Gu W - Search Results

1

Characterization of genotype-phenotype correlation with MORC2 mutated Axonal Charcot-Marie-Tooth disease in a cohort of Chinese patients.

Duan X, Liu X, Wang G, Gu W, Xu M, Hao Y, Dong M, Sun Q, Sun S, Chen Y, Wang W, Li J, Zhang Y, Cao Z, Fan D, Wang R, Da Y. Duan X, et al. Among authors: gu w. Orphanet J Rare Dis. 2021 May 31;16(1):244. doi: 10.1186/s13023-021-01881-7. Orphanet J Rare Dis. 2021. PMID: 34059105 Free PMC article.

2

[Genetics and clinical study of Chinese kindreds with dentatorubral pallidoluysian atrophy].

Zhang X, Hao Y, Gu WH, Chen YY, Zhang J, Wang GX, Wang K, Jin M, Duan XH. Zhang X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Feb;30(1):31-5. doi: 10.3760/cma.j.issn.1003-9406.2013.01.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23450475 Chinese.

3

Spinocerebellar ataxia 17: Inconsistency between phenotype and neuroimage findings.

Zhang J, Gu W, Hao Y, Chen Y. Zhang J, et al. Among authors: gu w. Ann Indian Acad Neurol. 2013 Oct;16(4):703-4. doi: 10.4103/0972-2327.120457. Ann Indian Acad Neurol. 2013. PMID: 24339615 Free PMC article.

4

Huntingtin gene CAG repeat numbers in Chinese patients with Huntington's disease and controls.

Jiang H, Sun YM, Hao Y, Yan YP, Chen K, Xin SH, Tang YP, Li XH, Jun T, Chen YY, Liu ZJ, Wang CR, Li H, Pei Z, Shang HF, Zhang BR, Gu WH, Wu ZY, Tang BS, Burgunder JM; Chinese HD Network. Jiang H, et al. Among authors: gu wh. Eur J Neurol. 2014 Apr;21(4):637-42. doi: 10.1111/ene.12366. Epub 2014 Jan 28. Eur J Neurol. 2014. PMID: 24471773

5

[Analysis of fragile X mental retardation 1 gene premutation in multiple system atrophy patients].

Zhang LW, Gu WH, Wang GX, Chen YY, Hao Y, Zhang J, Wang K, Jin M. Zhang LW, et al. Zhonghua Yi Xue Za Zhi. 2013 Dec 17;93(47):3744-7. Zhonghua Yi Xue Za Zhi. 2013. PMID: 24548388 Chinese.

6

Application of whole exome sequencing in undiagnosed inherited polyneuropathies.

Klein CJ, Middha S, Duan X, Wu Y, Litchy WJ, Gu W, Dyck PJ, Gavrilova RH, Smith DI, Kocher JP, Dyck PJ. Klein CJ, et al. Among authors: gu w. J Neurol Neurosurg Psychiatry. 2014 Nov;85(11):1265-72. doi: 10.1136/jnnp-2013-306740. Epub 2014 Mar 6. J Neurol Neurosurg Psychiatry. 2014. PMID: 24604904

7

Myotonic dystrophy type 1 associated with white matter hyperintense lesions: clinic, imaging, and genetic analysis.

Liu L, Liu HM, Liu ZJ, Zhang LW, Gu WH, Wang RB. Liu L, et al. Chin Med J (Engl). 2015 May 20;128(10):1412-4. doi: 10.4103/0366-6999.156812. Chin Med J (Engl). 2015. PMID: 25963366 Free PMC article. No abstract available.

8

Spinocerebellar ataxia type 10 in Chinese Han.

Wang K, McFarland KN, Liu J, Zeng D, Landrian I, Xia G, Hao Y, Jin M, Mulligan CJ, Gu W, Ashizawa T. Wang K, et al. Among authors: gu w. Neurol Genet. 2015 Oct 8;1(3):e26. doi: 10.1212/NXG.0000000000000026. eCollection 2015 Oct. Neurol Genet. 2015. PMID: 27066563 Free PMC article.

9

A Novel Asp121Asn Mutation of Myelin Protein Zero Is Associated with Late-Onset Axonal Charcot-Marie-Tooth Disease, Hearing Loss and Pupil Abnormalities.

Duan X, Gu W, Hao Y, Wang R, Wen H, Sun S, Jiao J, Fan D. Duan X, et al. Among authors: gu w. Front Aging Neurosci. 2016 Sep 22;8:222. doi: 10.3389/fnagi.2016.00222. eCollection 2016. Front Aging Neurosci. 2016. PMID: 27774063 Free PMC article.

10

Identification of a Splicing Mutation in ITPR1 via WES in a Chinese Early-Onset Spinocerebellar Ataxia Family.

Wang L, Hao Y, Yu P, Cao Z, Zhang J, Zhang X, Chen Y, Zhang H, Gu W. Wang L, et al. Among authors: gu w. Cerebellum. 2018 Jun;17(3):294-299. doi: 10.1007/s12311-017-0896-z. Cerebellum. 2018. PMID: 29196976 Free PMC article.

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