Compounds > s-adenosylmethionine
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s-adenosylmethionine and Bone Marrow Failure Syndromes, Congenital

s-adenosylmethionine has been researched along with Bone Marrow Failure Syndromes, Congenital in 13 studies

Research

Studies (13)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's10 (76.92)24.3611
2020's3 (23.08)2.80

Authors

AuthorsStudies
He, R; Huang, M; Kang, L; Li, X; Li, Y; Liu, Y; Ma, R; Men, J; Ren, J; Song, J; Yang, Y1
Bleeker, JC; Clarke, K; Cox, PJ; de Haan, FH; de Sain-van der Velden, MGM; Ferdinandusse, S; Houtkooper, RH; IJlst, L; Jeneson, JAL; Kok, IL; Langeveld, M; Sibeijn-Kuiper, A; Takken, T; van der Pol, WL; van der Woude, LH; van Weeghel, M; Visser, G; Wanders, RJA; Wijburg, FA; Wüst, RCI1
de Sain-van der Velden, MGM; Ferdinandusse, S; Houtkooper, RH; Knottnerus, SJG; Pras-Raves, ML; Schielen, PCJI; van der Ham, M; Visser, G; Wijburg, FA1
Cusmano-Ozog, K; McGuire, PJ; Tarasenko, TN1
Abdenur, JE; Au, SM; Barshop, BA; Feuchtbaum, L; Harding, CO; Hermerath, C; Lorey, F; Merritt, JL; Sesser, DE; Thompson, JD; Vedal, S; Yu, A1
Bastin, J; Bennett, MJ; Chen, J; Doulias, PT; Ischiropoulos, H; Tenopoulou, M1
Furuyama, H; Hisahara, S; Imai, T; Matsushita, T; Shigematsu, Y; Shimohama, S; Tajima, G1
Bick, DP; Burrage, LC; Craigen, WJ; Elsea, SH; Gibson, JB; Graham, BH; Lose, EJ; Miller, MJ; Strenk, ME; Sun, Q; Sutton, VR; Wong, LJ; Zhang, VW1
Burrage, LC; Elsea, SH; Graham, BH; Kennedy, AD; Miller, MJ; Sun, Q; Sutton, VR; Wong, LJ1
Arnold, GL; Berry, SA; Cameron, C; Edick, MJ; Hansen, J; Leslie, N; Mohsen, AW; Pena, LD; van Calcar, SC; Vockley, J; Walsh Vockley, C1
Marble, M; McGoey, RR1
Primassin, S; Spiekerkoetter, U; Tucci, S1
Conlon, T; Cossette, T; Dungtao, F; Erger, K; Flotte, TR; Keeler, AM; Mueller, C; Shaffer, SA; Tang, Q; Walter, G; Zeng, H1

Trials

1 trial(s) available for s-adenosylmethionine and Bone Marrow Failure Syndromes, Congenital

ArticleYear
Nutritional ketosis improves exercise metabolism in patients with very long-chain acyl-CoA dehydrogenase deficiency.
    Journal of inherited metabolic disease, 2020, Volume: 43, Issue:4

    Topics: Adolescent; Adult; Beverages; Blood Glucose; Carnitine; Congenital Bone Marrow Failure Syndromes; Cross-Over Studies; Diet, Ketogenic; Endurance Training; Esters; Exercise Test; Female; Humans; Ketones; Ketosis; Lipid Metabolism, Inborn Errors; Magnetic Resonance Spectroscopy; Male; Middle Aged; Mitochondrial Diseases; Muscle, Skeletal; Muscular Diseases; Netherlands; Pulmonary Gas Exchange; Young Adult

2020

Other Studies

12 other study(ies) available for s-adenosylmethionine and Bone Marrow Failure Syndromes, Congenital

ArticleYear
One potential hotspot ACADVL mutation in Chinese patients with very-long-chain acyl-coenzyme A dehydrogenase deficiency.
    Clinica chimica acta; international journal of clinical chemistry, 2020, Volume: 503

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Asian People; Carnitine; China; Congenital Bone Marrow Failure Syndromes; Female; Humans; Hypoglycemia; Infant, Newborn; Lipid Metabolism, Inborn Errors; Liver Diseases; Male; Mitochondrial Diseases; Muscular Diseases; Mutation

2020
Prediction of VLCAD deficiency phenotype by a metabolic fingerprint in newborn screening bloodspots.
    Biochimica et biophysica acta. Molecular basis of disease, 2020, 06-01, Volume: 1866, Issue:6

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Carnitine; Child; Child, Preschool; Congenital Bone Marrow Failure Syndromes; Dried Blood Spot Testing; Female; Humans; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Mass Spectrometry; Metabolomics; Mitochondrial Diseases; Muscular Diseases; Neonatal Screening; Phenotype

2020
Tissue acylcarnitine status in a mouse model of mitochondrial β-oxidation deficiency during metabolic decompensation due to influenza virus infection.
    Molecular genetics and metabolism, 2018, Volume: 125, Issue:1-2

