glutaric acid has been researched along with Muscular Diseases in 8 studies
glutaric acid: RN given refers to parent cpd
glutaric acid : An alpha,omega-dicarboxylic acid that is a linear five-carbon dicarboxylic acid.
Muscular Diseases: Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE.
Excerpt | Relevance | Reference |
---|---|---|
"Riboflavin and carnitine treatment corrected the metabolic abnormalities and she improved clinically." | 1.28 | Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adult. ( Bell, RB; Brownell, AK; Engel, AG; Frerman, FE; Goodman, SI; Roe, CR; Seccombe, DW; Snyder, FF, 1990) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (25.00) | 18.7374 |
1990's | 2 (25.00) | 18.2507 |
2000's | 4 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Beresford, MW | 2 |
Pourfarzam, M | 2 |
Turnbull, DM | 2 |
Davidson, JE | 2 |
Westermann, CM | 1 |
Dorland, L | 1 |
Votion, DM | 1 |
de Sain-van der Velden, MG | 1 |
Wijnberg, ID | 1 |
Wanders, RJ | 1 |
Spliet, WG | 1 |
Testerink, N | 1 |
Berger, R | 1 |
Ruiter, JP | 1 |
van der Kolk, JH | 1 |
Yamaguchi, S | 1 |
Enkhsaikhan, P | 1 |
Tomelleri, G | 1 |
Burlina, A | 1 |
Deotto, L | 1 |
Orrico, D | 1 |
Tonin, P | 1 |
Rizzuto, N | 1 |
Bell, RB | 1 |
Brownell, AK | 1 |
Roe, CR | 1 |
Engel, AG | 1 |
Goodman, SI | 1 |
Frerman, FE | 1 |
Seccombe, DW | 1 |
Snyder, FF | 1 |
Bartlett, K | 1 |
Eyre, JA | 1 |
Gardner-Medwin, D | 1 |
Johnson, MA | 1 |
Fisher, J | 1 |
Watmough, NJ | 1 |
de Visser, M | 1 |
Scholte, HR | 1 |
Schutgens, RB | 1 |
Bolhuis, PA | 1 |
Luyt-Houwen, IE | 1 |
Vaandrager-Verduin, MH | 1 |
Veder, HA | 1 |
Oey, PL | 1 |
1 review available for glutaric acid and Muscular Diseases
Article | Year |
---|---|
[Glutaric aciduria type 2].
Topics: Diagnosis, Differential; Electron-Transferring Flavoproteins; Fatty Acid Desaturases; Flavoproteins; | 2001 |
7 other studies available for glutaric acid and Muscular Diseases
Article | Year |
---|---|
So doctor, what exactly is wrong with my muscles? Glutaric aciduria type II presenting in a teenager.
Topics: Acyl-CoA Dehydrogenase; Adolescent; Carnitine; DNA Mutational Analysis; Electron-Transferring Flavop | 2006 |
"So doctor, what exactly is wrong with my muscles? Glutaric aciduria type II presenting in a teenager".
Topics: Adolescent; Confidentiality; Glutarates; Humans; Metabolic Diseases; Molecular Biology; Muscular Dis | 2006 |
Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Animals; Butyric Acid; Butyryl-CoA Dehydrogenase; C | 2008 |
[Myopathy with lipid accumulation and type-II glutaric aciduria].
Topics: Adolescent; Fatty Acid Desaturases; Female; Flavin-Adenine Dinucleotide; Glutarates; Humans; Lipid M | 1991 |
Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adult.
Topics: Acidosis; Adult; Carnitine; Electron-Transferring Flavoproteins; Fatty Acid Desaturases; Female; Glu | 1990 |
Lipid storage myopathy due to glutaric aciduria type II: treatment of a potentially fatal myopathy.
Topics: Carnitine; Female; Glutarates; Glutaryl-CoA Dehydrogenase; Glycine; Humans; Infant; Lipid Metabolism | 1988 |
Riboflavin-responsive lipid-storage myopathy and glutaric aciduria type II of early adult onset.
Topics: Adolescent; Carnitine; Child; Fatty Acids; Female; Fibroblasts; Glutarates; Humans; Infant; Lipid Me | 1986 |