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Items: 34

1.

Long-Term Neurobehavioral and Quality of Life Outcomes of Critically Ill Children after Glycemic Control.

Biagas KV, Hinton VJ, Hasbani NR, Luckett PM, Wypij D, Nadkarni VM, Agus MSD; HALF-PINT trial study investigators; PALISI Network.

J Pediatr. 2020 Jan 3. pii: S0022-3476(19)31466-0. doi: 10.1016/j.jpeds.2019.10.055. [Epub ahead of print]

PMID:
31910992
2.

Executive Functioning in the Dystrophinopathies and the Relation to Underlying Mutation Position.

Fee RJ, Montes J, Hinton VJ.

J Int Neuropsychol Soc. 2019 Feb;25(2):146-155. doi: 10.1017/S1355617718000942. Epub 2018 Dec 4.

PMID:
30511603
3.

Executive Skills and Academic Achievement in the Dystrophinopathies.

Fee RJ, Montes J, Stewart JL, Hinton VJ.

J Int Neuropsychol Soc. 2018 Oct;24(9):928-938. doi: 10.1017/S1355617717001333.

PMID:
30375314
4.

Zika Virus-Associated Cognitive Impairment in Adolescent, 2016.

Zucker J, Neu N, Chiriboga CA, Hinton VJ, Leonardo M, Sheikh A, Thakur K.

Emerg Infect Dis. 2017 Jun;23(6):1047-1048. doi: 10.3201/eid2306.162029.

5.

Cognitive functioning one month and one year following febrile status epilepticus.

Weiss EF, Masur D, Shinnar S, Hesdorffer DC, Hinton VJ, Bonner M, Rinaldi J, Van de Water V, Culbert J, Shinnar RC, Seinfeld S, Gallentine W, Nordli DR Jr, Frank LM, Epstein L, Moshé SL, Sun S; FEBSTAT study team.

Epilepsy Behav. 2016 Nov;64(Pt A):283-288. doi: 10.1016/j.yebeh.2016.09.013. Epub 2016 Oct 26.

6.

Digit Span Performance in Children with Dystrophinopathy: A Verbal Span or Working Memory Contribution?

Leaffer EB, Fee RJ, Hinton VJ.

J Int Neuropsychol Soc. 2016 Aug;22(7):777-84. doi: 10.1017/S1355617716000461. Epub 2016 Jun 8.

PMID:
27268852
7.

Long-term clinical course of Glut1 deficiency syndrome.

Alter AS, Engelstad K, Hinton VJ, Montes J, Pearson TS, Akman CI, De Vivo DC.

J Child Neurol. 2015 Feb;30(2):160-9. doi: 10.1177/0883073814531822. Epub 2014 Apr 30.

PMID:
24789115
8.

Longitudinal assessment of skill development in children with first febrile seizure.

Leaffer EB, Hinton VJ, Hesdorffer DC.

Epilepsy Behav. 2013 Jul;28(1):83-7. doi: 10.1016/j.yebeh.2013.03.034. Epub 2013 May 11.

9.

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

Pearson TS, Akman C, Hinton VJ, Engelstad K, De Vivo DC.

Curr Neurol Neurosci Rep. 2013 Apr;13(4):342. doi: 10.1007/s11910-013-0342-7. Review.

PMID:
23443458
10.

Resilience in children diagnosed with a chronic neuromuscular disorder.

Fee RJ, Hinton VJ.

J Dev Behav Pediatr. 2011 Nov;32(9):644-50. doi: 10.1097/DBP.0b013e318235d614.

11.

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.

Ann Neurol. 2010 Jan;67(1):31-40. doi: 10.1002/ana.21797.

PMID:
20186957
12.

Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort.

Flanigan KM, Dunn DM, von Niederhausern A, Soltanzadeh P, Gappmaier E, Howard MT, Sampson JB, Mendell JR, Wall C, King WM, Pestronk A, Florence JM, Connolly AM, Mathews KD, Stephan CM, Laubenthal KS, Wong BL, Morehart PJ, Meyer A, Finkel RS, Bonnemann CG, Medne L, Day JW, Dalton JC, Margolis MK, Hinton VJ; United Dystrophinopathy Project Consortium, Weiss RB.

Hum Mutat. 2009 Dec;30(12):1657-66. doi: 10.1002/humu.21114.

13.

Association of autistic spectrum disorders with dystrophinopathies.

Hinton VJ, Cyrulnik SE, Fee RJ, Batchelder A, Kiefel JM, Goldstein EM, Kaufmann P, De Vivo DC.

Pediatr Neurol. 2009 Nov;41(5):339-46. doi: 10.1016/j.pediatrneurol.2009.05.011. Erratum in: Pediatr Neurol. 2010 Jan;42(1):75.

PMID:
19818935
14.

Cognitive and adaptive deficits in young children with Duchenne muscular dystrophy (DMD).

Cyrulnik SE, Fee RJ, Batchelder A, Kiefel J, Goldstein E, Hinton VJ.

J Int Neuropsychol Soc. 2008 Sep;14(5):853-61. doi: 10.1017/S135561770808106X.

