citrulline has been researched along with Jaundice, Cholestatic in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bogdańska, A; Ciara, E; Jankowska, I; Jurkiewicz, D; Lipiński, P; Płoski, R; Rokicki, D; Socha, P; Stradomska, T; Tylki-Szymańska, A; Więcek, S | 1 |
| Balasubramaniam, S; Chew, HB; Hanifah, MJ; Keng, WT; Kobayashi, K; Ngu, LH; Zabedah, MY | 1 |
2 other study(ies) available for citrulline and Jaundice, Cholestatic
| Article | Year |
|---|---|
Neonatal cholestasis due to citrin deficiency: diagnostic pitfalls.
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 |
Neonatal intrahepatic cholestasis associated with citrin deficiency (NICCD): a case series of 11 Malaysian patients.
Topics: Asian People; Biomarkers; Citrulline; Citrullinemia; DNA Mutational Analysis; Exons; Fatal Outcome; Female; Genetic Predisposition to Disease; Heredity; Humans; Infant; Infant, Newborn; Jaundice, Obstructive; Liver Failure; Malaysia; Male; Mitochondrial Membrane Transport Proteins; Mutation; Pedigree; Phenotype; Prognosis; Time Factors | 2010 |