carnitine has been researched along with Cot Death in 28 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Infants with inborn errors of fatty acid metabolism may present with apnea, periodic breathing, and sudden infant death syndrome (SIDS)." | 7.69 | Familial infantile apnea and immature beta oxidation. ( Browning, IB; Iafolla, AK; Roe, CR, 1995) |
| "The accumulation of arrhythmogenic intermediary metabolites of fatty acids, such as long-chain acylcarnitines, may be responsible for arrhythmias." | 3.70 | Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children. ( Bonnet, D; Brivet, M; Jouvet, P; Martin, D; Rabier, D; Saudubray, JM; Villain, E, 1999) |
| "Infants with inborn errors of fatty acid metabolism may present with apnea, periodic breathing, and sudden infant death syndrome (SIDS)." | 3.69 | Familial infantile apnea and immature beta oxidation. ( Browning, IB; Iafolla, AK; Roe, CR, 1995) |
| "Many inborn errors of metabolism (IEMs) may present as sudden infant death (SID)." | 2.53 | Inborn Errors of Metabolism That Cause Sudden Infant Death: A Systematic Review with Implications for Population Neonatal Screening Programmes. ( Bekhof, J; de Koning, TJ; Derks, TG; Heiner Fokkema, MR; Koolhaas, GD; Schielen, PC; van Rijt, WJ; van Spronsen, FJ; Visser, G, 2016) |
| "Acyl-carnitine profiles were obtained from dried blood spot and/or from oxidation of (13) C-palmitate by cultured skin fibroblasts." | 1.42 | Familial very long chain acyl-CoA dehydrogenase deficiency as a cause of neonatal sudden infant death: improved survival by prompt diagnosis. ( Bottu, J; De Meirleir, L; Ferdinandusse, S; Scalais, E; Wanders, RJ; Waterham, HR, 2015) |
| "Carnitine treatment resulted in dramatic improvement of the cardiac symptoms, echocardiographic, and EKG findings in both cases." | 1.32 | Phenotypic manifestations of the OCTN2 V295X mutation: sudden infant death and carnitine-responsive cardiomyopathy in Roma families. ( Bene, J; Havasi, V; Kispál, G; Komlósi, K; Méhes, K; Melegh, B; Mogyorósy, G; Oláh, E; Pajor, L; Sumegi, B, 2004) |
| "Families with children who have had Reye syndrome or in which sudden infant death has occurred are at risk for MCAD deficiency." | 1.27 | Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes. ( Kinnebrew, P; Maltby, DA; Millington, DS; Roe, CR, 1986) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (14.29) | 18.7374 |
| 1990's | 10 (35.71) | 18.2507 |
| 2000's | 7 (25.00) | 29.6817 |
| 2010's | 7 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Scalais, E | 1 |
| Bottu, J | 1 |
| Wanders, RJ | 1 |
| Ferdinandusse, S | 1 |
| Waterham, HR | 1 |
| De Meirleir, L | 1 |
| van Rijt, WJ | 1 |
| Koolhaas, GD | 1 |
| Bekhof, J | 1 |
| Heiner Fokkema, MR | 1 |
| de Koning, TJ | 1 |
| Visser, G | 1 |
| Schielen, PC | 1 |
| van Spronsen, FJ | 1 |
| Derks, TG | 1 |
| Manoukian, AA | 1 |
| Ha, CE | 1 |
| Seaver, LH | 1 |
| Bhagavan, NV | 1 |
| Bouchireb, K | 1 |
| Teychene, AM | 1 |
| Rigal, O | 1 |
| de Lonlay, P | 1 |
| Valayannopoulos, V | 1 |
| Gaudelus, J | 1 |
| Sellier, N | 1 |
| Bonnefont, JP | 1 |
| Brivet, M | 2 |
| de Pontual, L | 1 |
| Yamamoto, T | 2 |
| Tanaka, H | 2 |
| Kobayashi, H | 1 |
| Okamura, K | 1 |
| Tanaka, T | 1 |
| Emoto, Y | 2 |
| Sugimoto, K | 1 |
| Nakatome, M | 1 |
| Sakai, N | 1 |
| Kuroki, H | 1 |
| Yamaguchi, S | 1 |
| Matoba, R | 2 |
| Pryce, JW | 2 |
| Weber, MA | 2 |
| Heales, S | 2 |
| Malone, M | 1 |
| Sebire, NJ | 2 |
| Krywawych, S | 1 |
| Ashworth, MT | 1 |
| Klein, NJ | 1 |
