Wang R - Search Results

1

[Clinical and genetic analysis of a patient with Krabbe disease presented as peripheral neuropathy].

Wang W, Qin Y, Wang R, Zhang W, Zhang L, Cui L, Jin M, Jiao Y, Jiao J. Wang W, et al. Among authors: wang r. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Aug 10;36(8):821-825. doi: 10.3760/cma.j.issn.1003-9406.2019.08.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31400137 Chinese.

2

[Clinical features of ultra longitudinally extensive transverse myelitis].

Zhang WH, Jiao YJ, Jiao JS, Liu ZJ, Wang RB. Zhang WH, et al. Zhonghua Yi Xue Za Zhi. 2011 Sep 20;91(35):2464-7. Zhonghua Yi Xue Za Zhi. 2011. PMID: 22321840 Chinese.

3

[Limb-girdle muscular dystrophy type 2G: clinical, pathological and genetic analysis of a case].

Wang W, Hao Y, Wang R, Jin M, Jiao J. Wang W, et al. Among authors: wang r. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Aug;31(4):476-8. doi: 10.3760/cma.j.issn.1003-9406.2014.04.014. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25119914 Chinese.

4

[Longitudinally extensive spinal cord lesion: etiology and imaging features].

Jiao Y, Zhang W, Li X, Wang W, Liu L, Zhang Z, Liu Z, Wang R, Xie S, Jiao J. Jiao Y, et al. Among authors: wang w, wang r. Zhonghua Yi Xue Za Zhi. 2014 Nov 11;94(41):3229-33. Zhonghua Yi Xue Za Zhi. 2014. PMID: 25604223 Chinese.

5

INF2 mutations associated with dominant inherited intermediate Charcot-Marie-Tooth neuropathy with focal segmental glomerulosclerosis in two Chinese patients.

Jin S, Wang W, Wang R, Lv H, Zhang W, Wang Z, Jiao J, Yuan Y. Jin S, et al. Among authors: wang w, wang z, wang r. Clin Neuropathol. 2015 Sep-Oct;34(5):275-81. doi: 10.5414/NP300835. Clin Neuropathol. 2015. PMID: 25943269

6

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.

7

[Carpal tunnel syndrome with cervical spondylotic radiculopathy: a clinical and electrophysiological study].

Wang R, Liu Z, Wang W, Dong M, Sun S, Mao K, Jiao J, Yan L. Wang R, et al. Among authors: wang w. Zhonghua Yi Xue Za Zhi. 2015 Sep 15;95(35):2846-50. Zhonghua Yi Xue Za Zhi. 2015. PMID: 26815187 Chinese.

8

[Clinical and genetic analysis of a patient with Perrault syndrome and additional neurological features].

Duan X, Wang W, Dong M, Wang L, Shao Z, Wang Z, Yuan Y, Wang R, Peng D. Duan X, et al. Among authors: wang w, wang l, wang z, wang r. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jun 10;36(6):577-580. doi: 10.3760/cma.j.issn.1003-9406.2019.06.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31055809 Chinese.

9

Questioning the existence of monophasic neuromyelitis optica spectrum disorder by defining a novel long-term relapse-free form from a large Chinese population.

Zhang W, Cui L, Zhang Y, Wang W, Wang R, Liu Z, Peng D, Jiao Y, Jiao J. Zhang W, et al. Among authors: wang w, wang r. J Neurol. 2020 Apr;267(4):1197-1205. doi: 10.1007/s00415-019-09685-3. Epub 2020 Jan 13. J Neurol. 2020. PMID: 31932912

10

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: wang g, wang w, wang r. 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.

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