Page last updated: 2024-08-21

ethylmalonic acid and Encephalomyopathies, Mitochondrial

ethylmalonic acid has been researched along with Encephalomyopathies, Mitochondrial 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
Fu, X; Hahn, SH; Kodama, H; Packman, S; Rinaldo, P	1

Other Studies

1 other study(ies) available for ethylmalonic acid and Encephalomyopathies, Mitochondrial

Article	Year
Mutation analysis of copper transporter genes in patients with ethylmalonic encephalopathy, mitochondriopathies and copper deficiency phenotypes. Journal of inherited metabolic disease, 2003, Volume: 26, Issue:1 Topics: Blotting, Northern; Brain Diseases, Metabolic; Cation Transport Proteins; Cells, Cultured; Child; Copper; Copper Transporter 1; DNA Mutational Analysis; DNA, Complementary; Fatty Acids; Female; Fibroblasts; Humans; Intellectual Disability; Lipid Metabolism, Inborn Errors; Lymphocytes; Male; Malonates; Mitochondrial Encephalomyopathies; Molecular Chaperones; Oxidation-Reduction; Phenotype	2003

Article

Year

Mutation analysis of copper transporter genes in patients with ethylmalonic encephalopathy, mitochondriopathies and copper deficiency phenotypes.

Journal of inherited metabolic disease, 2003, Volume: 26, Issue:1

Topics: Blotting, Northern; Brain Diseases, Metabolic; Cation Transport Proteins; Cells, Cultured; Child; Copper; Copper Transporter 1; DNA Mutational Analysis; DNA, Complementary; Fatty Acids; Female; Fibroblasts; Humans; Intellectual Disability; Lipid Metabolism, Inborn Errors; Lymphocytes; Male; Malonates; Mitochondrial Encephalomyopathies; Molecular Chaperones; Oxidation-Reduction; Phenotype

2003