Kenton Holden to Magnetic Resonance Imaging
This is a "connection" page, showing publications Kenton Holden has written about Magnetic Resonance Imaging.
Connection Strength
0.561
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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: 0.091
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Cystlike white matter lesions in tuberous sclerosis. AJNR Am J Neuroradiol. 1997 Aug; 18(7):1367-73.
Score: 0.077
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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: 0.068
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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: 0.066
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Mucolipidosis type IV: a subtle pediatric neurodegenerative disorder. Pediatr Neurol. 2010 Mar; 42(3):223-6.
Score: 0.046
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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: 0.042
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Sturge-Weber syndrome variant with atypical intracranial findings: case report. J Child Neurol. 2006 Feb; 21(2):155-7.
Score: 0.035
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Interferon beta-1b and childhood multiple sclerosis. Pediatr Neurol. 1999 Jul; 21(1):481-3.
Score: 0.022
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Neurologic outcomes in children with post-pump choreoathetosis. J Pediatr. 1998 Jan; 132(1):162-4.
Score: 0.020
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Transgenerational Inheritance of Familial Lipomyelomeningocele. J Child Neurol. 2017 Dec; 32(14):1118-1122.
Score: 0.020
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Unique cerebrovascular anomalies in Noonan syndrome with RAF1 mutation. J Child Neurol. 2014 Aug; 29(8):NP13-7.
Score: 0.015
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LIS1 duplication: expanding the phenotype. J Child Neurol. 2012 Jun; 27(6):791-5.
Score: 0.013
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Natural history of Christianson syndrome. Am J Med Genet A. 2010 Nov; 152A(11):2775-83.
Score: 0.012
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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: 0.009
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POMGnT1 gene alterations in a family with neurological abnormalities. Ann Neurol. 2004 Jul; 56(1):143-8.
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: 0.006
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Developmental neural abnormalities and seizures in epidermal nevus syndrome. Dev Med Child Neurol. 1996 Aug; 38(8):716-23.
Score: 0.005
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Neonatal hemangiomatosis associated with brachial plexus palsy. J Child Neurol. 1995 Sep; 10(5):411-3.
Score: 0.004
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Neurologic disease in a child with hepatoerythropoietic porphyria. Pediatr Dermatol. 1994 Sep; 11(3):216-21.
Score: 0.004