Colección: TEMAS
| Temas | Cantidad |
|---|---|
| Acute Necrotizing Encephalopathy; Epilepsy; Pediatrics | 1 |
| Antiepileptic drugs; Adverse reaction; Skin reaction | 1 |
| Biotinidase deficiency; Neurometabolic disorder; Developmental delay; Early diagnosis | 1 |
| Birth asphyxia; Neonates; Hospital outcome; Cameroon | 1 |
| Cerebral Palsy; Neuroimaging; Birth asphyxia; Children | 1 |
| Child; Cerebral palsy; Spastic diplegia; Equinus deformity; Orthosis; Rehabilitation | 1 |
| Children; Mitochondrial cytopathies; treatment | 1 |
| Chloral hydrate; Oral midazolam; Sleep; Sedation; Electroencephalography; Children | 1 |
| Clinical findings | 1 |
| Depression; Hospitalization; Pediatric patients | 1 |
| Electroencephalography; Spasms; West syndrome | 1 |
| Epilepsy | 1 |
| Episodic ataxia type 2; Downward vertical gaze palsy; Acetazolamide; Normal brain function | 1 |
| Etiology; Developmental Delay; Speech delay; Children | 1 |
| First; Unprovoked; Seizure; Children; Anti Epileptic Drugs (AED); Treatment | 1 |
| Friedreich’s ataxia; FXN gene; Mutation; PCR-SSCP | 1 |
| Headache; Migraine; Children; Hypothyroidism; Subclinical hypothyroidism | 1 |
| Infantile spasms; Topiramate; Nitrazepam; Seizure | 1 |
| Intractable Epilepsy; Antiepileptic drugs; Zonisamide | 1 |
| Joubert Syndrome; Developmental Delay; Respiratory Irregularity; Molar Tooth Sign | 1 |
| Joubert syndrome; Molar tooth sign; Vermian dysgenesis | 1 |
| Juvenile Systemic Lupus Erythematosus; Klinefelter’s syndrome; Cognitive Dysfunction; Neuropsychiatric | 1 |
| Kearns-Sayre; Hypoparathyroidism; Ophthalmoplegia;Mitochondrial cytopathy | 1 |
| Leber Hereditomy optic Neurophaty; Mitochondrial Disease; Children | 1 |
| Leigh disease; Mitochondropathy; Neurometabolic; Neurodegenerative | 1 |
| Methylmalonic acidemia; Neurometabolic disorder; Developmental delay; Early detection | 1 |
| Migraine; Children; Propranolol; Topiramate | 1 |
| Mirror movements; Cervical myelomeningocel; Diffusion tensor imaging | 1 |
| Mitochondria; Mitochondrial encephalomyopathy; NDNA; MDNA | 1 |
| Mitochondria; Structure; Function; Genetic | 1 |
| NCL; Causes; Dementia, Childhood | 1 |
| Nerometabolic disease; Registry site; Iran | 1 |
| Neurologic manifestations; Systemic Lupus erythematosus; Kawasaki disease; Seizures; Aseptic meningitis | 1 |
| Neurology; Epilepsy | 1 |
| No aplica | 6 |
| Oculodentodigital dysplasia; White matter lesions; Digital abnormality | 1 |
| Pediatric Neurology Clinic of Shahid Sadoughi University,Yazd,Iran | 1 |
| Pediatrics; Mitochondrial disease; Neuroimaging; Proton MR Spectroscopy | 1 |
| Propionic acidemia; Neurometabolic disorder; Developmental delay; Early detection | 1 |
| Seizure; First Unprovoked Seizure; Brain Imaging | 1 |
| Seizures; Febrile; Anemia; Iron deficiency | 1 |
| Simple; Complex; Febrile seizures; Electroencephalography; Epileptiform discharges | 1 |