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Results: 1-19 |
Results: 19
THE USEFULNESS OF SINGLE-STRAND DNA CONFORMATION POLYMORPHISM ANALYSIS TO DETECT MUTATIONS IN PROTEIN-C DEFICIENCY
Authors: GOMEZ E POORT SR BERTINA RM REITSMA PH
Citation: E. Gomez et al., THE USEFULNESS OF SINGLE-STRAND DNA CONFORMATION POLYMORPHISM ANALYSIS TO DETECT MUTATIONS IN PROTEIN-C DEFICIENCY, Blood coagulation & fibrinolysis, 8(8), 1997, pp. 497-502
CONTRIBUTION OF ADDITIONAL GENETIC RISK-FACTORS IN SYMPTOMATIC ANTITHROMBIN DEFICIENT INDIVIDUALS - FV 1691-A AND FII 20210-A
Authors: VANBOVEN HH POORT SR BERTINA RM ROSENDAAL FR
Citation: Hh. Vanboven et al., CONTRIBUTION OF ADDITIONAL GENETIC RISK-FACTORS IN SYMPTOMATIC ANTITHROMBIN DEFICIENT INDIVIDUALS - FV 1691-A AND FII 20210-A, Thrombosis and haemostasis, 1997, pp. 1548-1548
RAPID DETECTION OF THE PROTHROMBIN 20210-A VARIATION BY ALLELE-SPECIFIC PCR
Authors: POORT SR BERTINA RM VOS HL
Citation: Sr. Poort et al., RAPID DETECTION OF THE PROTHROMBIN 20210-A VARIATION BY ALLELE-SPECIFIC PCR, Thrombosis and haemostasis, 78(3), 1997, pp. 1157-1158
COMPOUND HETEROZYGOSITY FOR 2 NOVEL MISSENSE MUTATIONS IN THE PROTHROMBIN GENE IN A PATIENT WITH A SEVERE BLEEDING TENDENCY
Authors: POORT SR LANDOLFI R BERTINA RM
Citation: Sr. Poort et al., COMPOUND HETEROZYGOSITY FOR 2 NOVEL MISSENSE MUTATIONS IN THE PROTHROMBIN GENE IN A PATIENT WITH A SEVERE BLEEDING TENDENCY, Thrombosis and haemostasis, 77(4), 1997, pp. 610-615
MODIFICATION OF THE N-TERMINUS OF HUMAN FACTOR-IX BY DEFECTIVE PROPEPTIDE CLEAVAGE OR ACETYLATION RESULTS IN A DESTABILIZED CALCIUM-INDUCEDCONFORMATION - EFFECTS ON PHOSPHOLIPID-BINDING AND ACTIVATION BY FACTOR XIA
Authors: WOJCIK EGC VANDENBERG M POORT SR BERTINA RM
Citation: Egc. Wojcik et al., MODIFICATION OF THE N-TERMINUS OF HUMAN FACTOR-IX BY DEFECTIVE PROPEPTIDE CLEAVAGE OR ACETYLATION RESULTS IN A DESTABILIZED CALCIUM-INDUCEDCONFORMATION - EFFECTS ON PHOSPHOLIPID-BINDING AND ACTIVATION BY FACTOR XIA, Biochemical journal, 323, 1997, pp. 629-636
A COMMON GENETIC-VARIATION IN THE 3'-UNTRANSLATED REGION OF THE PROTHROMBIN GENE IS ASSOCIATED WITH ELEVATED PLASMA PROTHROMBIN LEVELS AND AN INCREASE IN VENOUS THROMBOSIS
Authors: POORT SR ROSENDAAL FR REITSMA PH BERTINA RM
Citation: Sr. Poort et al., A COMMON GENETIC-VARIATION IN THE 3'-UNTRANSLATED REGION OF THE PROTHROMBIN GENE IS ASSOCIATED WITH ELEVATED PLASMA PROTHROMBIN LEVELS AND AN INCREASE IN VENOUS THROMBOSIS, Blood, 88(10), 1996, pp. 3698-3703
IDENTIFICATION OF 8 POINT MUTATIONS IN PROTEIN-S DEFICIENCY TYPE-I - ANALYSIS OF 15 PEDIGREES
