Page last updated: 2024-08-23

s-adenosylmethionine and coenzyme q10

s-adenosylmethionine has been researched along with coenzyme q10 in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (33.33)	29.6817
2010's	2 (66.67)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bolar, NA; Bruhn, H; Freyer, C; Govaert, P; Jespers, A; Kishita, Y; Kohda, M; Lesko, N; Loeys, BL; Maffezzini, C; Marobbio, CM; Miniero, DV; Monné, M; Mourier, A; Murayama, K; Naess, K; Nennesmo, I; Ohtake, A; Okazaki, Y; Pajak, A; Palmieri, F; Stranneheim, H; Van Laer, L; Wedell, A; Wibom, R; Wredenberg, A	1
Driscoll, DJ; Lynn, CH; Miller, JL; Shuster, J	1

Reviews

1 review(s) available for s-adenosylmethionine and coenzyme q10

Article	Year
Anti-aging products, Part I. Can supplements rewind our body clocks? Harvard women's health watch, 2001, Volume: 9, Issue:4 Topics: Advertising; Aging; Antioxidants; Coenzymes; Dietary Supplements; Evidence-Based Medicine; Humans; Patient Education as Topic; S-Adenosylmethionine; Superoxide Dismutase; Thioctic Acid; Ubiquinone	2001

Other Studies

2 other study(ies) available for s-adenosylmethionine and coenzyme q10

Article	Year
Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26. American journal of human genetics, 2015, Nov-05, Volume: 97, Issue:5 Topics: Amino Acid Sequence; Amino Acid Transport Systems; Calcium-Binding Proteins; Child, Preschool; DNA Methylation; Female; Humans; Male; Mitochondrial Diseases; Molecular Sequence Data; Muscle Weakness; Mutation; Pedigree; Prognosis; RNA Stability; S-Adenosylmethionine; Sequence Homology, Amino Acid; Thioctic Acid; Ubiquinone	2015
Carnitine and coenzyme Q10 levels in individuals with Prader-Willi syndrome. American journal of medical genetics. Part A, 2011, Volume: 155A, Issue:3 Topics: Carnitine; Case-Control Studies; Child; Female; Humans; Male; Prader-Willi Syndrome; Siblings; Ubiquinone	2011

Article

Year

Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26.

American journal of human genetics, 2015, Nov-05, Volume: 97, Issue:5

Topics: Amino Acid Sequence; Amino Acid Transport Systems; Calcium-Binding Proteins; Child, Preschool; DNA Methylation; Female; Humans; Male; Mitochondrial Diseases; Molecular Sequence Data; Muscle Weakness; Mutation; Pedigree; Prognosis; RNA Stability; S-Adenosylmethionine; Sequence Homology, Amino Acid; Thioctic Acid; Ubiquinone

2015

Carnitine and coenzyme Q10 levels in individuals with Prader-Willi syndrome.

American journal of medical genetics. Part A, 2011, Volume: 155A, Issue:3

Topics: Carnitine; Case-Control Studies; Child; Female; Humans; Male; Prader-Willi Syndrome; Siblings; Ubiquinone

2011