threonine has been researched along with Inborn Errors of Metabolism in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (75.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Esteitie, N; Hance, N; Hinttala, R; Larsson, NG; Majamaa, K; Naess, K; Nilsson, H; Teär-Fahnehjelm, K; von Döbeln, U; Wibom, R | 1 |
| Celotto, AM; Frank, AC; Palladino, MJ; Seigle, JL | 1 |
| Constantopoulos, A; Najjar, VA | 1 |
| Gutman, AB; Yu, TF | 1 |
| Ando, T; Fawcett, N; Julius, RL; Nyhan, WL; Rennert, OM | 1 |
| Iivanainen, M; Palo, J; Savolainen, H | 1 |
| Anakura, M; Arashima, S; Matsuda, I; Nambu, H; Takekoshi, Y | 1 |
| Carton, D; De Schrijver, F; Delbeke, MJ; Dhondt, F; Hooft, C; Kint, J; Samyn, W | 1 |
8 other study(ies) available for threonine and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Secondary metabolic effects in complex I deficiency.
Topics: Adenosine Triphosphate; Adolescent; Adult; Blotting, Western; Child; Child, Preschool; DNA Mutational Analysis; DNA, Mitochondrial; Electron Transport Complex I; Female; Humans; Infant; Male; Metabolism, Inborn Errors; Models, Biological; Mutation; NADH Dehydrogenase; Threonine | 2005 |
Drosophila model of human inherited triosephosphate isomerase deficiency glycolytic enzymopathy.
Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Disease Models, Animal; Drosophila; Gene Expression Regulation, Enzymologic; Humans; Longevity; Metabolic Diseases; Metabolism, Inborn Errors; Molecular Sequence Data; Mutation, Missense; Reverse Transcriptase Polymerase Chain Reaction; Sequence Homology, Amino Acid; Threonine; Transgenes; Triose-Phosphate Isomerase | 2006 |
A new phagocytosis-stimulating tetrapeptide hormone, tuftsin, and its role in disease.
Topics: Adolescent; Animals; Arginine; Child, Preschool; Complement System Proteins; Dogs; Female; gamma-Globulins; Guinea Pigs; Humans; Immunoglobulin Fragments; Infant, Newborn; Leukocytes; Lysine; Male; Metabolism, Inborn Errors; Oligopeptides; Phagocytosis; Proline; Splenectomy; Splenic Diseases; Staphylococcal Infections; Staphylococcus; Streptococcal Infections; Threonine; Trypsin | 1972 |
Hyperglutamatemia in primary gout.
Topics: Adult; Aged; Alanine; Ammonia; Chromatography; Fasting; Glutamates; Glutamine; Glycine; Gout; Humans; Male; Metabolism, Inborn Errors; Middle Aged; Serine; Threonine; Uric Acid | 1973 |
Response to dietary therapy in B 12 unresponsive methylmalonic acidemia.
Topics: Acidosis; Agranulocytosis; Blood Glucose; Cephalometry; Child Development; Diet Therapy; Electroencephalography; Female; Growth Disorders; Humans; Infant; Intelligence; Isoleucine; Lymphocytosis; Malonates; Metabolism, Inborn Errors; Methionine; Otitis Media; Threonine; Valine; Vitamin B 12 | 1973 |
Free amino acids and carbohydrates in the cerebrospinal fluid of 305 mentally retarded patients: a screening study.
Topics: Adolescent; Adult; Alanine; Amino Acids; Arginine; Carbohydrates; Child; Child, Preschool; Chromatography, Thin Layer; Cystine; Epilepsy; Female; Glutamates; Glutamine; Humans; Intellectual Disability; Intelligence Tests; Isoleucine; Leucine; Lysine; Male; Metabolism, Inborn Errors; Methionine; Middle Aged; Ornithine; Phenylalanine; Pneumoencephalography; Threonine; Valine | 1973 |
Hyperammonemia due to a mutant enzyme of ornithine transcarbamylase.
Topics: Amino Acids; Ammonia; Animals; Autopsy; Clinical Enzyme Tests; Culture Techniques; Female; Humans; Infant; Liver; Metabolism, Inborn Errors; Mutation; Ornithine; Ornithine Carbamoyltransferase; Orotic Acid; Phosphotransferases; Rats; Threonine; Urea | 1971 |
Histidinemia.
Topics: Acetates; Acrylates; Adolescent; Alanine; Glycine; Histidine; Humans; Imidazoles; Lactates; Lyases; Male; Metabolism, Inborn Errors; Purpura, Thrombocytopenic; Pyruvates; Serine; Threonine | 1970 |