Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hua-Chuan Chao"'
Autor:
Jui-Yu Yeh, Hua-Chuan Chao, Cheng-Li Hong, Yu-Chien Hung, Fei-Yang Tzou, Cheng-Tsung Hsiao, Jeng-Lin Li, Wen-Jie Chen, Cheng-Ta Chou, Yu-Shuen Tsai, Yi-Chu Liao, Yu-Chun Lin, Suewei Lin, Shu-Yi Huang, Marina Kennerson, Yi-Chung Lee, Chih-Chiang Chan
Publikováno v:
EMBO Molecular Medicine, Vol 16, Iss 5, Pp 1091-1114 (2024)
Abstract PAR3/INSC/LGN form an evolutionarily conserved complex required for asymmetric cell division in the developing brain, but its post-developmental function and disease relevance in the peripheral nervous system (PNS) remains unknown. We mapped
Externí odkaz:
https://doaj.org/article/5359f09eb23c4e93a0c5ca897d7a0804
Autor:
Shao-Lun Hsu, Yi-Jiun Lu, Yu-Shuen Tsai, Hua-Chuan Chao, Jong-Ling Fuh, Yi-Chu Liao, Yi-Chung Lee
Publikováno v:
Journal of the Formosan Medical Association, Vol 121, Iss 1, Pp 126-133 (2022)
Background/purpose: Hereditary spastic paraplegia (HSP) is a heterogeneous group of inherited neurodegenerative disorders characterized by slowly progressive lower limbs spasticity and weakness. HSP type 15 (SPG15) is an autosomal recessive subtype c
Externí odkaz:
https://doaj.org/article/4f5761f3f14b409594563eb5b07a1944
Autor:
Hua‐Chuan Chao, Yi‐Chu Liao, Yo‐Tsen Liu, Yuh‐Cherng Guo, Fu‐Pang Chang, Yi‐Chung Lee, Kon‐Ping Lin
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 5, Pp 913-922 (2019)
Abstract Objective The clinical and genetic profiles of hereditary transthyretin amyloidosis (ATTR) in Chinese populations remain elusive. We aim to characterize the features of ATTR in a Taiwanese cohort of Han Chinese descent. Methods Seventy‐nin
Externí odkaz:
https://doaj.org/article/801a296b9e69416b84e888d92784b63f
Autor:
Hua-Chuan Chao, Cheng-Tsung Hsiao, Kuan-Lin Lai, Yu-Shuen Tsai, Kon-Ping Lin, Yi-Chu Liao, Yi-Chung Lee
Publikováno v:
Journal of the Formosan Medical Association = Taiwan yi zhi.
Mutations in the neurofilament light polypeptide gene (NEFL) are an uncommon cause of Charcot-Marie-Tooth disease (CMT). The aim of this study is to elucidate the clinical characteristics and genetic spectrum of NEFL-related neuropathy in a Taiwanese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::753c2254892e90b9aa054e73eacec8a3
https://pubmed.ncbi.nlm.nih.gov/36031490
https://pubmed.ncbi.nlm.nih.gov/36031490
Autor:
Kon-Ping Lin, Yuh-Cherng Guo, Yi-Chu Liao, Fu-Pang Chang, Yo-Tsen Liu, Yi-Chung Lee, Hua-Chuan Chao
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 5, Pp 913-922 (2019)
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology
Objective The clinical and genetic profiles of hereditary transthyretin amyloidosis (ATTR) in Chinese populations remain elusive. We aim to characterize the features of ATTR in a Taiwanese cohort of Han Chinese descent. Methods Seventy‐nine patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9e72c599df814354d9cc8fa73b7c46a
https://doaj.org/article/801a296b9e69416b84e888d92784b63f
https://doaj.org/article/801a296b9e69416b84e888d92784b63f
Autor:
Shao-Lun Hsu, Yi-Chu Liao, Jong Ling Fuh, Yu-Shuen Tsai, Yi-Jiun Lu, Hua-Chuan Chao, Yi-Chung Lee
Publikováno v:
Journal of the Formosan Medical Association, Vol 121, Iss 1, Pp 126-133 (2022)
Background/purpose Hereditary spastic paraplegia (HSP) is a heterogeneous group of inherited neurodegenerative disorders characterized by slowly progressive lower limbs spasticity and weakness. HSP type 15 (SPG15) is an autosomal recessive subtype ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e012d48c243e2ff3da3a2e44e57bb0a9
https://pubmed.ncbi.nlm.nih.gov/33637369
https://pubmed.ncbi.nlm.nih.gov/33637369
Publikováno v:
Journal of the Neurological Sciences. 358:213-220
Background Charcot Marie Tooth disease type 1A (CMT1A) is the most commonly inherited demyelinating polyneuropathy with variable phenotypes, affected by several comorbidities, especially diabetes mellitus (DM). Previous studies showed that DM exacerb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ffde871de9360476236dacd91808f27
https://doi.org/10.1016/j.jns.2015.08.1539
https://doi.org/10.1016/j.jns.2015.08.1539
Publikováno v:
Journal of the Neurological Sciences. 381:463-464
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3b0b5b854e9e2b50e8d90b899c9f412
https://doi.org/10.1016/j.jns.2017.08.3516
https://doi.org/10.1016/j.jns.2017.08.3516