ornithine has been researched along with Metabolic Diseases in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (16.67) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Hoeks, M; Huigen, M; IJzermans, T; Nijenhuis, T; Rennings, A; van der Meijden, W | 1 |
| J, J; K N, S; Sivashanmugam, M; V, U | 1 |
| ROBSON, EB; ROSE, GA | 1 |
| AVERY, GB; CONE, TE; FLEMING, WH; MORGAN, RI | 1 |
| Andrade, D; Camacho, JA; Cederbaum, SD; Derbeneva, O; Mardach, R; Qu, Y; Rioseco-Camacho, N; Ruiz-Pesini, E; Zaldivar, F | 1 |
| Goodwin, JF | 1 |
1 review(s) available for ornithine and Metabolic Diseases
| Article | Year |
|---|---|
Ornithine and its role in metabolic diseases: An appraisal.
Topics: Animals; Humans; Metabolic Diseases; Ornithine; Polyamines; Proline; Protein Binding; Protein Structure, Secondary | 2017 |
5 other study(ies) available for ornithine and Metabolic Diseases
| Article | Year |
|---|---|
Improving a Rare Metabolic Disorder Through Kidney Transplantation: A Case Report of a Patient With Lysinuric Protein Intolerance.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acid Transport System y+L; Arginine; Humans; Kidney Transplantation; Lysine; Metabolic Diseases; Ornithine | 2023 |
The effect of intravenous lysine on the renal clearances of cystine, arginine and ornithine in normal subjects, in patients with cystinuria and Fanconi syndrome and in their relatives.
Topics: Amino Acids; Arginine; Cystine; Cystinuria; Fanconi Syndrome; Humans; Lysine; Metabolic Diseases; Ornithine | 1957 |
GASTROINTESTINAL MALABSORPTION ASSOCIATED WITH CYSTINURIA. REPORT OF A CASE IN A NEGRO.
Topics: Adolescent; Anemia; Anemia, Hypochromic; Arginine; Black People; Celiac Disease; Cystine; Cystinuria; Emaciation; Humans; Lysine; Metabolic Diseases; Ornithine; Phosphorus Metabolism Disorders; Proteins; Rickets | 1963 |
Clinical and functional characterization of a human ORNT1 mutation (T32R) in the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome.
Topics: Adolescent; Adult; Amino Acid Transport Systems, Basic; Child; Citrullinemia; DNA, Mitochondrial; Female; Haplotypes; Humans; Hyperammonemia; Male; Metabolic Diseases; Mitochondrial Membrane Transport Proteins; Mutation; Ornithine; Pedigree; Phenotype; Polymorphism, Genetic; Proteins; RNA, Messenger; Syndrome | 2006 |
Spectrophotometry of proline in plasma and urine.
Topics: Amino Acids; Benzene; Chemical Phenomena; Chemistry; Creatinine; Evaluation Studies as Topic; Filtration; Humans; Hydrolysis; Hydroxyproline; Indenes; Indicators and Reagents; Infant; Ketones; Malabsorption Syndromes; Metabolic Diseases; Methods; Nitrites; Ornithine; Proline; Proteins; Spectrophotometry; Ultraviolet Rays | 1972 |