Compounds > s-adenosylmethionine
Page last updated: 2024-08-23

s-adenosylmethionine and Cot Death

s-adenosylmethionine has been researched along with Cot Death in 12 studies

Research

Studies (12)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (8.33)18.2507
2000's4 (33.33)29.6817
2010's7 (58.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bottu, J; De Meirleir, L; Ferdinandusse, S; Scalais, E; Wanders, RJ; Waterham, HR1
Bekhof, J; de Koning, TJ; Derks, TG; Heiner Fokkema, MR; Koolhaas, GD; Schielen, PC; van Rijt, WJ; van Spronsen, FJ; Visser, G1
Bhagavan, NV; Ha, CE; Manoukian, AA; Seaver, LH1
Bonnefont, JP; Bouchireb, K; Brivet, M; de Lonlay, P; de Pontual, L; Gaudelus, J; Rigal, O; Sellier, N; Teychene, AM; Valayannopoulos, V1
Emoto, Y; Kobayashi, H; Kuroki, H; Matoba, R; Nakatome, M; Okamura, K; Sakai, N; Sugimoto, K; Tanaka, H; Tanaka, T; Yamaguchi, S; Yamamoto, T1
Heales, S; Malone, M; Pryce, JW; Sebire, NJ; Weber, MA1
Ashworth, MT; Heales, S; Klein, NJ; Krywawych, S; Pryce, JW; Sebire, NJ; Weber, MA1
Emoto, Y; Kuriu, Y; Matoba, R; Murayama, K; Ohtake, A; Tanaka, H; Yamamoto, T1
Andresen, BS; Brooks, R; Gregersen, N; Gutman, A; Korman, SH; Sinnathamby, T1
Bonnet, D; Brivet, M; Jouvet, P; Martin, D; Rabier, D; Saudubray, JM; Villain, E1
Chace, DH; DiPerna, JC; Hofman, LF; Mitchell, BL; Naylor, EW; Sgroi, B1
Green, A; Hardy, D; Preece, MA1

Reviews

1 review(s) available for s-adenosylmethionine and Cot Death

ArticleYear
Inborn Errors of Metabolism That Cause Sudden Infant Death: A Systematic Review with Implications for Population Neonatal Screening Programmes.
    Neonatology, 2016, Volume: 109, Issue:4

    Topics: Amino Acids; Autopsy; Carnitine; Humans; Infant; Infant, Newborn; Metabolism, Inborn Errors; Neonatal Screening; Reye Syndrome; Sudden Infant Death

2016

Other Studies

11 other study(ies) available for s-adenosylmethionine and Cot Death

ArticleYear
Familial very long chain acyl-CoA dehydrogenase deficiency as a cause of neonatal sudden infant death: improved survival by prompt diagnosis.
    American journal of medical genetics. Part A, 2015, Volume: 167A, Issue:1

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Carnitine; Child; Family; Female; Fibroblasts; Humans; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Lymphocytes; Male; Oxidation-Reduction; Palmitates; Perinatal Death; Siblings; Sudden Infant Death; Survival Analysis

2015
A neonatal death due to medium-chain acyl-CoA dehydrogenase deficiency: utilization of the neonatal metabolic screen in a functional approach to sudden unexplained infant death.
    The American journal of forensic medicine and pathology, 2009, Volume: 30, Issue:3

    Topics: Acyl-CoA Dehydrogenase; Carnitine; Gene Deletion; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Neonatal Screening; Point Mutation; Sudden Infant Death

2009
Post-mortem MRI reveals CPT2 deficiency after sudden infant death.
    European journal of pediatrics, 2010, Volume: 169, Issue:12

    Topics: Carnitine; Carnitine O-Palmitoyltransferase; Cause of Death; Diagnosis; Fatty Liver; Hepatomegaly; Humans; Infant; Magnetic Resonance Imaging; Male; Metabolism, Inborn Errors; Postmortem Changes; Sudden Infant Death

2010
Retrospective review of Japanese sudden unexpected death in infancy: the importance of metabolic autopsy and expanded newborn screening.
    Molecular genetics and metabolism, 2011, Volume: 102, Issue:4

