL D VASSE M LEVEQUE H AIACH M GANDRILLE S
Citation: J. Duchemin et al., 5 NOVEL MUTATIONS OF THE PROTEIN-S ACTIVE GENE (PROS-1) IN 8 NORMAN FAMILIES, Thrombosis and haemostasis, 75(3), 1996, pp. 437-444
MOLECULAR-BASIS FOR PROTEIN-S HEREDITARY-DEFICIENCY - GENETIC-DEFECTSOBSERVED IN 118 PATIENTS WITH TYPE-I AND TYPE IIA DEFICIENCIES
Authors: BORGEL D DUCHEMIN J ALHENCGELAS M MATHERON C AIACH M GANDRILLE S
Citation: D. Borgel et al., MOLECULAR-BASIS FOR PROTEIN-S HEREDITARY-DEFICIENCY - GENETIC-DEFECTSOBSERVED IN 118 PATIENTS WITH TYPE-I AND TYPE IIA DEFICIENCIES, The Journal of laboratory and clinical medicine, 128(2), 1996, pp. 218-227
MOLECULAR DEFECTS RESPONSIBLE FOR TYPE-I AND TYPE IIA PROTEIN-S (PS) DEFICIENCIES IN A PANEL OF 120 FRENCH FAMILIES
Authors: BORGEL D DUCHEMIN J MATHERON C AIACH M GANDRILLE S
Citation: D. Borgel et al., MOLECULAR DEFECTS RESPONSIBLE FOR TYPE-I AND TYPE IIA PROTEIN-S (PS) DEFICIENCIES IN A PANEL OF 120 FRENCH FAMILIES, Thrombosis and haemostasis, 73(6), 1995, pp. 1256-1256
PRIMARY ANTIPHOSPHOLIPID SYNDROME IS NOT ASSOCIATED WITH ACTIVATED PROTEIN-C RESISTANCE CAUSED BY FACTOR-V ARG 506-]GLN MUTATION
Authors: BIOUSSE V PIETTE JC FRANCES C BLETRY O PAPO T TOURNIERLASSERVE E DUCHEMIN J AIACH M
Citation: V. Biousse et al., PRIMARY ANTIPHOSPHOLIPID SYNDROME IS NOT ASSOCIATED WITH ACTIVATED PROTEIN-C RESISTANCE CAUSED BY FACTOR-V ARG 506-]GLN MUTATION, Journal of rheumatology, 22(6), 1995, pp. 1215-1215
THE SER 460 TO PRO SUBSTITUTION OF THE PROTEIN-S-ALPHA (PROS1) GENE IS A FREQUENT MUTATION ASSOCIATED WITH FREE PROTEIN-S (TYPE-IIA) DEFICIENCY
Authors: DUCHEMIN J GANDRILLE S BORGEL D FEURGARD P ALHENCGELAS M MATHERON C DREYFUS M DUPUY E JUHANVAGUE I AIACH M
Citation: J. Duchemin et al., THE SER 460 TO PRO SUBSTITUTION OF THE PROTEIN-S-ALPHA (PROS1) GENE IS A FREQUENT MUTATION ASSOCIATED WITH FREE PROTEIN-S (TYPE-IIA) DEFICIENCY, Blood, 86(9), 1995, pp. 3436-3443
INFLUENCE OF 6 MUTATIONS OF THE PROTEIN-C GENE ON THE GLA DOMAIN CONFORMATION AND CALCIUM AFFINITY
Authors: GAUSSEM P GANDRILLE S DUCHEMIN J EMMERICH J ALHENCGELAS M AILLAUD MF AIACH M
Citation: P. Gaussem et al., INFLUENCE OF 6 MUTATIONS OF THE PROTEIN-C GENE ON THE GLA DOMAIN CONFORMATION AND CALCIUM AFFINITY, Thrombosis and haemostasis, 71(6), 1994, pp. 748-754
A NEW ASSAY BASED ON THROMBIN GENERATION INHIBITION TO DETECT BOTH PROTEIN-C AND PROTEIN-S DEFICIENCIES IN PLASMA
Authors: DUCHEMIN J PITTE JL TARTARY M BEGUIN S GAUSSEM P ALHENCGELAS M AIACH M
Citation: J. Duchemin et al., A NEW ASSAY BASED ON THROMBIN GENERATION INHIBITION TO DETECT BOTH PROTEIN-C AND PROTEIN-S DEFICIENCIES IN PLASMA, Thrombosis and haemostasis, 71(3), 1994, pp. 331-338
Risultati: 1-11 |