Using Omics to Understand and Treat Pulmonary Vascular Disease.

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Using Omics to Understand and Treat Pulmonary Vascular Disease.

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2018 nî lūn-bûn

@nan

2018年の論文

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2018年学术文章

@wuu

2018年学术文章

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2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

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2018年學術文章

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name

Using Omics to Understand and Treat Pulmonary Vascular Disease.

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Using Omics to Understand and Treat Pulmonary Vascular Disease.

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Item

label

Using Omics to Understand and Treat Pulmonary Vascular Disease.

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Using Omics to Understand and Treat Pulmonary Vascular Disease.

@nl

prefLabel

Using Omics to Understand and Treat Pulmonary Vascular Disease.

@en

Using Omics to Understand and Treat Pulmonary Vascular Disease.

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P1476

Using Omics to Understand and Treat Pulmonary Vascular Disease.

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P2093

Anna R Hemnes

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P2860

Ivacaftor for the treatment of patients with cystic fibrosis and the G551D mutation: a systematic review and cost-effectiveness analysis

Gene expression patterns in the lungs of patients with primary pulmonary hypertension: a gene microarray analysis

Initial Use of Ambrisentan plus Tadalafil in Pulmonary Arterial Hypertension

Clinical classification of pulmonary hypertension.

Gene expression in BMPR2 mutation carriers with and without evidence of pulmonary arterial hypertension suggests pathways relevant to disease penetrance

Identifying "super responders" in pulmonary arterial hypertension.

Shorter survival in familial versus idiopathic pulmonary arterial hypertension is associated with hemodynamic markers of impaired right ventricular function

BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertension.

An evaluation of long-term survival from time of diagnosis in pulmonary arterial hypertension from the REVEAL Registry.

Mutation in the gene for bone morphogenetic protein receptor II as a cause of primary pulmonary hypertension in a large kindred.

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157

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scholarly article

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10.3389/FMED.2018.00157

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2018-05-24T00:00:00Z

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29881726

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5976753

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