Clinical manifestations in a large hereditary hemorrhagic telangiectasia (HHT) type 2 kindred.
about
Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasiaALK5- and TGFBR2-independent role of ALK1 in the pathogenesis of hereditary hemorrhagic telangiectasia type 2Real-time imaging of de novo arteriovenous malformation in a mouse model of hereditary hemorrhagic telangiectasia.Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: data from the French-Italian HHT network.A retrospective analysis of low dose, intranasal injected bevacizumab (Avastin) in hereditary haemorrhagic telangiectasia.Optimal management of hereditary hemorrhagic telangiectasia.The pathobiology of vascular malformations: insights from human and model organism genetics.A case report of a patient with hereditary hemorrhagic telangiectasia treated successively with thalidomide and bevacizumabHereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century.Visceral manifestations in hereditary haemorrhagic telangiectasia type 2Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations.Fishing for novel angiogenic therapies.Hereditary hemorrhagic telangiectasia: an overview of diagnosis and management in the molecular era for clinicians.A long diagnostic delay in patients with Hereditary Haemorrhagic Telangiectasia: a questionnaire-based retrospective studyHereditary Haemorrhagic Telangiectasia Cerebrospinal Localization in Adults and Children. Review of 39 cases.The 'sweet' and 'bitter' involvement of glycosaminoglycans in lung diseases: pharmacotherapeutic relevance.Arteriovenous malformations in hereditary haemorrhagic telangiectasia: looking beyond ALK1-NOTCH interactions.How to identify pediatric cerebral and pulmonary arteriovenous malformation earlier: non-hereditary hemorrhagic telangiectasia case.Disease-associated mutations in conserved residues of ALK-1 kinase domain.Molecular screening of ALK1/ACVRL1 and ENG genes in hereditary hemorrhagic telangiectasia in France.Impact of genotype and mutation type on health-related quality of life in patients with hereditary hemorrhagic telangiectasia.
P2860
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P2860
Clinical manifestations in a large hereditary hemorrhagic telangiectasia (HHT) type 2 kindred.
description
2000 nî lūn-bûn
@nan
2000 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Clinical manifestations in a l ...... iectasia (HHT) type 2 kindred.
@ast
Clinical manifestations in a l ...... iectasia (HHT) type 2 kindred.
@en
Clinical manifestations in a large hereditary hemorrhagic telangiectasia
@nl
type
label
Clinical manifestations in a l ...... iectasia (HHT) type 2 kindred.
@ast
Clinical manifestations in a l ...... iectasia (HHT) type 2 kindred.
@en
Clinical manifestations in a large hereditary hemorrhagic telangiectasia
@nl
prefLabel
Clinical manifestations in a l ...... iectasia (HHT) type 2 kindred.
@ast
Clinical manifestations in a l ...... iectasia (HHT) type 2 kindred.
@en
Clinical manifestations in a large hereditary hemorrhagic telangiectasia
@nl
P2093
P2860
P1476
Clinical manifestations in a l ...... iectasia (HHT) type 2 kindred.
@en
P2093
P2860
P304
P356
10.1002/1096-8628(20000814)93:4<320::AID-AJMG12>3.0.CO;2-R
P577
2000-08-01T00:00:00Z