valine and Basal Ganglia Diseases

valine has been researched along with Basal Ganglia Diseases in 1 studies

Research

Studies (1)

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

Authors	Studies
Kremer, BP; Rabelink, GM; Sinke, RJ; van de Warrenburg, BP; Vlak, MH	1

Other Studies

1 other study(ies) available for valine and Basal Ganglia Diseases

Article	Year
Novel PRKCG/SCA14 mutation in a Dutch spinocerebellar ataxia family: expanding the phenotype. Movement disorders : official journal of the Movement Disorder Society, 2006, Volume: 21, Issue:7 Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Atrophy; Basal Ganglia Diseases; Cerebellum; DNA Mutational Analysis; Exons; Female; Glutamic Acid; Humans; Isoenzymes; Magnetic Resonance Imaging; Male; Middle Aged; Mutation, Missense; Myoclonus; Netherlands; Pedigree; Phenotype; Protein Kinase C; Spinocerebellar Ataxias; Tremor; Valine	2006

Article

Year

Novel PRKCG/SCA14 mutation in a Dutch spinocerebellar ataxia family: expanding the phenotype.

Movement disorders : official journal of the Movement Disorder Society, 2006, Volume: 21, Issue:7

Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Atrophy; Basal Ganglia Diseases; Cerebellum; DNA Mutational Analysis; Exons; Female; Glutamic Acid; Humans; Isoenzymes; Magnetic Resonance Imaging; Male; Middle Aged; Mutation, Missense; Myoclonus; Netherlands; Pedigree; Phenotype; Protein Kinase C; Spinocerebellar Ataxias; Tremor; Valine

2006