Wei CJ - Search Results

1

Multisystem involvement in Chinese patients with neuromyopathic phenotype of mitochondrial trifunctional protein deficiency.

Wei CJ, Chang XZ, Ge L, Fu XN, Fan YB, Liu JY, Wang S, Li HL, Yang YL, Xiong H. Wei CJ, et al. Chin Med J (Engl). 2020 Jun 5;133(11):1358-1360. doi: 10.1097/CM9.0000000000000805. Chin Med J (Engl). 2020. PMID: 32515919 Free PMC article. No abstract available.

2

Genotype/phenotype of 6 Chinese cases with Niemann-Pick disease type C.

Xiong H, Higaki K, Wei CJ, Bao XH, Zhang YH, Fu N, Qin J, Adachi K, Kumura Y, Ninomiya H, Nanba E, Wu XR. Xiong H, et al. Among authors: wei cj. Gene. 2012 May 1;498(2):332-5. doi: 10.1016/j.gene.2012.01.026. Epub 2012 Feb 4. Gene. 2012. PMID: 22326530

3

[Clinical and molecular genetic analysis of a family with normokalemic periodic paralysis].

Wei CJ, Wang D, Wang S, Jiao H, Hong DJ, Pu LH, Xiong H. Wei CJ, et al. Zhonghua Er Ke Za Zhi. 2013 Jan;51(1):47-51. Zhonghua Er Ke Za Zhi. 2013. PMID: 23527931 Chinese.

4

[Value of muscle enzyme analysis in differential diagnosis of childhood myopathic hyper-creatine kinase-emia].

Mao B, Xiong H, Jiao H, Wei CJ, Ding J, Chang XZ, Yang YL, Wang S, Wu Y, Liu XQ, Chen YH, DU JB, Li XY, Jiang YW, Qin J. Mao B, et al. Among authors: wei cj. Beijing Da Xue Xue Bao Yi Xue Ban. 2014 Feb 18;46(1):130-7. Beijing Da Xue Xue Bao Yi Xue Ban. 2014. PMID: 24535365 Free article. Chinese.

5

[Application of targeted capture technology and next generation sequencing in molecular diagnosis of inherited myopathy].

Fu X, Liu A, Yang H, Wei C, Ding J, Wang S, Wang J, Yuan Y, Jiang Y, Xiong H. Fu X, et al. Zhonghua Er Ke Za Zhi. 2015 Oct;53(10):741-6. Zhonghua Er Ke Za Zhi. 2015. PMID: 26758109 Chinese.

6

FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies.

Fu X, Yang H, Wei C, Jiao H, Wang S, Yang Y, Han C, Wu X, Xiong H. Fu X, et al. J Hum Genet. 2016 Dec;61(12):1013-1020. doi: 10.1038/jhg.2016.94. Epub 2016 Jul 21. J Hum Genet. 2016. PMID: 27439679

7

[Correlation between thigh muscle magnetic resonance imaging findings and clinical features of congenital muscular dystrophies: a preliminary study].

Wang LL, Du J, Fu XN, Fan YB, Wei CJ, Ding J, Tan DD, Xiao JX, Xiong H. Wang LL, et al. Among authors: wei cj. Zhonghua Er Ke Za Zhi. 2016 Oct 2;54(10):756-760. doi: 10.3760/cma.j.issn.0578-1310.2016.10.009. Zhonghua Er Ke Za Zhi. 2016. PMID: 27784478 Chinese.

8

[Peripheral nerve injury in LAMA2-related congenital muscular dystrophy patients].

Liang XP, Wang S, Zhang W, Yuan Y, Ding J, Chang XZ, Wei CJ, Liu JY, Xiong H. Liang XP, et al. Among authors: wei cj. Zhonghua Er Ke Za Zhi. 2017 Feb 2;55(2):95-99. doi: 10.3760/cma.j.issn.0578-1310.2017.02.008. Zhonghua Er Ke Za Zhi. 2017. PMID: 28173645 Chinese.

9

Genetic and clinical findings in a Chinese cohort of patients with collagen VI-related myopathies.

Fan Y, Liu A, Wei C, Yang H, Chang X, Wang S, Yuan Y, Bonnemann C, Wu Q, Wu X, Xiong H. Fan Y, et al. Clin Genet. 2018 Jun;93(6):1159-1171. doi: 10.1111/cge.13230. Epub 2018 Mar 12. Clin Genet. 2018. PMID: 29419890

10

Congenital muscular dystrophies in China.

Ge L, Zhang C, Wang Z, Chan SHS, Zhu W, Han C, Zhang X, Zheng H, Wu L, Jin B, Shan J, Mao B, Zhong J, Peng X, Cheng Y, Hu J, Sun Y, Lu J, Hua Y, Zhu S, Wei C, Wang S, Jiao H, Yang H, Fu X, Fan Y, Chang X, Wang S, Bao X, Zhang Y, Wang J, Wu Y, Jiang Y, Yuan Y, Rutkowski A, Bönnemann CG, Wei W, Wu X, Xiong H. Ge L, et al. Clin Genet. 2019 Sep;96(3):207-215. doi: 10.1111/cge.13560. Epub 2019 Jun 6. Clin Genet. 2019. PMID: 31066047

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