Wang JS - Search Results

1

Four New Cases of SLC35A2-CDG With Novel Mutations and Clinical Features.

Abuduxikuer K, Wang JS. Abuduxikuer K, et al. Among authors: wang js. Front Genet. 2021 May 27;12:658786. doi: 10.3389/fgene.2021.658786. eCollection 2021. Front Genet. 2021. PMID: 34122512 Free PMC article.

2

Zinc mono-therapy in pre-symptomatic Chinese children with Wilson disease: a single center, retrospective study.

Abuduxikuer K, Wang JS. Abuduxikuer K, et al. Among authors: wang js. PLoS One. 2014 Jan 24;9(1):e86168. doi: 10.1371/journal.pone.0086168. eCollection 2014. PLoS One. 2014. PMID: 24475083 Free PMC article.

3

JAG1 Mutation Spectrum and Origin in Chinese Children with Clinical Features of Alagille Syndrome.

Li L, Dong J, Wang X, Guo H, Wang H, Zhao J, Qiu Y, Abuduxikuer K, Wang J. Li L, et al. PLoS One. 2015 Jun 15;10(6):e0130355. doi: 10.1371/journal.pone.0130355. eCollection 2015. PLoS One. 2015. PMID: 26076142 Free PMC article.

4

Wilson disease with hepatic presentation in an eight-month-old boy.

Abuduxikuer K, Li LT, Qiu YL, Wang NL, Wang JS. Abuduxikuer K, et al. Among authors: wang nl, wang js. World J Gastroenterol. 2015 Aug 7;21(29):8981-4. doi: 10.3748/wjg.v21.i29.8981. World J Gastroenterol. 2015. PMID: 26269689 Free PMC article.

5

The Features of GGT in Patients with ATP8B1 or ABCB11 Deficiency Improve the Diagnostic Efficiency.

Wang NL, Li LT, Wu BB, Gong JY, Abuduxikuer K, Li G, Wang JS. Wang NL, et al. Among authors: wang js. PLoS One. 2016 Apr 6;11(4):e0153114. doi: 10.1371/journal.pone.0153114. eCollection 2016. PLoS One. 2016. PMID: 27050426 Free PMC article.

6

A fatal case of mitochondrial DNA depletion syndrome with novel compound heterozygous variants in the deoxyguanosine kinase gene.

Fang W, Song P, Xie X, Wang J, Lu Y, Li G, Abuduxikuer K. Fang W, et al. Oncotarget. 2017 Sep 15;8(48):84309-84319. doi: 10.18632/oncotarget.20905. eCollection 2017 Oct 13. Oncotarget. 2017. PMID: 29137425 Free PMC article.

7

A novel homozygous mutation in the glycerol-3-phosphate dehydrogenase 1 gene in a Chinese patient with transient infantile hypertriglyceridemia: a case report.

Li JQ, Xie XB, Feng JY, Chen L, Abuduxikuer K, Lu Y, Li YC, Wang JS. Li JQ, et al. Among authors: wang js. BMC Gastroenterol. 2018 Jun 25;18(1):96. doi: 10.1186/s12876-018-0827-6. BMC Gastroenterol. 2018. PMID: 29940878 Free PMC article.

8

Novel methionyl-tRNA synthetase gene variants/phenotypes in interstitial lung and liver disease: A case report and review of literature.

Abuduxikuer K, Feng JY, Lu Y, Xie XB, Chen L, Wang JS. Abuduxikuer K, et al. Among authors: wang js. World J Gastroenterol. 2018 Sep 28;24(36):4208-4216. doi: 10.3748/wjg.v24.i36.4208. World J Gastroenterol. 2018. PMID: 30271085 Free PMC article. Review.

9

UGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children: A retrospective analysis and quantitative correlation.

Abuduxikuer K, Fang LJ, Li LT, Gong JY, Wang JS. Abuduxikuer K, et al. Among authors: wang js. Medicine (Baltimore). 2018 Dec;97(49):e13576. doi: 10.1097/MD.0000000000013576. Medicine (Baltimore). 2018. PMID: 30544479 Free PMC article.

10

Risk factors associated with mortality in neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) and clinical implications.

Abuduxikuer K, Chen R, Wang ZL, Wang JS. Abuduxikuer K, et al. Among authors: wang zl, wang js. BMC Pediatr. 2019 Jan 14;19(1):18. doi: 10.1186/s12887-018-1383-5. BMC Pediatr. 2019. PMID: 30642297 Free PMC article.

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