Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Chao-Szu Wu"'
Publikováno v:
Journal of the Formosan Medical Association, Vol 121, Iss 11, Pp 2345-2350 (2022)
Episodic weakness is typically associated with a group of disorders so called periodic paralyses. Their major causes are mutation of ion channels, and have rarely been linked to mitochondrial disorders. We report a 20-year-old man with episodic weakn
Externí odkaz:
https://doaj.org/article/0591f6e481814ef6a172aa277306b63a
Autor:
Yin-Hsiu Chien, Ni-Chung Lee, Wen-Chin Weng, Li-Chu Chen, Yu-Hsuan Huang, Chao-Szu Wu, Wuh-Liang Hwu
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 43(7)
Background Duchenne muscular dystrophy (DMD/Duchenne) is a progressive X-linked muscular disease with an overall incidence of 1:5,000 live male births. Recent availability in treatment for DMD raised the need of early diagnosis, and DMD became as a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cda8cd99aae03b7fd0e12f82fb41eca7
https://pubmed.ncbi.nlm.nih.gov/35562557
https://pubmed.ncbi.nlm.nih.gov/35562557
Autor:
Ni-Chung Lee, Chao Szu Wu, Hung-Bin Tsai, Shao Yin Chu, Yin-Hsiu Chien, Chih Hung Chen, Wang-Tso Lee, Tzu Jou Wang, Shio Jean Lin, Chao Ching Huang, Wen-Chin Weng, Kun Long Hung, Pi-Chuan Fan, Pei-Lin Lee, Han Chung Hsiue, Chih-Chao Yang, Wuh-Liang Hwu, Chien Jung Lu
Publikováno v:
Intensive Care Medicine. 41:1493-1495
Dear Editor, Mitochondrial DNA 3243A[G is the most common pathogenic mutation of the tRNA gene, accounting for 80 % of mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) [1]. As a result of multi-organ involvement, patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7ddcda0f0881c43cf270100e8f59aba
https://doi.org/10.1007/s00134-015-3879-x
https://doi.org/10.1007/s00134-015-3879-x