Zhao J - Search Results

1

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. Among authors: zhao j. PLoS One. 2015 Jun 15;10(6):e0130355. doi: 10.1371/journal.pone.0130355. eCollection 2015. PLoS One. 2015. PMID: 26076142 Free PMC article.

2

Novel Melanocortin 2 Receptor Variant in a Chinese Infant With Familial Glucocorticoid Deficiency Type 1, Case Report and Review of Literature.

Abuduxikuer K, Li ZD, Xie XB, Li YC, Zhao J, Wang JS. Abuduxikuer K, et al. Among authors: zhao j. Front Endocrinol (Lausanne). 2019 Jun 6;10:359. doi: 10.3389/fendo.2019.00359. eCollection 2019. Front Endocrinol (Lausanne). 2019. PMID: 31244773 Free PMC article.

3

Primary ∆4-3-oxosteroid 5β-reductase deficiency: two cases in China.

Zhao J, Fang LJ, Setchell KD, Chen R, Li LT, Wang JS. Zhao J, et al. World J Gastroenterol. 2012 Dec 21;18(47):7113-7. doi: 10.3748/wjg.v18.i47.7113. World J Gastroenterol. 2012. PMID: 23323017 Free PMC article.

4

[Mutation analysis of FAH gene in patients with tyrosinemia type 1].

Dou LM, Fang LJ, Wang XH, Lu W, Chen R, Li LT, Zhao J, Wang JS. Dou LM, et al. Among authors: zhao j. Zhonghua Er Ke Za Zhi. 2013 Apr;51(4):302-7. Zhonghua Er Ke Za Zhi. 2013. PMID: 23927806 Chinese.

5

Two novel VPS33B mutations in a patient with arthrogryposis, renal dysfunction and cholestasis syndrome in mainland China.

Li LT, Zhao J, Chen R, Wang JS. Li LT, et al. Among authors: zhao j. World J Gastroenterol. 2014 Jan 7;20(1):326-9. doi: 10.3748/wjg.v20.i1.326. World J Gastroenterol. 2014. PMID: 24415890 Free PMC article.

6

ARC syndrome with high GGT cholestasis caused by VPS33B mutations.

Wang JS, Zhao J, Li LT. Wang JS, et al. Among authors: zhao j. World J Gastroenterol. 2014 Apr 28;20(16):4830-4. doi: 10.3748/wjg.v20.i16.4830. World J Gastroenterol. 2014. PMID: 24782640 Free PMC article.

7

Cholestasis as a dominating symptom of patients with CYP27A1 mutations: An analysis of 17 Chinese infants.

Zhang P, Zhao J, Peng XM, Qian YY, Zhao XM, Zhou WH, Wang JS, Wu BB, Wang HJ. Zhang P, et al. Among authors: zhao j, zhao xm. J Clin Lipidol. 2021 Jan-Feb;15(1):116-123. doi: 10.1016/j.jacl.2020.12.004. Epub 2020 Dec 14. J Clin Lipidol. 2021. PMID: 33414089

8

Pediatric Wilson disease presenting as acute liver failure: Prognostic indices.

Fang WY, Abuduxikuer K, Shi P, Qiu YL, Zhao J, Li YC, Zhang XY, Wang NL, Xie XB, Lu Y, Knisely AS, Wang JS. Fang WY, et al. Among authors: zhao j. World J Clin Cases. 2021 May 16;9(14):3273-3286. doi: 10.12998/wjcc.v9.i14.3273. World J Clin Cases. 2021. PMID: 34002136 Free PMC article.

9

Δ4-3-oxosteroid-5β-reductase deficiency: Responses to oral bile acid therapy and long-term outcomes.

Zhang MH, Setchell KD, Zhao J, Gong JY, Lu Y, Wang JS. Zhang MH, et al. Among authors: zhao j. World J Gastroenterol. 2019 Feb 21;25(7):859-869. doi: 10.3748/wjg.v25.i7.859. World J Gastroenterol. 2019. PMID: 30809085 Free PMC article.

10

Severe Neonatal Cholestasis in Cerebrotendinous Xanthomatosis: Genetics, Immunostaining, Mass Spectrometry.

Gong JY, Setchell KDR, Zhao J, Zhang W, Wolfe B, Lu Y, Lackner K, Knisely AS, Wang NL, Hao CZ, Zhang MH, Wang JS. Gong JY, et al. Among authors: zhao j. J Pediatr Gastroenterol Nutr. 2017 Nov;65(5):561-568. doi: 10.1097/MPG.0000000000001730. J Pediatr Gastroenterol Nutr. 2017. PMID: 28937538

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