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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1964 5
1994 1
1997 1
1998 4
2000 3
2001 9
2002 5
2003 6
2004 4
2005 6
2006 4
2007 2
2009 3
2010 19
2011 83
2012 73
2013 134
2014 50
2015 2
2016 6
2017 10
2018 10
2019 6
2020 7
2021 21
2022 32
2023 45
2024 15

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524 results

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Page 1
Pulmonary Hypertension: A Contemporary Review.
Johnson S, Sommer N, Cox-Flaherty K, Weissmann N, Ventetuolo CE, Maron BA. Johnson S, et al. Am J Respir Crit Care Med. 2023 Sep 1;208(5):528-548. doi: 10.1164/rccm.202302-0327SO. Am J Respir Crit Care Med. 2023. PMID: 37450768 Review.
Major advances in pulmonary arterial hypertension, pulmonary hypertension (PH) associated with lung disease, and chronic thromboembolic PH cast new light on the pathogenetic mechanisms, epidemiology, diagnostic approach, and therapeutic armamentarium f …
Major advances in pulmonary arterial hypertension, pulmonary hypertension (PH) associated with lung disease, and …
Pulmonary hypertension associated with lung disease: new insights into pathomechanisms, diagnosis, and management.
Olsson KM, Corte TJ, Kamp JC, Montani D, Nathan SD, Neubert L, Price LC, Kiely DG. Olsson KM, et al. Lancet Respir Med. 2023 Sep;11(9):820-835. doi: 10.1016/S2213-2600(23)00259-X. Epub 2023 Aug 14. Lancet Respir Med. 2023. PMID: 37591300 Review.
The pulmonary vasculopathy is distinct from that of other forms of pulmonary hypertension, with vascular ablation due to loss of small pulmonary vessels being a key feature. ...Most drugs approved for pulmonary arterial hypertension have …
The pulmonary vasculopathy is distinct from that of other forms of pulmonary hypertension, with vascular ablation due t …
Treatment of pulmonary arterial hypertension: recent progress and a look to the future.
Humbert M, Sitbon O, Guignabert C, Savale L, Boucly A, Gallant-Dewavrin M, McLaughlin V, Hoeper MM, Weatherald J. Humbert M, et al. Lancet Respir Med. 2023 Sep;11(9):804-819. doi: 10.1016/S2213-2600(23)00264-3. Epub 2023 Aug 14. Lancet Respir Med. 2023. PMID: 37591298 Review.
Pulmonary arterial hypertension (PAH) is a severe but treatable form of pre-capillary pulmonary hypertension caused by pulmonary vascular remodelling. ...In considering future directions for the field, our ambition is to identify therapies with
Pulmonary arterial hypertension (PAH) is a severe but treatable form of pre-capillary pulmonary hypertension cau
The physiological basis of pulmonary arterial hypertension.
Naeije R, Richter MJ, Rubin LJ. Naeije R, et al. Eur Respir J. 2022 Jun 16;59(6):2102334. doi: 10.1183/13993003.02334-2021. Print 2022 Jun. Eur Respir J. 2022. PMID: 34737219 Free PMC article. Review.
Pulmonary arterial hypertension (PAH) is a rare dyspnoea-fatigue syndrome caused by a progressive increase in pulmonary vascular resistance and eventual right ventricular (RV) failure. ...Exercise limitation in PAH is cardiovascular rather than ventilatory or
Pulmonary arterial hypertension (PAH) is a rare dyspnoea-fatigue syndrome caused by a progressive increase in pulmonary
Endothelial cells in the pathogenesis of pulmonary arterial hypertension.
Evans CE, Cober ND, Dai Z, Stewart DJ, Zhao YY. Evans CE, et al. Eur Respir J. 2021 Sep 2;58(3):2003957. doi: 10.1183/13993003.03957-2020. Print 2021 Sep. Eur Respir J. 2021. PMID: 33509961 Free PMC article. Review.
