Kenton Holden to Adult
This is a "connection" page, showing publications Kenton Holden has written about Adult.
Connection Strength
0.313
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The influence of traditional and complementary and alternative medicine on medication adherence in Honduras. Altern Ther Health Med. 2015 May-Jun; 21(3):26-35.
Score: 0.035
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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: 0.026
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Adult convulsive status epilepticus in the developing country of Honduras. Seizure. 2010 Jul; 19(6):363-7.
Score: 0.025
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A novel mutation in type II methemoglobinemia. J Child Neurol. 2010 Jan; 25(1):91-3.
Score: 0.023
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Adherence and complementary and alternative medicine use among Honduran people with epilepsy. Epilepsy Behav. 2009 Apr; 14(4):645-50.
Score: 0.023
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A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype. J Child Neurol. 2008 Dec; 23(12):1433-8.
Score: 0.022
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Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family. J Child Neurol. 2008 Aug; 23(8):901-5.
Score: 0.022
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Early onset alpha-mannosidosis with slow progression in three Hispanic males. Dev Med Child Neurol. 2007 Nov; 49(11):854-7.
Score: 0.021
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Unusual phenotypic expression of an XLRS1 mutation in X-linked juvenile retinoschisis. J Child Neurol. 2006 Apr; 21(4):331-3.
Score: 0.019
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Prevalence, incidence, and etiology of epilepsies in rural Honduras: the Salam? Study. Epilepsia. 2005 Jan; 46(1):124-31.
Score: 0.017
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Dietary intake and blood folate levels in Honduran women of childbearing age. J Child Neurol. 2002 May; 17(5):341-6.
Score: 0.014
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The use of hypothermia: a role in the treatment of neonatal asphyxia? Pediatr Neurol. 1999 Jul; 21(1):429-43.
Score: 0.012
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Topiramate for intractable childhood epilepsy. Seizure. 1999 Feb; 8(1):38-40.
Score: 0.011
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Cystlike white matter lesions in tuberous sclerosis. AJNR Am J Neuroradiol. 1997 Aug; 18(7):1367-73.
Score: 0.010
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?-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation. Brain. 2013 Jun; 136(Pt 6):1708-17.
Score: 0.008
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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: 0.007
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Natural history of Christianson syndrome. Am J Med Genet A. 2010 Nov; 152A(11):2775-83.
Score: 0.006
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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: 0.005
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X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28. Am J Hum Genet. 2002 May; 70(5):1349-56.
Score: 0.004
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Plasma pressors in the normal and stressed newborn infant. Pediatrics. 1972 Apr; 49(4):495-503.
Score: 0.002
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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: 0.001
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Stopping medication in children with epilepsy: predictors of outcome. N Engl J Med. 1981 May 07; 304(19):1125-9.
Score: 0.001