Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Wan-Jane Tsai"'
Publikováno v:
Pulmonary Circulation, Vol 13, Iss 2, Pp n/a-n/a (2023)
Abstract Approximately 25%–30% of patients diagnosed with idiopathic pulmonary arterial hypertension (PAH) have a clustered underlying Mendelian genetic cause and should be classified as heritable PAH (HPAH). The sixth World Symposium on Pulmonary
Externí odkaz:
https://doaj.org/article/2ee3f89cf93f4a5889fea0daf26aabd8
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
Cor triatriatum sinister is a rare congenital anomaly characterized by the left-sided triatrial form of the heart. Diverse theories have been proposed regarding its formation, and the failure of incorporation of the common pulmonary vein into the lef
Externí odkaz:
https://doaj.org/article/29cf2ef005a24e26a5899ca2ce933d1f
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
BackgroundGenetic variants could be identified in subjects with idiopathic and heritable pulmonary arterial hypertension (PAH). The 6th World Symposium on Pulmonary Hypertension (WSPH) provided a list of genes with evidence of association with PAH. H
Externí odkaz:
https://doaj.org/article/456145ef088f422eb411986357b6fe92
Autor:
Wan-Jane Tsai, 蔡宛真
100
The teratogenicity of antiepilepsy drug valproic acid (VPA) mostly is found in genetic and somatic levels, causing teratogenesis involving neurotubular defects (NTD), lumbosacral meningomyelocele, anencephaly, and leg dysfunction due to spin
The teratogenicity of antiepilepsy drug valproic acid (VPA) mostly is found in genetic and somatic levels, causing teratogenesis involving neurotubular defects (NTD), lumbosacral meningomyelocele, anencephaly, and leg dysfunction due to spin
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/95035127814166289143
Autor:
Hung-Chin Ho, Mey-Fann Lee, Chia-Chi Liu, Kuo-Yang Wang, Kae-Woei Liang, Wan-Jane Tsai, Wei-Wen Lin
Publikováno v:
BioMed Research International, Vol 2015 (2015)
BioMed Research International
BioMed Research International
Pulmonary arterial hypertension (PAH) is a rare disease but with significant morbidity and high mortality. There is no specific way to diagnose PAH. Thus, an easy used with good sensitivity and specificity biomarker of PAH is highly desirable to aid
Autor:
Chieh-Shou Su, Jin-Long Huang, Kae-Woei Liang, Hung-Tao Yi, Wan-Jane Tsai, Wei-Wen Lin, Tsu-Juey Wu, Yu-Cheng Hsieh, Kuo-Yang Wang
Publikováno v:
Heartlung : the journal of critical care. 43(6)
This aim of this study was to correlate heart rate variability (HRV) parameters to pulmonary arterial pressure (PAP) in patients with purely idiopathic pulmonary arterial hypertension (IPAH).HRV is decreased in patients with PAH. Whether HRV indices
Autor:
Chiu-Lan, Hsieh, Kuan-Chou, Chen, Chi-Yang, Ding, Wan-Jane, Tsai, Jia-Fong, Wu, Chiung-Chi, Peng
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 54(4)
Valproic acid induced teratogenicity at genetic and somatic levels, the action mechanism is still unclear. We hypothesized that folate receptor gene (folr1) and others may be interacting to elicit neural tube defect (NTD), while N-acetylcysteine (NAC
Publikováno v:
Toxicology. 291(1-3)
The teratogenicity of antiepilepsy drug valproic acid (VPA) mostly is found in genetic and somatic levels, causing teratogenesis involving neurotubular defects (NTDs), anencephaly, lumbosacral meningomyelocele, and leg dysfunction due to spina bifida
Publikováno v:
Romanian Journal of Morphology & Embryology; 2013, Vol. 54 Issue 4, p993-1004, 12p