Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Tian-Xinyu Xia"'
Autor:
Min Chu, Yue Cui, Liyong Wu, Jiali Meng, Zhuyi Jiang, Junjie Li, Hong Ye, Yang-Mingyue Ji, Wang Xin, Li Liu, Dong-Xin Wang, Jing Zhang, Haihan Yan, Lin Wang, Tian-Xinyu Xia, Kexin Xie, ZiChen Tian, Ye Zhao
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 93:291-297
ObjectiveElucidate the core clinical and genetic characteristics and identify the phenotypic variation between different regions and genotypes of fatal familial insomnia (FFI).MethodsA worldwide large sample of FFI patients from our case series and l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7a9966a8cc8cf07862cd52fd3ef1bd7
https://doi.org/10.1136/jnnp-2021-327247
https://doi.org/10.1136/jnnp-2021-327247
Autor:
Jing Zhang, Min Chu, ZiChen Tian, KeXin Xie, Yue Cui, Li Liu, JiaLi Meng, HaiHan Yan, Yang-Mingyue Ji, Zhuyi Jiang, Tian-Xinyu Xia, Dongxin Wang, Xin Wan, Ye Zhao, Hong Ye, Junjie Li, Lin Wang, Liyong Wu, Zhang, Jing, Chu, Min
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry; Mar2022, Vol. 93 Issue 3, p291-297, 7p
Autor:
Min Chu, Chaodong Wang, Tian-Xinyu Xia, Jing Zhang, Aihong Zhou, Kexin Xie, Yue Cui, Yu Kong, Ran Gao, Dong-Xin Wang, Li Liu, Liyong Wu
Publikováno v:
Ann Transl Med
Background CSF1R-related encephalopathy refers to adult-onset leukodystrophy with neuroaxonal spheroids and pigmented glia (ALSP) due to CSF1R mutations, which is a rare autosomal dominant white matter disease including two pathological entities, her
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9b61caa34f2455648f2fd370ed61cfd
https://doi.org/10.21037/atm-21-217
https://doi.org/10.21037/atm-21-217