๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

I14 Phenotypic and genotypic diagnosis of von Willebrand Disease

โœ Scribed by U. Budde; R. Schneppenheim


Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
66 KB
Volume
21
Category
Article
ISSN
0268-960X

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Type 2B von Willebrand's disease in thir
โœ Facey, D.A.; Favaloro, E.J.; Maxwell, E.; Baker, R.; Hertzberg, M.S. ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 21 KB ๐Ÿ‘ 1 views

Type 2B von Willebrand's disease (VWD) is due to a qualitative defect in von Willebrand factor (VWF) in which there is an increased affinity for the platelet glycoprotein Ib-IX-V receptor complex. Spontaneous binding of type 2B VWF to platelets and subsequent clearance from the plasma is thought to

Population differences in von Willebrand
โœ Connie H. Miller; Anne Dilley; Lisa Richardson; W. Craig Hooper; Bruce L. Evatt ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 67 KB ๐Ÿ‘ 2 views

## Abstract Diagnosis of von Willebrand disease (vWD) is based on a panel of laboratory tests that measure the amount and function of von Willebrand factor (vWF). In population studies, vWF is higher in African Americans than Caucasians. Bleeding time, factor VIII activity (FVIII), vWF antigen (vWF

Diagnosis of von Willebrand disease type
โœ Miller, Connie H.; Kelley, Leslie; Green, David ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 107 KB ๐Ÿ‘ 2 views

## Diagnosis of von Willebrand disease Type 2N (vWD 2N ), which mimics hemophilia A and its carrier state, is important for accurate genetic counseling and appropriate therapy. To make testing for the disorder more clinically applicable, we developed a simplified method for measurement of factor V

Genotypic and phenotypic characteristics
โœ Maria G. Macedo; Dagmar Verbaan; Yue Fang; Stephanie M. van Rooden; Martine Viss ๐Ÿ“‚ Article ๐Ÿ“… 2009 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 115 KB

## Abstract Early onset Parkinson's disease (EOPD) has been associated with mutations in the __Parkin__, __DJโ€1, PINK1, LRRK2,__ and __SNCA__ genes. The aim of this study is to assess the contribution of these genes in a Dutch EOPD cohort and the phenotypic characteristics of the mutation carriers.