Colección: TEMAS
| Temas | Cantidad |
|---|---|
| ARCMT; CMT 4A; GDAP1; Novel mutation | 1 |
| Acute Necrotizing Encephalopathy; Epilepsy; Pediatrics | 1 |
| Acute infantile Gaucher disease; Motor regression; Hypotonia | 1 |
| Antiepileptic drugs; Adverse reaction; Skin reaction | 1 |
| Autism spectrum disorders (ASDs); prevalence; etiology; diagnosis; treatment; Iran | 1 |
| Biotinidase deficiency; Neurometabolic disorder; Developmental delay; Early diagnosis | 1 |
| Birth asphyxia; Neonates; Hospital outcome; Cameroon | 1 |
| CIPNM; Insulin;Child | 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 |
| Epilepsy; Brain CT scan; Children; Neuroimaging | 1 |
| Episodic ataxia type 2; Downward vertical gaze palsy; Acetazolamide; Normal brain function | 1 |
| Ethylmalonic aciduria; neurodevelop-mental delay; report of a case. | 1 |
| Etiology; Developmental Delay; Speech delay; Children | 1 |
| Fabry disease; Childhood; Enzyme replacement therapy | 1 |
| First; Unprovoked; Seizure; Children; Anti Epileptic Drugs (AED); Treatment | 1 |
| Friedreich ataxia; tRNALeu (CUN) gene; mitochondrial DNA; Mutation; TTGE | 1 |
| Friedreich’s ataxia; FXN gene; Mutation; PCR-SSCP | 1 |
| Gastrointestinal Tract; Symptoms; Diagnosis; Child | 1 |
| Genetic; lysosomal storage disease; Child; Iran | 1 |
| Glutaric Aciduria; Iranian population;Mutation detection. | 1 |
| HSAN type IV; Congenital insensitivity to pain; Anhidrosis | 1 |
| Headache; Migraine; Children; Hypothyroidism; Subclinical hypothyroidism | 1 |
| Heart; Lysomoal disease; Treatment | 1 |
| Idiopathic generalized epilepsy; EEG; Seizure type | 1 |
| Imaging; organic acidemia; children, aminoacid. | 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 |
| Keywords: Organic academia; plasma acylcarnitine profile; diagnosis. | 1 |
| Leber Hereditomy optic Neurophaty; Mitochondrial Disease; Children | 1 |
| Leigh disease; Mitochondropathy; Neurometabolic; Neurodegenerative | 1 |
| Lysosomal Storage Diseases, Rheumatology, Bone pain; Arthropathy | 1 |
| Lysosomal disorders; Diagnosis; Approach | 1 |
| Lysosomal myopathy; Myopathy; Pompe; Acid maltase deficiency, Danon | 1 |
| Methadone; Intoxication; Children; Opioid; Acute hydrocephaly | 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 |
| Mucopolysaccharidosis 1; Child; Diagnosis; Therapy | 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 | 92 |
| Oculodentodigital dysplasia; White matter lesions; Digital abnormality | 1 |
| Oculodentodigitalis dysplasia; Epilepsy; Spasticity | 1 |
| Organic academia; Prenatal diagnosis; Amniocentesis; Chorionic villous sampling. | 1 |
| Organic academia; diagnosis; approach. | 1 |
| Pediatric Neurology Clinic of Shahid Sadoughi University,Yazd,Iran | 1 |
| Pediatrics; Mitochondrial disease; Neuroimaging; Proton MR Spectroscopy | 1 |
| Pompe disease; Children;EDX; EMG; Myotonic discharges | 1 |
| Postdural puncture headache; Children; Complication; Spinal needle | 1 |
| Posterior, Fossa; Tumor; Surgery | 1 |
| Propionic acidemia; Neurometabolic disorder; Developmental delay; Early detection | 1 |
| Regression; leukodystrophy; L-2-Hydroxyglutaric aciduria | 1 |
| School Teachers; Knowledge; Attitude; Perception; Epilepsy | 1 |
| Seizure; First Unprovoked Seizure; Brain Imaging | 1 |
| Seizure; Glucose 6 phospate dehydrogenase deficiency; Acute hemolysis; Methemoglobinemia | 1 |
| Seizure; childhood epilepsy; epidemiology of convulsion | 1 |
| Seizures, Refractory; Children; Midazolam; Diazepam | 1 |
| Seizures; Febrile; Anemia; Iron deficiency | 1 |
| Seizures; febrile; child; prevention and control | 1 |
| Simple; Complex; Febrile seizures; Electroencephalography; Epileptiform discharges | 1 |
| Status epilepticus; Refractory status epilepticus; Intravenous sodium valproate; Children | 1 |
| Treatments; organic acidemia; Children. | 1 |
| Tuberous sclerosis; Shagreen patch; Child; Cheek | 1 |
| febrile seizures; clonazepam | 1 |