Von willebrand disease and quantitative variation in von willebrand factor
- 1 September 1997
- journal article
- review article
- Published by Elsevier in Journal of Laboratory and Clinical Medicine
- Vol. 130 (3) , 252-261
- https://doi.org/10.1016/s0022-2143(97)90019-6
Abstract
No abstract availableThis publication has 81 references indexed in Scilit:
- A common frameshift mutation in von Willebrand factor does not alter mRNA stability but interferes with normal propeptide processingBritish Journal of Haematology, 1996
- Prevalence of von Willebrand disease in children: A multiethnic studyThe Journal of Pediatrics, 1993
- Type I von Willebrand disease, subtype ‘platelet low’: decreased platelet adhesion can be explained by low synthesis of von Willebrand factor in endothelial cellsBritish Journal of Haematology, 1993
- Rapid neonatal diagnosis of von Willebrand's disease by use of the polymerase chain reactionThe Lancet, 1990
- Inducible secretion of large, biologically potent von Willebrand factor multimersCell, 1986
- Carbohydrate moiety of von Willebrand factor is not necessary for maintaining multimeric structure and ristocetin cofactor activity but protects from proteolytic degradation.Journal of Clinical Investigation, 1984
- Incidence of Severe von Willebrand's DiseaseNew England Journal of Medicine, 1982
- Genetic analysis of von Willebrand's disease in two large pedigrees: A multivariate approachAmerican Journal of Medical Genetics, 1980
- Human blood platelet adhesion to artery subendothelium is mediated by factor VIII–Von Willebrand factor bound to the subendotheliumNature, 1979
- ABO BLOOD-GROUPS AND VENOUS THROMBOEMBOLIC DISEASEThe Lancet, 1970