| Murayama, K | 1 |
| Kuriu, Y | 1 |
| Ohtake, A | 1 |
| Korman, SH | 1 |
| Gutman, A | 1 |
| Brooks, R | 1 |
| Sinnathamby, T | 1 |
| Gregersen, N | 1 |
| Andresen, BS | 1 |
| Melegh, B | 1 |
| Bene, J | 1 |
| Mogyorósy, G | 1 |
| Havasi, V | 1 |
| Komlósi, K | 1 |
| Pajor, L | 1 |
| Oláh, E | 1 |
| Kispál, G | 1 |
| Sumegi, B | 1 |
| Méhes, K | 1 |
| Gordon, N | 1 |
| Rashed, MS | 1 |
| Ozand, PT | 1 |
| Bennett, MJ | 1 |
| Barnard, JJ | 1 |
| Govindaraju, DR | 1 |
| Rinaldo, P | 3 |
| Boles, RG | 2 |
| Martin, SK | 2 |
| Blitzer, MG | 2 |
| Iafolla, AK | 1 |
| Browning, IB | 1 |
| Roe, CR | 3 |
| Chalmers, RA | 1 |
| Stanley, CA | 1 |
| English, N | 1 |
| Wigglesworth, JS | 1 |
| Buck, EA | 1 |
| Platt, MS | 1 |
| Cowan, TM | 1 |
| Yoon, H | 1 |
| Madsen, JA | 1 |
| Reyes-Mugica, M | 1 |
| Bonnet, D | 1 |
| Martin, D | 1 |
| Villain, E | 1 |
| Jouvet, P | 1 |
| Rabier, D | 1 |
| Saudubray, JM | 1 |
| Treem, WR | 1 |
| Chace, DH | 1 |
| DiPerna, JC | 1 |
| Mitchell, BL | 1 |
| Sgroi, B | 1 |
| Hofman, LF | 1 |
| Naylor, EW | 1 |
| Green, A | 1 |
| Preece, MA | 1 |
| Hardy, D | 1 |
| Tameling, E | 1 |
| Touma, EH | 1 |
| Charpentier, C | 3 |
| Holton, JB | 1 |
| Allen, JT | 1 |
| Green, CA | 1 |
| Partington, S | 1 |
| Gilbert, RE | 1 |
| Berry, PJ | 1 |
| Harpey, JP | 2 |
| Paturneau-Jouas, M | 2 |
| Millington, DS | 2 |
| Maltby, DA | 2 |
| Wellman, RB | 1 |
| Coudé, M | 1 |
| Divry, P | 1 |
| Shaw, W | 1 |
| Kinnebrew, P | 1 |
4 reviews available for carnitine and Cot Death
| Article | Year |
|---|---|
Inborn Errors of Metabolism That Cause Sudden Infant Death: A Systematic Review with Implications for Population Neonatal Screening Programmes.
Topics: Amino Acids; Autopsy; Carnitine; Humans; Infant; Infant, Newborn; Metabolism, Inborn Errors; Neonata | 2016 |
New developments in the pathophysiology, clinical spectrum, and diagnosis of disorders of fatty acid oxidation.
Topics: Acetyl Coenzyme A; Carnitine; Fatty Acids; Female; Fetal Diseases; Humans; Infant; Lipid Metabolism, | 2000 |
Medium chain acyl-CoA dehydrogenase deficiency.
Topics: Acyl-CoA Dehydrogenases; Blood Glucose; Carnitine; Child, Preschool; Fasting; Fatty Acids; Female; H | 1992 |
Sudden infant death syndrome and inherited disorders of fatty acid beta-oxidation.
Topics: Adipates; Adolescent; Carnitine; Child; Child, Preschool; Fatty Acid Desaturases; Fatty Acids; Human | 1990 |
24 other studies available for carnitine and Cot Death
| Article | Year |
|---|---|
Familial very long chain acyl-CoA dehydrogenase deficiency as a cause of neonatal sudden infant death: improved survival by prompt diagnosis.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Carnitine; Child; Family; Female; Fibroblasts; Humans; Infant; I | 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.
Topics: Acyl-CoA Dehydrogenase; Carnitine; Gene Deletion; Humans; Infant, Newborn; Lipid Metabolism, Inborn | 2009 |
Post-mortem MRI reveals CPT2 deficiency after sudden infant death.
Topics: Carnitine; Carnitine O-Palmitoyltransferase; Cause of Death; Diagnosis; Fatty Liver; Hepatomegaly; H | 2010 |
Retrospective review of Japanese sudden unexpected death in infancy: the importance of metabolic autopsy and expanded newborn screening.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Carnitine; Carnitine Acyltransferases; Carnitine O-Palmitoyltran | 2011 |
Tandem mass spectrometry findings at autopsy for detection of metabolic disease in infant deaths: postmortem changes and confounding factors.
