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Volumn 21, Issue 6, 2010, Pages 334-337

Contemporary insights into the pathogenesis, diagnosis and therapy of pulmonary arterial hypertension

Author keywords

Mechanisms; Pulmonary hypertension; Therapy

Indexed keywords

AMBRISENTAN; BERAPROST; CALCIUM ANTAGONIST; DIGITALIS; DIHYDROPYRIDINE; DIURETIC AGENT; ENDOTHELIN RECEPTOR ANTAGONIST; ILOPROST; PHOSPHODIESTERASE V INHIBITOR; PROSTACYCLIN; PROSTANOID; SILDENAFIL; TADALAFIL; TRANSFORMING GROWTH FACTOR BETA RECEPTOR; WARFARIN;

EID: 78650801120     PISSN: 19951892     EISSN: None     Source Type: Journal    
DOI: 10.5830/CVJA-2010-088     Document Type: Review
Times cited : (12)

References (10)
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  • 2
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    • ACCF/AHA 2009 Expert Consensus Document on Pulmonary Hypertension - A Report of the American College of Cardiology Foundation Task Force on Expert Consensus Documents and the American Heart Association
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  • 3
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    • Guidelines for the Diagnosis and Treatment of Pulmonary Hypertension
    • The Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS) endorsed by the International Society of Heart and Lung Transplantation (ISHLT)
    • Guidelines for the Diagnosis and Treatment of Pulmonary Hypertension. The Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS) endorsed by the International Society of Heart and Lung Transplantation (ISHLT). Eur Heart J 2009; 30: 2493-2537.
    • (2009) Eur Heart J , vol.30 , pp. 2493-2537
  • 4
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  • 5
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    • Emerging concepts and translational priorities in pulmonary arterial hypertension
    • Michelakis ED, Wilkins MR, Rabinovitch M. Emerging concepts and translational priorities in pulmonary arterial hypertension. Circulation 2008; 118: 1486-1495.
    • (2008) Circulation , vol.118 , pp. 1486-1495
    • Michelakis, E.D.1    Wilkins, M.R.2    Rabinovitch, M.3
  • 6
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    • Heterozygous germ line mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension
    • Lane KB, Machado RD, Pauciulo MW, et al. Heterozygous germ line mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension. Nat Genet 2000; 26: 81-84.
    • (2000) Nat Genet , vol.26 , pp. 81-84
    • Lane, K.B.1    Machado, R.D.2    Pauciulo, M.W.3
  • 8
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    • Initial apoptosis is followed by increased proliferation of apoptosis -resistant endothelial cells
    • Sakoa S, Taraseviciene-Stewart L, Lee JD, et al. Initial apoptosis is followed by increased proliferation of apoptosis -resistant endothelial cells. FASEB J 2005; 19: 1178-1180.
    • (2005) FASEB J , vol.19 , pp. 1178-1180
    • Sakoa, S.1    Taraseviciene-Stewart, L.2    Lee, J.D.3
  • 9
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    • Uncertainties in the diagnosis and treatment of pulmonary arterial hypertension
    • Ghofrani HA, Wilkins MW, Rich S. Uncertainties in the diagnosis and treatment of pulmonary arterial hypertension. Circulation 2008; 118: 1195-1201.
    • (2008) Circulation , vol.118 , pp. 1195-1201
    • Ghofrani, H.A.1    Wilkins, M.W.2    Rich, S.3
  • 10
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    • Updated evidence-based treatment algorithm in pulmonary arterial hypertension
    • Barst RJ, Gibbs SR, Ghofrani HA, et al. Updated evidence-based treatment algorithm in pulmonary arterial hypertension. J Am Coll Cardiol 2009; 54: S78-84.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.