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Journal Articles

Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor

JC Eikenboom, T Matsushita, PH Reitsma, EA Tuley, G Castaman, E Briet, JE Sadler
Journal: Blood
Blood (1996) 88 (7): 2433–2441.
https://doi.org/10.1182/blood.V88.7.2433.bloodjournal8872433
Published: 1996
Journal Articles

Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients

VR Arruda, WC Pieneman, PH Reitsma, PP Deutz-Terlouw, JM Annichino-Bizzacchi, E Briet, FF Costa
Journal: Blood
Blood (1995) 86 (8): 3015–3020.
https://doi.org/10.1182/blood.V86.8.3015.3015
Published: 1995
Journal Articles

Protein C deficiency in a controlled series of unselected outpatients: an infrequent but clear risk factor for venous thrombosis (Leiden Thrombophilia Study) [see comments]

T Koster, FR Rosendaal, E Briet, FJ van der Meer, LP Colly, PH Trienekens, SR Poort, PH Reitsma, JP Vandenbroucke
Journal: Blood
Blood (1995) 85 (10): 2756–2761.
https://doi.org/10.1182/blood.V85.10.2756.bloodjournal85102756
Published: 1995
Journal Articles

Expression of the blood-clotting factor-VIII cDNA is repressed by a transcriptional silencer located in its coding region

RC Hoeben, FJ Fallaux, SJ Cramer, DJ van den Wollenberg, H van Ormondt, E Briet, AJ van der Eb
Journal: Blood
Blood (1995) 85 (9): 2447–2454.
https://doi.org/10.1182/blood.V85.9.2447.bloodjournal8592447
Published: 1995
Journal Articles

Hereditary antithrombin deficiency: heterogeneity of the molecular basis and mortality in Dutch families

HH van Boven, RJ Olds, SL Thein, PH Reitsma, DA Lane, E Briet, JP Vandenbroucke, FR Rosendaal
Journal: Blood
Blood (1994) 84 (12): 4209–4213.
https://doi.org/10.1182/blood.V84.12.4209.bloodjournal84124209
Published: 1994
Journal Articles

A sudden increase in factor VIII inhibitor development in multitransfused hemophilia A patients in The Netherlands. Dutch Hemophilia Study Group

FR Rosendaal, HK Nieuwenhuis, HM van den Berg, H Heijboer, EP Mauser- Bunschoten, J van der Meer, C Smit, PF Strengers, E Briet
Journal: Blood
Blood (1993) 81 (8): 2180–2186.
https://doi.org/10.1182/blood.V81.8.2180.2180
Published: 1993
Journal Articles

The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effects

PH Reitsma, SR Poort, CF Allaart, E Briet, RM Bertina
Journal: Blood
Blood (1991) 78 (4): 890–894.
https://doi.org/10.1182/blood.V78.4.890.890
Published: 1991
Journal Articles

Two novel point mutations correlate with an altered developmental expression of blood coagulation factor IX (hemophilia B Leyden phenotype)

PH Reitsma, T Mandalaki, CK Kasper, RM Bertina, E Briet
Journal: Blood
Blood (1989) 73 (3): 743–746.
https://doi.org/10.1182/blood.V73.3.743.743
Published: 1989
Journal Articles

The putative factor IX gene promoter in hemophilia B Leyden

PH Reitsma, RM Bertina, JK Ploos van Amstel, A Riemens, E Briet
Journal: Blood
Blood (1988) 72 (3): 1074–1076.
https://doi.org/10.1182/blood.V72.3.1074.1074
Published: 1988
Journal Articles

Carrier detection in hemophilia A: a cooperative international study. I. The carrier phenotype

JB Graham, CR Rizza, J Chediak, PM Mannucci, E Briet, R Ljung, CK Kasper, EM Essien, PP Green
Journal: Blood
Blood (1986) 67 (6): 1554–1559.
https://doi.org/10.1182/blood.V67.6.1554.1554
Published: 1986
Journal Articles

Carrier detection in hemophilia A: a cooperative international study. II. The efficacy of a universal discriminant

PP Green, PM Mannucci, E Briet, R Ljung, CK Kasper, EM Essien, J Chediak, CR Rizza, JB Graham
Journal: Blood
Blood (1986) 67 (6): 1560–1567.
https://doi.org/10.1182/blood.V67.6.1560.1560
Published: 1986