cystathionine has been researched along with Lesch-Nyhan Syndrome 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 |
| Harkness, RA | 1 |
| Harper, PS | 1 |
1 review(s) available for cystathionine and Lesch-Nyhan Syndrome
| 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 Lesch-Nyhan Syndrome
| Article | Year |
|---|---|
Lesch-Nyhan syndrome: reduced amino acid concentrations in CSF and brain.
Topics: Amino Acids; Brain; Cystathionine; gamma-Aminobutyric Acid; Humans; Hypoxanthine Phosphoribosyltransferase; Lesch-Nyhan Syndrome | 1989 |
Inborn errors of metabolism-the relationship of clinical and biochemical abnormalities.
Topics: Cystathionine; Diseases in Twins; Glutamine; Homocystinuria; Humans; Infant, Newborn; Intellectual Disability; Lesch-Nyhan Syndrome; Metabolism, Inborn Errors; NADH, NADPH Oxidoreductases; Phenotype; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias | 1973 |