Wang Z - Search Results

1

A novel compound heterozygous mutation in the COA7 gene responsible for a Chinese patient with spinocerebellar ataxia with axonal neuropathy type 3.

Tang Y, Yu M, Zhang W, Lv H, Deng J, Liu J, Shi X, Liang W, Jia Z, Yuan Y, Wang Z, Meng L. Tang Y, et al. Among authors: wang z. Clin Neuropathol. 2022 Sep-Oct;41(5):202-210. doi: 10.5414/NP301457. Clin Neuropathol. 2022. PMID: 35603692

2

[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.

3

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

4

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

5

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

6

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

7

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

8

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

9

Both hypokalaemic and normokalaemic periodic paralysis in different members of a single family with novel R1129Q mutation in SCN4A gene.

Hong D, Luan X, Chen B, Zheng R, Zhang W, Wang Z, Yuan Y. Hong D, et al. Among authors: wang z. J Neurol Neurosurg Psychiatry. 2010 Jun;81(6):703-4. doi: 10.1136/jnnp.2009.177451. J Neurol Neurosurg Psychiatry. 2010. PMID: 20522878 No abstract available.

10

NOTCH3 mutations and clinical features in 33 mainland Chinese families with CADASIL.

Wang Z, Yuan Y, Zhang W, Lv H, Hong D, Chen B, Liu Y, Luan X, Xie S, Wu S. Wang Z, et al. J Neurol Neurosurg Psychiatry. 2011 May;82(5):534-9. doi: 10.1136/jnnp.2010.209247. Epub 2010 Oct 9. J Neurol Neurosurg Psychiatry. 2011. PMID: 20935329

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