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pyruvic acid and Mitochondrial Myopathies

pyruvic acid has been researched along with Mitochondrial Myopathies in 14 studies

Pyruvic Acid: An intermediate compound in the metabolism of carbohydrates, proteins, and fats. In thiamine deficiency, its oxidation is retarded and it accumulates in the tissues, especially in nervous structures. (From Stedman, 26th ed)
pyruvic acid : A 2-oxo monocarboxylic acid that is the 2-keto derivative of propionic acid. It is a metabolite obtained during glycolysis.

Mitochondrial Myopathies: A group of muscle diseases associated with abnormal mitochondria function.

Research Excerpts

ExcerptRelevanceReference
"Five patients with McArdle's disease and five patients with mitochondrial myopathies performed the same incremental maximal exercise test."1.28Exercise intolerance in patients with McArdle's disease or mitochondrial myopathies. ( Camus, F; Chaussain, M; Defoligny, C; Eymard, B; Fardeau, M, 1992)

Research

Studies (14)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's9 (64.29)18.2507
2000's5 (35.71)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Axelson, HW1
Melberg, A1
Ronquist, G1
Askmark, H1
Smeitink, J1
Ruitenbeek, W2
Sengers, R1
Wevers, R1
van Lith, T1
Trijbels, F1
Folgerø, T1
Bertheussen, K1
Lindal, S1
Torbergsen, T1
Oian, P1
Dengler, R1
Wohlfarth, K1
Zierz, S1
Jobges, M1
Schubert, M1
Huizing, M1
Thinnes, FP1
DePinto, V1
Wendel, U1
Trijbels, FJ1
Smit, LM1
ter Laak, HJ1
van den Heuvel, LP1
Shorny, S1
Finsterer, J1
Bittner, RE1
Mamoli, B1
Chugani, HT1
Chan, A1
Gold, R1
Arp, S1
Pflughaupt, KW1
Toyka, KV1
Reichmann, H2
Sue, CM1
Hirano, M1
DiMauro, S1
De Vivo, DC1
Giordano, G1
Corradi, D1
D'Adda, T1
Melissari, M1
Damian, MS1
Sauter, W1
Murakami, N1
Sakuta, R1
Steiner, I1
Zeman, J1
Spacek, J1
Hansíková, H1
Wenchich, L1
Chaussain, M1
Camus, F1
Defoligny, C1
Eymard, B1
Fardeau, M1

Reviews

3 reviews available for pyruvic acid and Mitochondrial Myopathies

ArticleYear
Positron emission tomography in mitochondrial diseases.
    BioFactors (Oxford, England), 1998, Volume: 7, Issue:3

    Topics: Animals; Animals, Domestic; Brain; Glucose; Humans; Mitochondrial Myopathies; Oxygen Consumption; Py

1998
Neonatal presentations of mitochondrial metabolic disorders.
    Seminars in perinatology, 1999, Volume: 23, Issue:2

    Topics: DNA, Mitochondrial; Electron Transport; Humans; Infant; Infant, Newborn; Mitochondrial Myopathies; P

1999
[Pure mitochondrial myopathy].
    Ryoikibetsu shokogun shirizu, 2001, Issue:36

    Topics: Child; Cytochrome-c Oxidase Deficiency; Electron Transport Complex I; Electron Transport Complex II;

2001

Trials

2 trials available for pyruvic acid and Mitochondrial Myopathies

ArticleYear
Microdialysis and electromyography of experimental muscle fatigue in healthy volunteers and patients with mitochondrial myopathy.
    Muscle & nerve, 2002, Volume: 26, Issue:4

    Topics: Aconitate Hydratase; Adolescent; Adult; Aged; Electromyography; Exercise; Female; Humans; Isometric

2002
Subcutaneous microdialysis in mitochondrial cytopathy.
    Muscle & nerve, 2001, Volume: 24, Issue:5

    Topics: Adult; Aged; Circadian Rhythm; Female; Glucose; Humans; Kidney Failure, Chronic; Lactic Acid; Male;

2001

Other Studies

9 other studies available for pyruvic acid and Mitochondrial Myopathies

ArticleYear
Mitochondrial creatine kinase activity in patients with disturbed energy generation in muscle mitochondria.
    Journal of inherited metabolic disease, 1994, Volume: 17, Issue:1

    Topics: Adenosine Triphosphate; Adolescent; Adult; Child; Child, Preschool; Creatine Kinase; Energy Metaboli

1994
Mitochondrial disease and reduced sperm motility.
    Human reproduction (Oxford, England), 1993, Volume: 8, Issue:11

    Topics: Adenosine Triphosphate; Cells, Cultured; Culture Media; Glucose; Humans; Infertility, Male; Male; Mi

1993
Muscle fatigue, lactate, and pyruvate in mitochondrial myopathy with progressive external ophthalmoplegia.
    Muscle & nerve, 1996, Volume: 19, Issue:4

    Topics: Action Potentials; Adolescent; Adult; Aged; Exercise Test; Female; Humans; Lactates; Lactic Acid; Ma

1996
Deficiency of the voltage-dependent anion channel: a novel cause of mitochondriopathy.
    Pediatric research, 1996, Volume: 39, Issue:5

    Topics: Child, Preschool; Humans; Ion Channels; Magnetic Resonance Imaging; Male; Membrane Proteins; Microsc

1996
[Lactate determination at rest and during bicycle ergometry in healthy probands and in patients with mitochondrial myopathies].
    Wiener medizinische Wochenschrift (1946), 1996, Volume: 146, Issue:9-10

    Topics: Electron Transport; Exercise Test; Glycolysis; Humans; Lactic Acid; Mitochondrial Myopathies; Pyruvi

1996
[Standardized bicycle ergometry test in mitochondrial myopathies. Indications, interferences and clinical parameters].
    Der Nervenarzt, 1998, Volume: 69, Issue:6

    Topics: Adult; Energy Metabolism; Exercise Test; Female; Humans; Isometric Contraction; Lactic Acid; Male; M

1998
[An autopsy case of neonatal lactic acidosis].
    Pathologica, 2001, Volume: 93, Issue:1

    Topics: Acidosis, Lactic; Atrophy; Autopsy; Body Fluids; Brain; Cardiomegaly; Epilepsy, Generalized; Fatal O

2001
Mitochondrial cardiomyopathy--case report.
    Ceskoslovenska patologie, 2002, Volume: 38, Issue:1

    Topics: Adult; Cardiomyopathy, Hypertrophic; Energy Metabolism; Female; Humans; Infant; Lactic Acid; Male; M

2002
Exercise intolerance in patients with McArdle's disease or mitochondrial myopathies.
    The European journal of medicine, 1992, Volume: 1, Issue:8

    Topics: Adult; Alanine; Ammonia; Energy Metabolism; Exercise Test; Exercise Tolerance; Female; Glycogen Stor

1992