Pulmonary arterial hypertension (PAH) is a devastating disease that involves pulmonary vasoconstriction, small vessel obliteration, large vessel thickening and obstruction, and development of plexiform lesions. PAH vasculopathy leads to progressive increases
Pulmonary arterial hypertension (PAH) is a devastating disease that involves pulmonary vasoconstriction, small vessel o
2013 classification criteria for systemic sclerosis: an American college of rheumatology/European league against rheumatism collaborative initiative.
van den Hoogen F, Khanna D, Fransen J, Johnson SR, Baron M, Tyndall A, Matucci-Cerinic M, Naden RP, Medsger TA Jr, Carreira PE, Riemekasten G, Clements PJ, Denton CP, Distler O, Allanore Y, Furst DE, Gabrielli A, Mayes MD, van Laar JM, Seibold JR, Czirjak L, Steen VD, Inanc M, Kowal-Bielecka O, Müller-Ladner U, Valentini G, Veale DJ, Vonk MC, Walker UA, Chung L, Collier DH, Ellen Csuka M, Fessler BJ, Guiducci S, Herrick A, Hsu VM, Jimenez S, Kahaleh B, Merkel PA, Sierakowski S, Silver RM, Simms RW, Varga J, Pope JE. van den Hoogen F, et al. Ann Rheum Dis. 2013 Nov;72(11):1747-55. doi: 10.1136/annrheumdis-2013-204424. Ann Rheum Dis. 2013. PMID: 24092682 Free article.
RESULTS: It was determined that skin thickening of the fingers extending proximal to the metacarpophalangeal joints is sufficient for the patient to be classified as having SSc; if that is not present, seven additive items apply, with varying weights for each: skin thickening of …
RESULTS: It was determined that skin thickening of the fingers extending proximal to the metacarpophalangeal joints is sufficient for the pa …
Systemic Lupus Erythematosus and Pulmonary Hypertension.
Parperis K, Velidakis N, Khattab E, Gkougkoudi E, Kadoglou NPE. Parperis K, et al. Int J Mol Sci. 2023 Mar 7;24(6):5085. doi: 10.3390/ijms24065085. Int J Mol Sci. 2023. PMID: 36982160 Free PMC article. Review.
Pulmonary Hypertension (PH) is a common manifestation in patients with Systemic Lupus Erythematosus (SLE) and varies from asymptomatic to life-threatening disease. ...Prompt diagnosis of SLE-related PH and early identification of the underlying pathogenetic mechanis
Pulmonary Hypertension (PH) is a common manifestation in patients with Systemic Lupus Erythematosus (SLE) and varies from asym
Targeted therapies in pulmonary arterial hypertension.
Montani D, Chaumais MC, Guignabert C, Günther S, Girerd B, Jaïs X, Algalarrondo V, Price LC, Savale L, Sitbon O, Simonneau G, Humbert M. Montani D, et al. Pharmacol Ther. 2014 Feb;141(2):172-91. doi: 10.1016/j.pharmthera.2013.10.002. Epub 2013 Oct 14. Pharmacol Ther. 2014. PMID: 24134901 Free article. Review.
Pulmonary arterial hypertension (PAH) is a rare disorder characterized by progressive obliteration of small pulmonary arteries that leads to elevated pulmonary arterial pressure and right heart failure. ...
Pulmonary arterial hypertension (PAH) is a rare disorder characterized by progressive obliteration of small pulmonary a
New Drugs and Therapies in Pulmonary Arterial Hypertension.
Shah AJ, Beckmann T, Vorla M, Kalra DK. Shah AJ, et al. Int J Mol Sci. 2023 Mar 19;24(6):5850. doi: 10.3390/ijms24065850. Int J Mol Sci. 2023. PMID: 36982922 Free PMC article. Review.
Pulmonary arterial hypertension is a chronic, progressive disorder of the pulmonary vasculature with associated pulmonary and cardiac remodeling. ...
Pulmonary arterial hypertension is a chronic, progressive disorder of the pulmonary vasculature with associated pulm
Mechanisms of disease: pulmonary arterial hypertension.
Schermuly RT, Ghofrani HA, Wilkins MR, Grimminger F. Schermuly RT, et al. Nat Rev Cardiol. 2011 Jun 21;8(8):443-55. doi: 10.1038/nrcardio.2011.87. Nat Rev Cardiol. 2011. PMID: 21691314 Free PMC article. Review.
Our understanding of, and approach to, pulmonary arterial hypertension has undergone a paradigm shift in the past decade. Once a condition thought to be dominated by increased vasoconstrictor tone and thrombosis, pulmonary arterial hypertension is now …
Our understanding of, and approach to, pulmonary arterial hypertension has undergone a paradigm shift in the past decade. Once …
524 results