Fang LJ - Search Results

1

[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: fang lj. Zhonghua Er Ke Za Zhi. 2013 Apr;51(4):302-7. Zhonghua Er Ke Za Zhi. 2013. PMID: 23927806 Chinese.

2

[Progressive familial intrahepatic cholestasis type 3].

Fang LJ, Wang JS. Fang LJ, et al. Zhonghua Gan Zang Bing Za Zhi. 2010 Mar;18(3):238-40. doi: 10.3760/cma.j.issn.1007-3418.2010.03.023. Zhonghua Gan Zang Bing Za Zhi. 2010. PMID: 20380808 Review. Chinese. No abstract available.

3

A new frame-shifting mutation of UGT1A1 gene causes type I Crigler-Najjar syndrome.

Wang J, Fang LJ, Li L, Wang JS, Chen C. Wang J, et al. Among authors: fang lj. Chin Med J (Engl). 2011 Dec;124(23):4109-11. Chin Med J (Engl). 2011. PMID: 22340355 Clinical Trial.

4

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. J Pediatr Gastroenterol Nutr. 2012 Aug;55(2):150-6. doi: 10.1097/MPG.0b013e31824ef36f. J Pediatr Gastroenterol Nutr. 2012. PMID: 22343912

5

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: fang lj. 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.

6

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. Among authors: fang lj. 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.

7

[Characteristics of the plasma amino acid spectrum of neonatal intrahepatic cholestasis caused by citrin deficiency].

Fu HY, Wang XH, Lu Y, Zhang SR, Fang LJ, Chen R, Yu H, Zhu QR, Wang JS. Fu HY, et al. Among authors: fang lj. Zhonghua Gan Zang Bing Za Zhi. 2013 Dec;21(12):934-9. doi: 10.3760/cma.j.issn.1007-3418.2013.12.012. Zhonghua Gan Zang Bing Za Zhi. 2013. PMID: 24636297 Chinese.

8

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: fang lj. Medicine (Baltimore). 2018 Dec;97(49):e13576. doi: 10.1097/MD.0000000000013576. Medicine (Baltimore). 2018. PMID: 30544479 Free PMC article.

9

NTCP Deficiency Causes Gallbladder Abnormalities in Mice and Human Beings.

Mao F, Wang MX, Hou X, Zhou Z, Yan YY, Fang LJ, Tan Z, Fang WY, Liu T, He W, Li C, Xie XB, Lu SQ, Sui J, Wang F, Han J, Wang JS, Li W. Mao F, et al. Among authors: fang wy, fang lj. Cell Mol Gastroenterol Hepatol. 2021;11(3):831-839. doi: 10.1016/j.jcmgh.2020.09.001. Epub 2020 Sep 9. Cell Mol Gastroenterol Hepatol. 2021. PMID: 32919083 Free PMC article. No abstract available.

10

Genetic spectrum and clinical characteristics of 3β-hydroxy-Δ⁵-C₂₇-steroid oxidoreductase (HSD3B7) deficiency in China.

Zhao J, Setchell KDR, Gong Y, Sun Y, Zhang P, Heubi JE, Fang L, Lu Y, Xie X, Gong J, Wang JS. Zhao J, et al. Orphanet J Rare Dis. 2021 Oct 9;16(1):417. doi: 10.1186/s13023-021-02041-7. Orphanet J Rare Dis. 2021. PMID: 34627351 Free PMC article.

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