ethylmalonic acid has been researched along with Cot Death in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Gordon, N | 1 |
| Ang, D; Bolund, L; Bross, P; Corydon, TJ; Eiberg, H; Georgopoulos, C; Gregersen, N; Hansen, J; Hansen, JJ; Kølvraa, S; Li, Z; Lundemose, JB; Nielsen, MN; Niezen-Koning, K; Yang, H | 1 |
| Charpentier, C; Harpey, JP; Paturneau-Jouas, M | 1 |
| Charpentier, C; Coudé, M; Divry, P; Harpey, JP; Paturneau-Jouas, M | 1 |
1 review(s) available for ethylmalonic acid and Cot Death
| Article | Year |
|---|---|
Sudden infant death syndrome and inherited disorders of fatty acid beta-oxidation.
Topics: Adipates; Adolescent; Carnitine; Child; Child, Preschool; Fatty Acid Desaturases; Fatty Acids; Humans; Infant; Lipid Metabolism, Inborn Errors; Malonates; Oxidation-Reduction; Sudden Infant Death | 1990 |
3 other study(ies) available for ethylmalonic acid and Cot Death
| Article | Year |
|---|---|
Acyl-CoA dehydrogenase deficiency: varieties with neurological involvement.
Topics: Acyl-CoA Dehydrogenase; Carnitine; Child; Child, Preschool; Chromosome Aberrations; Developmental Disabilities; Diagnosis, Differential; Electron-Transferring Flavoproteins; Female; Genes, Recessive; Genetic Variation; Humans; Hypoglycemia; Infant; Infant, Newborn; Male; Malonates; Mass Spectrometry; Metabolism, Inborn Errors; Neonatal Screening; Nervous System Diseases; Pregnancy; Prenatal Diagnosis; Prognosis; Succinates; Sudden Infant Death | 2005 |
Single-nucleotide variations in the genes encoding the mitochondrial Hsp60/Hsp10 chaperone system and their disease-causing potential.
Topics: Butyryl-CoA Dehydrogenase; Chaperonin 10; Chaperonin 60; Child; Child, Preschool; Genetic Predisposition to Disease; Humans; Infant; Infant, Newborn; Malonates; Mitochondrial Proteins; Polymorphism, Single Nucleotide; Promoter Regions, Genetic; Sudden Infant Death | 2007 |
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; Malonates; Metabolism, Inborn Errors; Risk; Sudden Infant Death | 1987 |