Yang Y - Search Results

1

Exercise intolerance and developmental delay associated with a novel mitochondrial ND5 mutation.

Fang H, Shi H, Li X, Sun D, Li F, Li B, Ding Y, Ma Y, Liu Y, Zhang Y, Shen L, Bai Y, Yang Y, Lu J. Fang H, et al. Among authors: yang y. Sci Rep. 2015 May 27;5:10480. doi: 10.1038/srep10480. Sci Rep. 2015. PMID: 26014388 Free PMC article.

2

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. Chin Med J (Engl). 2006 Mar 5;119(5):373-7. Chin Med J (Engl). 2006. PMID: 16542579

3

Screening of common mitochondrial mutations in Chinese patients with mitochondrial encephalomyopathies.

Qi Y, Zhang Y, Wang Z, Yang Y, Yuan Y, Niu S, Pei P, Wang S, Ma Y, Bu D, Zou L, Fang F, Xiao J, Sun F, Zhang Y, Wu Y, Wang S, Xiong H, Wu X. Qi Y, et al. Among authors: yang y. Mitochondrion. 2007 Feb-Apr;7(1-2):147-50. doi: 10.1016/j.mito.2006.11.019. Epub 2006 Dec 9. Mitochondrion. 2007. PMID: 17276742

4

[Leigh syndrome due to pyruvate dehydrogenase E1 alpha subunit gene mutation: a complicated and difficult case study].

Zhang Y, Sun F, Yang YL, Chang XZ, Qi Y, Qi ZY, Xiao JX, Qin J, Wu XR. Zhang Y, et al. Among authors: yang yl. Zhongguo Dang Dai Er Ke Za Zhi. 2007 Jun;9(3):216-9. Zhongguo Dang Dai Er Ke Za Zhi. 2007. PMID: 17582259 Chinese.

5

Spinal cord demyelination associated with biotinidase deficiency in 3 Chinese patients.

Yang Y, Li C, Qi Z, Xiao J, Zhang Y, Yamaguchi S, Hasegawa Y, Tagami Y, Jiang Y, Xiong H, Zhang Y, Qin J, Wu XR. Yang Y, et al. J Child Neurol. 2007 Feb;22(2):156-60. doi: 10.1177/0883073807300307. J Child Neurol. 2007. PMID: 17621476

6

[Clinical studies on fifty-seven Chinese patients with combined methylmalonic aciduria and homocysteinemia].

Zhang Y, Song JQ, Liu P, Yan R, Dong JH, Yang YL, Wang LF, Jiang YW, Zhang YH, Qin J, Wu XR. Zhang Y, et al. Among authors: yang yl. Zhonghua Er Ke Za Zhi. 2007 Jul;45(7):513-7. Zhonghua Er Ke Za Zhi. 2007. PMID: 17953808 Clinical Trial. Chinese.

7

Prenatal diagnosis of methylmalonic aciduria by analysis of organic acids and total homocysteine in amniotic fluid.

Zhang Y, Yang YL, Hasegawa Y, Yamaguchi S, Shi CY, Song JQ, Sayami S, Liu P, Yan R, Dong JH, Qin J. Zhang Y, et al. Among authors: yang yl. Chin Med J (Engl). 2008 Feb 5;121(3):216-9. Chin Med J (Engl). 2008. PMID: 18298912

8

[A case of Leigh syndrome associated with respiratory chain complex I deficiency due to mitochondrial gene 13513G>A mutation].

Wei XQ, Kong QP, Zhang Y, Yang YL, Chang XZ, Qi Y, Qi ZY, Xiao JX, Qin J, Wu XR. Wei XQ, et al. Among authors: yang yl. Zhongguo Dang Dai Er Ke Za Zhi. 2009 May;11(5):333-6. Zhongguo Dang Dai Er Ke Za Zhi. 2009. PMID: 19470250 Chinese.

9

[Clinical and molecular genetic investigations on mitochondrial respiratory chain complex-I deficiency].

Wei XQ, Zhang Y, Yang YL. Wei XQ, et al. Among authors: yang yl. Zhonghua Er Ke Za Zhi. 2009 Feb;47(2):156-8. Zhonghua Er Ke Za Zhi. 2009. PMID: 19573469 Review. Chinese. No abstract available.

10

[Mitochondrial respiratory chain complex III deficiency and diseases].

Ma YY, Yang YL. Ma YY, et al. Zhonghua Er Ke Za Zhi. 2010 Nov;48(11):878-80. Zhonghua Er Ke Za Zhi. 2010. PMID: 21215041 Review. Chinese. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

108,563 results

Search Page

Filters