Bernard-Soulier Syndrome
Author:
Affiliation:
1. From the Departments of Medicine and Molecular and Human Genetics, Baylor College of Medicine and VA Medical Center, Houston, TX; and the Hazel and Pip Appel Vascular Biology Laboratory, Baker Medical Research Institute, Prahran, Australia.
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Reference219 articles.
1. Sur une nouvelle variété de dystrophie thrombocytaire-hémorragipare congénitale.;Bernard;Semin Hop Paris,1948
2. Congenital thrombocytopenia with giant platelets: A defect in the platelet membrane.;Gröttum;Br J Haematol,1969
3. Hereditary giant platelet syndrome: A disorder of a new aspect of platelet function.;Howard;Br Med J,1973
4. Interaction between platelets and von Willebrand factor provides a new scheme for primary haemostasis.;Caen;Nature,1973
5. Decreased adhesion of giant (Bernard-Soulier) platelets to subendothelium. Further implications on the role of the von Willebrand factor in hemostasis.;Weiss;Am J Med,1974
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1. Bernard–Soulier Syndrome: A Review of Epidemiology, Molecular Pathology, Clinical Features, Laboratory Diagnosis, and Therapeutic Management;Seminars in Thrombosis and Hemostasis;2024-08-27
2. The compound pathogenic effects of a homozygous frameshift variant in the transmembrane region of GP9, causing Bernard–Soulier syndrome, with a missense variant in GP1BB;British Journal of Haematology;2024-06-25
3. Binding Mechanism between Platelet Glycoprotein and Cyclic Peptide Elucidated by McMD-Based Dynamic Docking;Journal of Chemical Information and Modeling;2024-05-16
4. Platelet Physiology;Seminars in Thrombosis and Hemostasis;2024-04-23
5. Bernard–Soulier syndrome caused by two novel heterozygous GP1BA gene mutations: a case report and literature review;Hematology;2024-04-02
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