Kenton Holden to Infant
This is a "connection" page, showing publications Kenton Holden has written about Infant.
Connection Strength
0.717
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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: 0.089
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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: 0.078
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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: 0.058
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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: 0.055
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The modified Atkins diet: a potential treatment for developing countries. Epilepsia. 2008 Sep; 49(9):1646-7.
Score: 0.049
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Prevalence, incidence, and etiology of epilepsies in rural Honduras: the Salam? Study. Epilepsia. 2005 Jan; 46(1):124-31.
Score: 0.038
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Facial hemangioma, and associated malformations: a case report. Neuropediatrics. 2004 Jun; 35(3):194-7.
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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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: 0.023
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Long-term outcomes of conventional therapy for infantile spasms. Seizure. 1997 Jun; 6(3):201-5.
Score: 0.022
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Benign familial neonatal convulsions; psychosocial adjustment to the threat of recurrent seizures. Seizure. 1996 Sep; 5(3):243-5.
Score: 0.021
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A novel familial autosomal dominant mutation in ARID1B causing neurodevelopmental delays, short stature, and dysmorphic features. Am J Med Genet A. 2016 12; 170(12):3313-3318.
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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LIS1 duplication: expanding the phenotype. J Child Neurol. 2012 Jun; 27(6):791-5.
Score: 0.015
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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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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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A novel in-frame deletion in ARX is associated with lissencephaly with absent corpus callosum and hypoplastic genitalia. Am J Med Genet A. 2005 Sep 15; 138(1):70-2.
Score: 0.010
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POMGnT1 gene alterations in a family with neurological abnormalities. Ann Neurol. 2004 Jul; 56(1):143-8.
Score: 0.009
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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: 0.007
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X-linked myotubular myopathy: clinical observations in ten additional cases. Am J Med Genet. 1995 Nov 06; 59(2):168-73.
Score: 0.005
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Neonatal hemangiomatosis associated with brachial plexus palsy. J Child Neurol. 1995 Sep; 10(5):411-3.
Score: 0.005
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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