Page last updated: 2024-08-17

methionine and Encephalomyelitis, Subacute Necrotizing

methionine has been researched along with Encephalomyelitis, Subacute Necrotizing in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Antonicka, H; Brunel-Guitton, C; Fahiminiya, S; Faubert, D; Hinttala, R; Majewski, J; Nishimura, T; Ostergaard, E; Sasarman, F; Schwartzentruber, J; Shoubridge, EA; Smeitink, JA	1
Borrone, C; Caruso, U; Di Rocco, M; Fantasia, AR; Gibson, KM; Lamantea, E; Lupino, S; Moroni, I	1

Other Studies

2 other study(ies) available for methionine and Encephalomyelitis, Subacute Necrotizing

Article	Year
An N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidase. Human molecular genetics, 2015, Jul-15, Volume: 24, Issue:14 Topics: Cells, Cultured; Chromatography, Liquid; Cyclooxygenase 1; Electron Transport Complex IV; Exome; Fibroblasts; Gene Expression Regulation; Gene Silencing; Heterozygote; Humans; Leigh Disease; Methionine; Mitochondria; Mutation; Oxidative Phosphorylation; Protein Biosynthesis; RNA, Transfer, Met; Sequence Analysis, DNA; Tandem Mass Spectrometry	2015
3-Methylglutaconic aciduria and hypermethioninaemia in a child with clinical and neuroradiological findings of Leigh disease. Journal of inherited metabolic disease, 1999, Volume: 22, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Glutarates; Humans; Leigh Disease; Male; Methionine; Skull; Tomography, X-Ray Computed	1999

Article

Year

An N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidase.

Human molecular genetics, 2015, Jul-15, Volume: 24, Issue:14

Topics: Cells, Cultured; Chromatography, Liquid; Cyclooxygenase 1; Electron Transport Complex IV; Exome; Fibroblasts; Gene Expression Regulation; Gene Silencing; Heterozygote; Humans; Leigh Disease; Methionine; Mitochondria; Mutation; Oxidative Phosphorylation; Protein Biosynthesis; RNA, Transfer, Met; Sequence Analysis, DNA; Tandem Mass Spectrometry

2015

3-Methylglutaconic aciduria and hypermethioninaemia in a child with clinical and neuroradiological findings of Leigh disease.

Journal of inherited metabolic disease, 1999, Volume: 22, Issue:5

Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Glutarates; Humans; Leigh Disease; Male; Methionine; Skull; Tomography, X-Ray Computed

1999