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Animals; Cardiomyopathies; Carnitine; Congenital Bone Marrow Failure Syndromes; Disease Models, Animal; Fatty Acids; Female; Humans; Hypoglycemia; Lipid Metabolism, Inborn Errors; Lipid Peroxidation; Liver; Liver Failure; Metabolic Diseases; Mice; Mitochondrial Diseases; Muscle, Skeletal; Muscular Diseases; Myocardium; Oxidation-Reduction

2018
Infants suspected to have very-long chain acyl-CoA dehydrogenase deficiency from newborn screening.
    Molecular genetics and metabolism, 2014, Volume: 111, Issue:4

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Carnitine; Congenital Bone Marrow Failure Syndromes; Demography; DNA Mutational Analysis; Fatty Acids; Female; Genotype; Humans; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Mitochondrial Diseases; Muscular Diseases; Neonatal Screening; Phenotype; Reproducibility of Results

2014
Strategies for correcting very long chain acyl-CoA dehydrogenase deficiency.
    The Journal of biological chemistry, 2015, Apr-17, Volume: 290, Issue:16

    Topics: Acetylcysteine; Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenase, Long-Chain; Amino Acid Sequence; Carnitine; Congenital Bone Marrow Failure Syndromes; Cysteine; Dose-Response Relationship, Drug; Fatty Acids; Fibroblasts; Genetic Therapy; Humans; Kinetics; Lipid Metabolism, Inborn Errors; Mitochondrial Diseases; Molecular Sequence Data; Muscular Diseases; Mutation; Oxidation-Reduction; Primary Cell Culture; Skin

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
Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States.
    Molecular genetics and metabolism, 2015, Volume: 116, Issue:3

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Alleles; Carnitine; Computer Simulation; Congenital Bone Marrow Failure Syndromes; Exons; Female; Genetic Carrier Screening; Genotype; Humans; Hypoglycemia; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Mitochondrial Diseases; Muscular Diseases; Mutation, Missense; Neonatal Screening; Oligonucleotide Array Sequence Analysis; Sequence Analysis, DNA; Tandem Mass Spectrometry; United States

2015
Elevations of C14:1 and C14:2 Plasma Acylcarnitines in Fasted Children: A Diagnostic Dilemma.
    The Journal of pediatrics, 2016, Volume: 169

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Adolescent; Carnitine; Child; Child, Preschool; Congenital Bone Marrow Failure Syndromes; Fasting; Female; Humans; Infant; Lipid Metabolism, Inborn Errors; Male; Mitochondrial Diseases; Muscular Diseases; Retrospective Studies

2016
Outcomes and genotype-phenotype correlations in 52 individuals with VLCAD deficiency diagnosed by NBS and enrolled in the IBEM-IS database.
    Molecular genetics and metabolism, 2016, Volume: 118, Issue:4

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Adolescent; Carnitine; Child; Child, Preschool; Congenital Bone Marrow Failure Syndromes; Creatine Kinase; Female; Genetic Association Studies; Genotype; Humans; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Mitochondrial Diseases; Muscular Diseases; Mutation; Neonatal Screening; Retrospective Studies

2016
Positive newborn screen in a normal infant of a mother with asymptomatic very long-chain Acyl-CoA dehydrogenase deficiency.
    The Journal of pediatrics, 2011, Volume: 158, Issue:6

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Carnitine; Congenital Bone Marrow Failure Syndromes; Female; Genotype; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Metabolism, Inborn Errors; Mitochondrial Diseases; Mothers; Muscular Diseases; Neonatal Screening; Phenotype

2011
Hepatic and muscular effects of different dietary fat content in VLCAD deficient mice.
    Molecular genetics and metabolism, 2011, Volume: 104, Issue:4

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Animals; Carnitine; Congenital Bone Marrow Failure Syndromes; Diet; Dietary Fats; Energy Metabolism; Glycogen; Lipid Metabolism; Lipid Metabolism, Inborn Errors; Lipids; Lipogenesis; Liver; Mice; Mice, 129 Strain; Mice, Inbred C57BL; Mice, Knockout; Mitochondrial Diseases; Muscle, Skeletal; Muscular Diseases; Physical Exertion; Up-Regulation

2011
Long-term correction of very long-chain acyl-coA dehydrogenase deficiency in mice using AAV9 gene therapy.
    Molecular therapy : the journal of the American Society of Gene Therapy, 2012, Volume: 20, Issue:6

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Animals; Carnitine; Congenital Bone Marrow Failure Syndromes; Dependovirus; Gene Expression; Genetic Therapy; Genetic Vectors; Lipid Metabolism; Lipid Metabolism, Inborn Errors; Liver; Mice; Mice, Knockout; Mitochondrial Diseases; Muscle, Skeletal; Muscular Diseases; Phenotype; Tissue Distribution; Transduction, Genetic

2012