Lu Y - Search Results

1

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: lu y. Hum Mutat. 2020 Feb;41(2):502-511. doi: 10.1002/humu.23947. Epub 2019 Nov 28. Hum Mutat. 2020. PMID: 31696999

2

[Clinical features of hepatolenticular degeneration in children].

Lu Y, Wang XH, Wang JS. Lu Y, et al. Zhonghua Gan Zang Bing Za Zhi. 2008 Mar;16(3):224-6. Zhonghua Gan Zang Bing Za Zhi. 2008. PMID: 18364085 Chinese.

3

Urinary copper/zinc ratio: a promising parameter for replacement of 24-hour urinary copper excretion for diagnosis of Wilson's disease in children.

Wang JS, Lu Y, Wang XH, Zhu QR. Wang JS, et al. Among authors: lu y. World J Pediatr. 2010 May;6(2):148-53. doi: 10.1007/s12519-010-0023-4. Epub 2010 Feb 1. World J Pediatr. 2010. PMID: 20127216

4

[The reassessment of the diagnostic value of 24-hour urinary copper excretion in children with Wilson's disease].

Lu Y, Liu XQ, Wang XH, Wang JS. Lu Y, et al. Zhonghua Gan Zang Bing Za Zhi. 2010 Jan;18(1):49-53. doi: 10.3760/cma.j.issn.1007-3418.2010.01.012. Zhonghua Gan Zang Bing Za Zhi. 2010. PMID: 20128970 Chinese.

5

[Clinical characteristics of autoimmune hepatitis in 11 children].

Lu Y, Wang XH, Wang JS. Lu Y, et al. Zhonghua Er Ke Za Zhi. 2010 Oct;48(10):758-63. Zhonghua Er Ke Za Zhi. 2010. PMID: 21176485 Chinese.

6

Clinical and molecular characterization of Wilson's disease in China: identification of 14 novel mutations.

Li XH, Lu Y, Ling Y, Fu QC, Xu J, Zang GQ, Zhou F, De-Min Y, Han Y, Zhang DH, Gong QM, Lu ZM, Kong XF, Wang JS, Zhang XX. Li XH, et al. Among authors: lu y, lu zm. BMC Med Genet. 2011 Jan 11;12:6. doi: 10.1186/1471-2350-12-6. BMC Med Genet. 2011. PMID: 21219664 Free PMC article.

7

Chinese children with chronic intrahepatic cholestasis and high γ-glutamyl transpeptidase: clinical features and association with ABCB4 mutations.

Fang LJ, Wang XH, Knisely AS, Yu H, Lu Y, Liu LY, Wang JS. Fang LJ, et al. Among authors: lu y. J Pediatr Gastroenterol Nutr. 2012 Aug;55(2):150-6. doi: 10.1097/MPG.0b013e31824ef36f. J Pediatr Gastroenterol Nutr. 2012. PMID: 22343912

8

Biochemical characteristics of neonatal cholestasis induced by citrin deficiency.

Wang JS, Wang XH, Zheng YJ, Fu HY, Chen R, Lu Y, Fang LJ, Saheki T, Kobayashi K. Wang JS, et al. Among authors: lu y. World J Gastroenterol. 2012 Oct 21;18(39):5601-7. doi: 10.3748/wjg.v18.i39.5601. World J Gastroenterol. 2012. PMID: 23112554 Free PMC article.

9

Association of variants of ABCB11 with transient neonatal cholestasis.

Liu LY, Wang XH, Lu Y, Zhu QR, Wang JS. Liu LY, et al. Among authors: lu y. Pediatr Int. 2013 Apr;55(2):138-44. doi: 10.1111/ped.12049. Pediatr Int. 2013. PMID: 23279303

10

Hypothyroidism Associated with ATP8B1 Deficiency.

Li L, Deheragoda M, Lu Y, Gong J, Wang J. Li L, et al. Among authors: lu y. J Pediatr. 2015 Dec;167(6):1334-9.e1. doi: 10.1016/j.jpeds.2015.08.037. Epub 2015 Sep 15. J Pediatr. 2015. PMID: 26382629

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