Huang ZH - Search Results

1

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: huang zh. Medicine (Baltimore). 2019 Sep;98(39):e17305. doi: 10.1097/MD.0000000000017305. Medicine (Baltimore). 2019. PMID: 31574858 Free PMC article.

2

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. J Pediatr Endocrinol Metab. 2015 Mar;28(3-4):471-5. doi: 10.1515/jpem-2014-0278. J Pediatr Endocrinol Metab. 2015. PMID: 25381944

3

[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. Zhonghua Er Ke Za Zhi. 2015 May;53(5):360-5. Zhonghua Er Ke Za Zhi. 2015. PMID: 26080666 Review. Chinese.

4

Fecal microbiota transplantation induces remission of infantile allergic colitis through gut microbiota re-establishment.

Liu SX, Li YH, Dai WK, Li XS, Qiu CZ, Ruan ML, Zou B, Dong C, Liu YH, He JY, Huang ZH, Shu SN. Liu SX, et al. Among authors: huang zh. World J Gastroenterol. 2017 Dec 28;23(48):8570-8581. doi: 10.3748/wjg.v23.i48.8570. World J Gastroenterol. 2017. PMID: 29358865 Free PMC article.

5

Clinical Assessment of Differential Diagnostic Methods in Infants with Cholestasis due to Biliary Atresia or Non-Biliary Atresia.

Dong C, Zhu HY, Chen YC, Luo XP, Huang ZH. Dong C, et al. Among authors: huang zh. Curr Med Sci. 2018 Feb;38(1):137-143. doi: 10.1007/s11596-018-1857-6. Epub 2018 Mar 15. Curr Med Sci. 2018. PMID: 30074163

6

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: huang zh. 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

7

[A novel SLC25A13 variant and the resultant aberrant transcript identified in a pedigree affected with citrin deficiency].

Deng M, Cheng Y, Shu S, Huang Z, Song Y. Deng M, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Feb 10;36(2):116-119. doi: 10.3760/cma.j.issn.1003-9406.2019.02.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30703226 Chinese.

8

Biliary atresia combined with progressive familial intrahepatic cholestasis type 3: A case report and review of the literature.

Zhang BP, Huang ZH, Dong C. Zhang BP, et al. Among authors: huang zh. Medicine (Baltimore). 2019 May;98(19):e15593. doi: 10.1097/MD.0000000000015593. Medicine (Baltimore). 2019. PMID: 31083246 Free PMC article. Review.

9

Case Report: Be Aware of "New" Features of Niemann-Pick Disease: Insights From Two Pediatric Cases.

Chen F, Guo S, Li X, Liu S, Wang L, Zhang VW, Xu H, Huang Z, Ying Y, Shu S. Chen F, et al. Front Genet. 2022 Mar 11;13:845246. doi: 10.3389/fgene.2022.845246. eCollection 2022. Front Genet. 2022. PMID: 35360843 Free PMC article.

10

Long-term safety and efficacy of fecal microbiota transplantation in 74 children: A single-center retrospective study.

Zou B, Liu SX, Li XS, He JY, Dong C, Ruan ML, Xu L, Bai T, Huang ZH, Shu SN. Zou B, et al. Among authors: huang zh. Front Pediatr. 2022 Oct 11;10:964154. doi: 10.3389/fped.2022.964154. eCollection 2022. Front Pediatr. 2022. PMID: 36304525 Free PMC article.

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