Familial Primary Pulmonary Hypertension
"Familial Primary Pulmonary Hypertension" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Familial or idiopathic hypertension in the PULMONARY CIRCULATION which is not secondary to other disease.
Descriptor ID |
D065627
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MeSH Number(s) |
C08.381.423.847
|
Concept/Terms |
Idiopathic Pulmonary Arterial Hypertension- Idiopathic Pulmonary Arterial Hypertension
- Primary Pulmonary Hypertension
- Hypertension, Primary Pulmonary
- Hypertensions, Primary Pulmonary
- Primary Pulmonary Hypertensions
- Pulmonary Hypertension, Primary
- Pulmonary Hypertensions, Primary
- Pulmonary Hypertension, Primary, 1
- Idiopathic Pulmonary Hypertension
- Hypertension, Idiopathic Pulmonary
- Hypertensions, Idiopathic Pulmonary
- Idiopathic Pulmonary Hypertensions
- Pulmonary Hypertension, Idiopathic
- Pulmonary Hypertensions, Idiopathic
Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia- Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia
- Pph1 With Hht
- Hht, Pph1 With
- Hhts, Pph1 With
- Pph1 With Hhts
- With Hht, Pph1
- With Hhts, Pph1
|
Below are MeSH descriptors whose meaning is more general than "Familial Primary Pulmonary Hypertension".
Below are MeSH descriptors whose meaning is more specific than "Familial Primary Pulmonary Hypertension".
This graph shows the total number of publications written about "Familial Primary Pulmonary Hypertension" by people in this website by year, and whether "Familial Primary Pulmonary Hypertension" was a major or minor topic of these publications.
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click here.
Year | Major Topic | Minor Topic | Total |
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2011 | 0 | 1 | 1 |
2012 | 0 | 1 | 1 |
2013 | 0 | 1 | 1 |
2014 | 0 | 1 | 1 |
2015 | 1 | 0 | 1 |
2018 | 0 | 1 | 1 |
2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Familial Primary Pulmonary Hypertension" by people in Profiles.
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Katz MG, Hadas Y, Vincek A, Freage-Kahn L, Shtraizent N, Madjarov JM, Pastuszko P, Eliyahu E. Acid ceramidase gene therapy ameliorates pulmonary arterial hypertension with right heart dysfunction. Respir Res. 2023 Aug 11; 24(1):197.
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Cohen JL, Nees SN, Valencia GA, Rosenzweig EB, Krishnan US. Sildenafil Use in Children with Pulmonary Hypertension. J Pediatr. 2019 02; 205:29-34.e1.
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Dardi F, Manes A, Palazzini M, Bachetti C, Mazzanti G, Rinaldi A, Albini A, Gotti E, Monti E, Bacchi Reggiani ML, Galiè N. Combining bosentan and sildenafil in pulmonary arterial hypertension patients failing monotherapy: real-world insights. Eur Respir J. 2015 Aug; 46(2):414-21.
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Khan MA, Pitcher JD, Kawut SM, Ho AC. Bilateral cotton wool spots after use of an endothelin receptor antagonist. Ophthalmic Surg Lasers Imaging Retina. 2014 Mar-Apr; 45(2):156-9.
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Derrett-Smith EC, Dooley A, Gilbane AJ, Trinder SL, Khan K, Baliga R, Holmes AM, Hobbs AJ, Abraham D, Denton CP. Endothelial injury in a transforming growth factor ß-dependent mouse model of scleroderma induces pulmonary arterial hypertension. Arthritis Rheum. 2013 Nov; 65(11):2928-39.
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Trapp CM, Elder RW, Gerken AT, Sopher AB, Lerner S, Aranoff GS, Rosenzweig EB. Pediatric pulmonary arterial hypertension and hyperthyroidism: a potentially fatal combination. J Clin Endocrinol Metab. 2012 Jul; 97(7):2217-22.
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Sachdev V, Kato GJ, Gibbs JS, Barst RJ, Machado RF, Nouraie M, Hassell KL, Little JA, Schraufnagel DE, Krishnamurti L, Novelli EM, Girgis RE, Morris CR, Rosenzweig EB, Badesch DB, Lanzkron S, Castro OL, Taylor JG, Hannoush H, Goldsmith JC, Gladwin MT, Gordeuk VR. Echocardiographic markers of elevated pulmonary pressure and left ventricular diastolic dysfunction are associated with exercise intolerance in adults and adolescents with homozygous sickle cell anemia in the United States and United Kingdom. Circulation. 2011 Sep 27; 124(13):1452-60.