framycetin has been researched along with Amino Acid Metabolism Disorders, Inborn in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (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 |
|---|---|
| BARNESS, LA; BESSELMAN, D; MELLMAN, WJ; TEDESCO, TA | 1 |
| DELAEY, P; HOOFT, C; SNOECK, J; TIMMERMANS, J | 1 |
| FOIS, A; LECCHINI, L | 1 |
| BRENTON, DP; CUSWORTH, DC; GAULL, GE | 1 |
| McMurray, WC; Mohyuddin, F; Rathbun, JC | 1 |
| Hill, A; Hoag, GN; Zaleski, W | 1 |
| Campbell, AG; Nuzum, CT; Rosenberg, LE; Snodgrass, PJ | 1 |
7 other study(ies) available for framycetin and Amino Acid Metabolism Disorders, Inborn
| Article | Year |
|---|---|
INDOLYLACROYL GLYCINE EXCRETION IN A FAMILY WITH MENTAL RETARDATION.
Topics: Amino Acid Metabolism, Inborn Errors; Body Fluids; Child; Glycine; Humans; Hydrogen-Ion Concentration; Indoles; Intellectual Disability; Kidney; Neomycin; Pharmacology; Proteins; Renal Aminoacidurias; Tryptophan; Urine | 1963 |
BIOCHEMICAL ASPECTS OF THE HARTNUP DISEASE. I. RESULTS OF INTRAVENOUS AND ORAL TRYPTOPHAN LOADING TESTS IN A CASE OF HARTNUP DISEASE.
Topics: Amino Acid Metabolism, Inborn Errors; Biomedical Research; Friedreich Ataxia; Genetics, Medical; Hartnup Disease; Humans; Indican; Indoles; Infant; Intestines; Metabolic Diseases; Neomycin; Niacin; Niacinamide; Nicotinic Acids; Nystatin; Pellagra; Renal Aminoacidurias; Tryptophan; Urine | 1964 |
ACUTE CEREBELLAR ATAXIA ASSOCIATED WITH SOME FEATURES OF THE HARTNUP SYNDROME. PRESENTATION OF A CASE.
Topics: Amino Acid Metabolism, Inborn Errors; Cerebellar Ataxia; Child; Chromatography; Drug Therapy; Electroencephalography; Friedreich Ataxia; Hartnup Disease; Humans; Indoles; Italy; Neomycin; Niacin; Nicotinic Acids; Nystagmus, Pathologic; Renal Aminoacidurias; Tryptophan; Urine | 1964 |
HOMOCYSTINURIA: METABOLIC STUDIES ON 3 PATIENTS.
Topics: Amino Acid Metabolism, Inborn Errors; Blood; Child; Genetics, Medical; Homocysteine; Homocystine; Homocystinuria; Humans; Intellectual Disability; Metabolism; Methionine; Neomycin; Urine | 1965 |
Studies on amino acid metabolism in citrullinuria.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Blood Chemical Analysis; Caseins; Child; Citrulline; Diet Therapy; Humans; Infant; Intellectual Disability; Ligases; Male; Neomycin; Urea | 1967 |
Urinary p-tyramine in hereditary tyrosinemia: II. Origin of urinary p-tyramine.
Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Administration, Oral; Adolescent; Amino Acid Metabolism, Inborn Errors; Diet; Female; Humans; Neomycin; Oxygenases; Tyramine; Tyrosine | 1977 |
Ornithine transcarbamylase deficiency: a cause of lethal neonatal hyperammonemia in males.
Topics: Alkalosis, Respiratory; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Blood Urea Nitrogen; Diagnosis, Differential; Exchange Transfusion, Whole Blood; Humans; Hyperventilation; Infant, Newborn; Infant, Newborn, Diseases; Liver; Male; Neomycin; Nitrogen; Ornithine Carbamoyltransferase; Peritoneal Dialysis; Urea | 1973 |