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carnitine and Complex IV Deficiency

carnitine has been researched along with Complex IV Deficiency in 15 studies

Research Excerpts

ExcerptRelevanceReference
"The effects of a single oral dose of carnitine on fasting-induced ketosis was investigated in four normal individuals, five patients with muscular dystrophy, and one patient with a generalized cytochrome c oxidase deficiency."7.67Ketogenic effects of carnitine in patients with muscular dystrophy and cytochrome oxidase deficiency. ( Hoganson, GE; Paulson, DJ; Peters, H; Shug, AL; Sufit, R; Traxler, J, 1988)
"The effects of a single oral dose of carnitine on fasting-induced ketosis was investigated in four normal individuals, five patients with muscular dystrophy, and one patient with a generalized cytochrome c oxidase deficiency."3.67Ketogenic effects of carnitine in patients with muscular dystrophy and cytochrome oxidase deficiency. ( Hoganson, GE; Paulson, DJ; Peters, H; Shug, AL; Sufit, R; Traxler, J, 1988)
"Carnitine uptake was normal in the intramitochondrial beta-oxidation cases, suggesting other mechanisms for their carnitine deficiency."1.29Skin fibroblast carnitine uptake in secondary carnitine deficiency disorders. ( De Vivo, DC; DiMauro, S; Ranucci, D; Tein, I, 1993)
"Treatment with sodium bicarbonate, riboflavin, and carnitine led to considerable improvement in growth and a significant reduction in the dicarboxylic aciduria."1.28Cytochrome c oxidase deficiency in muscle with dicarboxylic aciduria and renal tubular acidosis. ( DiMauro, S; Haas, R; Nyhan, WL; Pintos-Morell, G; Prodanos, C, 1990)

Research

Studies (15)

TimeframeStudies, this research(%)All Research%
pre-19908 (53.33)18.7374
1990's7 (46.67)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Schaub, J1
Heiman-Patterson, TD1
Bonilla, E2
DiMauro, S5
Foreman, J1
Schotland, DL1
Müller-Höcker, J1
Pongratz, D1
Deufel, T1
Trijbels, JM1
Endres, W1
Hübner, G1
Christensen, E1
Brandt, NJ1
Schmalbruch, H1
Kamieniecka, Z1
Hertz, B1
Ruitenbeek, W1
Tein, I1
De Vivo, DC1
Ranucci, D1
Romero, NB1
Marsac, C1
Paturneau-Jouas, M1
Ogier, H1
Magnier, S1
Fardeau, M1
Wada, H1
Nishio, H1
Nagaki, S1
Yanagawa, H1
Imamura, A1
Yokoyama, S1
Sano, T1
Woo, M1
Matsuo, M1
Itoh, H1
Nakamura, H1
Salo, MK1
Rapola, J1
Somer, H1
Pihko, H1
Koivikko, M1
Tritschler, HJ1
Pintos-Morell, G1
Haas, R1
Prodanos, C1
Nyhan, WL1
Hoffmann, GF1
Hunneman, DH1
Jakobs, C1
Wilichowski, E1
Eber, SW1
Hanefeld, F1
Rating, D1
Reichmann, H1
Zeviani, M1
Servidei, S1
DeVivo, DC1
Schon, EA1
Scholte, HR1
Busch, HF1
Luyt-Houwen, IE1
Vaandrager-Verduin, MH1
Przyrembel, H1
Arts, WF1
Sengers, RC1
Stadhouders, AM1
Paulson, DJ1
Hoganson, GE1
Traxler, J1
Sufit, R1
Peters, H1
Shug, AL1
Schmidt-Sommerfeld, E1
Penn, D1

Reviews

4 reviews available for carnitine and Complex IV Deficiency

ArticleYear
[Metabolic myopathies in childhood. A review in summarized form].
    Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde, 1984, Volume: 132, Issue:8

    Topics: Carnitine; Carnitine O-Palmitoyltransferase; Child; Child, Preschool; Cytochrome-c Oxidase Deficienc

1984
Infantile familial cardiomyopathy due to mitochondrial complex I and IV associated deficiency.
    Neuromuscular disorders : NMD, 1993, Volume: 3, Issue:1

