Qiu YL - Search Results

1

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: qiu yl. 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.

2

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.

3

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: qiu yl. 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.

4

A Specially Designed Multi-Gene Panel Facilitates Genetic Diagnosis in Children with Intrahepatic Cholestasis: Simultaneous Test of Known Large Insertions/Deletions.

Wang NL, Lu YL, Zhang P, Zhang MH, Gong JY, Lu Y, Xie XB, Qiu YL, Yan YY, Wu BB, Wang JS. Wang NL, et al. Among authors: qiu yl. PLoS One. 2016 Oct 5;11(10):e0164058. doi: 10.1371/journal.pone.0164058. eCollection 2016. PLoS One. 2016. PMID: 27706244 Free PMC article.

5

Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ-glutamyltransferase cholestasis.

Qiu YL, Gong JY, Feng JY, Wang RX, Han J, Liu T, Lu Y, Li LT, Zhang MH, Sheps JA, Wang NL, Yan YY, Li JQ, Chen L, Borchers CH, Sipos B, Knisely AS, Ling V, Xing QH, Wang JS. Qiu YL, et al. Hepatology. 2017 May;65(5):1655-1669. doi: 10.1002/hep.29020. Epub 2017 Mar 23. Hepatology. 2017. PMID: 28027573 Free PMC article.

6

Novel NBAS mutations and fever-related recurrent acute liver failure in Chinese children: a retrospective study.

Li JQ, Qiu YL, Gong JY, Dou LM, Lu Y, Knisely AS, Zhang MH, Luan WS, Wang JS. Li JQ, et al. Among authors: qiu yl. BMC Gastroenterol. 2017 Jun 19;17(1):77. doi: 10.1186/s12876-017-0636-3. BMC Gastroenterol. 2017. PMID: 28629372 Free PMC article.

7

Splicing analysis of rare/novel synonymous or intronic variants identified in ABCB11 heterozygotes presenting as progressive intrahepatic cholestasis with low γ-glutamyltransferase.

Wang NL, Qiu YL, Guan WC, Li G, Lu Y, Zhang MH, Luan WS, Wang JS. Wang NL, et al. Among authors: qiu yl. Hepatol Res. 2018 Jun;48(7):574-584. doi: 10.1111/hepr.13055. Epub 2018 Feb 12. Hepatol Res. 2018. PMID: 29316097

8

Comprehensive bile acid profiling in hereditary intrahepatic cholestasis: Genetic and clinical correlations.

Liu T, Wang RX, Han J, Hao CZ, Qiu YL, Yan YY, Li LT, Wang NL, Gong JY, Lu Y, Zhang MH, Xie XB, Yang JC, You YJ, Li JQ, Knisely AS, Borchers CH, Ling V, Wang JS. Liu T, et al. Among authors: qiu yl. Liver Int. 2018 Sep;38(9):1676-1685. doi: 10.1111/liv.13714. Epub 2018 Mar 12. Liver Int. 2018. PMID: 29412511

9

Novel missense mutation in VPS33B is associated with isolated low gamma-glutamyltransferase cholestasis: Attenuated, incomplete phenotype of arthrogryposis, renal dysfunction, and cholestasis syndrome.

Qiu YL, Liu T, Abuduxikuer K, Hao CZ, Gong JY, Zhang MH, Li LT, Yan YY, Li JQ, Wang JS. Qiu YL, et al. Hum Mutat. 2019 Dec;40(12):2247-2257. doi: 10.1002/humu.23770. Epub 2019 Sep 3. Hum Mutat. 2019. PMID: 31479177

10

TJP2 hepatobiliary disorders: Novel variants and clinical diversity.

Zhang J, Liu LL, Gong JY, Hao CZ, Qiu YL, Lu Y, Feng JY, Li JQ, Li ZD, Wang MX, Xing QH, Knisely AS, Wang JS. Zhang J, et al. Among authors: qiu yl. Hum Mutat. 2020 Feb;41(2):502-511. doi: 10.1002/humu.23947. Epub 2019 Nov 28. Hum Mutat. 2020. PMID: 31696999

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