Pulmonary Arterial Hypertension-Reference-Cited by-同舟云学术

Pulmonary Arterial Hypertension

Published:2004-06-22 Issue:24 Volume:109 Page:2947-2952
ISSN:0009-7322
Container-title:Circulation
language:en
Short-container-title:Circulation

Author:

Newman John H.¹,Fanburg Barry L.¹,Archer Stephen L.¹,Badesch David B.¹,Barst Robyn J.¹,Garcia Joe G.N.¹,Kao Peter N.¹,Knowles James A.¹,Loyd James E.¹,McGoon Michael D.¹,Morse Jane H.¹,Nichols William C.¹,Rabinovitch Marlene¹,Rodman David M.¹,Stevens Troy¹,Tuder Rubin M.¹,Voelkel Norbert F.¹,Gail Dorothy B.¹

Affiliation:

1. From the Departments of Medicine, Nashville VA Medical Center (GRECC), and Vanderbilt University, Nashville, Tenn (J.H.N., J.E.L.); Department of Medicine, New England Medical Center, Boston, Mass (B.L.F.); Division of Cardiology, University of Alberta Hospital, Edmonton, Alberta, Canada (S.L.A.); Department of Medicine, University of Colorado Health Science Center, Denver, Colo (D.B.B., D.M.R., N.F.V.); Pulmonary Hypertension Center (R.J.B.) and Department of Medicine (J.A.K., J.M.), Columbia...

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Link

https://www.ahajournals.org/doi/pdf/10.1161/01.CIR.0000132476.87231.6F

Reference57 articles.

1. Familial Primary Pulmonary Hypertension (Gene PPH1) Is Caused by Mutations in the Bone Morphogenetic Protein Receptor–II Gene

2. Heterozygous germline mutations in BMPR2, encoding a TGF-β receptor, cause familial primary pulmonary hypertension

3. Clinical and Molecular Genetic Features of Pulmonary Hypertension in Patients with Hereditary Hemorrhagic Telangiectasia

4. Mutation in the Gene for Bone Morphogenetic Protein Receptor II as a Cause of Primary Pulmonary Hypertension in a Large Kindred

5. Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta family

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