相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease
Paula D. James et al.
BLOOD ADVANCES (2021)
Characterization of large in-frame von Willebrand factor deletions highlights differing pathogenic mechanisms
Ashley Cartwright et al.
BLOOD ADVANCES (2020)
Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): comprehensive genetic analysis by next-generation sequencing of 480 patients
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THROMBOSIS RESEARCH (2017)
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MEDICINE (2016)
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NEW ENGLAND JOURNAL OF MEDICINE (2016)
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THROMBOSIS AND HAEMOSTASIS (2016)
von Willebrand factor propeptide and the phenotypic classification of von Willebrand disease
Yvonne V. Sanders et al.
BLOOD (2015)
von Willebrand factor biosynthesis, secretion, and clearance: connecting the far ends
Peter J. Lenting et al.
BLOOD (2015)
The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine
Peter D. Stenson et al.
HUMAN GENETICS (2014)
VWF propeptide and ratios between VWF, VWF propeptide, and FVIII in the characterization of type 1 von Willebrand disease
Jeroen Eikenboom et al.
BLOOD (2013)
Variation in the VWF Gene in Swedish Patients with Type 1 von Willebrand Disease
Anna M. Johansson et al.
ANNALS OF HUMAN GENETICS (2011)
Expanded phenotype-genotype correlations in a pediatric population with type 1 von Willebrand disease
J. D. Robertson et al.
JOURNAL OF THROMBOSIS AND HAEMOSTASIS (2011)
Management of Inherited von Willebrand Disease in Italy: Results from the Retrospective Study on 1234 Patients
Augusto B. Federici et al.
SEMINARS IN THROMBOSIS AND HEMOSTASIS (2011)
Health-related quality of life among adult patients with moderate and severe von Willebrand disease
E. M. de Wee et al.
JOURNAL OF THROMBOSIS AND HAEMOSTASIS (2010)
Reduced von Willebrand factor survival in von Willebrand disease: pathophysiologic and clinical relevance
G. Castaman et al.
JOURNAL OF THROMBOSIS AND HAEMOSTASIS (2009)
An assessment of the pathogenic significance of the R924Q von Willebrand factor substitution
E. Berber et al.
JOURNAL OF THROMBOSIS AND HAEMOSTASIS (2009)
Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: Molecular and Clinical Markers for the Diagnosis and Management of Type 1 VWD (MCMDM-1VWD)
Sandra L. Haberichter et al.
BLOOD (2008)
Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD)
U. Budde et al.
JOURNAL OF THROMBOSIS AND HAEMOSTASIS (2008)
The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort study
Paula D. James et al.
BLOOD (2007)
Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)
Anne Goodeve et al.
BLOOD (2007)
Assay of the von Willebrand factor (VWF) propeptide to identify patients with type 1 von Willebrand disease with decreased VWF survival
Sandra L. Haberichter et al.
BLOOD (2006)
An investigation of the von Willebrand factor genotype in UK patients diagnosed to have type I von Willebrand disease
Anthony Cumming et al.
THROMBOSIS AND HAEMOSTASIS (2006)