Hinton VJ - Search Results

1

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. Hinton VJ, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):87-95. doi: 10.1002/ajmg.1320430113. Am J Med Genet. 1992. PMID: 1605240

2

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

Hinton VJ, Brown WT, Wisniewski K, Rudelli RD. Hinton VJ, et al. Am J Med Genet. 1991 Dec 1;41(3):289-94. doi: 10.1002/ajmg.1320410306. Am J Med Genet. 1991. PMID: 1724112

3

Cognitive and molecular aspects of fragile X.

Hinton VJ, Halperin JM, Dobkin CS, Ding XH, Brown WT, Miezejeski CM. Hinton VJ, et al. J Clin Exp Neuropsychol. 1995 Aug;17(4):518-28. doi: 10.1080/01688639508405142. J Clin Exp Neuropsychol. 1995. PMID: 7593472

4

Brief screening questionnaire for determining affected state in fragile X syndrome: a consensus recommendation.

Reiss AL, Cianchetti C, Cohen IL, DeVries B, Hagerman R, Hinton V, Froster U, Lachiewicz A, Mazzocco M, Sobesky W, et al. Reiss AL, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):61-4. doi: 10.1002/ajmg.1320430109. Am J Med Genet. 1992. PMID: 1605236

5

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. Schapiro MB, et al. Among authors: hinton vj. Am J Med Genet. 1995 Dec 18;60(6):480-93. doi: 10.1002/ajmg.1320600603. Am J Med Genet. 1995. PMID: 8825884

6

Premutation female carriers of fragile X syndrome: a pilot study on brain anatomy and metabolism.

Murphy DG, Mentis MJ, Pietrini P, Grady CL, Moore CJ, Horwitz B, Hinton V, Dobkin CS, Schapiro MB, Rapoport SI. Murphy DG, et al. J Am Acad Child Adolesc Psychiatry. 1999 Oct;38(10):1294-301. doi: 10.1097/00004583-199910000-00019. J Am Acad Child Adolesc Psychiatry. 1999. PMID: 10517063

7

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.

8

Visual memory failure presages conversion to MELAS phenotype.

Leaffer EB, De Vivo DC, Engelstad K, Fryer RH, Gu Y, Shungu DC, Hirano M, DiMauro S, Hinton VJ. Leaffer EB, et al. Among authors: hinton vj. Ann Clin Transl Neurol. 2022 Jun;9(6):841-852. doi: 10.1002/acn3.51564. Epub 2022 May 6. Ann Clin Transl Neurol. 2022. PMID: 35522125 Free PMC article.

9

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

Kern JH, Hinton VJ, Nereo NE, Hayes CJ, Gersony WM. Kern JH, et al. Among authors: hinton vj. Pediatrics. 1998 Nov;102(5):1148-52. doi: 10.1542/peds.102.5.1148. Pediatrics. 1998. PMID: 9794947

10

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

Cyrulnik SE, Fee RJ, Batchelder A, Kiefel J, Goldstein E, Hinton VJ. Cyrulnik SE, et al. Among authors: hinton vj. J Int Neuropsychol Soc. 2008 Sep;14(5):853-61. doi: 10.1017/S135561770808106X. J Int Neuropsychol Soc. 2008. PMID: 18764980

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