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methionine and Autosomal Dominant Cerebellar Ataxia, Type II

methionine has been researched along with Autosomal Dominant Cerebellar Ataxia, Type II in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (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

Other Studies

2 other study(ies) available for methionine 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