Topics: Autopsy; Bile; Carnitine; Humans; Infant; Infant, Newborn; Liver; Metabolic Diseases; Organ Size; Po | 2011 |
Postmortem tandem mass spectrometry profiling for detection of infection in unexpected infant death.
Topics: Autopsy; Bile; Biomarkers; Carnitine; Cause of Death; Communicable Diseases; Forensic Toxicology; Hu | 2012 |
Metabolic autopsy with postmortem cultured fibroblasts in sudden unexpected death in infancy: diagnosis of mitochondrial respiratory chain disorders.
Topics: Autopsy; Carnitine; Cells, Cultured; Electron Transport; Enzyme Assays; Female; Fibroblasts; Humans; | 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
Topics: Acyl-CoA Dehydrogenase; Adult; Alternative Splicing; Arabs; Base Sequence; Carnitine; Child; Codon, | 2004 |
Phenotypic manifestations of the OCTN2 V295X mutation: sudden infant death and carnitine-responsive cardiomyopathy in Roma families.
Topics: Amino Acid Sequence; Base Sequence; Cardiomyopathies; Carnitine; Child, Preschool; DNA; DNA Mutation | 2004 |
Acyl-CoA dehydrogenase deficiency: varieties with neurological involvement.
Topics: Acyl-CoA Dehydrogenase; Carnitine; Child; Child, Preschool; Chromosome Aberrations; Developmental Di | 2005 |
Inborn errors of metabolism diagnosed in sudden death cases by acylcarnitine analysis of postmortem bile.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acylation; Bile; Carnitine; Child; Fatty Acids; Glutaryl-CoA Dehyd | 1995 |
Biochemical diagnosis of fatty acid oxidation disorders by metabolite analysis of postmortem liver.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenase, Long-Chain; Animals; Caprylates; Carnitine; Child, P | 1994 |
Familial infantile apnea and immature beta oxidation.
Topics: Apnea; Carnitine; Diseases in Twins; Fatty Acids; Female; Humans; Infant, Newborn; Lipid Metabolism, | 1995 |
Mitochondrial carnitine-acylcarnitine translocase deficiency presenting as sudden neonatal death.
Topics: Adult; Amnion; Breast Feeding; Carnitine; Carnitine Acyltransferases; Carnitine O-Palmitoyltransfera | 1997 |
Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenase, Long-Chain; Carnit | 1998 |
Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenase, Long-Chain; Arrhyt | 1999 |
Electrospray tandem mass spectrometry for analysis of acylcarnitines in dried postmortem blood specimens collected at autopsy from infants with unexplained cause of death.
Topics: Autopsy; Bile; Blood Specimen Collection; Canada; Carnitine; Fatty Acids; Humans; Infant; Infant, Ne | 2001 |
More on the metabolic autopsy.
Topics: Amino Acids; Autopsy; Biopsy; Carnitine; Humans; Infant, Newborn; Metabolism, Inborn Errors; Skin; S | 2002 |
New organization targets carnitine deficiency.
Topics: Adult; Carnitine; Child; Humans; Infant; Sudden Infant Death; United States; Voluntary Health Agenci | 1992 |
Inherited metabolic diseases in the sudden infant death syndrome.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Carnitine; Child, Preschool; Female; Glycogen Stora | 1991 |
Post-mortem recognition of inherited metabolic disorders from specific acylcarnitines in tissue in cases of sudden infant death.
Topics: Acyl-CoA Dehydrogenase; Carnitine; Fatty Acid Desaturases; Female; Humans; Infant; Infant, Newborn; | 1987 |
Sudden infant death syndrome and multiple acyl-coenzyme A dehydrogenase deficiency, ethylmalonic-adipic aciduria, or systemic carnitine deficiency.
Topics: Acyl-CoA Dehydrogenase; Adipates; Carnitine; Fatty Acid Desaturases; Humans; Infant; Infant, Newborn | 1987 |
Possible role of lysolecithins and nonesterified fatty acids in the pathogenesis of Reye's syndrome, sudden infant death syndrome, acute pancreatitis, and diabetic ketoacidosis.
Topics: Acute Disease; Barbiturates; Blood Transfusion; Carnitine; Diabetic Ketoacidosis; Fasting; Fatty Aci | 1985 |
Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Adult; Breast Feeding; Carnitine; Child, Preschool; | 1986 |