Page last updated: 2024-08-21

ethylmalonic acid and Developmental Disabilities

ethylmalonic acid has been researched along with Developmental Disabilities in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Biberoglu, G; Ezgü, FS; Okuyaz, C; Tiranti, V; Yilgör, E; Zeviani, M	1
Gordon, N	1

Other Studies

2 other study(ies) available for ethylmalonic acid and Developmental Disabilities

Article	Year
Severe infantile hypotonia with ethylmalonic aciduria: case report. Journal of child neurology, 2008, Volume: 23, Issue:6 Topics: Alleles; Butyryl-CoA Dehydrogenase; Developmental Disabilities; Diagnosis, Differential; DNA Mutational Analysis; Female; Genotype; Humans; Infant; Lipid Metabolism, Inborn Errors; Malonates; Muscle Hypotonia; Muscle Weakness; Neurologic Examination; Phenotype; Polymorphism, Genetic	2008
Acyl-CoA dehydrogenase deficiency: varieties with neurological involvement. Developmental medicine and child neurology, 2005, Volume: 47, Issue:3 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

Article

Year

Severe infantile hypotonia with ethylmalonic aciduria: case report.

Journal of child neurology, 2008, Volume: 23, Issue:6

Topics: Alleles; Butyryl-CoA Dehydrogenase; Developmental Disabilities; Diagnosis, Differential; DNA Mutational Analysis; Female; Genotype; Humans; Infant; Lipid Metabolism, Inborn Errors; Malonates; Muscle Hypotonia; Muscle Weakness; Neurologic Examination; Phenotype; Polymorphism, Genetic

2008

Acyl-CoA dehydrogenase deficiency: varieties with neurological involvement.

Developmental medicine and child neurology, 2005, Volume: 47, Issue:3

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