Kenton Holden to Male
This is a "connection" page, showing publications Kenton Holden has written about Male.
Connection Strength
0.586
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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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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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Unbalanced translocation involving partial trisomy 9p and partial monosomy yq with neurodevelopmental delays. J Child Neurol. 2013 Apr; 28(4):524-6.
Score: 0.022
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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: 0.021
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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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Novel CLCN1 mutation in carbamazepine-responsive myotonia congenita. Pediatr Neurol. 2010 May; 42(5):365-8.
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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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: 0.019
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Utilization of blood spot testing for metabolic-genetic disorders in Honduras: is it time for newborn screening? J Child Neurol. 2010 Mar; 25(3):306-11.
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: 0.018
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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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The modified Atkins diet: a potential treatment for developing countries. Epilepsia. 2008 Sep; 49(9):1646-7.
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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Early onset alpha-mannosidosis with slow progression in three Hispanic males. Dev Med Child Neurol. 2007 Nov; 49(11):854-7.
Score: 0.016
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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: 0.014
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Sturge-Weber syndrome variant with atypical intracranial findings: case report. J Child Neurol. 2006 Feb; 21(2):155-7.
Score: 0.014
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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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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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Interferon beta-1b and childhood multiple sclerosis. Pediatr Neurol. 1999 Jul; 21(1):481-3.
Score: 0.009
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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: 0.009
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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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Transgenerational Inheritance of Familial Lipomyelomeningocele. J Child Neurol. 2017 Dec; 32(14):1118-1122.
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 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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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: 0.006
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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: 0.006
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Unique cerebrovascular anomalies in Noonan syndrome with RAF1 mutation. J Child Neurol. 2014 Aug; 29(8):NP13-7.
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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Roberts/pseudothalidomide syndrome and normal intelligence: approaches to diagnosis and management. Dev Med Child Neurol. 1992 Jun; 34(6):534-9.
Score: 0.006
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LIS1 duplication: expanding the phenotype. J Child Neurol. 2012 Jun; 27(6):791-5.
Score: 0.005
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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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Pediatric convulsive status epilepticus in Honduras, Central America. Epilepsia. 2009 Oct; 50(10):2314-9.
Score: 0.005
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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: 0.004
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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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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: 0.003
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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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Neurologic complications following bone marrow transplantation for sickle cell disease. Bone Marrow Transplant. 1996 Mar; 17(3):405-7.
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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Neonatal hemangiomatosis associated with brachial plexus palsy. J Child Neurol. 1995 Sep; 10(5):411-3.
Score: 0.002
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Progressive venous occlusion in a neonate with Sturge-Weber syndrome: demonstration with MR venography. AJNR Am J Neuroradiol. 1995 Aug; 16(7):1539-42.
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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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