Compounds > s-adenosylmethionine

Page last updated: 2024-08-23

s-adenosylmethionine and Rhabdomyolysis

s-adenosylmethionine has been researched along with Rhabdomyolysis in 15 studies

Research

Studies (15)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	5 (33.33)	29.6817
2010's	8 (53.33)	24.3611
2020's	2 (13.33)	2.80

Authors

Authors	Studies
Adam, T; Chrastina, P; Farolfi, M; Foltenová, H; Friedecký, D; Hanák, P; Honzík, T; Hrubá, E; Ješina, P; Kousal, B; Kožich, V; Pavlíková, M; Rücklová, K; Smolka, V; Vlášková, H; Zeman, J	1
Hayashida, S; Isobe, N; Shiraishi, W; Tajima, G; Tateishi, T; Tsumura, M	1
Balogh, L; Berenténé Bene, J; Hidvégi, T; Komoly, S; Melegh, B; Molnár, GA; Pál, E; Sebők, Á; Szabó, A; Wittmann, I; Zsidegh, P	1
Hussain, S; Prasad, M	1
Ask, S; Gustafsson, J; Haglind, CB; Nordenström, A; Stenlid, MH; von Döbeln, U	1
Furuyama, H; Hisahara, S; Imai, T; Matsushita, T; Shigematsu, Y; Shimohama, S; Tajima, G	1
Acquaviva-Bourdain, C; Attarian, S; Bassez, G; Béhin, A; Brivet, M; Eymard, B; Fouilhoux, A; Kaminsky, P; Labarre-Villa, A; Laforêt, P; Laquerrière, A; Pérard, L; Pouget, J; Rigal, O; Souvannanorath, S; Streichenberger, N; Vanhulle, C; Vianey-Saban, C	1
Hiramatsu, Y; Izumi, Y; Kaji, R; Matsui, N; Miyazaki, Y; Nodera, H; Takashima, H; Yamamoto, Y	1
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, C	1
Jumma, O; Ogundare, O; Turnbull, DM; Woywodt, A	1
Chang, YS; Jin, DK; Ki, CS; Kim, SR; Lee, SY; Park, HD; Park, WS	1
Aagaard-Tillery, K; Mendez-Figueroa, H; Shaibani, A; Shchelochkov, OA; Shinawi, MS	1
Al-Thihli, K; Mezei, M; Nelson, J; Sinclair, G; Sirrs, S; Vallance, H	1
Andresen, BS; Bischoff, C; Bonham, JR; Chakrapani, A; Clark, S; Downing, M; Gregersen, N; Manning, NJ; Muntoni, F; Olpin, SE; Olsen, RK; Pourfarzam, M; Sharrard, M; Turnbull, DN	1
de Sain, MG; Dorland, L; Engbers, HM; Eskes, PF; Visser, G	1

