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Clinical features of NOTCH2NLC-related neuronal intranuclear inclusion disease.
Tian Y, Zhou L, Gao J, Jiao B, Zhang S, Xiao Q, Xue J, Wang Y, Liang H, Liu Y, Ji G, Mao C, Liu C, Dong L, Zhang L, Zhang S, Yi J, Zhao G, Luo Y, Sun Q, Zhou Y, Yi F, Chen X, Zhou C, Xie N, Luo M, Yao L, Hu Y, Zhang M, Zeng Q, Fang L, Long HY, Xie Y, Weng L, Chen S, Du J, Xu Q, Feng L, Huang Q, Hou X, Wang J, Xie B, Zhou L, Long L, Guo JF, Wang J, Yan X, Jiang H, Xu H, Duan R, Tang B, Shen L. Tian Y, et al. Among authors: jiang h. J Neurol Neurosurg Psychiatry. 2022 Dec;93(12):1289-1298. doi: 10.1136/jnnp-2022-329772. Epub 2022 Sep 23. J Neurol Neurosurg Psychiatry. 2022. PMID: 36150844 Free PMC article.
UBA5 Mutations Cause a New Form of Autosomal Recessive Cerebellar Ataxia.
Duan R, Shi Y, Yu L, Zhang G, Li J, Lin Y, Guo J, Wang J, Shen L, Jiang H, Wang G, Tang B. Duan R, et al. Among authors: jiang h. PLoS One. 2016 Feb 12;11(2):e0149039. doi: 10.1371/journal.pone.0149039. eCollection 2016. PLoS One. 2016. PMID: 26872069 Free PMC article.
Safety and efficacy of valproic acid treatment in SCA3/MJD patients.
Lei LF, Yang GP, Wang JL, Chuang DM, Song WH, Tang BS, Jiang H. Lei LF, et al. Among authors: jiang h. Parkinsonism Relat Disord. 2016 May;26:55-61. doi: 10.1016/j.parkreldis.2016.03.005. Epub 2016 Mar 12. Parkinsonism Relat Disord. 2016. PMID: 26997655 Clinical Trial.
ATXN2 polymorphism modulates age at onset in Machado-Joseph disease.
Ding D, Li K, Wang C, Chen Z, Long Z, Peng Y, Zhou X, Peng H, Qiu R, Xia K, Tang B, Jiang H. Ding D, et al. Among authors: jiang h. Brain. 2016 Oct 1;139(10):e59. doi: 10.1093/brain/aww176. Brain. 2016. PMID: 27452601 No abstract available.
Rare GCH1 heterozygous variants contributing to Parkinson's disease.
Xu Q, Li K, Sun Q, Ding D, Zhao Y, Yang N, Luo Y, Liu Z, Zhang Y, Wang C, Xia K, Yan X, Jiang H, Shen L, Tang B, Guo J. Xu Q, et al. Among authors: jiang h. Brain. 2017 Jul 1;140(7):e41. doi: 10.1093/brain/awx110. Brain. 2017. PMID: 28582483 No abstract available.
27,184 results
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