Pulmonary arteriovenous malformations and migraine: a new vision. - Wikidata - awgldk - TriplyDB

Pulmonary arteriovenous malformations and migraine: a new vision.

Pulmonary arteriovenous malformations and migraine: a new vision.

http://www.wikidata.org/entity/Q37168913

about

Hereditary hemorrhagic telangiectasia: an overview of diagnosis, management, and pathogenesis Optimal management of hereditary hemorrhagic telangiectasia.Headache and cardiovascular disease: old symptoms, new proposals.Asymptomatic pulmonary arteriovenous malformations in children with hereditary hemorrhagic telangiectasia.

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Pulmonary arteriovenous malformations and migraine: a new vision.

http://www.wikidata.org/entity/Q37168913

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 20 May 2008

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Pulmonary arteriovenous malformations and migraine: a new vision.

@en

Pulmonary arteriovenous malformations and migraine: a new vision.

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type

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Pulmonary arteriovenous malformations and migraine: a new vision.

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Pulmonary arteriovenous malformations and migraine: a new vision.

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prefLabel

Pulmonary arteriovenous malformations and migraine: a new vision.

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Pulmonary arteriovenous malformations and migraine: a new vision.

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Pulmonary arteriovenous malformations and migraine: a new vision.

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C J J Westermann

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H W M Plokker

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J J Mager

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M C Post

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M W F van Gent

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R J Snijder

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W J Schonewille

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P2860

Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

Aspirin is efficacious for the treatment of acute migraine

Risk of ischaemic stroke in people with migraine: systematic review and meta-analysis of observational studies.

Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).

Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.

Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century.

Embolotherapy of pulmonary arteriovenous malformations: long-term results in 112 patients.

Migraine, headache, and the risk of stroke in women: a prospective study.

Pulmonary vascular manifestations of hereditary hemorrhagic telangiectasia (rendu-osler disease).

Neurological manifestations of hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease): report of 2 cases and review of the literature.

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228-233

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10.1159/000134011

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2

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2008-05-20T00:00:00Z

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P921

migraine disorder

arteriovenous malformation

pulmonary arteriovenous malformations