Experimental Investigation Of The Role Of Endothelin‐1 In Idiopathic Portal Hypertension
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Immune and inflammatory mechanisms in pulmonary arterial
subcategorized as idiopathic PAH, familial PAH, pulmo-nary hypertension associated with other diseases such as connective tissue diseases (CTD, e.g., systemic sclerosis (SSc), lupus erythematosus, and mixed CTD), portal hypertension and pulmonary hypertension related to HIV infection, drugs and toxins.1 PAH is characterized by
3,700 108,500 1.7 M
Pulmonary hypertension (PH) was first described over 100 years ago, but a thorough understanding of its pathogenesis and a successful approach to curing the disease still remain under investigation. Advanced research in the field of PH has enhanced our understanding of this entity and has led to new therapies.
消化器・総合外科学 - med.shimane-u.ac.jp
Experimental investigation of the role of endothelin-1 in idiopathic portal hypertension. Journal of Gastroenterology and Hepatology 22:1134-1140,2007 17）Dipok Kumar Dhar, Shinji Hattori, Yasuhito Tonomoto, Tadakazu Shimoda, Hoichi Kato,Mitsuo Tachibana, Kosho Matsura,Yojiro Mitsumoto, Alex G.Little, Naofumi Naga sue.
Functionalized cerium oxide nanoparticles mitigate the
rhotic patients and experimental models of liver diseases has been demonstrated. However, the pathological role of the portal vein endothelium in this clinical context is scarcely studied and, therefore, deserves attention. In this context, we aimed to investigate whether patho-logical endothelial activation occurs in the portal vein of
The role of sex in the pathophysiology of pulmonary hypertension
R. (2018) The role of sex in the pathophysiology of pulmonary hypertension. In: Kerkhof, P. L.M. and Miller, V. M. (eds.) Sex-Specific Analysis of Cardiovascular Function. Series: Advances in experimental medicine and biology (1065). Springer: Cham, pp. 511-528. ISBN 9783319779317. There may be differences between this version and the published
HDL Cholesterol as a Marker of Disease Severity and Prognosis
Jul 18, 2019 intake and portal hypertension. In patients without any known predisposing factors or positive family history, idiopathic PAH (IPAH) can be diagnosed . The ﬁrst symptoms of PAH are mostly related to right ventricular dysfunction and are typically present during exertion. Most common