Wang ZX - Search Results

1

Study of Enhanced Depth Imaging Optical Coherence Tomography in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.

Fang XJ, Yu M, Wu Y, Zhang ZH, Wang WW, Wang ZX, Yuan Y. Fang XJ, et al. Among authors: wang zx, wang ww. Chin Med J (Engl). 2017 May 5;130(9):1042-1048. doi: 10.4103/0366-6999.204935. Chin Med J (Engl). 2017. PMID: 28469098 Free PMC article.

2

Clinical and Brain Magnetic Resonance Imaging Features in a Cohort of Chinese Patients with Kearns-Sayre Syndrome.

Yu M, Zhang Z, Wang QQ, Liu J, Zuo YH, Yu L, Xiao JX, Zhang W, Yuan Y, Wang ZX. Yu M, et al. Among authors: wang zx, wang qq. Chin Med J (Engl). 2016 Jun 20;129(12):1419-24. doi: 10.4103/0366-6999.183417. Chin Med J (Engl). 2016. PMID: 27270536 Free PMC article.

3

"Target" and "Sandwich" Signs in Thigh Muscles have High Diagnostic Values for Collagen VI-related Myopathies.

Fu J, Zheng YM, Jin SQ, Yi JF, Liu XJ, Lyn H, Wang ZX, Zhang W, Xiao JX, Yuan Y. Fu J, et al. Among authors: wang zx. Chin Med J (Engl). 2016 Aug 5;129(15):1811-6. doi: 10.4103/0366-6999.186638. Chin Med J (Engl). 2016. PMID: 27453230 Free PMC article.

4

Compound Heterozygote Mutation of C12orf65 Causes Distal Motor Neuropathy and Optic Atrophy.

Fang XJ, Zhang W, Lyu H, Wang ZX, Wang WW, Yuan Y. Fang XJ, et al. Among authors: wang zx, wang ww. Chin Med J (Engl). 2017 Jan 20;130(2):242-244. doi: 10.4103/0366-6999.198019. Chin Med J (Engl). 2017. PMID: 28091420 Free PMC article. No abstract available.

5

Muscle Magnetic Resonance Imaging for the Differentiation of Multiple Acyl-CoA Dehydrogenase Deficiency and Immune-mediated Necrotizing Myopathy.

Zhao YW, Liu XJ, Zhang W, Wang ZX, Yuan Y. Zhao YW, et al. Among authors: wang zx. Chin Med J (Engl). 2018 Jan 20;131(2):144-150. doi: 10.4103/0366-6999.222323. Chin Med J (Engl). 2018. PMID: 29336361 Free PMC article.

6

Optical coherence tomography findings in chronic progressive external ophthalmoplegia.

Wu Y, Kang L, Wu HL, Hou Y, Wang ZX. Wu Y, et al. Among authors: wang zx. Chin Med J (Engl). 2019 May 20;132(10):1202-1207. doi: 10.1097/CM9.0000000000000262. Chin Med J (Engl). 2019. PMID: 31140991 Free PMC article.

7

[NOTCH3 gene mutations in four Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].

Wang ZX, Lu H, Zhang Y, Bu DF, Niu XY, Zhang Z, Huang YN, Yuan Y. Wang ZX, et al. Zhonghua Yi Xue Za Zhi. 2004 Jul 17;84(14):1175-80. Zhonghua Yi Xue Za Zhi. 2004. PMID: 15387979 Chinese.

8

[Clinical features in 4 Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].

Lv H, Yao S, Zhang W, Wang ZX, Huang YN, Niu XY, Zhang Z, Yuan Y. Lv H, et al. Among authors: wang zx. Beijing Da Xue Xue Bao Yi Xue Ban. 2004 Oct;36(5):496-500. Beijing Da Xue Xue Bao Yi Xue Ban. 2004. PMID: 15489930 Free article. Chinese.

9

Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome.

Yang YL, Sun F, Zhang Y, Qian N, Yuan Y, Wang ZX, Qi Y, Xiao JX, Wang XY, Qi ZY, Zhang YH, Jiang YW, Bao XH, Qin J, Wu XR. Yang YL, et al. Among authors: wang zx, wang xy. Chin Med J (Engl). 2006 Mar 5;119(5):373-7. Chin Med J (Engl). 2006. PMID: 16542579

10

Hereditary Transthyretin Amyloidosis in Eight Chinese Families.

Meng LC, Lyu H, Zhang W, Liu J, Wang ZX, Yuan Y. Meng LC, et al. Among authors: wang zx. Chin Med J (Engl). 2015 Nov 5;128(21):2902-5. doi: 10.4103/0366-6999.168048. Chin Med J (Engl). 2015. PMID: 26521788 Free PMC article.

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