Compounds > s-adenosylmethionine
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s-adenosylmethionine and Muscular Weakness

s-adenosylmethionine has been researched along with Muscular Weakness in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (12.50)18.2507
2000's2 (25.00)29.6817
2010's5 (62.50)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Han, J; Ji, G; Lu, S; Song, X; Wu, H; Xie, Y1
Bo, R; Fukuda, S; Hasegawa, Y; Ishii, A; Kobayashi, H; Mizusawa, H; Ohkubo, T; Purevsuren, J; Shigematsu, Y; Shioya, A; Sugie, H; Takahashi, T; Taketani, T; Takuma, H; Tamaoka, A; Tsunemi, T; Watanabe, M; Yamada, K; Yamaguchi, S; Yokota, T1
Fu, HX; He, JJ; Jin, M; Lin, MT; Liu, XY; Wang, DN; Wang, N; Wang, ZQ1
Acquaviva-Bourdain, C; Andresen, BS; Bedat-Millet, AL; Behin, A; Boespflug-Tanguy, O; Brivet, M; Chabrol, B; Chaigne, D; Delevaux, I; Eymard, B; Laforêt, P; Laroche, C; Lombès, A; Penisson-Besnier, I; Rigal, O; Vianey-Saban, C1
Acquaviva-Bourdain, C; Brivet, M; Eymard, B; Jardel, C; Laforêt, P; Lombès, A; Maillart, E; Rigal, O; Vianey-Saban, C1
Liapi-Adamidou, G; Tsagris, V1
Georgala, C; Georgala, S; Michas, T; Schulpis, KH1
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, A1

Trials

1 trial(s) available for s-adenosylmethionine and Muscular Weakness

ArticleYear
L-carnitine supplementation in patients with cystic acne on isotretinoin therapy.
    Journal of the European Academy of Dermatology and Venereology : JEADV, 1999, Volume: 13, Issue:3

    Topics: Acne Vulgaris; Adult; Alanine Transaminase; Alkaline Phosphatase; Aspartate Aminotransferases; Carnitine; Case-Control Studies; Cholesterol; Female; Follow-Up Studies; Humans; Isotretinoin; Keratolytic Agents; Liver; Male; Muscle Weakness; Muscular Diseases; Pain; Placebos; Triglycerides

1999

Other Studies

7 other study(ies) available for s-adenosylmethionine and Muscular Weakness

ArticleYear
Adolescent Hyperuricemia with Lipid Storage Myopathy: A Clinical Study.
    Medical science monitor : international medical journal of experimental and clinical research, 2019, Nov-30, Volume: 25

    Topics: Adolescent; Adult; Carnitine; Child; China; Electron-Transferring Flavoproteins; Female; Humans; Hyperuricemia; Iron-Sulfur Proteins; Lipid Metabolism, Inborn Errors; Male; Muscle Weakness; Muscle, Skeletal; Muscular Diseases; Muscular Dystrophies; Oxidoreductases Acting on CH-NH Group Donors; Quality of Life; Riboflavin; Young Adult

2019
Clinical, biochemical and molecular investigation of adult-onset glutaric acidemia type II: Characteristics in comparison with pediatric cases.
    Brain & development, 2016, Volume: 38, Issue:3

    Topics: Adult; Age Factors; Carnitine; Humans; Male; Multiple Acyl Coenzyme A Dehydrogenase Deficiency; Muscle Weakness; Muscular Diseases

2016
Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency.
    Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2016, Volume: 37, Issue:7

    Topics: Adolescent; Adult; Aged; Carnitine; Computational Biology; DNA Mutational Analysis; Electron-Transferring Flavoproteins; Genotype; Humans; Iron-Sulfur Proteins; Magnetic Resonance Imaging; Male; Multiple Acyl Coenzyme A Dehydrogenase Deficiency; Muscle Weakness; Muscular Diseases; Mutation; Oxidoreductases Acting on CH-NH Group Donors

2016
Diagnostic assessment and long-term follow-up of 13 patients with Very Long-Chain Acyl-Coenzyme A dehydrogenase (VLCAD) deficiency.
    Neuromuscular disorders : NMD, 2009, Volume: 19, Issue:5

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Adolescent; Adult; Biomarkers; Carnitine; Cells, Cultured; Child; DNA Mutational Analysis; Exercise Tolerance; Female; Genetic Testing; Genotype; Heterozygote; Homozygote; Humans; Male; Metabolism, Inborn Errors; Middle Aged; Mitochondrial Diseases; Muscle Weakness; Muscular Diseases; Mutation; Rhabdomyolysis; Young Adult

2009
[Multiple acyl-CoA dehydrogenase deficiency (MADD): a curable cause of genetic muscular lipidosis].
    Revue neurologique, 2010, Volume: 166, Issue:3

    Topics: Acyl-CoA Dehydrogenases; Adult; Biopsy; Brain Diseases, Metabolic; Carnitine; Coloring Agents; DNA Mutational Analysis; Electron Transport; Electron-Transferring Flavoproteins; Female; Humans; Lipid Metabolism, Inborn Errors; Lipidoses; Male; Middle Aged; Muscle Weakness; Muscle, Skeletal; Riboflavin; Tandem Mass Spectrometry; Young Adult

2010
Serum carnitine levels in patients with homozygous beta thalassemia: a possible new role for carnitine?
    European journal of pediatrics, 2005, Volume: 164, Issue:3

    Topics: Adolescent; Adult; beta-Thalassemia; Carnitine; Case-Control Studies; Child; Child, Preschool; Fatty Acids; Female; Homozygote; Humans; Male; Muscle Weakness; Surveys and Questionnaires

2005
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