Kenton Holden to Female
This is a "connection" page, showing publications Kenton Holden has written about Female.
Connection Strength
0.534
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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: 0.031
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Progressive increase of T1 signal intensity in the dentate nucleus and globus pallidus on unenhanced T1-weighted MR images in the pediatric brain exposed to multiple doses of gadolinium contrast. Brain Dev. 2016 Mar; 38(3):331-6.
Score: 0.027
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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: 0.027
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Heads you win, tails you lose: measuring head circumference. Dev Med Child Neurol. 2014 Aug; 56(8):705.
Score: 0.025
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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: 0.020
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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: 0.020
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Adult convulsive status epilepticus in the developing country of Honduras. Seizure. 2010 Jul; 19(6):363-7.
Score: 0.019
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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: 0.019
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Mucolipidosis type IV: a subtle pediatric neurodegenerative disorder. Pediatr Neurol. 2010 Mar; 42(3):223-6.
Score: 0.019
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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: 0.018
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A novel mutation in type II methemoglobinemia. J Child Neurol. 2010 Jan; 25(1):91-3.
Score: 0.018
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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: 0.017
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A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype. J Child Neurol. 2008 Dec; 23(12):1433-8.
Score: 0.017
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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: 0.017
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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: 0.016
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Expansion of the deletion 13q syndrome phenotype: a case report. J Child Neurol. 2007 Sep; 22(9):1124-7.
Score: 0.016
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Prevalence, incidence, and etiology of epilepsies in rural Honduras: the Salam? Study. Epilepsia. 2005 Jan; 46(1):124-31.
Score: 0.013
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Facial hemangioma, and associated malformations: a case report. Neuropediatrics. 2004 Jun; 35(3):194-7.
Score: 0.012
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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: 0.011
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Cranial magnetic resonance imaging examination of normal term neonates: a pilot study. J Child Neurol. 1999 Nov; 14(11):708-10.
Score: 0.009
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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: 0.009
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Topiramate for intractable childhood epilepsy. Seizure. 1999 Feb; 8(1):38-40.
Score: 0.009
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Neurologic outcomes in children with post-pump choreoathetosis. J Pediatr. 1998 Jan; 132(1):162-4.
Score: 0.008
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Cystlike white matter lesions in tuberous sclerosis. AJNR Am J Neuroradiol. 1997 Aug; 18(7):1367-73.
Score: 0.008
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Long-term outcomes of conventional therapy for infantile spasms. Seizure. 1997 Jun; 6(3):201-5.
Score: 0.008
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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: 0.008
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Benign familial neonatal convulsions; psychosocial adjustment to the threat of recurrent seizures. Seizure. 1996 Sep; 5(3):243-5.
Score: 0.007
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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: 0.007
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Hemolytic jaundice due to G6PD deficiency causing kernicterus in a female newborn. South Med J. 1995 Jul; 88(7):776-9.
Score: 0.007
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Opsoclonus-myoclonus and recurrent neuroblastoma. J Pediatr. 1995 May; 126(5 Pt 1):847-8.
Score: 0.007
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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: 0.006
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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: 0.006
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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: 0.006
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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: 0.005
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Natural history of Christianson syndrome. Am J Med Genet A. 2010 Nov; 152A(11):2775-83.
Score: 0.005
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Expanding CEP290 mutational spectrum in ciliopathies. Am J Med Genet A. 2009 Oct; 149A(10):2173-80.
Score: 0.005
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Pediatric convulsive status epilepticus in Honduras, Central America. Epilepsia. 2009 Oct; 50(10):2314-9.
Score: 0.004
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What do future (female) pediatricians value? J Pediatr. 2007 Nov; 151(5):443-4, 444.e1-2.
Score: 0.004
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A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family. Mol Vis. 2006 Jul 20; 12:791-5.
Score: 0.004
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The "slurp" test: bedside evaluation of bulbar muscle fatigue. Pediatrics. 2006 Aug; 118(2):e530-3.
Score: 0.004
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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: 0.003
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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: 0.003
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POMGnT1 gene alterations in a family with neurological abnormalities. Ann Neurol. 2004 Jul; 56(1):143-8.
Score: 0.003
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Peripheral leukocytosis in children with febrile seizures. J Child Neurol. 2004 Jan; 19(1):47-50.
Score: 0.003
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X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome. Eur J Hum Genet. 2003 Dec; 11(12):937-44.
Score: 0.003
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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: 0.003
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Neonatal seizures. I. Correlation of prenatal and perinatal events with outcomes. Pediatrics. 1982 Aug; 70(2):165-76.
Score: 0.003
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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: 0.003
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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: 0.002
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Use of the pediatric symptom checklist in the pediatric neurology population. Pediatr Neurol. 1999 Feb; 20(2):116-20.
Score: 0.002
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Developmental neural abnormalities and seizures in epidermal nevus syndrome. Dev Med Child Neurol. 1996 Aug; 38(8):716-23.
Score: 0.002
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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: 0.002
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Neurologic disease in a child with hepatoerythropoietic porphyria. Pediatr Dermatol. 1994 Sep; 11(3):216-21.
Score: 0.002
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Neurological involvement in nevus unis lateris and nevus linearis sebaceus. Neurology. 1972 Sep; 22(9):879-87.
Score: 0.001
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Plasma pressors in the normal and stressed newborn infant. Pediatrics. 1972 Apr; 49(4):495-503.
Score: 0.001
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Diffuse neonatal hemangiomatosis. Pediatrics. 1970 Sep; 46(3):411-21.
Score: 0.001
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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: 0.000
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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: 0.000