Wei Q - Search Results

1

Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia.

Wei Q, Dong HL, Pan LY, Chen CX, Yan YT, Wang RM, Li HF, Liu ZJ, Tao QQ, Wu ZY. Wei Q, et al. Transl Neurodegener. 2019 Jun 26;8:19. doi: 10.1186/s40035-019-0157-9. eCollection 2019. Transl Neurodegener. 2019. PMID: 31289639 Free PMC article.

2

Sensory nerve disturbance in amyotrophic lateral sclerosis.

Tao QQ, Wei Q, Wu ZY. Tao QQ, et al. Among authors: wei q. Life Sci. 2018 Jun 15;203:242-245. doi: 10.1016/j.lfs.2018.04.052. Epub 2018 Apr 27. Life Sci. 2018. PMID: 29709651 Review.

3

Targeted next-generation sequencing improves diagnosis of hereditary spastic paraplegia in Chinese patients.

Lu C, Li LX, Dong HL, Wei Q, Liu ZJ, Ni W, Gitler AD, Wu ZY. Lu C, et al. Among authors: wei q. J Mol Med (Berl). 2018 Jul;96(7):701-712. doi: 10.1007/s00109-018-1655-4. Epub 2018 Jun 11. J Mol Med (Berl). 2018. PMID: 29934652

4

Motor neuron disease-like phenotype associated with anti-IgLON5 disease.

Tao QQ, Wei Q, Song SJ, Yin XZ. Tao QQ, et al. Among authors: wei q. CNS Neurosci Ther. 2018 Dec;24(12):1305-1308. doi: 10.1111/cns.13038. Epub 2018 Aug 13. CNS Neurosci Ther. 2018. PMID: 30105827 Free PMC article. No abstract available.

5

Clinical and genetic characterization of a cohort of Chinese patients with hereditary spastic paraplegia.

Yan YT, Wei Q, Zheng Y, Luo WJ, Dong HL, Lu C, Zhang J, Chen MJ, Bao YX, Li HF. Yan YT, et al. Among authors: wei q. Clin Genet. 2019 May;95(5):637-639. doi: 10.1111/cge.13517. Epub 2019 Feb 19. Clin Genet. 2019. PMID: 30780198

6

Identification and functional analysis of novel mutations in the SOD1 gene in Chinese patients with amyotrophic lateral sclerosis.

Lin HX, Tao QQ, Wei Q, Chen CX, Chen YC, Li HF, Gitler AD, Wu ZY. Lin HX, et al. Among authors: wei q. Amyotroph Lateral Scler Frontotemporal Degener. 2019 May;20(3-4):222-228. doi: 10.1080/21678421.2019.1582668. Epub 2019 Mar 19. Amyotroph Lateral Scler Frontotemporal Degener. 2019. PMID: 30887850

7

Genetic spectrum and clinical profiles in a southeast Chinese cohort of Charcot-Marie-Tooth disease.

Chen CX, Dong HL, Wei Q, Li LX, Yu H, Li JQ, Liu GL, Li HF, Bai G, Ma H, Wu ZY. Chen CX, et al. Among authors: wei q. Clin Genet. 2019 Nov;96(5):439-448. doi: 10.1111/cge.13616. Epub 2019 Aug 8. Clin Genet. 2019. PMID: 31372974

8

Spastic paraplegia as the predominant phenotype in a cohort of Chinese patients with adrenoleukodystrophy.

Luo WJ, Wei Q, Dong HL, Yan YT, Chen MJ, Li HF. Luo WJ, et al. Among authors: wei q. Mol Genet Genomic Med. 2020 Jan;8(1):e1065. doi: 10.1002/mgg3.1065. Epub 2019 Nov 27. Mol Genet Genomic Med. 2020. PMID: 31777199 Free PMC article.

9

Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral Sclerosis.

Liu ZJ, Lin HX, Wei Q, Zhang QJ, Chen CX, Tao QQ, Liu GL, Ni W, Gitler AD, Li HF, Wu ZY. Liu ZJ, et al. Among authors: wei q. Aging Dis. 2019 Dec 1;10(6):1199-1206. doi: 10.14336/AD.2019.0215. eCollection 2019 Dec. Aging Dis. 2019. PMID: 31788332 Free PMC article.

10

New clinical characteristics and novel pathogenic variants of patients with hereditary leukodystrophies.

Xie JJ, Ni W, Wei Q, Ma H, Bai G, Shen Y, Wu ZY. Xie JJ, et al. Among authors: wei q. CNS Neurosci Ther. 2020 May;26(5):567-575. doi: 10.1111/cns.13284. Epub 2019 Dec 29. CNS Neurosci Ther. 2020. PMID: 31885218 Free PMC article.

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