Connection

Kenton Holden to Brain

This is a "connection" page, showing publications Kenton Holden has written about Brain.
Connection Strength

0.627
  1. 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.
    View in: PubMed
    Score: 0.236
  2. Cranial magnetic resonance imaging examination of normal term neonates: a pilot study. J Child Neurol. 1999 Nov; 14(11):708-10.
    View in: PubMed
    Score: 0.081
  3. ?-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation. Brain. 2013 Jun; 136(Pt 6):1708-17.
    View in: PubMed
    Score: 0.052
  4. Mucolipidosis type IV: a subtle pediatric neurodegenerative disorder. Pediatr Neurol. 2010 Mar; 42(3):223-6.
    View in: PubMed
    Score: 0.041
  5. Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family. J Child Neurol. 2008 Aug; 23(8):901-5.
    View in: PubMed
    Score: 0.037
  6. Expansion of the deletion 13q syndrome phenotype: a case report. J Child Neurol. 2007 Sep; 22(9):1124-7.
    View in: PubMed
    Score: 0.035
  7. 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.
    View in: PubMed
    Score: 0.030
  8. POMGnT1 gene alterations in a family with neurological abnormalities. Ann Neurol. 2004 Jul; 56(1):143-8.
    View in: PubMed
    Score: 0.028
  9. ATP6AP2 variant impairs CNS development and neuronal survival to cause fulminant neurodegeneration. J Clin Invest. 2019 04 15; 129(5):2145-2162.
    View in: PubMed
    Score: 0.019
  10. Neurologic outcomes in children with post-pump choreoathetosis. J Pediatr. 1998 Jan; 132(1):162-4.
    View in: PubMed
    Score: 0.018
  11. Cystlike white matter lesions in tuberous sclerosis. AJNR Am J Neuroradiol. 1997 Aug; 18(7):1367-73.
    View in: PubMed
    Score: 0.017
  12. Unique cerebrovascular anomalies in Noonan syndrome with RAF1 mutation. J Child Neurol. 2014 Aug; 29(8):NP13-7.
    View in: PubMed
    Score: 0.013
  13. Seizures and X-linked intellectual disability. Eur J Med Genet. 2012 May; 55(5):307-12.
    View in: PubMed
    Score: 0.012
  14. X-linked lissencephaly with absent corpus callosum and ambiguous genitalia. Am J Med Genet. 1999 Oct 08; 86(4):331-7.
    View in: PubMed
    Score: 0.005
  15. Developmental neural abnormalities and seizures in epidermal nevus syndrome. Dev Med Child Neurol. 1996 Aug; 38(8):716-23.
    View in: PubMed
    Score: 0.004
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.