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Holden, Kenton
One or more keywords matched the following items that are connected to Holden, Kenton
Item TypeName
Academic Article Neurologic outcomes in children with post-pump choreoathetosis.
Academic Article The effect of tiagabine on spasticity in children with intractable epilepsy: a pilot study.
Academic Article Use of the pediatric symptom checklist in the pediatric neurology population.
Academic Article Topiramate for intractable childhood epilepsy.
Academic Article X-linked lissencephaly with absent corpus callosum and ambiguous genitalia.
Academic Article Persistent growth failure in Prader-Willi syndrome associated with short-chain acyl-CoA dehydrogenase gene variant.
Academic Article A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype.
Academic Article Pediatric convulsive status epilepticus in Honduras, Central America.
Academic Article Diagnosis, treatment, and long-term outcomes of late-onset (type III) multiple acyl-CoA dehydrogenase deficiency.
Academic Article United States head circumference growth reference charts: birth to 21 years.
Academic Article Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short stature.
Academic Article Severe Hunter syndrome (mucopolysaccharidosis II) phenotype secondary to large deletion in the X chromosome encompassing IDS, FMR1, and AFF2 (FMR2).
Academic Article Unbalanced translocation involving partial trisomy 9p and partial monosomy yq with neurodevelopmental delays.
Academic Article Novel mutation in Sjogren-Larsson syndrome is associated with divergent neurologic phenotypes.
Academic Article Opsoclonus-myoclonus and recurrent neuroblastoma.
Academic Article A deletion in the long arm of chromosome 18 in a child with serum carnosinase deficiency.
Academic Article Epidemiology of childhood Guillain-Barr? syndrome as a cause of acute flaccid paralysis in Honduras: 1989-1999.
Academic Article Peripheral leukocytosis in children with febrile seizures.
Academic Article Cystlike white matter lesions in tuberous sclerosis.
Academic Article Prevalence, incidence, and etiology of epilepsies in rural Honduras: the Salam? Study.
Academic Article X-linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype.
Academic Article Carriers and patients with muscle-eye-brain disease can be rapidly diagnosed by enzymatic analysis of fibroblasts and lymphoblasts.
Academic Article The "slurp" test: bedside evaluation of bulbar muscle fatigue.
Academic Article Mucolipidosis type IV: a subtle pediatric neurodegenerative disorder.
Academic Article Natural history of Christianson syndrome.
Academic Article Reduction in rate of epilepsy from neurocysticercosis by community interventions: the Salam?, Honduras study.
Academic Article Autism in two females with duplications involving Xp11.22-p11.23.
Academic Article Discontinuing antiepileptic medication in children with epilepsy after two years without seizures. A prospective study.
Academic Article Neurological involvement in nevus unis lateris and nevus linearis sebaceus.
Academic Article Effects of fresh plasma or whole blood transfusions on patients with various types of mucopolysaccharidosis.
Academic Article Medroxprogesterone acetate in the treatment of seizures associated with menstruation.
Academic Article Neonatal seizures. I. Correlation of prenatal and perinatal events with outcomes.
Academic Article Neonatal seizures. II. A multivariate analysis of factors associated with outcome.
Academic Article Neurologic disease in a child with hepatoerythropoietic porphyria.
Concept Child, Preschool
Academic Article Neurodevelopmental delays and macrocephaly in 17p13.1 microduplication syndrome.
Academic Article Redefining the Pediatric Phenotype of X-Linked Monocarboxylate Transporter 8 (MCT8) Deficiency: Implications for Diagnosis and Therapies.
Academic Article Clinical Features and Neurologic Complications of Children Hospitalized With Chikungunya Virus in Honduras.
Academic Article ATP6AP2 variant impairs CNS development and neuronal survival to cause fulminant neurodegeneration.
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  • Child Preschool