Von Willebrand's disease in the year 2003: towards the complete identification of gene defects for correct diagnosis and treatment, Haematologica, vol.88, issue.1, pp.94-108, 2003. ,
A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease, Medicine, vol.95, issue.11, p.3038, 2016. ,
DOI : 10.1097/MD.0000000000003038
Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor, Journal of Thrombosis and Haemostasis, vol.93, issue.10, pp.2103-2114, 2006. ,
DOI : 10.1111/j.1538-7836.2006.01847.x
Heightened Interaction between Platelets and Factor VIII/von Willebrand Factor in a New Subtype of von Willebrand's Disease, New England Journal of Medicine, vol.302, issue.19, pp.1047-1051, 1980. ,
DOI : 10.1056/NEJM198005083021902
Von Willebrand factor, platelets and endothelial cell interactions, Journal of Thrombosis and Haemostasis, vol.101, issue.7, pp.1335-1342, 2003. ,
DOI : 10.1161/01.CIR.101.19.2290
The molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding domain., Journal of Clinical Investigation, vol.87, issue.4, pp.1227-1233, 1991. ,
DOI : 10.1172/JCI115123
Type IIB Tampa: a variant of von Willebrand disease with chronic thrombocytopenia, circulating platelet aggregates, and spontaneous platelet aggregation, Blood, vol.66, issue.2, pp.282-286, 1985. ,
von Willebrand disease type 2B must be always considered in the differential diagnosis of genetic thrombocytopenias with giant platelets, Platelets, vol.27, issue.3, pp.149-152, 2006. ,
DOI : 10.1002/ajh.2830270412
Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients, Blood, vol.113, issue.3, pp.526-534, 2009. ,
DOI : 10.1182/blood-2008-04-152280
Management of pregnancy in type 2B von Willebrand disease: case report and literature review, Haemophilia, vol.32, issue.1, pp.98-103, 2015. ,
DOI : 10.1016/j.annfar.2012.10.032
Thrombocytopenia associated with pregnancy in a patient with type IIB von Willebrand's disease, Blood, vol.69, issue.3, pp.786-789, 1987. ,
Maternal and fetal outcomes in pregnancies affected by von Willebrand disease type 2, American Journal of Obstetrics and Gynecology, vol.184, issue.2, pp.229-230, 2001. ,
DOI : 10.1067/mob.2001.106764
Type 2B vWD: the varied clinical manifestations in two kindreds, Haemophilia, vol.89, issue.1, pp.137-144, 2003. ,
DOI : 10.1136/adc.78.3.257
Severe Thrombocytopenia, Type 2B von Willebrand Disease and Pregnancy, Anesthesiology, vol.101, issue.6, pp.1465-1467, 2004. ,
DOI : 10.1097/00000542-200412000-00029
Pregnancy in type 2B VWD: a case series, Haemophilia, vol.115, issue.3, pp.406-412, 2012. ,
DOI : 10.1182/blood-2009-11-253120
Summary, Thrombosis and Haemostasis, vol.106, issue.11, pp.885-892, 2011. ,
DOI : 10.1160/TH11-03-0180
Management of type 2b von Willebrand disease in the neonatal period, Pediatric Blood & Cancer, vol.113, issue.3, pp.103-105, 2017. ,
DOI : 10.1182/blood-2008-04-152280
A family having type 2B von Willebrand disease with a novel P a g e, p.34 ,
Differential diagnosis of neonatal alloimmune thrombocytopenia: Type 2B von Willebrand disease, Platelets, vol.69, issue.8, pp.1-4 ,
DOI : 10.1111/hae.12733
Summary, Thrombosis and Haemostasis, vol.116, issue.12, pp.1070-1078, 2016. ,
DOI : 10.1160/TH16-06-0438
Effects of different amino-acid substitutions in the leucine 694-proline 708 segment of recombinant von Willebrand factor, Br. J. Haematol, vol.91, issue.4, pp.983-990, 1995. ,
Influence of mutations and size of multimers in type II von Willebrand disease upon the function of von Willebrand factor, Blood, vol.83, issue.12, pp.3553-3561, 1994. ,
A type 2b von Willebrand disease mutation (Ile546-->Val) associated with an unusual phenotype, Thromb. Haemost, vol.78, issue.3, pp.1132-1137, 1997. ,
Functional analysis of a type IIB von Willebrand disease missense mutation: increased binding of large von Willebrand factor multimers to platelets., Proceedings of the National Academy of Sciences, vol.89, issue.7, pp.2869-2872, 1992. ,
DOI : 10.1073/pnas.89.7.2869
Molecular basis of von Willebrand disease type IIB. Candidate mutations cluster in one disulfide loop between proposed platelet glycoprotein Ib binding sequences., Journal of Clinical Investigation, vol.87, issue.4, pp.1220-1226, 1991. ,
DOI : 10.1172/JCI115122
Comparative analysis of type 2b von Willebrand disease mutations: implications for the mechanism of von Willebrand factor binding to platelets, Blood, vol.87, issue.6, pp.2322-2328, 1996. ,
Heterogeneity in type IIB von Willebrand disease: Two unrelated cases with no family history and mild abnormalities of ristocetin-induced interaction between von willebrand factor and platelets, American Journal of Hematology, vol.63, issue.4, pp.381-390, 1986. ,
DOI : 10.1002/ajh.2830230410
Type 2B von Willebrand's disease due to Val1316Met mutation. Heterogeneity in the same sibship, Ann. Hematol, vol.80, issue.6, pp.354-360, 2001. ,
Normal vaginal delivery is to be recommended for haemophilia carrier gravidae, Acta Paediatrica, vol.158, issue.6, pp.609-611, 1992. ,
DOI : 10.1016/0002-9378(88)90098-1
[Epidemiology of hereditary bleeding disorders: input of FranceCoag Network], Arch. Pediatr. Organe Off. Soc. Francaise Pediatr, vol.17, issue.6, pp.618-619, 2010. ,