arginine has been researched along with Adult Neuroaxonal Dystrophy 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 | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Battini, R; Catania, A; Chiapparini, ML; Garavaglia, B; Ghezzi, D; Nardocci, N; Pasquariello, R; Pippucci, T; Seri, M; Tiranti, V; Zorzi, G | 1 |
1 other study(ies) available for arginine and Adult Neuroaxonal Dystrophy
Article | Year |
---|---|
R106C TFG variant causes infantile neuroaxonal dystrophy "plus" syndrome.
Topics: Adult; Amino Acid Substitution; Arginine; Case-Control Studies; Cells, Cultured; Child; Child, Preschool; Consanguinity; Cysteine; Female; Follow-Up Studies; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Mutation, Missense; Neuroaxonal Dystrophies; Pedigree; Proteins; Siblings; Spastic Paraplegia, Hereditary | 2018 |