Genetic heterogeneity of severe von Willebrand disease type III in the German population.
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Critical von Willebrand factor A1 domain residues influence type VI collagen binding.Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor.The molecular biology of von Willebrand disease.Assessment of the olfactory function in Italian patients with type 3 von Willebrand disease caused by a homozygous 253 Kb deletion involving VWF and TMEM16B/ANO2Genetic heterogeneity in a large cohort of Indian type 3 von Willebrand disease patients.Characterization of recessive severe type 1 and 3 von Willebrand Disease (VWD), asymptomatic heterozygous carriers versus bloodgroup O-related von Willebrand factor deficiency, and dominant type 1 VWD.Bleeding scores in inherited bleeding disorders: clinical or research tools?von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA).The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles.von Willebrand factor: the complex molecular genetics of a multidomain and multifunctional protein.Current management of patients with severe von Willebrand disease type 3: a 2012 update.Phenotypic and genotypic characterization of 10 Finnish patients with von Willebrand disease type 3: discovery of two main mutations.Pathogenesis, clinical picture and treatment of von Willebrand's disease.The role of exon 45 and 16 in the pathogenesis of Von Willebrand disease in Iranian Patients.Guidelines for the diagnosis and management of von Willebrand disease in Italy.Expression studies of missense mutations p.D141Y, p.C275S located in the propeptide of von Willebrand factor in patients with type 3 von Willebrand disease.Massive retroperitoneal pseudotumour in a patient with type 3 von Willebrand disease.Gene conversions are a common cause of von Willebrand disease.Hemorrhagic symptoms and bleeding risk in obligatory carriers of type 3 von Willebrand disease: an international, multicenter study.A common 253-kb deletion involving VWF and TMEM16B in German and Italian patients with severe von Willebrand disease type 3
P2860
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P2860
Genetic heterogeneity of severe von Willebrand disease type III in the German population.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Genetic heterogeneity of severe von Willebrand disease type III in the German population.
@en
Genetic heterogeneity of severe von Willebrand disease type III in the German population.
@nl
type
label
Genetic heterogeneity of severe von Willebrand disease type III in the German population.
@en
Genetic heterogeneity of severe von Willebrand disease type III in the German population.
@nl
prefLabel
Genetic heterogeneity of severe von Willebrand disease type III in the German population.
@en
Genetic heterogeneity of severe von Willebrand disease type III in the German population.
@nl
P2093
P356
P1433
P1476
Genetic heterogeneity of severe von Willebrand disease type III in the German population.
@en
P2093
F Bergmann
R Schneppenheim
P2888
P304
P356
10.1007/BF00206958
P577
1994-12-01T00:00:00Z
P6179
1013480210