Compounds > methionine
Page last updated: 2024-08-17

methionine and Myositis, Inclusion Body

methionine has been researched along with Myositis, Inclusion Body in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's2 (66.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Amouri, R; Driss, A; Hentati, F; Kefi, M; Murayama, K; Nishino, I1
Kitzler, H; Lampe, J; Lochmüller, H; Reichmann, H; Walter, MC1
Orth, M; Schapira, AH; Tabrizi, SJ1

Other Studies

3 other study(ies) available for methionine and Myositis, Inclusion Body

ArticleYear
Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy.
    Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:5

    Topics: Adult; DNA Mutational Analysis; Dystonic Disorders; Extremities; Family Health; Female; Histidine; Humans; Leucine; Male; Methionine; Middle Aged; Multienzyme Complexes; Muscle, Skeletal; Mutation; Myositis, Inclusion Body; Staining and Labeling; Threonine; Tunisia

2005
Methionine homozygosity at prion gene codon 129 may predispose to sporadic inclusion-body myositis.
    Lancet (London, England), 1999, Feb-06, Volume: 353, Issue:9151

    Topics: Codon; Genetic Predisposition to Disease; Homozygote; Humans; Methionine; Middle Aged; Myositis, Inclusion Body; Prions

1999
Sporadic inclusion body myositis not linked to prion protein codon 129 methionine homozygosity.
    Neurology, 2000, Oct-24, Volume: 55, Issue:8

    Topics: Genetic Linkage; Homozygote; Humans; Methionine; Middle Aged; Myositis, Inclusion Body; Prions

2000