(Q45886373)

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Appendix II: A revised classification of Von Willebrand disease*: For The Subcommittee on Von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis

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17 December 2017

http://europepmc.org/abstract/MED/27213751

Appendix II: A revised classification of Von Willebrand disease*: For The Subcommittee on Von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis (English)

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17 December 2017

http://europepmc.org/abstract/MED/27213751

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author name string

J E Sadler

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17 December 2017

http://europepmc.org/abstract/MED/27213751

publication date

1 July 1997

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Europe PubMed Central

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17 December 2017

http://europepmc.org/abstract/MED/27213751

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Europe PubMed Central

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17 December 2017

http://europepmc.org/abstract/MED/27213751

3 Suppl 2

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11-18

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17 December 2017

http://europepmc.org/abstract/MED/27213751

Genetic Variants of von Willebrand's Disease

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

A variant of factor 8 related antigen

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

Platelet aggregation induced by 1-desamino-8-D-arginine vasopressin (DDAVP) in Type IIB von Willebrand's disease

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

Structure and function of von Willebrand factor: relationship to von Willebrand's disease

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

International system for human gene nomenclature (1979) ISGN (1979).

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

Pseudo-von Willebrand's disease. An intrinsic platelet defect with aggregation by unmodified human factor VIII/von Willebrand factor and enhanced adsorption of its high-molecular-weight multimers

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

Apparent ‘dominant’ and ‘recessive’ inheritance of von Willebrand's disease within the same kindreds. Possible biochemical mechanisms

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

Aberrant multimeric structure of von Willebrand factor in a new variant of von Willebrand's disease (type IIC)

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

Investigation of a kindred with a new autosomal dominantly inherited variant type von Willebrand's disease (possible type IID).

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

Subunit composition of plasma von Willebrand factor. Cleavage is present in normal individuals, increased in IIA and IIB von Willebrand disease, but minimal in variants with aberrant structure of individual oligomers (types IIC, IID, and IIE).

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

Type II H von Willebrand disease: new structural abnormality of plasma and platelet von Willebrand factor in a patient with prolonged bleeding time and borderline levels of ristocetin cofactor activity

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

von Willebrand disease type B: a missense mutation selectively abolishes ristocetin-induced von Willebrand factor binding to platelet glycoprotein Ib

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

The human von Willebrand factor gene. Structure of the 5' region

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

The human gene for von Willebrand factor. Identification of repetitive Alu sequences 5' to the transcription initiation site

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

Clinical indications for desmopressin (DDAVP) in congenital and acquired von Willebrand disease

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

Further evidence for recessive inheritance of von Willebrand disease with abnormal binding of von Willebrand factor to factor VIII

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

IIB von Willebrand's disease: pathogenetic and therapeutic studies

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

Evidence for a von Willebrand factor defect in factor VIII binding in three members of a family previously misdiagnosed mild haemophilia A and haemophilia A carriers: consequences for therapy and genetic counselling

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.1997.TB00175.X

21 January 2018

Identifiers

10.1111/J.1365-2516.1997.TB00175.X

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/27213751

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/27213751

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