tryptophan has been researched along with Hallervorden-Spatz Disease in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Annesi, F; Annesi, G; Carrideo, S; CirĂ² Candiano, IC; Civitelli, D; Consoli, D; De Marco, EV; Gambardella, A; Naso, F; Quattrone, A; Spadafora, P; Tarantino, P; Valentino, P; Zappia, M | 1 |
1 other study(ies) available for tryptophan and Hallervorden-Spatz Disease
Article | Year |
---|---|
Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern.
Topics: Adult; Amino Acid Substitution; Arginine; Brain; Chromosome Mapping; Female; Genetic Heterogeneity; Genetic Markers; Genotype; Globus Pallidus; Humans; Magnetic Resonance Imaging; Male; Microsatellite Repeats; Middle Aged; Neurologic Examination; Nucleotides; Pantothenate Kinase-Associated Neurodegeneration; Pedigree; Phenotype; Phosphotransferases (Alcohol Group Acceptor); Tryptophan | 2006 |