Authors: GOMEZ E POORT SR BERTINA RM REITSMA PH
Citation: E. Gomez et al., IDENTIFICATION OF 8 POINT MUTATIONS IN PROTEIN-S DEFICIENCY TYPE-I - ANALYSIS OF 15 PEDIGREES, Thrombosis and haemostasis, 73(5), 1995, pp. 750-755
PROTEIN-C DEFICIENCY - A DATABASE OF MUTATIONS, 1995 UPDATE
Authors: REITSMA PH BERNARDI F DOIG RG GANDRILLE S GREENGARD JS IRELAND H KRAWCZAK M LIND B LONG GL POORT SR SAITO H SALA N WITT I COOPER DN
Citation: Ph. Reitsma et al., PROTEIN-C DEFICIENCY - A DATABASE OF MUTATIONS, 1995 UPDATE, Thrombosis and haemostasis, 73(5), 1995, pp. 876-889
PREVALENCE OF PROTEIN-C DEFICIENCY IN THE HEALTHY POPULATION
Authors: TAIT RC WALKER ID REITSMA PH ISLAM SIAM MCCALL F POORT SR CONKIE JA BERTINA RM
Citation: Rc. Tait et al., PREVALENCE OF PROTEIN-C DEFICIENCY IN THE HEALTHY POPULATION, Thrombosis and haemostasis, 73(1), 1995, pp. 87-93
FACTOR-IX ZUTPHEN - A CYS(18)-]ARG MUTATION RESULTS IN FORMATION OF AHETERODIMER WITH ALPHA(1)-MICROGLOBULIN AND THE INABILITY TO FORM A CALCIUM-INDUCED CONFORMATION
Authors: WOJCIK EGC VANDENBERG M VANDERLINDEN IK POORT SR CUPERS R BERTINA RM
Citation: Egc. Wojcik et al., FACTOR-IX ZUTPHEN - A CYS(18)-]ARG MUTATION RESULTS IN FORMATION OF AHETERODIMER WITH ALPHA(1)-MICROGLOBULIN AND THE INABILITY TO FORM A CALCIUM-INDUCED CONFORMATION, Biochemical journal, 311, 1995, pp. 753-759
FULMINANT MENINGOCOCCAL SEPTIC SHOCK IN A BOY WITH COMBINED INHERITEDPROPERDIN AND PROTEIN-C DEFICIENCY
Authors: FIJEN CAP DERKX BHF KUIJPER EJ MANNENS M POORT SR PETERS M DAHA MR DANKER J
Citation: Cap. Fijen et al., FULMINANT MENINGOCOCCAL SEPTIC SHOCK IN A BOY WITH COMBINED INHERITEDPROPERDIN AND PROTEIN-C DEFICIENCY, Clinical and experimental immunology, 102(2), 1995, pp. 290-296
PROTEIN-C DEFICIENCY IN A CONTROLLED SERIES OF UNSELECTED OUTPATIENTS- AN INFREQUENT BUT CLEAR RISK FACTOR FOR VENOUS THROMBOSIS (LEIDEN THROMBOPHILIA STUDY)
Authors: KOSTER T ROSENDAAL FR BRIET E VANDERMEER FJM COLLY LP TRIENEKENS PH POORT SR REITSMA PH VANDENBROUCKE JP
Citation: T. Koster et al., PROTEIN-C DEFICIENCY IN A CONTROLLED SERIES OF UNSELECTED OUTPATIENTS- AN INFREQUENT BUT CLEAR RISK FACTOR FOR VENOUS THROMBOSIS (LEIDEN THROMBOPHILIA STUDY), Blood, 85(10), 1995, pp. 2756-2761
DETERMINATION OF THE ALLELIC AND HAPLOTYPE FREQUENCIES OF 3 POLYMORPHISMS IN THE PROMOTER REGION OF THE HUMAN PROTEIN-C GENE
Authors: SPEK CA POORT SR BERTINA RM REITSMA PH
Citation: Ca. Spek et al., DETERMINATION OF THE ALLELIC AND HAPLOTYPE FREQUENCIES OF 3 POLYMORPHISMS IN THE PROMOTER REGION OF THE HUMAN PROTEIN-C GENE, Blood coagulation & fibrinolysis, 5(2), 1994, pp. 309-311
