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

Year Number of Results
1934 1
1948 2
1949 3
1950 1
1951 2
1952 5
1953 8
1954 3
1955 5
1956 8
1957 11
1958 27
1959 16
1960 14
1961 9
1962 6
1963 15
1964 16
1965 17
1966 18
1967 10
1968 15
1969 19
1970 19
1971 18
1972 30
1973 27
1974 25
1975 71
1976 78
1977 71
1978 78
1979 90
1980 100
1981 104
1982 115
1983 125
1984 161
1985 164
1986 160
1987 175
1988 196
1989 233
1990 199
1991 230
1992 215
1993 217
1994 206
1995 239
1996 232
1997 253
1998 224
1999 206
2000 241
2001 239
2002 270
2003 305
2004 429
2005 552
2006 619
2007 685
2008 742
2009 818
2010 923
2011 999
2012 1107
2013 1273
2014 1384
2015 1419
2016 1493
2017 1532
2018 1586
2019 1590
2020 1804
2021 1940
2022 1896
2023 1754
2024 1827
2025 801

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29,558 results

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Page 1
Diagnosis and Treatment of Pulmonary Arterial Hypertension: A Review.
Ruopp NF, Cockrill BA. Ruopp NF, et al. JAMA. 2022 Apr 12;327(14):1379-1391. doi: 10.1001/jama.2022.4402. JAMA. 2022. PMID: 35412560 Review.
IMPORTANCE: Pulmonary arterial hypertension (PAH) is a subtype of pulmonary hypertension (PH), characterized by pulmonary arterial remodeling. ...Pulmonary arterial hypertension is 1 of the 5 groups of PH and i …
IMPORTANCE: Pulmonary arterial hypertension (PAH) is a subtype of pulmonary hypertension (PH), characteri …
Pulmonary arterial hypertension.
Luna-López R, Ruiz Martín A, Escribano Subías P. Luna-López R, et al. Med Clin (Barc). 2022 Jun 24;158(12):622-629. doi: 10.1016/j.medcli.2022.01.003. Epub 2022 Mar 9. Med Clin (Barc). 2022. PMID: 35279313 Review. English, Spanish.
Pulmonary arterial hypertension (PAH) is a rare disease characterized by adverse remodeling of the arterial tree leading to increased vascular resistance with subsequent increase in right ventricular afterload and eventual development of heart failure.
Pulmonary arterial hypertension (PAH) is a rare disease characterized by adverse remodeling of the arterial tree
Pulmonary Arterial Hypertension.
Hassoun PM. Hassoun PM. N Engl J Med. 2021 Dec 16;385(25):2361-2376. doi: 10.1056/NEJMra2000348. N Engl J Med. 2021. PMID: 34910865 Review. No abstract available.
Contemporary Treatment of Pulmonary Arterial Hypertension: A U.S. Perspective.
Sahay S, Chakinala MM, Kim NH, Preston IR, Thenappan T, Mclaughlin VV. Sahay S, et al. Am J Respir Crit Care Med. 2024 Sep 1;210(5):581-592. doi: 10.1164/rccm.202405-0914SO. Am J Respir Crit Care Med. 2024. PMID: 38984912 Review.
Pulmonary arterial hypertension (PAH) is a complex fatal condition that requires aggressive treatment with close monitoring. ...
Pulmonary arterial hypertension (PAH) is a complex fatal condition that requires aggressive treatment with close monito
Paediatric pulmonary arterial hypertension: updates on definition, classification, diagnostics and management.
Rosenzweig EB, Abman SH, Adatia I, Beghetti M, Bonnet D, Haworth S, Ivy DD, Berger RMF. Rosenzweig EB, et al. Eur Respir J. 2019 Jan 24;53(1):1801916. doi: 10.1183/13993003.01916-2018. Print 2019 Jan. Eur Respir J. 2019. PMID: 30545978 Free PMC article. Review.
Paediatric pulmonary arterial hypertension (PAH) shares common features of adult disease, but is associated with several additional disorders and challenges that require unique approaches. This article discusses recent advances, ongoing challenges and distinc …
Paediatric pulmonary arterial hypertension (PAH) shares common features of adult disease, but is associated with severa …
Pulmonary arterial hypertension.
Boucly A, Gerges C, Savale L, Jaïs X, Jevnikar M, Montani D, Sitbon O, Humbert M. Boucly A, et al. Presse Med. 2023 Sep;52(3):104168. doi: 10.1016/j.lpm.2023.104168. Epub 2023 Jul 28. Presse Med. 2023. PMID: 37516248 Review.
Pulmonary arterial hypertension (PAH) is a rare and progressive disease characterised by remodelling of the pulmonary arteries and progressive narrowing of the pulmonary vasculature. This leads to a progressive increase in pulmonary vascu
Pulmonary arterial hypertension (PAH) is a rare and progressive disease characterised by remodelling of the pulmonar
Pulmonary Arterial Hypertension: Diagnosis, Treatment, and Novel Advances.
Maron BA, Abman SH, Elliott CG, Frantz RP, Hopper RK, Horn EM, Nicolls MR, Shlobin OA, Shah SJ, Kovacs G, Olschewski H, Rosenzweig EB. Maron BA, et al. Am J Respir Crit Care Med. 2021 Jun 15;203(12):1472-1487. doi: 10.1164/rccm.202012-4317SO. Am J Respir Crit Care Med. 2021. PMID: 33861689 Free PMC article.
The diagnosis and management of pulmonary arterial hypertension (PAH) includes several advances, such as a broader recognition of extrapulmonary vascular organ system involvement, validated point-of-care clinical assessment tools, and focus on the early initi …
The diagnosis and management of pulmonary arterial hypertension (PAH) includes several advances, such as a broader reco …
Perivascular Inflammation in Pulmonary Arterial Hypertension.
Hu Y, Chi L, Kuebler WM, Goldenberg NM. Hu Y, et al. Cells. 2020 Oct 22;9(11):2338. doi: 10.3390/cells9112338. Cells. 2020. PMID: 33105588 Free PMC article. Review.
Perivascular inflammation is a prominent pathologic feature in most animal models of pulmonary hypertension (PH) as well as in pulmonary arterial hypertension (PAH) patients. Accumulating evidence suggests a functional role of perivascular infla …
Perivascular inflammation is a prominent pathologic feature in most animal models of pulmonary hypertension (PH) as well as in …
Pediatric Pulmonary Arterial Hypertension.
Frank BS, Ivy DD. Frank BS, et al. Pediatr Clin North Am. 2020 Oct;67(5):903-921. doi: 10.1016/j.pcl.2020.06.005. Pediatr Clin North Am. 2020. PMID: 32888689 Review.
Pulmonary hypertension (PH), the syndrome of increased pressure in the pulmonary arteries, is associated with significant morbidity and mortality for affected children and is associated with a variety of potential underlying causes. Several pulmonary
Pulmonary hypertension (PH), the syndrome of increased pressure in the pulmonary arteries, is associated with significa
Evaluation and management of pulmonary arterial hypertension.
Beshay S, Sahay S, Humbert M. Beshay S, et al. Respir Med. 2020 Sep;171:106099. doi: 10.1016/j.rmed.2020.106099. Epub 2020 Aug 19. Respir Med. 2020. PMID: 32829182 Free article. Review.
Pulmonary arterial hypertension is a devastating progressive disease mediated by different pathophysiologic pathways that result in progressive increase in pulmonary vascular resistance along with right ventricular failure and eventually premature deat
Pulmonary arterial hypertension is a devastating progressive disease mediated by different pathophysiologic pathways th
29,558 results
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