Page last updated: 2024-10-18

glutaric acid and Muscular Diseases

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.

Research Excerpts

ExcerptRelevanceReference
"Riboflavin and carnitine treatment corrected the metabolic abnormalities and she improved clinically."1.28Electron 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)

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19902 (25.00)18.7374
1990's2 (25.00)18.2507
2000's4 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Beresford, MW2
Pourfarzam, M2
Turnbull, DM2
Davidson, JE2
Westermann, CM1
Dorland, L1
Votion, DM1
de Sain-van der Velden, MG1
Wijnberg, ID1
Wanders, RJ1
Spliet, WG1
Testerink, N1
Berger, R1
Ruiter, JP1
van der Kolk, JH1
Yamaguchi, S1
Enkhsaikhan, P1
Tomelleri, G1
Burlina, A1
Deotto, L1
Orrico, D1
Tonin, P1
Rizzuto, N1
Bell, RB1
Brownell, AK1
Roe, CR1
Engel, AG1
Goodman, SI1
Frerman, FE1
Seccombe, DW1
Snyder, FF1
Bartlett, K1
Eyre, JA1
Gardner-Medwin, D1
Johnson, MA1
Fisher, J1
Watmough, NJ1
de Visser, M1
Scholte, HR1
Schutgens, RB1
Bolhuis, PA1
Luyt-Houwen, IE1
Vaandrager-Verduin, MH1
Veder, HA1
Oey, PL1

Reviews

1 review available for glutaric acid and Muscular Diseases

ArticleYear
[Glutaric aciduria type 2].
    Ryoikibetsu shokogun shirizu, 2001, Issue:36

    Topics: Diagnosis, Differential; Electron-Transferring Flavoproteins; Fatty Acid Desaturases; Flavoproteins;

2001

Other Studies

7 other studies available for glutaric acid and Muscular Diseases

ArticleYear
So doctor, what exactly is wrong with my muscles? Glutaric aciduria type II presenting in a teenager.
    Neuromuscular disorders : NMD, 2006, Volume: 16, Issue:4

    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".
    Neuromuscular disorders : NMD, 2006, Volume: 16, Issue:9-10

    Topics: Adolescent; Confidentiality; Glutarates; Humans; Metabolic Diseases; Molecular Biology; Muscular Dis

2006
Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy.
    Neuromuscular disorders : NMD, 2008, Volume: 18, Issue:5

    Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Animals; Butyric Acid; Butyryl-CoA Dehydrogenase; C

2008
[Myopathy with lipid accumulation and type-II glutaric aciduria].
    Minerva pediatrica, 1991, Volume: 43, Issue:3

    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.
    Neurology, 1990, Volume: 40, Issue:11

    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.
    Developmental medicine and child neurology, 1988, Volume: 30, Issue:5

    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.
    Neurology, 1986, Volume: 36, Issue:3

    Topics: Adolescent; Carnitine; Child; Fatty Acids; Female; Fibroblasts; Glutarates; Humans; Infant; Lipid Me

1986