methionine has been researched along with Citrullinemia 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 | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Avdjieva-Tzavella, DM; Ivanova, MB; Kathom, HM; Lazarova, EA; Panteleeva, EI; Tincheva, RS; Tincheva, SS; Todorov, TP; Todorova, AP; Yaneva, PG | 1 |
| Abukawa, D; Aikawa, J; Iinuma, K; Kobayashi, K; Ohura, T; Saheki, T; Sakamoto, O; Tazawa, Y | 1 |
2 other study(ies) available for methionine and Citrullinemia
| Article | Year |
|---|---|
First Bulgarian case of citrin deficiency caused by one novel and one recurrent mutation in the SLC25A13 gene.
Topics: Arginine; Bulgaria; Calcium-Binding Proteins; Citrulline; Citrullinemia; DNA Mutational Analysis; Female; Follow-Up Studies; Galactose; Genetic Carrier Screening; Humans; Infant, Newborn; Male; Methionine; Mitochondrial Membrane Transport Proteins; Mutation, Missense; Organic Anion Transporters; Phenotype; Pregnancy; White People | 2014 |
A novel inborn error of metabolism detected by elevated methionine and/or galactose in newborn screening: neonatal intrahepatic cholestasis caused by citrin deficiency.
Topics: Cholestasis, Intrahepatic; Citrullinemia; Diagnosis, Differential; DNA Mutational Analysis; Galactose; Humans; Infant, Newborn; Mass Screening; Methionine; Neonatal Screening; Phenylalanine; Retrospective Studies | 2003 |