Hinton V - Search Results

1

Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment, and prognosis.

Pons R, Ford B, Chiriboga CA, Clayton PT, Hinton V, Hyland K, Sharma R, De Vivo DC. Pons R, et al. Among authors: hinton v. Neurology. 2004 Apr 13;62(7):1058-65. doi: 10.1212/wnl.62.7.1058. Neurology. 2004. PMID: 15079002 Review.

2

Phenotypic spectrum of glucose transporter type 1 deficiency syndrome (Glut1 DS).

Pearson TS, Akman C, Hinton VJ, Engelstad K, De Vivo DC. Pearson TS, et al. Curr Neurol Neurosci Rep. 2013 Apr;13(4):342. doi: 10.1007/s11910-013-0342-7. Curr Neurol Neurosci Rep. 2013. PMID: 23443458 Review.

3

Long-term clinical course of Glut1 deficiency syndrome.

Alter AS, Engelstad K, Hinton VJ, Montes J, Pearson TS, Akman CI, De Vivo DC. Alter AS, et al. J Child Neurol. 2015 Feb;30(2):160-9. doi: 10.1177/0883073814531822. Epub 2014 Apr 30. J Child Neurol. 2015. PMID: 24789115

4

Poor verbal working memory across intellectual level in boys with Duchenne dystrophy.

Hinton VJ, De Vivo DC, Nereo NE, Goldstein E, Stern Y. Hinton VJ, et al. Neurology. 2000 Jun 13;54(11):2127-32. doi: 10.1212/wnl.54.11.2127. Neurology. 2000. PMID: 10851376 Free PMC article.

5

Verbal and memory skills in males with Duchenne muscular dystrophy.

Hinton VJ, Fee RJ, Goldstein EM, De Vivo DC. Hinton VJ, et al. Dev Med Child Neurol. 2007 Feb;49(2):123-8. doi: 10.1111/j.1469-8749.2007.00123.x. Dev Med Child Neurol. 2007. PMID: 17254000 Free PMC article.

6

Brain glucose supply and the syndrome of infantile neuroglycopenia.

Pascual JM, Wang D, Hinton V, Engelstad K, Saxena CM, Van Heertum RL, De Vivo DC. Pascual JM, et al. Among authors: hinton v. Arch Neurol. 2007 Apr;64(4):507-13. doi: 10.1001/archneur.64.4.noc60165. Epub 2007 Feb 12. Arch Neurol. 2007. PMID: 17296829

7

Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers.

Weiduschat N, Kaufmann P, Mao X, Engelstad KM, Hinton V, DiMauro S, De Vivo D, Shungu D. Weiduschat N, et al. Among authors: hinton v. Neurology. 2014 Mar 4;82(9):798-805. doi: 10.1212/WNL.0000000000000169. Epub 2014 Jan 29. Neurology. 2014. PMID: 24477106 Free PMC article.

8

Association of autistic spectrum disorders with dystrophinopathies.

Hinton VJ, Cyrulnik SE, Fee RJ, Batchelder A, Kiefel JM, Goldstein EM, Kaufmann P, De Vivo DC. Hinton VJ, et al. Pediatr Neurol. 2009 Nov;41(5):339-46. doi: 10.1016/j.pediatrneurol.2009.05.011. Pediatr Neurol. 2009. PMID: 19818935

9

Acute hyperglycemia produces transient improvement in glucose transporter type 1 deficiency.

Akman CI, Engelstad K, Hinton VJ, Ullner P, Koenigsberger D, Leary L, Wang D, De Vivo DC. Akman CI, et al. Ann Neurol. 2010 Jan;67(1):31-40. doi: 10.1002/ana.21797. Ann Neurol. 2010. PMID: 20186957

10

Selective deficits in verbal working memory associated with a known genetic etiology: the neuropsychological profile of duchenne muscular dystrophy.

Hinton VJ, De Vivo DC, Nereo NE, Goldstein E, Stern Y. Hinton VJ, et al. J Int Neuropsychol Soc. 2001 Jan;7(1):45-54. doi: 10.1017/s1355617701711058. J Int Neuropsychol Soc. 2001. PMID: 11253841 Free PMC article.

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