leucine has been researched along with Cerebellar Diseases in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (25.00) | 29.6817 |
2010's | 2 (50.00) | 24.3611 |
2020's | 1 (25.00) | 2.80 |
Authors | Studies |
---|---|
Pan, AYH; Taylor, RM; Wade, CM; Williamson, P | 1 |
Kalla, R; Strupp, M | 1 |
Feil, K; Kalla, R; Muth, C; Strupp, M; Teufel, J | 1 |
Accili, E; Armstrong, L; Chapman, K; Demos, MK; Farrell, K; Macri, V; Nelson, TN | 1 |
2 review(s) available for leucine and Cerebellar Diseases
Article | Year |
---|---|
Aminopyridines and Acetyl-DL-leucine: New Therapies in Cerebellar Disorders.
Topics: Aminopyridines; Animals; Cerebellar Ataxia; Cerebellar Diseases; Humans; Leucine | 2019 |
Update on the pharmacotherapy of cerebellar and central vestibular disorders.
Topics: 4-Aminopyridine; Cerebellar Diseases; Humans; Leucine; Male; Nystagmus, Pathologic; Potassium Channel Blockers; Potassium Channels, Voltage-Gated; Vestibular Diseases | 2016 |
2 other study(ies) available for leucine and Cerebellar Diseases
Article | Year |
---|---|
Cerebellar Abiotrophy in Australian Working Kelpies Is Associated with Two Major Risk Loci.
Topics: Animals; Australia; Cerebellar Ataxia; Cerebellar Diseases; Dog Diseases; Dogs; Genome-Wide Association Study; Leucine; Mammals; Membrane Proteins; Neurodegenerative Diseases | 2022 |
A novel KCNA1 mutation associated with global delay and persistent cerebellar dysfunction.
Topics: Adult; Animals; Cerebellar Diseases; Child, Preschool; CHO Cells; Cricetinae; Cricetulus; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Humans; Kv1.1 Potassium Channel; Leucine; Magnetic Resonance Imaging; Male; Membrane Potentials; Mutation; Transfection; Valine | 2009 |