نتایج جستجو برای: ژن ipah

تعداد نتایج: 16248  

Journal: :Patria : Jurnal Pengabdian Kepada Masyarakat 2021

Pemberdayaan dilakukan dalam kerangka model triple helix, yang terdiri dari akademik, pemerintah, dan komunitas petani daerah urban. Naskah ini merupakan refleksi pelaksanaan program tahun pertama kedua 2019–2020 pengembangan desa mitra (PPDM). Tujuan pengabdian: masyarakat sadar pentingnya melakukan adaptasi terhadap perubahan iklim, menangkap air hujan dimasukkan kembali ke tanah, kelompok ta...

Journal: :Circulation journal : official journal of the Japanese Circulation Society 2009
Zhulanqiqige Do e Yoshihiro Fukumoto Aya Takaki Shunsuke Tawara Junko Ohashi Makoto Nakano Tomohiro Tada Kenya Saji Kohichiro Sugimura Hiroshi Fujita Yasushi Hoshikawa Jun Nawata Takashi Kondo Hiroaki Shimokawa

BACKGROUND Direct evidence for Rho-kinase activation in patients with pulmonary hypertension (PH) is still lacking. METHODS AND RESULTS Rho-kinase activity in circulating neutrophils was examined by determining the ratio of phosphorylated/total forms of myosin-binding subunit, a substrate of Rho-kinase, in 40 consecutive PH patients and 40 healthy controls. Next, Rho-kinase expression and act...

Journal: :The European respiratory journal 2011
C J Rhodes J Wharton L Howard J S R Gibbs A Vonk-Noordegraaf M R Wilkins

Iron deficiency is known to be common and detrimental in chronic left heart failure, where parenteral iron treatment has been shown to improve exercise capacity, New York Heart Association functional class and patient wellbeing. There is now increasing interest in the role of iron in the natural history of pulmonary arterial hypertension (PAH). Iron availability influences the pulmonary vasocon...

2016
YE YUAN YINGYING ZHANG XIAOXU ZHANG YANAN YU BING LI PENGQIAN WANG HAIXIA LI YIJUN ZHAO CHUNTI SHEN ZHONG WANG

Coronary heart disease (CHD), idiopathic pulmonary arterial hypertension (IPAH) and pulmonary heart disease (PHD) are circulatory system diseases that may simultaneously emerge in a patient and they are often treated together in clinical practice. However, the molecular mechanisms connecting these three diseases remain unclear. In order to determine the multidimensional characteristic correlati...

2012
Ying-Hua Guo Long-Xiang Su Na Guo Chang-Ting Liu

Idiopathic pulmonary arterial hypertension (IPAH) is a progressive, nearly fatal condition that until recently has had very few treatment options. Median survival time for untreated IPAH was 2.8 years without effective drug intervention. IPAH is characterized by deregulated proliferation of pulmonary arterial endothelial and intimal smooth muscle cells resulting in progressive pulmonary vascula...

Journal: :The European respiratory journal 2009
F S de Man M L Handoko H Groepenhoff A J van 't Hul J Abbink R J H Koppers H P Grotjohan J W R Twisk H-J Bogaard A Boonstra P E Postmus N Westerhof W J van der Laarse A Vonk-Noordegraaf

We determined the physiological effects of exercise training on exercise capacity and quadriceps muscle function in patients with idiopathic pulmonary arterial hypertension (iPAH). In total, 19 clinically stable iPAH patients (New York Heart Association II-III) underwent a supervised exercise training programme for the duration of 12 weeks. Maximal capacity, endurance capacity and quadriceps fu...

Journal: :Chest 2006
Anna Fijalkowska Marcin Kurzyna Adam Torbicki Grzegorz Szewczyk Michal Florczyk Piotr Pruszczyk Monika Szturmowicz

STUDY OBJECTIVES Baseline prognostic assessment in patients with pulmonary hypertension (PH) may help in the selection of treatment. High plasma levels of natriuretic peptide type B have been reported in patients with right ventricular (RV) dysfunction and suggest poor prognosis in patients with idiopathic pulmonary arterial hypertension (IPAH). We prospectively assessed the correlation of N-te...

2017
Changwei Wu Jian Guo Hui Liu Bigyan Pudasaini Wenlan Yang Qinhua Zhao Lan Wang Jinming Liu

We show by this study that a decrease in HRR1 in IPAH patients is associated with severe limitation of exercise capacity. HRR1 < 16 beats and CI just after completion of a CPET could be an indicator of poor prognosis.

Journal: :Annals of the Rheumatic Diseases 2023

Background Abnormal production of various cytokines is involved in the pathogenesis CTD, and cytokine abnormalities vary according to type organ lesion. Recent reports indicate that are also iPAH.1) The differences between PH associated with CTD other PH-associated cytokines, including iPAH, not well defined. relationship severity each clear. Objectives purpose this study was determine profile ...

Journal: :The European respiratory journal 2015
Melanie J Brewis Alistair C Church Martin K Johnson Andrew J Peacock

Pulmonary hypertension (PH) due to lung disease (World Health Organization (WHO) group 3) is common, but severe PH, arbitrarily defined as mean pulmonary artery pressure ≥35 mmHg is reported in only a small proportion. Whether these should be treated as patients in WHO group 1 (i.e. pulmonary arterial hypertension) with PH-targeted therapies is unknown. We compared the phenotypic characteristic...

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