Wang H - Search Results

1

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.

2

[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.

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

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.

5

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

6

Noninvasive diagnosis of hereditary transthyretin-related cardiac amyloidosis: A case report.

Qin J, Zhan C, Li H, Han Y, Wang H, Li R, Ma F, Yan J. Qin J, et al. Among authors: wang h. Medicine (Baltimore). 2019 Jul;98(30):e16566. doi: 10.1097/MD.0000000000016566. Medicine (Baltimore). 2019. PMID: 31348283 Free PMC article.

7

Temporal echocardiography findings in patients with fulminant myocarditis: beyond ejection fraction decline.

Zuo H, Li R, Ma F, Jiang J, Miao K, Li H, Nagel E, Tadic M, Wang H, Wang DW. Zuo H, et al. Among authors: wang h, wang dw. Front Med. 2020 Jun;14(3):284-292. doi: 10.1007/s11684-019-0713-9. Epub 2019 Dec 19. Front Med. 2020. PMID: 31858367

8

Trimetazidine Inhibits Renal Tubular Epithelial Cells to Mesenchymal Transition in Diabetic Rats via Upregulation of Sirt1.

Yang Y, Wang Y, He Z, Liu Y, Chen C, Wang Y, Wang DW, Wang H. Yang Y, et al. Among authors: wang h, wang y, wang dw. Front Pharmacol. 2020 Jul 29;11:1136. doi: 10.3389/fphar.2020.01136. eCollection 2020. Front Pharmacol. 2020. PMID: 32848753 Free PMC article.

9

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

10

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.

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