Yuan Y - Search Results

1

Clinical, muscle imaging, and genetic characteristics of dystrophinopathies with deep-intronic DMD variants.

Xie Z, Sun C, Liu C, Xie Z, Wei L, Yu J, Ling C, Guo X, Liu Y, Yu M, Leng Y, Meng L, Sun Y, Deng J, Leal SM, Schrauwen I, Wang Z, Yuan Y. Xie Z, et al. Among authors: yuan y. J Neurol. 2023 Feb;270(2):925-937. doi: 10.1007/s00415-022-11432-0. Epub 2022 Nov 2. J Neurol. 2023. PMID: 36319768

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. Among authors: yuan y. Chin Med J (Engl). 2002 Jul;115(7):995-7. Chin Med J (Engl). 2002. PMID: 12150728

3

[Mitochondrial DNA mutations in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome].

Wang ZX, Yuan Y, Gao F, Qi Y, Shen DG, Chen QT. Wang ZX, et al. Among authors: yuan y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Aug;20(4):273-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12903032 Chinese.

4

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

Wang Z, Zhang Y, Zhang W, Yuan Y. Wang Z, et al. Among authors: yuan y. 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.

5

[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. Among authors: yuan y. Zhonghua Yi Xue Za Zhi. 2004 Jul 17;84(14):1175-80. Zhonghua Yi Xue Za Zhi. 2004. PMID: 15387979 Chinese.

6

[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: yuan y. 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.

7

[Phenotype heterogeneity associated with mitochondrial DNA A3243G mutation].

Zhang Y, Wang ZX, Niu SL, Xu YF, Pei P, Yuan Y, Yang YL, Qi Y. Zhang Y, et al. Among authors: yuan y. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2005 Feb;27(1):77-80. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2005. PMID: 15782498 Chinese.

8

Novel GLA gene mutations in two Chinese families with classic Fabry disease.

Wang ZX, Zhang Y, Bu DF, Zhang W, Yuan Y. Wang ZX, et al. Among authors: yuan y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Oct;22(5):489-92. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16215932

9

[Two novel mutations in palmitoyl-protein thioesterase gene in two Chinese babies with infantile neuronal ceroid lipofuscinosis].

Bi HY, Yao S, Bu DF, Wang ZX, Zhang Y, Qin J, Yang YL, Yuan Y. Bi HY, et al. Among authors: yuan y. Zhonghua Er Ke Za Zhi. 2006 Jul;44(7):496-9. Zhonghua Er Ke Za Zhi. 2006. PMID: 17044973 Chinese.

10

Cerebrotendinous xanthomatosis with a compound heterozygote mutation and severe polyneuropathy.

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

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