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Journal Article
Journal of Child Neurology, ISSN 0883-0738, 4/2011, Volume 26, Issue 4, pp. 507 - 509
Ohtahara syndrome is a rare epileptic encephalopathy in infants; the underlying etiology is generally thought to be structural brain malformations. The authors... 
biotinidase deficiency | Ohtahara syndrome | epileptic encephalopathy | PEDIATRICS | CLINICAL NEUROLOGY | MANIFESTATIONS | Infant | Male | Biotinidase Deficiency - complications | Brain Diseases - complications | Humans | Epilepsy - complications | Index Medicus
Journal Article
Epilepsia, ISSN 0013-9580, 08/2012, Volume 53, Issue 8, pp. 1441 - 1449
Journal Article
08/2007
Early infantile epileptic encephalopathy or EIEE (Ohtahara syndrome; OS) is a kind of intractable seizure that begins in neonatal age with sudden onset of... 
EIEE | Early myoclonic encephalopathy | Ohtahara syndrome | Intractable infantile seizure | Early infantile epilepsy with suppression-bursts
Web Resource
Journal of Child Neurology, ISSN 0883-0738, 12/2013, Volume 28, Issue 12, pp. 1607 - 1617
Journal Article
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 6, pp. 640 - 645
Journal Article
Revista de Neurologia, ISSN 0210-0010, 2018, Volume 66, pp. S61 - S69
Journal Article
Epilepsia, ISSN 0013-9580, 5/2013, Volume 54, Issue 5, pp. e81 - e85
Mutations in SCN2A gene cause a variety of epilepsy syndromes. We report a novel SCN2A -associated epilepsy phenotype in monozygotic twins with tonic seizures... 
Ohtahara syndrome | SCN2A | Whole genome sequencing | Seizures
Journal Article