Wei Q - Search Results

1

Clinical characterization and founder effect analysis in Chinese amyotrophic lateral sclerosis patients with SOD1 common variants.

Wang PS, Yang XX, Wei Q, Lv YT, Wu ZY, Li HF. Wang PS, et al. Among authors: wei q. Ann Med. 2024 Dec;56(1):2407522. doi: 10.1080/07853890.2024.2407522. Epub 2024 Oct 1. Ann Med. 2024. PMID: 39351695 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

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

4

Clinical feature difference between juvenile amyotrophic lateral sclerosis with SPTLC1 and FUS mutations.

Wang P, Wei Q, Li H, Wu ZY. Wang P, et al. Among authors: wei q. Chin Med J (Engl). 2023 Jan 20;136(2):176-183. doi: 10.1097/CM9.0000000000002495. Chin Med J (Engl). 2023. PMID: 36801857 Free PMC article. Review.

5

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

6

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

7

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.

8

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

9

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.

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

9,057 results

Search Page

Filters