Wang Z - Search Results

1

GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathy.

Yu J, Luan XH, Yu M, Zhang W, Lv H, Cao L, Meng L, Zhu M, Zhou B, Wu XR, Li P, Gang Q, Liu J, Shi X, Liang W, Jia Z, Yao S, Yuan Y, Deng J, Hong D, Wang Z. Yu J, et al. Among authors: wang z. Ann Clin Transl Neurol. 2021 Jun;8(6):1330-1342. doi: 10.1002/acn3.51371. Epub 2021 May 4. Ann Clin Transl Neurol. 2021. PMID: 33943039 Free PMC article.

2

Detection of A3243G point mutation in mitochondrial DNA from 10 cases of MELAS.

Wang Z, Liu S, Yang Y, Yuan Y, Wu L, Qi Y, Chen Q. Wang Z, et al. Chin Med J (Engl). 2002 Jul;115(7):995-7. Chin Med J (Engl). 2002. PMID: 12150728

3

[Clinical pathology and molecular genetics on familial amyloidotic polyneuropathy].

Wang Z, Zhang Y, Zhang W, Yuan Y. Wang Z, et al. Beijing Da Xue Xue Bao Yi Xue Ban. 2003 Aug;35(4):408-11. Beijing Da Xue Xue Bao Yi Xue Ban. 2003. PMID: 12947559 Free article. Chinese.

4

Cerebrotendinous xanthomatosis with a compound heterozygote mutation and severe polyneuropathy.

Wang Z, Yuan Y, Zhang W, Zhang Y, Feng L. Wang Z, et al. Neuropathology. 2007 Feb;27(1):62-6. doi: 10.1111/j.1440-1789.2006.00739.x. Neuropathology. 2007. PMID: 17319284

5

The overlap of corticobasal degeneration and Alzheimer changes: an autopsy case.

Zhang W, Zheng R, Wang Z, Yuan Y. Zhang W, et al. Among authors: wang z. Neuropathology. 2009 Dec;29(6):720-6. doi: 10.1111/j.1440-1789.2009.01012.x. Epub 2009 Mar 23. Neuropathology. 2009. PMID: 19323789

6

Clincial and pathological study of distal motor neuropathy with N88S mutation in BSCL2.

Chen B, Zheng R, Luan X, Zhang W, Wang Z, Yuan Y. Chen B, et al. Among authors: wang z. Neuropathology. 2009 Oct;29(5):543-7. doi: 10.1111/j.1440-1789.2009.01011.x. Epub 2009 Mar 23. Neuropathology. 2009. PMID: 19323790

7

Clinical phenotype of autosomal dominant progressive external ophthalmoplegia in a family with a novel mutation in the C10orf2 gene.

Hong D, Bi H, Yao S, Wang Z, Yuan Y. Hong D, et al. Among authors: wang z. Muscle Nerve. 2010 Jan;41(1):92-9. doi: 10.1002/mus.21439. Muscle Nerve. 2010. PMID: 19705478

8

Novel human pathological mutations. Gene symbol: SCN4A. Disease: Periodic paralysis.

Hong D, Luan X, Chen B, Zheng R, Wang Z, Yuan Y. Hong D, et al. Among authors: wang z. Hum Genet. 2010 Jan;127(1):113. Hum Genet. 2010. PMID: 20108424 No abstract available.

9

Phenotypic patterns of MELAS/LS overlap syndrome associated with m.13513G>A mutation, and neuropathological findings in one autopsy case.

Wang Z, Qi XK, Yao S, Chen B, Luan X, Zhang W, Han M, Yuan Y. Wang Z, et al. Neuropathology. 2010 Dec;30(6):606-14. doi: 10.1111/j.1440-1789.2010.01115.x. Neuropathology. 2010. PMID: 20408961

10

A novel heterozygous deletion-insertion mutation (2695-2712 del/GTTTGT ins) in exon 18 of the filamin C gene causes filaminopathy in a large Chinese family.

Luan X, Hong D, Zhang W, Wang Z, Yuan Y. Luan X, et al. Among authors: wang z. Neuromuscul Disord. 2010 Jun;20(6):390-6. doi: 10.1016/j.nmd.2010.03.009. Epub 2010 Apr 22. Neuromuscul Disord. 2010. PMID: 20417099

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