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
|
| 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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| Year | Major Topic | Minor Topic | Total |
|---|
| 2011 | 0 | 1 | 1 |
| 2012 | 0 | 2 | 2 |
| 2013 | 0 | 3 | 3 |
| 2017 | 14 | 2 | 16 |
| 2018 | 7 | 8 | 15 |
| 2019 | 2 | 1 | 3 |
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Below are the most recent publications written about "Familial Primary Pulmonary Hypertension" by people in Profiles.
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Reply: COVID-19 Experience and Pulmonary Arterial Hypertension: Do Earlier Theses and New Data Still Match? Ann Am Thorac Soc. 2021 06; 18(6):1081-1082.
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Dysbalance of ACE2 levels - a possible cause for severe COVID-19 outcome in COPD. J Pathol Clin Res. 2021 09; 7(5):446-458.
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Outpatient Inhaled Nitric Oxide in a Patient with Vasoreactive Idiopathic Pulmonary Arterial Hypertension and COVID-19 Infection. Am J Respir Crit Care Med. 2020 07 01; 202(1):130-132.
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Still puzzling about a clear definition of pulmonary arterial hypertension in newborns. Eur Respir J. 2019 03; 53(3).
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Widening the landscape of heritable pulmonary hypertension mutations in paediatric and adult cases. Eur Respir J. 2019 03; 53(3).
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Germline BMP9 mutation causes idiopathic pulmonary arterial hypertension. Eur Respir J. 2019 03; 53(3).
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Validation of a risk assessment instrument for pulmonary arterial hypertension. Eur Heart J. 2018 12 14; 39(47):4182-4185.
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Risk assessment in patients with systemic sclerosis and pulmonary arterial hypertension. Eur Respir J. 2018 10; 52(4).
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Use of TAPSE/PASP ratio in pulmonary arterial hypertension: An easy shortcut in a congested road. Int J Cardiol. 2018 09 01; 266:242-244.
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CCL21 as a Potential Serum Biomarker for Pulmonary Arterial Hypertension in Systemic Sclerosis. Arthritis Rheumatol. 2018 10; 70(10):1644-1653.