tryptophan has been researched along with Choreoathetosis Self-Mutilation Hyperuricemia Syndrome in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 2 (66.67) | 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 |
|---|---|
| Gaigl, Z; Gathof, BS; Gresser, U; Micheli, V; Rocchigiani, M | 1 |
| Gathof, BS; Jacomelli, G; Manzoni, F; Micheli, V; Peruzzi, L; Pompucci, G; Rocchigiani, M; Sestini, S; Zammarchi, E | 1 |
| Mizuno, TI; Yugari, Y | 1 |
1 trial(s) available for tryptophan and Choreoathetosis Self-Mutilation Hyperuricemia Syndrome
| Article | Year |
|---|---|
Letter: Self mutilation in Lesch-Nyhan syndrome.
Topics: 5-Hydroxytryptophan; Administration, Oral; Child; Dihydroxyphenylalanine; Humans; Hydroxyindoleacetic Acid; Infant; Lesch-Nyhan Syndrome; Placebos; Self Mutilation; Tryptophan | 1974 |
2 other study(ies) available for tryptophan and Choreoathetosis Self-Mutilation Hyperuricemia Syndrome
| Article | Year |
|---|---|
HPRT-mutations in Italian Lesch-Nyhan patients.
Topics: Base Sequence; Exons; Female; Glycine; Humans; Hypoxanthine Phosphoribosyltransferase; Italy; Lesch-Nyhan Syndrome; Male; Nuclear Family; Point Mutation; Polymerase Chain Reaction; Sequence Deletion; Tryptophan | 1998 |
Hypoxanthine-guanine phosphoribosyltransferase deficiency and erythrocyte synthesis of pyridine coenzymes.
Topics: Adolescent; Adult; Amide Synthases; Child; Child, Preschool; Erythrocytes; Female; Humans; Hypoxanthine Phosphoribosyltransferase; Infant; Kinetics; Lesch-Nyhan Syndrome; Male; Middle Aged; NAD; Nicotinic Acids; Pentosyltransferases; Purine Nucleotides; Purines; Pyridines; Pyrimidine Nucleotides; Tryptophan | 1999 |