Cheng J - Search Results

1

Phenotype and molecular characteristics in 45 Chinese children with 5α-reductase type 2 deficiency from South China.

Cheng J, Lin R, Zhang W, Liu G, Sheng H, Li X, Zhou Z, Mao X, Liu L. Cheng J, et al. Clin Endocrinol (Oxf). 2015 Oct;83(4):518-26. doi: 10.1111/cen.12799. Epub 2015 May 7. Clin Endocrinol (Oxf). 2015. PMID: 25899528

2

[Gene mutation analysis in four Chinese patients with multiple carboxylase deficiency].

Li D, Liu L, Li XZ, Cheng J, Zhao XY, Zhou R. Li D, et al. Among authors: cheng j. Zhonghua Er Ke Za Zhi. 2006 Nov;44(11):865-8. Zhonghua Er Ke Za Zhi. 2006. PMID: 17274881 Chinese.

3

[Persistent hyperinsulinemic hypoglycemia of infancy: clinical analysis of 12 cases].

Wu AW, Liu L, Li XZ, Cheng J, Zhou ZH, Zhang W. Wu AW, et al. Among authors: cheng j. Zhongguo Dang Dai Er Ke Za Zhi. 2009 Oct;11(10):809-12. Zhongguo Dang Dai Er Ke Za Zhi. 2009. PMID: 19849938 Free article. Chinese.

4

[Neonatal diabetes mellitus: a clinical analysis of 13 cases].

Li XZ, Zhang XH, Liu L, Cheng J, Zhang W. Li XZ, et al. Among authors: cheng j. Zhonghua Er Ke Za Zhi. 2010 Oct;48(10):775-8. Zhonghua Er Ke Za Zhi. 2010. PMID: 21176489 Chinese.

5

[Clinical and gene mutation analyses of three patients with ornithine carbamoyltransferase deficiency].

Mo WQ, Liu L, Chen YY, Cheng J, Li XZ, Zhou ZH, Mao XJ, Zhang W. Mo WQ, et al. Among authors: cheng j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Jun;28(3):328-31. doi: 10.3760/cma.j.issn.1003-9406.2011.03.020. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21644234 Chinese.

6

[Enzymatic diagnosis and clinical characteristics of 52 children with mucopolysaccharidosis].

Huang YL, Li SY, Zhao XY, Fan LP, Lin WC, Zhou ZH, Cheng J, Liu L. Huang YL, et al. Among authors: cheng j. Zhongguo Dang Dai Er Ke Za Zhi. 2012 Jul;14(7):510-4. Zhongguo Dang Dai Er Ke Za Zhi. 2012. PMID: 22809603 Free article. Chinese.

7

[Gene mutations and clinical manifestations in children with glycogen storage disease type Ib].

Liang CL, Liu L, Sheng HY, Jiang MY, Yin X, Mei HF, Cheng J, Zhang W, Fan LP. Liang CL, et al. Among authors: cheng j. Zhongguo Dang Dai Er Ke Za Zhi. 2013 Aug;15(8):661-5. Zhongguo Dang Dai Er Ke Za Zhi. 2013. PMID: 23965881 Free article. Chinese.

8

[Analysis of clinical features and arylsulfatase B gene mutation in thirteen Chinese children with mucopolysaccharidosis type VI].

Zheng J, Huang Y, Zhao X, Sheng H, Cheng J, Zhou Z, Li X, Mao X, Liu L. Zheng J, et al. Among authors: cheng j. Zhonghua Er Ke Za Zhi. 2014 Jun;52(6):403-8. Zhonghua Er Ke Za Zhi. 2014. PMID: 25190157 Chinese.

9

A novel ABCD1 gene mutation in a Chinese patient with X-linked adrenoleukodystrophy.

Cai YN, Jiang MY, Liang CL, Peng MZ, Cheng J, Sheng HY, Fan LP, Chen XQ, Liu L. Cai YN, et al. Among authors: cheng j. J Pediatr Endocrinol Metab. 2015 May;28(5-6):725-9. doi: 10.1515/jpem-2013-0441. J Pediatr Endocrinol Metab. 2015. PMID: 25423669

10

[Clinical features of pyruvate dehydrogenase complex deficiency and gene testing in one case].

Wu M, Liu L, Cai Y, Sheng H, Cheng J, Li X, Yin X, Lu Z, Lin R, Zhou Z, Fan L, Liu H. Wu M, et al. Among authors: cheng j. Zhonghua Er Ke Za Zhi. 2014 Nov;52(11):863-6. Zhonghua Er Ke Za Zhi. 2014. PMID: 25582476 Chinese.

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

22,647 results

Search Page

Filters