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Carnitine; Carnitine Acyltransferases; Carnitine O-Palmitoyltransferase; Case-Control Studies; Female; Haplotypes; Humans; Infant; Infant, Newborn; Japan; Liver; Male; Mitochondrial Trifunctional Protein; Multienzyme Complexes; Mutation, Missense; Neonatal Screening; Retrospective Studies; Sudden Infant Death

2011
Tandem mass spectrometry findings at autopsy for detection of metabolic disease in infant deaths: postmortem changes and confounding factors.
    Journal of clinical pathology, 2011, Volume: 64, Issue:11

    Topics: Autopsy; Bile; Carnitine; Humans; Infant; Infant, Newborn; Liver; Metabolic Diseases; Organ Size; Postmortem Changes; Sudden Infant Death; Tandem Mass Spectrometry

2011
Postmortem tandem mass spectrometry profiling for detection of infection in unexpected infant death.
    Forensic science, medicine, and pathology, 2012, Volume: 8, Issue:3

    Topics: Autopsy; Bile; Biomarkers; Carnitine; Cause of Death; Communicable Diseases; Forensic Toxicology; Humans; Infant; Infant Mortality; Infant, Newborn; Linear Models; London; Postmortem Changes; Predictive Value of Tests; Reference Standards; Retrospective Studies; Risk Factors; Sudden Infant Death; Tandem Mass Spectrometry

2012
Metabolic autopsy with postmortem cultured fibroblasts in sudden unexpected death in infancy: diagnosis of mitochondrial respiratory chain disorders.
    Molecular genetics and metabolism, 2012, Volume: 106, Issue:4

    Topics: Autopsy; Carnitine; Cells, Cultured; Electron Transport; Enzyme Assays; Female; Fibroblasts; Humans; Infant; Infant, Newborn; Liver; Male; Mitochondrial Diseases; Myocardium; Postmortem Changes; Sudden Infant Death

2012
Homozygosity for a severe novel medium-chain acyl-CoA dehydrogenase (MCAD) mutation IVS3-1G > C that leads to introduction of a premature termination codon by complete missplicing of the MCAD mRNA and is associated with phenotypic diversity ranging from s
    Molecular genetics and metabolism, 2004, Volume: 82, Issue:2

    Topics: Acyl-CoA Dehydrogenase; Adult; Alternative Splicing; Arabs; Base Sequence; Carnitine; Child; Codon, Nonsense; Female; Homozygote; Humans; Infant, Newborn; Male; Mutation; Oxidation-Reduction; Pedigree; Phenotype; RNA, Messenger; Sudden Infant Death

2004
Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children.
    Circulation, 1999, Nov-30, Volume: 100, Issue:22

    Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenase, Long-Chain; Arrhythmias, Cardiac; Carnitine; Carnitine Acyltransferases; Carnitine O-Palmitoyltransferase; Fatty Acid Desaturases; Fatty Acids; Female; Heart Conduction System; Humans; Infant; Infant, Newborn; Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase; Male; Mitochondria, Heart; Mitochondrial Myopathies; Models, Biological; Oxidation-Reduction; Sudden Infant Death; Tachycardia, Ventricular

1999
Electrospray tandem mass spectrometry for analysis of acylcarnitines in dried postmortem blood specimens collected at autopsy from infants with unexplained cause of death.
    Clinical chemistry, 2001, Volume: 47, Issue:7

    Topics: Autopsy; Bile; Blood Specimen Collection; Canada; Carnitine; Fatty Acids; Humans; Infant; Infant, Newborn; Metabolism, Inborn Errors; Oxidation-Reduction; Paper; Reference Values; Spectrometry, Mass, Electrospray Ionization; Sudden Infant Death; United States

2001
More on the metabolic autopsy.
    Clinical chemistry, 2002, Volume: 48, Issue:6 Pt 1

    Topics: Amino Acids; Autopsy; Biopsy; Carnitine; Humans; Infant, Newborn; Metabolism, Inborn Errors; Skin; Sudden Infant Death; Urine

2002