(Q46704794)

24 December 2017

title

Clinical symptoms according to genotype amongst patients with hereditary haemorrhagic telangiectasia (English)

1 reference

24 December 2017

author

Klaus Brusgaard

3

1 reference

24 December 2017

author name string

A D Kjeldsen

1

1 reference

24 December 2017

T R Møller

2

1 reference

24 December 2017

P Vase

4

1 reference

24 December 2017

P E Andersen

5

1 reference

24 December 2017

language of work or name

English

0 references

publication date

1 October 2005

1 reference

24 December 2017

Journal of Internal Medicine

published in

1 reference

24 December 2017

volume

258

1 reference

24 December 2017

issue

4

1 reference

24 December 2017

page(s)

349-355

1 reference

24 December 2017

Should asymptomatic patients with hereditary haemorrhagic telangiectasia (HHT) be screened for cerebral vascular malformations? Data from 22,061 years of HHT patient life

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2005.01555.X

Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2005.01555.X

A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2005.01555.X

Hereditary haemorrhagic telangiectasia: a population-based study of prevalence and mortality in Danish patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2005.01555.X

Pulmonary arteriovenous malformations: screening procedures and pulmonary angiography in patients with hereditary hemorrhagic telangiectasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2005.01555.X

Mutations in endoglin and in activin receptor-like kinase 1 among Danish patients with hereditary haemorrhagic telangiectasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2005.01555.X

Cerebral symptoms in pulmonary arteriovenous fistula. A result of paradoxical emboli (?).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2005.01555.X

Visceral manifestations in hereditary haemorrhagic telangiectasia type 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2005.01555.X

10.1111/J.1365-2796.2005.01555.X

21 January 2018

Identifiers

DOI

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/rwwk5lnhnrgpfcj7p7v6udtiw4

mapped directly with Wikidata item

30 July 2022

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Fatcat ID

release_rwwk5lnhnrgpfcj7p7v6udtiw4

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/rwwk5lnhnrgpfcj7p7v6udtiw4

mapped directly with Wikidata item

30 July 2022

based on heuristic

https://api.fatcat.wiki/v0/release/rwwk5lnhnrgpfcj7p7v6udtiw4

1 reference