Other Studies

15 other study(ies) available for s-adenosylmethionine and Rhabdomyolysis

Article	Year
Impact of Newborn Screening and Early Dietary Management on Clinical Outcome of Patients with Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency and Medium Chain Acyl-CoA Dehydrogenase Deficiency-A Retrospective Nationwide Study. Nutrients, 2021, Aug-24, Volume: 13, Issue:9 Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acyl-CoA Dehydrogenase; Cardiomyopathies; Carnitine; Child; Child, Preschool; Czech Republic; Female; Humans; Incidence; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Metabolism, Inborn Errors; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; Neonatal Screening; Nervous System Diseases; Outcome Assessment, Health Care; Retrospective Studies; Rhabdomyolysis; Severity of Illness Index	2021
[A case of very long chain acyl-CoA dehydrogenase deficiency diagnosed due to a trigger of hyperemesis gravidarum during pregnancy]. Rinsho shinkeigaku = Clinical neurology, 2023, Oct-25, Volume: 63, Issue:10 Topics: Acyl-CoA Dehydrogenase, Long-Chain; Adult; Carnitine; Fatty Acids; Female; Humans; Hyperemesis Gravidarum; Infant, Newborn; Lipid Metabolism, Inborn Errors; Pregnancy; Rhabdomyolysis	2023
[Rhabdomyolysis - may it be a metabolic myopathy? Case report and diagnostic algorithm]. Orvosi hetilap, 2017, Volume: 158, Issue:47 Topics: Algorithms; Carnitine; Diagnosis, Differential; Female; Humans; Middle Aged; Muscular Diseases; Rhabdomyolysis	2017
Glutaric aciduria type II presenting as myopathy and rhabdomyolysis in a teenager. Journal of child neurology, 2015, Volume: 30, Issue:1 Topics: Adolescent; Carnitine; Humans; Male; Multiple Acyl Coenzyme A Dehydrogenase Deficiency; Muscular Diseases; Rhabdomyolysis	2015
Increased and early lipolysis in children with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency during fast. Journal of inherited metabolic disease, 2015, Volume: 38, Issue:2 Topics: 3-Hydroxyacyl CoA Dehydrogenases; Age Factors; Biomarkers; Blood Glucose; Calorimetry, Indirect; Cardiomyopathies; Carnitine; Child; Child, Preschool; Energy Metabolism; Fasting; Female; Glycerol; Humans; Hyperglycemia; Isotope Labeling; Lipid Metabolism, Inborn Errors; Lipolysis; Male; Microdialysis; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; Nervous System Diseases; Postprandial Period; Rhabdomyolysis; Time Factors	2015
A heterozygous missense mutation in adolescent-onset very long-chain acyl-CoA dehydrogenase deficiency with exercise-induced rhabdomyolysis. The Tohoku journal of experimental medicine, 2015, Volume: 235, Issue:4 Topics: Acyl-CoA Dehydrogenase, Long-Chain; Adolescent; Amino Acid Sequence; Base Sequence; Carnitine; Congenital Bone Marrow Failure Syndromes; Exercise; Heterozygote; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Mitochondrial Diseases; Models, Molecular; Molecular Sequence Data; Muscular Diseases; Mutation, Missense; Protein Structure, Tertiary; Rhabdomyolysis; Sequence Alignment	2015
Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic disease. Revue neurologique, 2016, Volume: 172, Issue:3 Topics: Adult; Age of Onset; Biopsy; Carnitine; Electromyography; Electron-Transferring Flavoproteins; Exercise; Female; France; Humans; Iron-Sulfur Proteins; Lipid Metabolism, Inborn Errors; Male; Middle Aged; Multiple Acyl Coenzyme A Dehydrogenase Deficiency; Muscle, Skeletal; Mutation; Neuromuscular Diseases; Oxidation-Reduction; Oxidoreductases Acting on CH-NH Group Donors; Rhabdomyolysis; Young Adult	2016
Mitochondrial trifunctional protein deficiency: an adult patient with similar progress to Charcot-Marie-Tooth disease. Rinsho shinkeigaku = Clinical neurology, 2017, 02-25, Volume: 57, Issue:2 Topics: Biomarkers; Cardiomyopathies; Carnitine; Charcot-Marie-Tooth Disease; Diagnosis, Differential; Disease Progression; Genetic Testing; Humans; Lipid Metabolism, Inborn Errors; Male; Middle Aged; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; Mitochondrial Trifunctional Protein, beta Subunit; Mutation; Nervous System Diseases; Peripheral Nervous System Diseases; Recurrence; Rhabdomyolysis	2017
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
Searching for the needle in the Haystacks. Lancet (London, England), 2009, Sep-05, Volume: 374, Issue:9692 Topics: Acyl-CoA Dehydrogenase, Long-Chain; Age of Onset; Biopsy; Carnitine; Creatine Kinase; Creatinine; Histocytochemistry; Humans; Male; Middle Aged; Mitochondrial Myopathies; Prognosis; Rare Diseases; Recurrence; Rhabdomyolysis; Walking	2009
Two novel HADHB gene mutations in a Korean patient with mitochondrial trifunctional protein deficiency. Annals of clinical and laboratory science, 2009,Fall, Volume: 39, Issue:4 Topics: 3-Hydroxyacyl CoA Dehydrogenases; Cardiomyopathies; Carnitine; DNA Mutational Analysis; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Mitochondria; Mitochondrial Myopathies; Mitochondrial Proteins; Mitochondrial Trifunctional Protein; Mitochondrial Trifunctional Protein, beta Subunit; Multienzyme Complexes; Mutation; Nervous System Diseases; Peripheral Nervous System Diseases; Republic of Korea; Retinitis Pigmentosa; Rhabdomyolysis	2009
Clinical and biochemical improvement of very long-chain acyl-CoA dehydrogenase deficiency in pregnancy. Journal of perinatology : official journal of the California Perinatal Association, 2010, Volume: 30, Issue:8 Topics: Acyl-CoA Dehydrogenase, Long-Chain; Carnitine; Female; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Pregnancy; Pregnancy Complications; Prenatal Care; Rhabdomyolysis; Term Birth; Young Adult	2010
Performance of serum and dried blood spot acylcarnitine profiles for detection of fatty acid β-oxidation disorders in adult patients with rhabdomyolysis. Journal of inherited metabolic disease, 2014, Volume: 37, Issue:2 Topics: Adolescent; Adult; Biopsy; Carnitine; Carnitine O-Palmitoyltransferase; Dried Blood Spot Testing; Fatty Acids; Female; Humans; Lipid Metabolism, Inborn Errors; Male; Middle Aged; Mitochondrial Diseases; Oxidation-Reduction; Retrospective Studies; Rhabdomyolysis; Young Adult	2014
Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiency. Journal of inherited metabolic disease, 2005, Volume: 28, Issue:4 Topics: Acyl-CoA Dehydrogenase, Long-Chain; Cardiomyopathies; Carnitine; Exons; Fatty Acids; Fibroblasts; Homozygote; Humans; Lipid Metabolism, Inborn Errors; Male; Mitochondria; Mitochondrial Trifunctional Protein; Multienzyme Complexes; Mutation; Phenotype; Polyneuropathies; Prognosis; Rhabdomyolysis	2005
Rhabdomyolysis in early-onset very long-chain acyl-CoA dehydrogenase deficiency despite normal glucose after fasting. Journal of inherited metabolic disease, 2005, Volume: 28, Issue:6 Topics: Acyl-CoA Dehydrogenase, Long-Chain; Blood Glucose; Carnitine; Fasting; Glucose; Humans; Hypoglycemia; Infant; Metabolism, Inborn Errors; Rhabdomyolysis	2005