Heart failure and pulmonary arteriovenous malformations in a patient with hereditary hemorrhagic telangiectasia type 2.

about

Heart failure and pulmonary arteriovenous malformations in a patient with hereditary hemorrhagic telangiectasia type 2.

Item

http://www.wikidata.org/entity/Q50998123

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh-hant

name

Heart failure and pulmonary ar ...... rrhagic telangiectasia type 2.

@en

Heart failure and pulmonary ar ...... rrhagic telangiectasia type 2.

@nl

type

Item

label

Heart failure and pulmonary ar ...... rrhagic telangiectasia type 2.

@en

Heart failure and pulmonary ar ...... rrhagic telangiectasia type 2.

@nl

prefLabel

Heart failure and pulmonary ar ...... rrhagic telangiectasia type 2.

@en

Heart failure and pulmonary ar ...... rrhagic telangiectasia type 2.

@nl

P1476

Heart failure and pulmonary ar ...... rrhagic telangiectasia type 2.

@en

P2093

Jing Huang

http://www.w3.org/2001/XMLSchema#string

Juan Du

http://www.w3.org/2001/XMLSchema#string

Lin Liu

http://www.w3.org/2001/XMLSchema#string

Sha Li

http://www.w3.org/2001/XMLSchema#string

Xiao-Hua Luo

http://www.w3.org/2001/XMLSchema#string

Yan Zhu

http://www.w3.org/2001/XMLSchema#string

Yu-Lin Zhang

http://www.w3.org/2001/XMLSchema#string

P2860

Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia

Identification of BMP9 and BMP10 as functional activators of the orphan activin receptor-like kinase 1 (ALK1) in endothelial cells

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

A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5

Endoglin and activin receptor-like-kinase 1 are co-expressed in the distal vessels of the lung: implications for two familial vascular dysplasias, HHT and PAH.

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

International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia.

Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia.

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

A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12.

P2888

s11239-015-1253-z

P304

515-519

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1007/S11239-015-1253-Z

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2015-08-06T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

26245826

http://www.w3.org/2001/XMLSchema#string

P921

arteriovenous malformation

heart failure

hereditary hemorrhagic telangiectasia