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Page 1
Adventitial Fibroblast Nox4 Expression and ROS Signaling in Pulmonary Arterial Hypertension.
Barman SA, Fulton D. Barman SA, et al. Adv Exp Med Biol. 2017;967:1-11. doi: 10.1007/978-3-319-63245-2_1. Adv Exp Med Biol. 2017. PMID: 29047077 Review.
Pulmonary arterial hypertension (PAH) is a progressive disease arising from remodeling and narrowing of pulmonary arteries (PA) resulting in high pulmonary arterial blood pressure and ultimately right ventricular failure. ...In the vascular wall, Nox4 is pres …
Pulmonary arterial hypertension (PAH) is a progressive disease arising from remodeling and narrowing of pulmonary arteries (PA …
Smoking-Related "Interstitial" Lung Disease.
Franks TJ, Galvin JR. Franks TJ, et al. Arch Pathol Lab Med. 2015 Aug;139(8):974-7. doi: 10.5858/arpa.2013-0384-RA. Epub 2014 Nov 21. Arch Pathol Lab Med. 2015. PMID: 25415179 Free article. Review.
CONTEXT: Emphysema, respiratory bronchiolitis, desquamative interstitial pneumonia, pulmonary Langerhans' cell histiocytosis, small-airway injury including submucosal and adventitial fibrosis, increased bronchus-associated lymphoid tissue, and small artery …
CONTEXT: Emphysema, respiratory bronchiolitis, desquamative interstitial pneumonia, pulmonary Langerhans' cell histiocytosis, small-a …
Pulmonary veno-occlusive disease: An important consideration in patients with pulmonary hypertension.
Balko R, Edriss H, Nugent K, Test V. Balko R, et al. Respir Med. 2017 Nov;132:203-209. doi: 10.1016/j.rmed.2017.10.015. Epub 2017 Oct 20. Respir Med. 2017. PMID: 29229098 Free article. Review.
High resolution computed tomography scans reveal ground glass opacities, interlobular septal thickening, and lymphadenopathy. Echocardiography can estimate the level of pulmonary artery pressures; right heart catheterization is needed for complete hemodynamic charac …
High resolution computed tomography scans reveal ground glass opacities, interlobular septal thickening, and lymphadenopathy. Echocardiograp …
Inhaled prostanoids in the therapy of pulmonary hypertension.
Gessler T, Seeger W, Schmehl T. Gessler T, et al. J Aerosol Med Pulm Drug Deliv. 2008 Mar;21(1):1-12. doi: 10.1089/jamp.2007.0657. J Aerosol Med Pulm Drug Deliv. 2008. PMID: 18518827 Review.
These properties qualify them as efficient drugs for the treatment of pulmonary hypertension, a life-threatening illness characterized by an increase in artery pressure and vascular resistance in the pulmonary circulation. Diseased pulmonary vessels sh …
These properties qualify them as efficient drugs for the treatment of pulmonary hypertension, a life-threatening illness characterize …
Takayasu's truncoarteritis. Pulseless disease or aortitis syndrome.
Nasu T. Nasu T. Acta Pathol Jpn. 1982;32 Suppl 1:117-31. Acta Pathol Jpn. 1982. PMID: 6139930 Review.
Based on the summary of autopsy findings and taking clinical features into consideration, the current criteria for the pathological diagnosis of this condition might be summarized as follows. 1) Non-syphilitic truncoarteritis frequently occurring in young females. 2) Frequent man …
Based on the summary of autopsy findings and taking clinical features into consideration, the current criteria for the pathological diagnosi …
Takayasu's arteritis: a cell-mediated large-vessel vasculitis.
Rizzi R, Bruno S, Stellacci C, Dammacco R. Rizzi R, et al. Int J Clin Lab Res. 1999;29(1):8-13. doi: 10.1007/s005990050055. Int J Clin Lab Res. 1999. PMID: 10356657 Review.
Early or active-stage pathology consists of continuous or patchy granulomatous inflammation, which progresses to intimal and adventitial fibrosis and scarring of the media. Multiple focal or segmental stenoses result and aneurysms may occasionally occur. ...Specific …
Early or active-stage pathology consists of continuous or patchy granulomatous inflammation, which progresses to intimal and adventitial …
[Update on the pathomorphological assessment of vasculopathies in pulmonary arterial hypertension].
Dorfmüller P, Humbert M, Capron F. Dorfmüller P, et al. Pathologe. 2006 Mar;27(2):140-6. doi: 10.1007/s00292-006-0822-5. Pathologe. 2006. PMID: 16450085 Review. German.
Pulmonary arterial hypertension (PAH) is a term which has recently been redefined and includes idiopathic pulmonary arterial hypertension, familial pulmonary arterial hypertension PAH related to specific pathological conditions (e.g. connective tissue disease …
Pulmonary arterial hypertension (PAH) is a term which has recently been redefined and includes idiopathic pulmonary arterial h …