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Query Trace: von Willebrand Disease, Type 1 and VWF[orginal query]

Genetic Variation in the Syntaxin-Binding Protein STXBP5 in Type 1 von Willebrand Disease Patients. Thrombosis and haemostasis 2018 Jul . Lind-Halldén Christina, Manderstedt Eric, Carlberg Daniel, Lethagen Stefan, Halldén Christ Similar articles in PubMed
Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients. PloS one 2018 13 (2): e0192024. Manderstedt Eric, Lind-Halldén Christina, Lethagen Stefan, Halldén Christ Similar articles in PubMed
Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States. Blood 2016 05 127 (20): 2481-8. Flood Veronica H, Christopherson Pamela A, Gill Joan Cox, Friedman Kenneth D, Haberichter Sandra L, Bellissimo Daniel B, Udani Rupa A, Dasgupta Mahua, Hoffmann Raymond G, Ragni Margaret V, Shapiro Amy D, Lusher Jeanne M, Lentz Steven R, Abshire Thomas C, Leissinger Cindy, Hoots W Keith, Manco-Johnson Marilyn J, Gruppo Ralph A, Boggio Lisa N, Montgomery Kate T, Goodeve Anne C, James Paula D, Lillicrap David, Peake Ian R, Montgomery Robert Similar articles in PubMed
Effect of Genetic Variation in STXBP5 and STX2 on von Willebrand Factor and Bleeding Phenotype in Type 1 von Willebrand Disease Patients. PloS one 2012 7 (7): 7. van Loon JE, Sanders YV, de Wee EM, Kruip MJ, de Maat MP, Leebeek FW Similar articles in PubMed