ethylmalonic acid has been researched along with Nervous System Disorders in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (50.00) | 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 |
Belanger-Quintana, A; Bischoff, C; de la Mota, JL; Ferrer, I; García, MJ; Gregersen, N; Martin-Hernández, E; Martínez Pardo, M; Merinero, B; Pérez-Cerdá, C; Ruiz Sala, P; Ugarte, M; Vianey-Saban, C | 1 |
Lehnert, W; Ruitenbeek, W | 1 |
al Odaib, A; Gascon, GG; Hazzaa, S; Mazrou, A; Millington, DS; Ozand, PT; Rahbeeni, Z; Rashed, M; Sakati, N; Youssef, N | 1 |
4 other study(ies) available for ethylmalonic acid and Nervous System Disorders
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 |
Persistent increase of plasma butyryl/isobutyrylcarnitine concentrations as marker of SCAD defect and ethylmalonic encephalopathy.
Topics: Brain Diseases; Butyryl-CoA Dehydrogenase; Carnitine; Humans; Malonates; Mitochondrial Proteins; Nervous System Diseases; Nucleocytoplasmic Transport Proteins | 2006 |
Ethylmalonic aciduria associated with progressive neurological disease and partial cytochrome c oxidase deficiency.
Topics: Child; Child, Preschool; Cytochrome-c Oxidase Deficiency; Female; Humans; Male; Malonates; Muscles; Nervous System Diseases | 1993 |
Ethylmalonic aciduria: an organic acidemia with CNS involvement and vasculopathy.
Topics: Acidosis; Brain Edema; Female; Fibroblasts; Gas Chromatography-Mass Spectrometry; Humans; Infant; Infant, Newborn; Magnetic Resonance Imaging; Male; Malonates; Mass Spectrometry; Metabolism, Inborn Errors; Nervous System Diseases; Pedigree; Tomography, X-Ray Computed; Vascular Diseases | 1994 |