citrulline and Cholestasis, Intrahepatic

citrulline has been researched along with Cholestasis, Intrahepatic in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's1 (20.00)24.3611
2020's2 (40.00)2.80

Authors

AuthorsStudies
Cai, Y; Jiang, M; Li, X; Lin, Y; Liu, L; Liu, Z; Lu, Z; Peng, M; Shao, Y; Zhang, W1
Bogdańska, A; Ciara, E; Jankowska, I; Jurkiewicz, D; Lipiński, P; Płoski, R; Rokicki, D; Socha, P; Stradomska, T; Tylki-Szymańska, A; Więcek, S1
Guo, L; Han, LS; Kobayashi, K; Saheki, T; Song, YZ; Yang, YL1
Kobayashi, K; Ngu, HL; Zabedah, MY1
Begum, L; Gao, HZ; Iijima, M; Jalil, MA; Kobayashi, K; Li, MX; Nishi, I; Saheki, T; Yamaguchi, N; Yasuda, T1

Reviews

1 review(s) available for citrulline and Cholestasis, Intrahepatic

ArticleYear
Pathogenesis and pathophysiology of citrin (a mitochondrial aspartate glutamate carrier) deficiency.
    Metabolic brain disease, 2002, Volume: 17, Issue:4

    Topics: Calcium-Binding Proteins; Cholestasis, Intrahepatic; Citrulline; Humans; Infant, Newborn; Infant, Newborn, Diseases; Membrane Transport Proteins; Metabolism, Inborn Errors; Mitochondrial Membrane Transport Proteins; Mitochondrial Proteins; Mutation; Organic Anion Transporters

2002

Other Studies

4 other study(ies) available for citrulline and Cholestasis, Intrahepatic

ArticleYear
Features of liver injury in 138 Chinese patients with NICCD.
    Journal of pediatric endocrinology & metabolism : JPEM, 2023, Dec-15, Volume: 36, Issue:12

    Topics: Cholestasis, Intrahepatic; Citrulline; Citrullinemia; East Asian People; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Mitochondrial Membrane Transport Proteins; Mutation; Tyrosine

2023
Neonatal cholestasis due to citrin deficiency: diagnostic pitfalls.
    Acta biochimica Polonica, 2020, May-21, Volume: 67, Issue:2

    Topics: Blood Coagulation Disorders; Cholagogues and Choleretics; Cholestasis, Intrahepatic; Citrulline; Citrullinemia; Early Diagnosis; Exome Sequencing; Follow-Up Studies; Humans; Hypoalbuminemia; Infant; Infant, Low Birth Weight; Infant, Newborn; Jaundice, Obstructive; Male; Neonatal Screening; Retrospective Studies; Tandem Mass Spectrometry; Treatment Outcome; Ursodeoxycholic Acid; Vitamins

2020
[Failure to thrive and dyslipidemia caused by citrin deficiency: a novel clinical phenotype].
    Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, 2009, Volume: 11, Issue:5

    Topics: Body Weight; Calcium-Binding Proteins; Cholestasis, Intrahepatic; Citrulline; Dyslipidemias; Failure to Thrive; Humans; Infant; Lipids; Male; Mitochondrial Membrane Transport Proteins; Mutation; Organic Anion Transporters; Phenotype

2009
Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) in three Malay children.
    The Malaysian journal of pathology, 2010, Volume: 32, Issue:1

    Topics: Child; Child, Preschool; Cholestasis, Intrahepatic; Citrulline; Citrullinemia; Female; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Malaysia; Male; Mitochondrial Membrane Transport Proteins; Mutagenesis, Insertional; Polymerase Chain Reaction

2010