arginine has been researched along with Ambulation Disorders, Neurologic in 2 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 (50.00) | 24.3611 |
2020's | 1 (50.00) | 2.80 |
Authors | Studies |
---|---|
Afrantou, T; Bakirtzis, C; Boziki, MK; Grigoriadis, N; Smyrni, N | 1 |
Camargos, ST; Cardoso, F; DiMauro, S; Gurgel-Giannetti, J; Hirano, M | 1 |
2 other study(ies) available for arginine and Ambulation Disorders, Neurologic
Article | Year |
---|---|
Spastic gait, intellectual disability and seizures due to a rare mutation causing hyperargininemia.
Topics: Arginine; Exome Sequencing; Gait Disorders, Neurologic; Humans; Hyperargininemia; Intellectual Disability; Male; Mutation; Seizures; Young Adult | 2021 |
POLG1 Arg953Cys mutation: expanded phenotype and recessive inheritance in a Brazilian family.
Topics: Adult; Arginine; Brazil; Cardiomyopathies; Cysteine; Depression; DNA Mutational Analysis; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Electromyography; Female; Gait Disorders, Neurologic; Humans; Male; Muscle, Skeletal; Mutation; Neural Conduction; Ophthalmoplegia, Chronic Progressive External; Parkinson Disease; Phenotype; Succinate Dehydrogenase | 2012 |