tryptophan and Hallervorden-Spatz Disease

tryptophan has been researched along with Hallervorden-Spatz Disease in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
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, M1

Other Studies

1 other study(ies) available for tryptophan and Hallervorden-Spatz Disease

ArticleYear
Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern.
    Movement disorders : official journal of the Movement Disorder Society, 2006, Volume: 21, Issue:2

    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