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Journal of Child Neurology, ISSN 0883-0738, 11/2019, Volume 34, Issue 13, pp. 830 - 836
Perinatal stroke is a significant cause of severe epilepsy, including epileptic spasms. Although epileptic spasms due to underlying structural lesion often... 
Journal Article
Epilepsy and Behavior, ISSN 1525-5050, 2015, Volume 47, pp. 75 - 77
Journal Article
Expert Opinion on Orphan Drugs, ISSN 2167-8707, 12/2018, Volume 6, Issue 12, pp. 741 - 751
Journal Article
Journal of Child Neurology, ISSN 0883-0738, 2/2017, Volume 32, Issue 2, pp. 170 - 176
The SCN1A gene has been implicated in the etiology of various forms of epilepsy. New research has linked this gene to specific types of epilepsy, all of which... 
focal seizures | genetic epilepsy | SCN1A
Journal Article
Valproic acid use in pediatric partial epilepsy after initial medication failure, 10/2004
We retrospectively identified 46 children and adolescents with partial epilepsy, who failed prior treatment with phenytoin, carbamazepine, phenobarbital and/or... 
Neurology | Pediatrics | partial seizures, valproic acid, children, magnetic resonance imaging, anti-epileptic medication. pn04039
Journal
11/2015, ISBN 0128008776
Mitochondrial Case Studies: Underlying Mechanisms and Diagnosis offers the science behind mitochondrial disease with a case studies approach. Since... 
Pre-clinical Medicine: Basic Sciences | Mitochondrial pathology
eBook
Epilepsy & Behavior Case Reports, ISSN 2213-3232, 2018, Volume 11, pp. 1 - 3
Abstract Congenital TORCH infections are a significant cause of epileptic spasms, an infantile epileptic encephalopathy, through disruptions to several... 
Neurology
Journal Article
Epilepsy & behavior case reports, ISSN 2213-3232, 2019, Volume 11, p. 1
Congenital TORCH infections are a significant cause of epileptic spasms, an infantile epileptic encephalopathy, through disruptions to several pathways in... 
Journal Article
Application of Clinical Genetics, ISSN 1178-704X, 12/2014, Volume 7, pp. 221 - 234
Leigh syndrome, also referred to as subacute necrotizing encephalomyelopathy, is a severe, early-onset neurodegenerative disorder that is relentlessly... 
Neuroimaging | Multisystemic disease | Neurodegeneration | Oxidative phos-phorylation | Mitochondrial DNA | Mitochondrial disorder | Seizures | Care and treatment | Leigh disease | Genetic aspects | Risk management | Health aspects | Risk factors | Methods | Convulsions & seizures | Dehydrogenases | Nuclear magnetic resonance--NMR | Population | Ataxia | Mutation | Patients | Age
Journal Article
Journal of child neurology, 07/2019, p. 883073819863278
Perinatal stroke is a significant cause of severe epilepsy, including epileptic spasms. Although epileptic spasms due to underlying structural lesion often... 
Journal Article
Journal of Pediatric Biochemistry, ISSN 1879-5390, 2014, Volume 4, Issue 4, pp. 201 - 215
Journal Article
Pediatric Neurology, ISSN 0887-8994, 03/2013, Volume 48, Issue 3, pp. 167 - 178
Alpers-Huttenlocher syndrome is an uncommon mitochondrial disease most often associated with mutations in the mitochondrial DNA replicase, polymerase-[gamma].... 
Enzymes | replicase | Mitochondria | Liver diseases | Epilepsy | Liver | Degeneration | Mitochondrial DNA | Mutation | Genotypes | Seizures
Journal Article
Pediatrics, ISSN 0031-4005, 12/2007, Volume 120, Issue 6, pp. 1326 - 1333
Journal Article
Journal of neurosurgery. Pediatrics, ISSN 1933-0707, 01/2014, Volume 13, Issue 1, pp. 95 - 100
Functional hemispherectomy is a well-recognized surgical option for the treatment of unihemispheric medically intractable epilepsy. While the resultant motor... 
Humans | Child, Preschool | Infant | Male | Incidence | Hemispherectomy - adverse effects | Adolescent | Deglutition Disorders - etiology | Female | Hemispherectomy - methods | Retrospective Studies | Child | Epilepsy, Tonic-Clonic - surgery | Infant, Newborn
Journal Article
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