Huang Z - Search Results

1

Repeated and multiple fecal microbiota transplantations plus partial enteral nutrition as the first-line treatment in active pediatric Crohn's disease.

Zou B, Liu S, Li X, He J, Dong C, Ruan M, Huang Z, Shu S. Zou B, et al. Among authors: huang z. Front Cell Infect Microbiol. 2023 Feb 23;13:1083236. doi: 10.3389/fcimb.2023.1083236. eCollection 2023. Front Cell Infect Microbiol. 2023. PMID: 36909725 Free PMC article.

2

The value of radionuclide hepatobiliary scintigraphy in combination with determination of bilirubin from duodenal drainage in differential diagnosis of infantile persistent jaundice.

Liu SX, Huang ZH. Liu SX, et al. Front Med China. 2010 Sep;4(3):342-5. doi: 10.1007/s11684-010-0099-1. Epub 2010 Aug 10. Front Med China. 2010. PMID: 21191842

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. Among authors: huang z. 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. 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. 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. 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. Among authors: huang z. 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. Medicine (Baltimore). 2019 May;98(19):e15593. doi: 10.1097/MD.0000000000015593. Medicine (Baltimore). 2019. PMID: 31083246 Free PMC article. Review.

9

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

10

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. Among authors: huang z. Front Genet. 2022 Mar 11;13:845246. doi: 10.3389/fgene.2022.845246. eCollection 2022. Front Genet. 2022. PMID: 35360843 Free PMC article.

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