PMID:
18764980
15.

Are MRI-detected brain abnormalities associated with febrile seizure type?

Hesdorffer DC, Chan S, Tian H, Allen Hauser W, Dayan P, Leary LD, Hinton VJ.

Epilepsia. 2008 May;49(5):765-71. Epub 2007 Dec 6.

16.

Duchenne muscular dystrophy: a cerebellar disorder?

Cyrulnik SE, Hinton VJ.

Neurosci Biobehav Rev. 2008;32(3):486-96. Epub 2007 Oct 4. Review.

PMID:
18022230
17.

Investigation of Poor Academic Achievement in Children with Duchenne Muscular Dystrophy.

Hinton VJ, De Vivo DC, Fee R, Goldstein E, Stern Y.

Learn Disabil Res Pract. 2004 Aug;19(3):146-154.

18.

Delayed developmental language milestones in children with Duchenne's muscular dystrophy.

Cyrulnik SE, Fee RJ, De Vivo DC, Goldstein E, Hinton VJ.

J Pediatr. 2007 May;150(5):474-8.

19.

Verbal and memory skills in males with Duchenne muscular dystrophy.

Hinton VJ, Fee RJ, Goldstein EM, De Vivo DC.

Dev Med Child Neurol. 2007 Feb;49(2):123-8.

20.

Poor facial affect recognition among boys with duchenne muscular dystrophy.

Hinton VJ, Fee RJ, De Vivo DC, Goldstein E.

J Autism Dev Disord. 2007 Nov;37(10):1925-33. Epub 2006 Dec 20.

21.

Social behavior problems in boys with Duchenne muscular dystrophy.

Hinton VJ, Nereo NE, Fee RJ, Cyrulnik SE.

J Dev Behav Pediatr. 2006 Dec;27(6):470-6.

22.

Influence of breastfeeding on cognitive outcomes at age 6-8 years: follow-up of very low birth weight infants.

Smith MM, Durkin M, Hinton VJ, Bellinger D, Kuhn L.

Am J Epidemiol. 2003 Dec 1;158(11):1075-82.

PMID:
14630603
23.

Parental stress in mothers of boys with duchenne muscular dystrophy.

Nereo NE, Fee RJ, Hinton VJ.

J Pediatr Psychol. 2003 Oct-Nov;28(7):473-84.

24.

Initiation of breastfeeding among mothers of very low birth weight infants.

Smith MM, Durkin M, Hinton VJ, Bellinger D, Kuhn L.

Pediatrics. 2003 Jun;111(6 Pt 1):1337-42.

PMID:
12777550
25.

Three wishes and psychological functioning in boys with duchenne muscular dystrophy.

Nereo NE, Hinton VJ.

J Dev Behav Pediatr. 2003 Apr;24(2):96-103.

26.

Ethics of neuroimaging in pediatric development.

Hinton VJ.

Brain Cogn. 2002 Dec;50(3):455-68.

PMID:
12480490
27.

Long-term cognitive benefits of antenatal corticosteroids for prematurely born children with cranial ultrasound abnormalities.

Arad I, Durkin MS, Hinton VJ, Kuhn L, Chiriboga C, Kuban K, Bellinger D.

Am J Obstet Gynecol. 2002 Apr;186(4):818-25.

PMID:
11967514
28.
29.

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

Hinton VJ, De Vivo DC, Nereo NE, Goldstein E, Stern Y.

Neurology. 2000 Jun 13;54(11):2127-32.

30.

Early developmental outcome after the Norwood procedure for hypoplastic left heart syndrome.

Kern JH, Hinton VJ, Nereo NE, Hayes CJ, Gersony WM.

Pediatrics. 1998 Nov;102(5):1148-52.

PMID:
9794947
31.

Adult fragile X syndrome: neuropsychology, brain anatomy, and metabolism.

Schapiro MB, Murphy DG, Hagerman RJ, Azari NP, Alexander GE, Miezejeski CM, Hinton VJ, Horwitz B, Haxby JV, Kumar A, et al.

Am J Med Genet. 1995 Dec 18;60(6):480-93.

PMID:
8825884
32.

Cognitive and molecular aspects of fragile X.

Hinton VJ, Halperin JM, Dobkin CS, Ding XH, Brown WT, Miezejeski CM.

J Clin Exp Neuropsychol. 1995 Aug;17(4):518-28.

PMID:
7593472
33.

Mode of inheritance influences behavioral expression and molecular control of cognitive deficits in female carriers of the fragile X syndrome.

Hinton VJ, Dobkin CS, Halperin JM, Jenkins EC, Brown WT, Ding XH, Cohen IL, Rousseau F, Miezejeski CM.

Am J Med Genet. 1992 Apr 15-May 1;43(1-2):87-95.

PMID:
1605240
34.

Analysis of neocortex in three males with the fragile X syndrome.

Hinton VJ, Brown WT, Wisniewski K, Rudelli RD.

Am J Med Genet. 1991 Dec 1;41(3):289-94.

PMID:
1724112

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