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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.
(CAG)n loci as genetic modifiers of age-at-onset in patients with Machado-Joseph disease from mainland China.
Chen Z, Zheng C, Long Z, Cao L, Li X, Shang H, Yin X, Zhang B, Liu J, Ding D, Peng Y, Wang C, Peng H, Ye W, Qiu R, Pan Q, Xia K, Chen S, Sequeiros J, Ashizawa T, Klockgether T, Tang B, Jiang H; Chinese Clinical Research Cooperative Group for Spinocerebellar Ataxias (CCRCG-SCA). Chen Z, et al. Among authors: jiang h. Brain. 2016 Aug;139(Pt 8):e41. doi: 10.1093/brain/aww087. Epub 2016 Apr 16. Brain. 2016. PMID: 27085188 No abstract available.
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.
Ubiquitin-related network underlain by (CAG)n loci modulate age at onset in Machado-Joseph disease.
Chen Z, Wang C, Zheng C, Long Z, Cao L, Li X, Shang H, Yin X, Zhang B, Liu J, Ding D, Peng Y, Peng H, Ye W, Qiu R, Pan Q, Xia K, Chen S, Sequeiros J, Ashizawa T, Tang B, Jiang H; Chinese Clinical Research Cooperative Group for Spinocerebellar Ataxias (CCRCG-SCA). Chen Z, et al. Among authors: jiang h. Brain. 2017 Apr 1;140(4):e25. doi: 10.1093/brain/awx028. Brain. 2017. PMID: 28334945 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.
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