Endoglin germline mutation in a patient with hereditary haemorrhagic telangiectasia and dexfenfluramine associated pulmonary arterial hypertension.

Chaouat, A; Coulet, F; Favre, C; Simonneau, G; Weitzenblum, E; Soubrier, F; Humbert, M

Chaouat, A; Coulet, F; Favre, C; Simonneau, G; Weitzenblum, E; Soubrier, F; Humbert, M.

Affiliation

Chaouat A; Service de Pneumologie, Hôpital de Hautepierre, Strasbourg, France. ari.chaouat@chru-strasbourg.fr

Thorax ; 59(5): 446-8, 2004 May.

Article in En | MEDLINE | ID: mdl-15115879

Subject(s)

Dexfenfluramine/adverse effects; Germ-Line Mutation/genetics; Hypertension, Pulmonary/chemically induced; Serotonin Receptor Agonists/adverse effects; Telangiectasia, Hereditary Hemorrhagic/genetics; Vascular Cell Adhesion Molecule-1/genetics; Adult; Antigens, CD; Endoglin; Female; Gene Deletion; Heterozygote; Humans; Pedigree; Receptors, Cell Surface

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Telangiectasia, Hereditary Hemorrhagic / Serotonin Receptor Agonists / Germ-Line Mutation / Vascular Cell Adhesion Molecule-1 / Dexfenfluramine / Hypertension, Pulmonary Type of study: Risk_factors_studies Limits: Adult / Female / Humans Language: En Journal: Thorax Year: 2004 Document type: Article Affiliation country: France Country of publication: United kingdom

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