HOMOZYGOSITY FOR A NOVEL MISSENSE MUTATION IN THE PROTHROMBIN GENE CAUSING A SEVERE BLEEDING DISORDER
Authors: POORT SR MICHIELS JJ REITSMA PH BERTINA RM
Citation: Sr. Poort et al., HOMOZYGOSITY FOR A NOVEL MISSENSE MUTATION IN THE PROTHROMBIN GENE CAUSING A SEVERE BLEEDING DISORDER, Thrombosis and haemostasis, 72(6), 1994, pp. 819-824
HOMOZYGOSITY FOR A NOVEL MISSENSE MUTATION IN THE PROTHROMBIN GENE CAUSING A SEVERE BLEEDING DISORDER
Authors: POORT SR MICHIELS JJ REITSMA PH BERTINA RM
Citation: Sr. Poort et al., HOMOZYGOSITY FOR A NOVEL MISSENSE MUTATION IN THE PROTHROMBIN GENE CAUSING A SEVERE BLEEDING DISORDER, Blood, 84(10), 1994, pp. 10000240-10000240
FACTOR-IZ ZUTPHEN - A CYS18 -] AGR MUTATION RESULTS IN FORMATION OF AHETERODIMER WITH ALPHA-1-MICROGLOBULIN AND THE INABILITY TO FORM A CALCIUM-INDUCED CONFORMATION
Authors: WOJCIK EGC VANDENBERG M VANDERLINDEN IK POORT SR CUPERS R BERTINA RM
Citation: Egc. Wojcik et al., FACTOR-IZ ZUTPHEN - A CYS18 -] AGR MUTATION RESULTS IN FORMATION OF AHETERODIMER WITH ALPHA-1-MICROGLOBULIN AND THE INABILITY TO FORM A CALCIUM-INDUCED CONFORMATION, Thrombosis and haemostasis, 69(6), 1993, pp. 615-615
OVERLAP IN PROTEIN-C LEVELS BETWEEN HETEROZYGOTES AND CONTROLS ON ORAL ANTICOAGULANT-THERAPY - USE OF PROTEIN-C AND FACTOR-X ANTIGEN IN THECALCULATION OF A LIKELIHOOD RATIO ON CARRIERSHIP
Authors: ALLAART CFR HERMANS J POORT SR BRIET E BERTINA RM
Citation: Cfr. Allaart et al., OVERLAP IN PROTEIN-C LEVELS BETWEEN HETEROZYGOTES AND CONTROLS ON ORAL ANTICOAGULANT-THERAPY - USE OF PROTEIN-C AND FACTOR-X ANTIGEN IN THECALCULATION OF A LIKELIHOOD RATIO ON CARRIERSHIP, Thrombosis and haemostasis, 69(6), 1993, pp. 1257-1257
OVERLAP IN PROTEIN-C LEVELS BETWEEN HETEROZYGOTES AND NORMALS - USE OF PROTEIN-C ACTIVITY OR ANTIGEN AND FACTOR-II ANTIGEN TO CALCULATE A LIKELIHOOD RATIO ON CARRIERSHIP
Authors: ALLAART CFR HERMANS J POORT SR BRIET E BERTINA RM
Citation: Cfr. Allaart et al., OVERLAP IN PROTEIN-C LEVELS BETWEEN HETEROZYGOTES AND NORMALS - USE OF PROTEIN-C ACTIVITY OR ANTIGEN AND FACTOR-II ANTIGEN TO CALCULATE A LIKELIHOOD RATIO ON CARRIERSHIP, Thrombosis and haemostasis, 69(6), 1993, pp. 1258-1258
DIAGNOSIS OF PROTEIN-C DEFICIENCY BY ANALYSIS OF SINGLE-STRAND DNA CONFORMATION POLYMORPHISMS
Authors: GOMEZ E REITSMA PH POORT SR RODRIGUEZ C NICOLAS C BERTINA RM
Citation: E. Gomez et al., DIAGNOSIS OF PROTEIN-C DEFICIENCY BY ANALYSIS OF SINGLE-STRAND DNA CONFORMATION POLYMORPHISMS, Blood, 82(10), 1993, pp. 10000406-10000406
Risultati: 1-19 |