citrulline has been researched along with Classic Galactosemia in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (100.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
COFFEY, VP | 1 |
Bloom, A; Spector, E; Streeter, S | 1 |
O'Reilly, S | 1 |
3 other study(ies) available for citrulline and Classic Galactosemia
Article | Year |
---|---|
MENTAL RETARDATION AND THE INBORN ERRORS OF METABOLISM.
Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Arginine; Citrulline; Fructose; Galactosemias; Histidine; Homocysteine; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Renal Aminoacidurias; Vitamin B 6 Deficiency | 1964 |
Growth of establishes lymphocytes in selective media: application to studies of inborn metabolic errors and somatic mutations.
Topics: Amino Acid Metabolism, Inborn Errors; Cell Line; Citrulline; Culture Media; DNA, Viral; Galactosemias; Herpesvirus 4, Human; Humans; Hybrid Cells; Lesch-Nyhan Syndrome; Lymphocytes; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Mutation; Pentosyltransferases | 1973 |
Neurologic disorders and liver disease.
Topics: Adipose Tissue; Ammonia; Brain Diseases; Citrulline; Fatty Liver; Galactosemias; Hepatic Encephalopathy; Hepatitis; Hepatolenticular Degeneration; Humans; Hyperbilirubinemia, Hereditary; Kidney Diseases; Liver; Liver Diseases; Metabolism, Inborn Errors; Mucopolysaccharidoses; Nervous System Diseases; Neurologic Manifestations; Paraplegia; Phenylketonurias; Quadriplegia; Urea | 1971 |