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Results: 1-15 |
Results: 15
PROTEIN-S DEFICIENCY - DIFFERENT BIOLOGICAL PHENOTYPES ACCORDING TO THE ASSAYS USED
Authors: BRUNET D BARTHET MC MORANGE PE ALESSI MC BORGEL D GANDRILLE S AILLAUD MF JUHANVAGUE I
Citation: D. Brunet et al., PROTEIN-S DEFICIENCY - DIFFERENT BIOLOGICAL PHENOTYPES ACCORDING TO THE ASSAYS USED, Thrombosis and haemostasis, 79(2), 1998, pp. 446-447
ABERRANT SPLICED TRANSCRIPTS GENERATED DURING PROS1 GENE-EXPRESSION IN A FAMILY WITH TYPE-II PROTEIN-S (PS) DEFICIENCY
Authors: LEROYMATHERON C GOUAULTHEILMANN M BORGEL D AIACH M GANDRILLE S
Citation: C. Leroymatheron et al., ABERRANT SPLICED TRANSCRIPTS GENERATED DURING PROS1 GENE-EXPRESSION IN A FAMILY WITH TYPE-II PROTEIN-S (PS) DEFICIENCY, Thrombosis and haemostasis, 1997, pp. 759-759
PROTEIN-S DEFICIENCY
Authors: BORGEL D GANDRILLE S AIACH M
Citation: D. Borgel et al., PROTEIN-S DEFICIENCY, Thrombosis and haemostasis, 78(1), 1997, pp. 351-356
PROTEIN-S DEFICIENCY - A DATABASE OF MUTATIONS - FOR THE PLASMA COAGULATION INHIBITORS SUBCOMMITTEE OF THE SCIENTIFIC AND STANDARDIZATION COMMITTEE OF THE INTERNATIONAL-SOCIETY-ON-THROMBOSIS-AND-HEMOSTASIS
Authors: GANDRILLE S BORGEL D IRELAND H LANE DA SIMMONDS R REITSMA PH MANNHALTER C PABINGER I SAITO H SUZUKI K FORMSTONE C COOPER DN ESPINOSA Y SALA N BERNARDI F ALACH M
Citation: S. Gandrille et al., PROTEIN-S DEFICIENCY - A DATABASE OF MUTATIONS - FOR THE PLASMA COAGULATION INHIBITORS SUBCOMMITTEE OF THE SCIENTIFIC AND STANDARDIZATION COMMITTEE OF THE INTERNATIONAL-SOCIETY-ON-THROMBOSIS-AND-HEMOSTASIS, Thrombosis and haemostasis, 77(6), 1997, pp. 1201-1214
PROTEIN-C AND PROTEIN-S DEFICIENCIES
Authors: AIACH M BORGEL D GAUSSEM P EMMERICH J ALHENCGELAS M GANDRILLE S
Citation: M. Aiach et al., PROTEIN-C AND PROTEIN-S DEFICIENCIES, Seminars in hematology, 34(3), 1997, pp. 205-216
FIRST CASE OF SPORADIC PROTEIN-S DEFICIENCY DUE TO A NOVEL CANDIDATE MUTATION, ALA484-]PRO, IN THE PROTEIN-S ACTIVE GENE (PROS1)
Authors: BORGEL D JUDE B AIACH M GANDRILLE S
Citation: D. Borgel et al., FIRST CASE OF SPORADIC PROTEIN-S DEFICIENCY DUE TO A NOVEL CANDIDATE MUTATION, ALA484-]PRO, IN THE PROTEIN-S ACTIVE GENE (PROS1), Thrombosis and haemostasis, 75(6), 1996, pp. 883-886
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
ROLL WRAPPING OF PULP AND PAPER WITH HIGH-PERFORMANCE STRETCH FILMS
Authors: CLIMENHAGE D HEIJMANS F BORGEL D
Citation: D. Climenhage et al., ROLL WRAPPING OF PULP AND PAPER WITH HIGH-PERFORMANCE STRETCH FILMS, Pulp & paper Canada, 97(4), 1996, pp. 24-28
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
INCIDENCE OF ACTIVATED PROTEIN-C RESISTANCE DUE TO ARG 506 GLN MUTATION IN FACTOR-V IN 116 UNRELATED PROPOSITUS FROM FAMILIES WITH PROTEIN-S DEFICIENCY
Authors: GANDRILLE S BORGEL D AIACH M
Citation: S. Gandrille et al., INCIDENCE OF ACTIVATED PROTEIN-C RESISTANCE DUE TO ARG 506 GLN MUTATION IN FACTOR-V IN 116 UNRELATED PROPOSITUS FROM FAMILIES WITH PROTEIN-S DEFICIENCY, Thrombosis and haemostasis, 73(6), 1995, pp. 1372-1372
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
IDENTIFICATION OF 15 DIFFERENT CANDIDATE CAUSAL POINT MUTATIONS AND 3POLYMORPHISMS IN 19 PATIENTS WITH PROTEIN-S DEFICIENCY USING A SCANNING METHOD FOR THE ANALYSIS OF THE PROTEIN-S ACTIVE GENE
Authors: GANDRILLE S BORGEL D ESCHWEGEGUFFLET V AILLAUD M DREYFUS M MATHERON C GAUSSEM P ABGRALL JF JUDE B SIE P TOULON P AIACH M
Citation: S. Gandrille et al., IDENTIFICATION OF 15 DIFFERENT CANDIDATE CAUSAL POINT MUTATIONS AND 3POLYMORPHISMS IN 19 PATIENTS WITH PROTEIN-S DEFICIENCY USING A SCANNING METHOD FOR THE ANALYSIS OF THE PROTEIN-S ACTIVE GENE, Blood, 85(1), 1995, pp. 130-138
FIRST FRAMESHIFT MUTATION IN THE ACTIVE PROTEIN-S GENE ASSOCIATED WITH A QUANTITATIVE HEREDITARY-DEFICIENCY
Authors: BORGEL D GANDRILLE S GOUAULTHEILMANN M AIACH M
Citation: D. Borgel et al., FIRST FRAMESHIFT MUTATION IN THE ACTIVE PROTEIN-S GENE ASSOCIATED WITH A QUANTITATIVE HEREDITARY-DEFICIENCY, Blood coagulation & fibrinolysis, 5(4), 1994, pp. 593-600
IDENTIFICATION OF 14 NOVEL PUNCTUAL MUTATIONS IN THE PS-ALPHA-GENE OFSUBJECTS WITH SYMPTOMATIC PROTEIN-S (PS) DEFICIENCY
Authors: GANDRILLE S BORGEL D GUFFLET V AIACH M
Citation: S. Gandrille et al., IDENTIFICATION OF 14 NOVEL PUNCTUAL MUTATIONS IN THE PS-ALPHA-GENE OFSUBJECTS WITH SYMPTOMATIC PROTEIN-S (PS) DEFICIENCY, Thrombosis and haemostasis, 69(6), 1993, pp. 790-790
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