Page last updated: 2024-08-17

coenzyme a and Complex IV Deficiency

coenzyme a has been researched along with Complex IV Deficiency in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (100.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Arts, WF; Busch, HF; Luyt-Houwen, IE; Przyrembel, H; Scholte, HR; Vaandrager-Verduin, MH	1
Penn, D; Schmidt-Sommerfeld, E	1

Other Studies

2 other study(ies) available for coenzyme a and Complex IV Deficiency

Article	Year
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; Cytochrome-c Oxidase Deficiency; Electron Transport Complex III; Female; Fibroblasts; Humans; Infant; Male; Metabolism, Inborn Errors; Mitochondria; Mitochondria, Liver; Mitochondria, Muscle; Mitochondrial ADP, ATP Translocases; NAD(P)H Dehydrogenase (Quinone); Oxidative Phosphorylation; Quinone Reductases	1987
[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; Cytochrome-c Oxidase Deficiency; Fatty Acid Desaturases; Fatty Acids; Humans; Ketones; Lipid Metabolism, Inborn Errors; Mitochondria, Liver; Mitochondria, Muscle; Muscular Diseases; Renal Aminoacidurias; Renal Dialysis; Transferases	1986

Article

Year

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; Cytochrome-c Oxidase Deficiency; Electron Transport Complex III; Female; Fibroblasts; Humans; Infant; Male; Metabolism, Inborn Errors; Mitochondria; Mitochondria, Liver; Mitochondria, Muscle; Mitochondrial ADP, ATP Translocases; NAD(P)H Dehydrogenase (Quinone); Oxidative Phosphorylation; Quinone Reductases

1987

[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; Cytochrome-c Oxidase Deficiency; Fatty Acid Desaturases; Fatty Acids; Humans; Ketones; Lipid Metabolism, Inborn Errors; Mitochondria, Liver; Mitochondria, Muscle; Muscular Diseases; Renal Aminoacidurias; Renal Dialysis; Transferases

1986