Kenton Holden to Child, Preschool
This is a "connection" page, showing publications Kenton Holden has written about Child, Preschool.
Connection Strength
1.009
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Clinical Features and Neurologic Complications of Children Hospitalized With Chikungunya Virus in Honduras. J Child Neurol. 2017 07; 32(8):712-716.
Score: 0.087
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Redefining the Pediatric Phenotype of X-Linked Monocarboxylate Transporter 8 (MCT8) Deficiency: Implications for Diagnosis and Therapies. J Child Neurol. 2015 Oct; 30(12):1664-8.
Score: 0.076
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Unbalanced translocation involving partial trisomy 9p and partial monosomy yq with neurodevelopmental delays. J Child Neurol. 2013 Apr; 28(4):524-6.
Score: 0.062
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Severe Hunter syndrome (mucopolysaccharidosis II) phenotype secondary to large deletion in the X chromosome encompassing IDS, FMR1, and AFF2 (FMR2). J Child Neurol. 2012 Jun; 27(6):786-90.
Score: 0.060
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Autism in two females with duplications involving Xp11.22-p11.23. Dev Med Child Neurol. 2011 May; 53(5):463-6.
Score: 0.057
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Reduction in rate of epilepsy from neurocysticercosis by community interventions: the Salam?, Honduras study. Epilepsia. 2011 Jun; 52(6):1177-85.
Score: 0.057
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United States head circumference growth reference charts: birth to 21 years. J Pediatr. 2010 Jun; 156(6):907-913.e2.
Score: 0.053
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Mucolipidosis type IV: a subtle pediatric neurodegenerative disorder. Pediatr Neurol. 2010 Mar; 42(3):223-6.
Score: 0.053
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Diagnosis, treatment, and long-term outcomes of late-onset (type III) multiple acyl-CoA dehydrogenase deficiency. J Child Neurol. 2010 Aug; 25(8):954-60.
Score: 0.052
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A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype. J Child Neurol. 2008 Dec; 23(12):1433-8.
Score: 0.049
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Persistent growth failure in Prader-Willi syndrome associated with short-chain acyl-CoA dehydrogenase gene variant. J Child Neurol. 2008 Jan; 23(1):112-7.
Score: 0.046
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Prevalence, incidence, and etiology of epilepsies in rural Honduras: the Salam? Study. Epilepsia. 2005 Jan; 46(1):124-31.
Score: 0.037
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The effect of tiagabine on spasticity in children with intractable epilepsy: a pilot study. Pediatr Neurol. 1999 Oct; 21(4):728-30.
Score: 0.026
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ATP6AP2 variant impairs CNS development and neuronal survival to cause fulminant neurodegeneration. J Clin Invest. 2019 04 15; 129(5):2145-2162.
Score: 0.025
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Topiramate for intractable childhood epilepsy. Seizure. 1999 Feb; 8(1):38-40.
Score: 0.025
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Neurologic outcomes in children with post-pump choreoathetosis. J Pediatr. 1998 Jan; 132(1):162-4.
Score: 0.023
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Cystlike white matter lesions in tuberous sclerosis. AJNR Am J Neuroradiol. 1997 Aug; 18(7):1367-73.
Score: 0.022
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A deletion in the long arm of chromosome 18 in a child with serum carnosinase deficiency. Pediatr Res. 1997 Feb; 41(2):210-3.
Score: 0.021
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Opsoclonus-myoclonus and recurrent neuroblastoma. J Pediatr. 1995 May; 126(5 Pt 1):847-8.
Score: 0.019
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Neurodevelopmental delays and macrocephaly in 17p13.1 microduplication syndrome. Am J Med Genet A. 2014 Nov; 164A(11):2887-91.
Score: 0.018
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Novel mutation in Sjogren-Larsson syndrome is associated with divergent neurologic phenotypes. J Child Neurol. 2013 Oct; 28(10):1259-65.
Score: 0.016
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Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short stature. Am J Med Genet A. 2011 Sep; 155A(9):2146-53.
Score: 0.015
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Natural history of Christianson syndrome. Am J Med Genet A. 2010 Nov; 152A(11):2775-83.
Score: 0.014
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Pediatric convulsive status epilepticus in Honduras, Central America. Epilepsia. 2009 Oct; 50(10):2314-9.
Score: 0.013
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The "slurp" test: bedside evaluation of bulbar muscle fatigue. Pediatrics. 2006 Aug; 118(2):e530-3.
Score: 0.010
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Carriers and patients with muscle-eye-brain disease can be rapidly diagnosed by enzymatic analysis of fibroblasts and lymphoblasts. Neuromuscul Disord. 2006 Feb; 16(2):132-6.
Score: 0.010
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X-linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype. J Child Neurol. 2005 Oct; 20(10):852-7.
Score: 0.010
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Peripheral leukocytosis in children with febrile seizures. J Child Neurol. 2004 Jan; 19(1):47-50.
Score: 0.009
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Epidemiology of childhood Guillain-Barr? syndrome as a cause of acute flaccid paralysis in Honduras: 1989-1999. J Child Neurol. 2003 Nov; 18(11):741-7.
Score: 0.009
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Neonatal seizures. I. Correlation of prenatal and perinatal events with outcomes. Pediatrics. 1982 Aug; 70(2):165-76.
Score: 0.008
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X-linked lissencephaly with absent corpus callosum and ambiguous genitalia. Am J Med Genet. 1999 Oct 08; 86(4):331-7.
Score: 0.006
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Use of the pediatric symptom checklist in the pediatric neurology population. Pediatr Neurol. 1999 Feb; 20(2):116-20.
Score: 0.006
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Neurologic disease in a child with hepatoerythropoietic porphyria. Pediatr Dermatol. 1994 Sep; 11(3):216-21.
Score: 0.005
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Neurological involvement in nevus unis lateris and nevus linearis sebaceus. Neurology. 1972 Sep; 22(9):879-87.
Score: 0.004
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Discontinuing antiepileptic medication in children with epilepsy after two years without seizures. A prospective study. N Engl J Med. 1985 Oct 17; 313(16):976-80.
Score: 0.002
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Neonatal seizures. II. A multivariate analysis of factors associated with outcome. Pediatrics. 1982 Aug; 70(2):177-85.
Score: 0.002
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Medroxprogesterone acetate in the treatment of seizures associated with menstruation. J Pediatr. 1973 Dec; 83(6):959-63.
Score: 0.001
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Effects of fresh plasma or whole blood transfusions on patients with various types of mucopolysaccharidosis. Pediatrics. 1972 Nov; 50(5):688-92.
Score: 0.001