cystathionine has been researched along with Alkaptonuria 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 |
|---|---|
| Martin-DeLeon, PA | 1 |
| Kroll, S; Toussaint, W; Zebisch, P | 2 |
1 review(s) available for cystathionine and Alkaptonuria
| Article | Year |
|---|---|
Differential diagnosis and diseases due to enzyme changes.
Topics: Adrenal Hyperplasia, Congenital; Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Biological Transport, Active; Cell Membrane; Cystathionine; Diagnosis, Differential; Enzymes; Feedback; Galactosemias; Glycogen Storage Disease; Humans; Lesch-Nyhan Syndrome; Metabolism, Inborn Errors; Mucopolysaccharidoses; Mutation; Phenylketonurias; Tay-Sachs Disease; Vitamins | 1979 |
2 other study(ies) available for cystathionine and Alkaptonuria
| Article | Year |
|---|---|
[Hereditary amino acid metabolism disorders. Indications for early diagnosis].
Topics: Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Cystathionine; Cystinosis; Diagnosis, Differential; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Maple Syrup Urine Disease; Methods; Methylmalonic Acid; Phenylketonurias; Proline; Propionates; Tyrosine | 1972 |
[Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods].
Topics: Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Clinical Laboratory Techniques; Cystathionine; Cystinosis; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Maple Syrup Urine Disease; Methods; Methylmalonic Acid; Phenylketonurias; Proline; Propionates; Tyrosine | 1972 |