glutamic acid and Rhabdomyolysis

glutamic acid has been researched along with Rhabdomyolysis 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	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Horváth, R; Jaksch, M; Lochmüller, H; Müller-Höcker, J; Schoser, BG; Völpel, M	1
Davé, V; de Barsy, T; Martin, JJ; Matthys, E; Ookawara, T; Willems, P; Yoshida, A	1

Other Studies

2 other study(ies) available for glutamic acid and Rhabdomyolysis

Article	Year
Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathy. Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:12 Topics: Adult; DNA Mutational Analysis; Electron Transport Complex IV; Glutamic Acid; Humans; Immunohistochemistry; Male; Mitochondrial Encephalomyopathies; Muscle, Skeletal; Muscular Diseases; Mutation; Proline; Reverse Transcriptase Polymerase Chain Reaction; Rhabdomyolysis; RNA, Messenger; Serine	2005
Retarded and aberrant splicings caused by single exon mutation in a phosphoglycerate kinase variant. Archives of biochemistry and biophysics, 1996, Mar-01, Volume: 327, Issue:1 Topics: Adolescent; Alanine; Alternative Splicing; Amino Acid Sequence; Base Sequence; Codon; DNA Primers; Exons; Genetic Variation; Glutamic Acid; Humans; Introns; Lymphocytes; Male; Molecular Sequence Data; Phosphoglycerate Kinase; Point Mutation; Polymerase Chain Reaction; Rhabdomyolysis; RNA, Messenger	1996

Article

Year

Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathy.

Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:12

Topics: Adult; DNA Mutational Analysis; Electron Transport Complex IV; Glutamic Acid; Humans; Immunohistochemistry; Male; Mitochondrial Encephalomyopathies; Muscle, Skeletal; Muscular Diseases; Mutation; Proline; Reverse Transcriptase Polymerase Chain Reaction; Rhabdomyolysis; RNA, Messenger; Serine

2005

Retarded and aberrant splicings caused by single exon mutation in a phosphoglycerate kinase variant.

Archives of biochemistry and biophysics, 1996, Mar-01, Volume: 327, Issue:1

Topics: Adolescent; Alanine; Alternative Splicing; Amino Acid Sequence; Base Sequence; Codon; DNA Primers; Exons; Genetic Variation; Glutamic Acid; Humans; Introns; Lymphocytes; Male; Molecular Sequence Data; Phosphoglycerate Kinase; Point Mutation; Polymerase Chain Reaction; Rhabdomyolysis; RNA, Messenger

1996