Kenton Holden to Child
This is a "connection" page, showing publications Kenton Holden has written about Child.
Connection Strength
0.851
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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: 0.066
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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: 0.057
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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: 0.043
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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: 0.040
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Mucolipidosis type IV: a subtle pediatric neurodegenerative disorder. Pediatr Neurol. 2010 Mar; 42(3):223-6.
Score: 0.040
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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: 0.039
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Pediatric convulsive status epilepticus in Honduras, Central America. Epilepsia. 2009 Oct; 50(10):2314-9.
Score: 0.039
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A novel mutation in type II methemoglobinemia. J Child Neurol. 2010 Jan; 25(1):91-3.
Score: 0.038
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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: 0.037
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A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype. J Child Neurol. 2008 Dec; 23(12):1433-8.
Score: 0.037
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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: 0.036
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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: 0.034
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Expansion of the deletion 13q syndrome phenotype: a case report. J Child Neurol. 2007 Sep; 22(9):1124-7.
Score: 0.034
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Sturge-Weber syndrome variant with atypical intracranial findings: case report. J Child Neurol. 2006 Feb; 21(2):155-7.
Score: 0.030
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Febrile and afebrile or provoked and unprovoked seizures? Pediatr Neurol. 2005 Apr; 32(4):291; author reply 291-2.
Score: 0.028
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Prevalence, incidence, and etiology of epilepsies in rural Honduras: the Salam? Study. Epilepsia. 2005 Jan; 46(1):124-31.
Score: 0.028
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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: 0.019
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Interferon beta-1b and childhood multiple sclerosis. Pediatr Neurol. 1999 Jul; 21(1):481-3.
Score: 0.019
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Topiramate for intractable childhood epilepsy. Seizure. 1999 Feb; 8(1):38-40.
Score: 0.019
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Neurologic outcomes in children with post-pump choreoathetosis. J Pediatr. 1998 Jan; 132(1):162-4.
Score: 0.017
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Cystlike white matter lesions in tuberous sclerosis. AJNR Am J Neuroradiol. 1997 Aug; 18(7):1367-73.
Score: 0.017
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Deletion of 16q24.1 supports a role for the ATP2C2 gene in specific language impairment. J Child Neurol. 2015 Mar; 30(4):517-21.
Score: 0.014
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Acquired microcephaly in blepharophimosis-ptosis-epicanthus inversus syndrome because of an interstitial 3q22.3q23 deletion. Pediatr Neurol. 2014 Jun; 50(6):636-9.
Score: 0.013
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Unique cerebrovascular anomalies in Noonan syndrome with RAF1 mutation. J Child Neurol. 2014 Aug; 29(8):NP13-7.
Score: 0.013
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Childhood epilepsy: an overview. J S C Med Assoc. 1992 May; 88(5):251-5.
Score: 0.012
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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: 0.011
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Natural history of Christianson syndrome. Am J Med Genet A. 2010 Nov; 152A(11):2775-83.
Score: 0.010
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Finding new etiologies of mental retardation and hypotonia: X marks the spot. Dev Med Child Neurol. 2008 Feb; 50(2):104-11.
Score: 0.009
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The "slurp" test: bedside evaluation of bulbar muscle fatigue. Pediatrics. 2006 Aug; 118(2):e530-3.
Score: 0.008
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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: 0.008
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POMGnT1 gene alterations in a family with neurological abnormalities. Ann Neurol. 2004 Jul; 56(1):143-8.
Score: 0.007
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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: 0.006
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Neonatal seizures. I. Correlation of prenatal and perinatal events with outcomes. Pediatrics. 1982 Aug; 70(2):165-76.
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: 0.005
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Neurologic complications following bone marrow transplantation for sickle cell disease. Bone Marrow Transplant. 1996 Mar; 17(3):405-7.
Score: 0.004
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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: 0.004
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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: 0.001
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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
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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