(Q36500518)

14 August 2017

Mutations of von Willebrand factor gene in families with von Willebrand disease in the Aland Islands (English)

1 reference

14 August 2017

Zhang ZP

1

1 reference

14 August 2017

Blombäck M

series ordinal

2

1 reference

14 August 2017

Nyman D

series ordinal

3

1 reference

14 August 2017

Anvret M

series ordinal

4

1 reference

14 August 2017

language of work or name

English

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publication date

1 September 1993

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Proceedings of the National Academy of Sciences of the United States of America

14 August 2017

1 reference

14 August 2017

90

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14 August 2017

17

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14 August 2017

7937-7940

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Structure of the gene for human von Willebrand factor

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=47262

Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand disease type III and type I

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=47262

Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=47262

Dinucleotide repeat polymorphism in the promoter region of the human von Willebrand factor gene (vWF gene)

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=47262

A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=47262

On an inherited autosomal hemorrhagic diathesis with antihemophilic globulin (AHG) deficiency and prolonged bleeding time.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=47262

Inherited defective platelet aggregation with arachidonate as the main expression of a defective metabolism of arachidonic acid

21 September 2018

1 reference

12 December 2020

v. Willebrand's disease in Sweden; its pathogenesis and treatment

1 reference

12 December 2020

Influence of age, sex and blood groups on 15 blood coagulation laboratory variables in a reference material composed of 80 blood donors

1 reference

12 December 2020

On laboratory problems in diagnosing mild von Willebrand's disease

1 reference

12 December 2020

Genetic and blood coagulation characterization of "Swedish" families with von Willebrand's disease types I and III: new aspects of heredity

1 reference

12 December 2020

[On Willebrand-Jürgens constitutional thrombopathy in the Aland Islands.]

1 reference

12 December 2020

Von Willebrand's disease and its correction with human plasma fraction 1-0

1 reference

12 December 2020

Studies on antihemophilic globulin

1 reference

12 December 2020

[Antihemophilic globulin (factor VIII) deficiency in Aland (Willebrand-Jürgens) thrombopathy.]

1 reference

12 December 2020

[Willebrand's disease. Clinical, genetic and biological study (apropos of 22 cases)]

1 reference

12 December 2020

Pseudohemophilia type B; hereditary hemorrhagic diathesis characterized by prolonged bleeding time and decrease in antihemophilic factor

1 reference

12 December 2020

Recent investigations of the first bleeder family in Aland (Finland) described by von Willebrand

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.90.17.7937

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14 August 2017

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1 reference

14 August 2017

PubMed publication ID

8367445

1 reference