Compounds > valine

valine and Autosomal Dominant Cerebellar Ataxia, Type II

valine has been researched along with Autosomal Dominant Cerebellar Ataxia, Type II in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Banoei, MM; Houshmand, M; Nafisi, S; Panahi, MS; Parivar, K; Rostami, M; Safaei, S; Shariati, P1
Arima, K; Hanyu, N; Ikeda, S; Oide, T; Yamazaki, M1
Kremer, BP; Rabelink, GM; Sinke, RJ; van de Warrenburg, BP; Vlak, MH1

Other Studies

3 other study(ies) available for valine and Autosomal Dominant Cerebellar Ataxia, Type II

ArticleYear
Mitochondrial tRNALeu/Lys and ATPase 6/8 gene variations in spinocerebellar ataxias.
    Neuro-degenerative diseases, 2009, Volume: 6, Issue:1-2

    Topics: Alanine; Amino Acid Substitution; Ataxin-3; Ataxin-7; Ataxins; Calcium Channels; DNA; DNA Primers; Gene Amplification; Genetic Variation; Glycine; Humans; Methionine; Mitochondrial Proton-Translocating ATPases; Nerve Tissue Proteins; Nuclear Proteins; Repressor Proteins; RNA, Transfer, Leu; RNA, Transfer, Lys; Spinocerebellar Ataxias; Threonine; Trinucleotide Repeats; Valine

2009
Coexistence of familial transthyretin amyloidosis ATTR Val30Met and spinocerebellar ataxia type 1 in a Japanese family--a follow-up autopsy report.
    Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2004, Volume: 11, Issue:3

    Topics: Amino Acid Substitution; Amyloid Neuropathies, Familial; Family; Humans; Japan; Male; Methionine; Middle Aged; Pedigree; Point Mutation; Prealbumin; Spinocerebellar Ataxias; Tomography, X-Ray Computed; Valine

2004
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