Huang Y - Search Results

1

[Abnormal findings during newborn period of 160 patients with early-onset methylmalonic aciduria].

Liu YP, Ma YY, Wu TF, Wang Q, Li XY, Ding Y, Song JQ, Huang Y, Yang YL. Liu YP, et al. Among authors: huang y. Zhonghua Er Ke Za Zhi. 2012 Jun;50(6):410-4. Zhonghua Er Ke Za Zhi. 2012. PMID: 22931934 Chinese.

2

[Skin lesions induced by malnutrition in an infant with methylmalonic aciduria and homocysteic acidemia].

Liu YP, Song JQ, Ma YY, Wu TF, Wang Q, Huang Y, Yang YL. Liu YP, et al. Among authors: huang y. Zhongguo Dang Dai Er Ke Za Zhi. 2012 Mar;14(3):233-4. Zhongguo Dang Dai Er Ke Za Zhi. 2012. PMID: 22433417 Free article. Chinese. No abstract available.

3

[Analysis of clinical features of 6 patients with infantile type glycogen storage disease type II].

Ding J, Huang Y, Yang H, Zhang Q, Hou X, Liu X, Yang Y, Xiong H. Ding J, et al. Among authors: huang y. Zhonghua Er Ke Za Zhi. 2015 Jun;53(6):436-41. Zhonghua Er Ke Za Zhi. 2015. PMID: 26310554 Chinese.

4

[A boy with Fabry disease with the onset at the age of four].

Liu YP, Huang Y, Wang Q, Wu TF, Ma YY, Li XY, Song JQ, Yang YL. Liu YP, et al. Among authors: huang y. Beijing Da Xue Xue Bao Yi Xue Ban. 2013 Apr 18;45(2):307-11. Beijing Da Xue Xue Bao Yi Xue Ban. 2013. PMID: 23591357 Free article. Chinese.

5

Molecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type A.

Wang X, Huang Y, Yan M, Li J, Ding C, Jin H, Fang F, Yang Y, Wu B, Chen D. Wang X, et al. Among authors: huang y. Sci Rep. 2017 Oct 20;7(1):13686. doi: 10.1038/s41598-017-14034-3. Sci Rep. 2017. PMID: 29057985 Free PMC article.

6

[Clinical and genetic analysis for two children with congenital disturbance of glycosylation with PMM2 gene mutations].

Ren C, Fang F, Huang Y, Cheng H, Dai L. Ren C, et al. Among authors: huang y. Zhonghua Er Ke Za Zhi. 2015 Dec;53(12):938-42. Zhonghua Er Ke Za Zhi. 2015. PMID: 26887550 Chinese.

7

[Clinical and genetic features of Schwartz-Jampel syndrome in a Chinese child: case report and literature review].

Dai L, Fang F, Huang Y, Cheng H, Ren C. Dai L, et al. Among authors: huang y. Zhonghua Er Ke Za Zhi. 2015 Nov;53(11):855-9. Zhonghua Er Ke Za Zhi. 2015. PMID: 26758326 Review. Chinese.

8

Clinical study in Chinese patients with late-infantile form neuronal ceroid lipofuscinoses.

Chang X, Huang Y, Meng H, Jiang Y, Wu Y, Xiong H, Wang S, Qin J. Chang X, et al. Among authors: huang y. Brain Dev. 2012 Oct;34(9):739-45. doi: 10.1016/j.braindev.2011.12.005. Epub 2012 Jan 14. Brain Dev. 2012. PMID: 22245569

9

Clinical and GAA gene mutation analysis in mainland Chinese patients with late-onset Pompe disease: identifying c.2238G > C as the most common mutation.

Liu X, Wang Z, Jin W, Lv H, Zhang W, Que C, Huang Y, Yuan Y. Liu X, et al. Among authors: huang y. BMC Med Genet. 2014 Dec 20;15:141. doi: 10.1186/s12881-014-0141-2. BMC Med Genet. 2014. PMID: 25526786 Free PMC article.

10

[Clinical and genetic study on familial idiopathic pulmonary fibrosis in a Chinese family].

Yan W, Zhu X, Wang J, Huang Y, He B. Yan W, et al. Among authors: huang y. Zhonghua Jie He He Hu Xi Za Zhi. 2015 Nov;38(11):833-8. Zhonghua Jie He He Hu Xi Za Zhi. 2015. PMID: 26850772 Chinese.

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