Ling-juan Fang

109 Xueyuan Western Road
Wenzhou, China

Last Updated: 09/26/2026

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Found 10 publications

NTCP Deficiency Causes Gallbladder Abnormalities in Mice and Human Beings.

NTCP Deficiency Causes Gallbladder Abnormalities in Mice and Human Beings.

Journal: Cellular and molecular gastroenterology and hepatology

Published: December 28, 2019

1H NMR-based metabolomics analyses in children with Helicobacter pylori infection and the alteration of serum metabolites after treatment.

1H NMR-based metabolomics analyses in children with Helicobacter pylori infection and the alteration of serum metabolites after treatment.

Journal: Microbial pathogenesis

Published: September 11, 2019

An infant presenting with extreme hypertriglyceridemia diagnosed as glycogen storage disease type Ia.

An infant presenting with extreme hypertriglyceridemia diagnosed as glycogen storage disease type Ia.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: August 18, 2019

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

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

Journal: Medicine

Published: December 14, 2018

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

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

Journal: Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology

Published: March 19, 2014

Mutation analysis of FAH gene in patients with tyrosinemia type 1

Mutation analysis of FAH gene in patients with tyrosinemia type 1

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: August 10, 2013

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

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

Journal: World journal of gastroenterology

Published: July 25, 2012

Biochemical characteristics of neonatal cholestasis induced by citrin deficiency.

Biochemical characteristics of neonatal cholestasis induced by citrin deficiency.

Journal: World journal of gastroenterology

Published: April 12, 2012

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

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

Journal: Journal of pediatric gastroenterology and nutrition

Published: February 21, 2012

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

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

Journal: Chinese medical journal

Published: February 21, 2012

Showing 1-10 of 10

Last Updated: 09/26/2026