    Topics: Biopsy; Cardiomyopathies; Carnitine; Consanguinity; Cytochrome-c Oxidase Deficiency; Electron Transp

1993
Mitochondrial myopathies.
    Journal of inherited metabolic disease, 1987, Volume: 10 Suppl 1

    Topics: Adenosine Triphosphatases; Biological Transport; Carnitine; Citric Acid Cycle; Cytochrome-c Oxidase

1987
Secondary mitochondrial pathology.
    Journal of inherited metabolic disease, 1987, Volume: 10 Suppl 1

    Topics: Carnitine; Cytochrome-c Oxidase Deficiency; Drug-Related Side Effects and Adverse Reactions; Humans;

1987

Other Studies

11 other studies available for carnitine and Complex IV Deficiency

ArticleYear
Cytochrome-c-oxidase deficiency in a floppy infant.
    Neurology, 1982, Volume: 32, Issue:8

    Topics: Carnitine; Cytochrome-c Oxidase Deficiency; Female; Humans; Infant, Newborn; Microscopy, Electron; M

1982
Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle.
    Virchows Archiv. A, Pathological anatomy and histopathology, 1983, Volume: 399, Issue:1

    Topics: Carnitine; Cytochrome-c Oxidase Deficiency; Female; Histocytochemistry; Humans; Hypertrophy; Infant;

1983
Muscle cytochrome c oxidase deficiency accompanied by a urinary organic acid pattern mimicking multiple acyl-CoA dehydrogenase deficiency.
    Journal of inherited metabolic disease, 1993, Volume: 16, Issue:3

    Topics: Acids; Acyl-CoA Dehydrogenases; Carnitine; Cytochrome-c Oxidase Deficiency; Epilepsy; Humans; Infant

1993
Skin fibroblast carnitine uptake in secondary carnitine deficiency disorders.
    Journal of inherited metabolic disease, 1993, Volume: 16, Issue:1

    Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acyl-CoA Dehydrogenase, Long-Chain; Adolescent; Carnitine; Cytochr

1993
[Benign infantile mitochondrial myopathy caused by reversible cytochrome c oxidase deficiency].
    No to hattatsu = Brain and development, 1996, Volume: 28, Issue:5

    Topics: Carnitine; Cytochrome-c Oxidase Deficiency; Female; Humans; Infant; Mitochondrial Myopathies; Ubiqui

1996
Reversible mitochondrial myopathy with cytochrome c oxidase deficiency.
    Archives of disease in childhood, 1992, Volume: 67, Issue:8

    Topics: Biopsy; Carnitine; Cells, Cultured; Combined Modality Therapy; Cytochrome-c Oxidase Deficiency; Ente

1992
Cytochrome c oxidase deficiency in muscle with dicarboxylic aciduria and renal tubular acidosis.
    Journal of child neurology, 1990, Volume: 5, Issue:2

    Topics: Acidosis, Renal Tubular; Amino Acids, Dicarboxylic; Bicarbonates; Carnitine; Cytochrome-c Oxidase De

1990
Progressive fatal pancytopenia, psychomotor retardation and muscle carnitine deficiency in a child with ethylmalonic aciduria and ethylmalonic acidaemia.
    Journal of inherited metabolic disease, 1990, Volume: 13, Issue:3

    Topics: Carnitine; Cytochrome-c Oxidase Deficiency; DNA, Mitochondrial; Fatty Acid Desaturases; Female; Huma

1990
Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells.
    Journal of inherited metabolic disease, 1987, Volume: 10 Suppl 1

    Topics: Adolescent; Adult; Biotin; Brain; Carnitine; Cells, Cultured; Child, Preschool; Coenzyme A; Cytochro

1987
Ketogenic effects of carnitine in patients with muscular dystrophy and cytochrome oxidase deficiency.
    Biochemical medicine and metabolic biology, 1988, Volume: 39, Issue:1

    Topics: Adult; Blood Glucose; Carnitine; Cytochrome-c Oxidase Deficiency; Fasting; Fatty Acids, Nonesterifie

1988
[Carnitine deficiency].
    Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde, 1986, Volume: 134, Issue:5

    Topics: Carnitine; Carnitine Acyltransferases; Carnitine O-Palmitoyltransferase; Child; Coenzyme A; Cytochro

1986