Wang H - Search Results

1

[Infant with 3β-hydroxy-Δ(5)-C27 steroid dehydrogenase deficiency: report of two cases and literatures review].

Li X, Huang Z, Wang H. Li X, et al. Among authors: wang h. Zhonghua Er Ke Za Zhi. 2015 May;53(5):360-5. Zhonghua Er Ke Za Zhi. 2015. PMID: 26080666 Review. Chinese.

2

Clinical Features and Genetic Analysis of Pediatric Patients with Alagille Syndrome Presenting Initially with Liver Function Abnormalities.

Liu Y, Wang H, Dong C, Feng JX, Huang ZH. Liu Y, et al. Among authors: wang h. Curr Med Sci. 2018 Apr;38(2):304-309. doi: 10.1007/s11596-018-1879-0. Epub 2018 Apr 30. Curr Med Sci. 2018. PMID: 30074189

3

Clinical and histopathologic features of sodium taurocholate cotransporting polypeptide deficiency in pediatric patients.

Dong C, Zhang BP, Wang H, Xu H, Zhang C, Cai ZS, Wang DW, Shu SN, Huang ZH, Luo XP. Dong C, et al. Among authors: wang h, wang dw. Medicine (Baltimore). 2019 Sep;98(39):e17305. doi: 10.1097/MD.0000000000017305. Medicine (Baltimore). 2019. PMID: 31574858 Free PMC article.

4

A Case Report: Can Citrin Deficiency Lead to Hepatocellular Carcinoma in Children?

He J, Zhang J, Li X, Wang H, Feng C, Fang F, Shu S. He J, et al. Among authors: wang h. Front Pediatr. 2019 Sep 18;7:371. doi: 10.3389/fped.2019.00371. eCollection 2019. Front Pediatr. 2019. PMID: 31620407 Free PMC article.

5

Novel Mutations in the 3β-hydroxy-∆5-C27-steroid Dehydrogenase Gene (HSD3B7) in a Patient with Neonatal Cholestasis.

Huang HY, Zhou H, Wang H, Chen YX, Fang F. Huang HY, et al. Among authors: wang h. Chin Med J (Engl). 2016 Jan 5;129(1):98-100. doi: 10.4103/0366-6999.172603. Chin Med J (Engl). 2016. PMID: 26712441 Free PMC article. No abstract available.

6

Novel mutations in the SLC25A13 gene in a patient with NICCD and severe manifestations.

Wang H, Shu S, Chen C, Huang Z, Wang D. Wang H, et al. Among authors: wang d. J Pediatr Endocrinol Metab. 2015 Mar;28(3-4):471-5. doi: 10.1515/jpem-2014-0278. J Pediatr Endocrinol Metab. 2015. PMID: 25381944

7

[Mutation analysis of a family with 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency].

Shu JB, Zhang YQ, Jiang SZ, Zhang CH, Meng YT, Wang H, Song L. Shu JB, et al. Among authors: wang h. Zhonghua Er Ke Za Zhi. 2013 Oct;51(10):783-6. Zhonghua Er Ke Za Zhi. 2013. PMID: 24406234 Chinese.

8

Effects of 100-μT extremely low frequency electromagnetic fields exposure on hematograms and blood chemistry in rats.

Lai J, Zhang Y, Zhang J, Liu X, Ruan G, Chaugai S, Tang J, Wang H, Chen C, Wang DW. Lai J, et al. Among authors: wang h, wang dw. J Radiat Res. 2016 Jan;57(1):16-24. doi: 10.1093/jrr/rrv059. Epub 2015 Sep 23. J Radiat Res. 2016. PMID: 26404558 Free PMC article.

9

A splicing LMNA mutation causing laminopathies accompanied by aortic valve malformation.

Tao J, Duan J, Pi X, Wang H, Li S. Tao J, et al. Among authors: wang h. J Clin Lab Anal. 2021 Apr;35(4):e23736. doi: 10.1002/jcla.23736. Epub 2021 Feb 24. J Clin Lab Anal. 2021. PMID: 33626194 Free PMC article.

10

[Analysis of gene variant in an infant with succinic semialdehyde dehydrogenase deficiency].

Yan D, Xu X, Wang X, Zhang X, Zhi X, Wang H, Zhang Y, Shu J. Yan D, et al. Among authors: wang x, wang h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Feb 10;39(2):216-221. doi: 10.3760/cma.j.cn511374-20201120-00818. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35076924 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

152,277 results

Search Page

Filters