ornithine has been researched along with BCKD Deficiency in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (85.71) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Gibson, KM; Knerr, I; Vockley, J; Weinhold, N | 1 |
| WOODY, NC | 1 |
| Kim, S; Nochumson, S; Paik, WK | 1 |
| Ampola, MG | 1 |
| Levy, HL | 1 |
| Barkin, E; Levy, HL | 1 |
| Antener, I | 1 |
3 review(s) available for ornithine and BCKD Deficiency
| Article | Year |
|---|---|
Advances and challenges in the treatment of branched-chain amino/keto acid metabolic defects.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Branched-Chain; Animals; Creatinine; Humans; Maple Syrup Urine Disease; Mass Spectrometry; Metabolomics; Mice; Mice, Knockout; Mice, Transgenic; Ornithine; Phenotype; Risk | 2012 |
Phenylketonuria and other disorders of amino acid metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Child, Preschool; Counseling; Cystathionine; Cystinosis; Cystinuria; Diet Therapy; Dietary Proteins; Family; Female; Hartnup Disease; Histidine; Homocystinuria; Humans; Hyperglycemia; Infant; Infant, Newborn; Lysine; Maple Syrup Urine Disease; Ornithine; Phenylketonurias; Pregnancy; Proline; Tyrosine | 1973 |
Genetic screening.
Topics: Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Arginine; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Erythrocytes; Fanconi Syndrome; Galactosemias; Genetics, Population; Glucosephosphate Dehydrogenase; Glycine; Hartnup Disease; Heterozygote; Histidine; Homocystine; Humans; Lysine; Maple Syrup Urine Disease; Mass Screening; Methods; Ornithine; Phenylalanine; Phenylketonurias; Succinates; Tyrosine | 1973 |
4 other study(ies) available for ornithine and BCKD Deficiency
| Article | Year |
|---|---|
HYPERLYSINEMIA.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Alcohols; Aminobutyrates; Anemia; Arginine; Asthenia; Blood Chemical Analysis; Child; Chromatography; Genetics, Medical; Growth; Humans; Hyperlysinemias; Infant; Lysine; Maple Syrup Urine Disease; Muscular Diseases; Ornithine; Seizures; Urine | 1964 |
Effect of modification on inhibitory amino acids on arginase activity.
Topics: Amino Acids; Animals; Arginase; Cattle; Humans; Keto Acids; Liver; Lysine; Maple Syrup Urine Disease; Methylation; Ornithine; Structure-Activity Relationship | 1978 |
Comparison of amino acid concentrations between plasma and erythrocytes. Studies in normal human subjects and those with metabolic disorders.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Aspartic Acid; Biological Transport; Child; Chromatography, Ion Exchange; Cystine; Erythrocytes; Glutamates; Glutathione; Glycine; Histidine; Homocystine; Homocystinuria; Humans; Infant; Maple Syrup Urine Disease; Methionine; Ornithine; Phenylketonurias; Plasma; Renal Tubular Transport, Inborn Errors; Serine; Spectrophotometry; Threonine; Tyrosine | 1971 |
[Biochemical studies on inherited disorders of amino acid metabolism in pediatrics].
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Chemistry, Clinical; Child; Child, Preschool; Chromatography, Paper; Cystine; Cystinosis; Cystinuria; Electrophoresis; Fanconi Syndrome; Feces; Histidine; Humans; Keto Acids; Lysine; Maple Syrup Urine Disease; Ornithine; Phenylketonurias | 1970 |