Hall DA - Search Results

1

Clinical Phenotype of Adult Fragile X Gray Zone Allele Carriers: a Case Series.

Debrey SM, Leehey MA, Klepitskaya O, Filley CM, Shah RC, Kluger B, Berry-Kravis E, Spector E, Tassone F, Hall DA. Debrey SM, et al. Among authors: hall da. Cerebellum. 2016 Oct;15(5):623-31. doi: 10.1007/s12311-016-0809-6. Cerebellum. 2016. PMID: 27372099

2

A French accent after corpus callosum infarct.

Hall DA, Anderson CA, Filley CM, Newcombe J, Hughes RL. Hall DA, et al. Neurology. 2003 May 13;60(9):1551-2. doi: 10.1212/01.wnl.0000058762.73309.39. Neurology. 2003. PMID: 12743256 No abstract available.

3

Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population.

Jacquemont S, Hagerman RJ, Leehey MA, Hall DA, Levine RA, Brunberg JA, Zhang L, Jardini T, Gane LW, Harris SW, Herman K, Grigsby J, Greco CM, Berry-Kravis E, Tassone F, Hagerman PJ. Jacquemont S, et al. Among authors: hall da. JAMA. 2004 Jan 28;291(4):460-9. doi: 10.1001/jama.291.4.460. JAMA. 2004. PMID: 14747503

4

Aging in individuals with the FMR1 mutation.

Jacquemont S, Farzin F, Hall D, Leehey M, Tassone F, Gane L, Zhang L, Grigsby J, Jardini T, Lewin F, Berry-Kravis E, Hagerman PJ, Hagerman RJ. Jacquemont S, et al. Am J Ment Retard. 2004 Mar;109(2):154-64. doi: 10.1352/0895-8017(2004)109<154:AIIWTF>2.0.CO;2. Am J Ment Retard. 2004. PMID: 15000674 Free PMC article.

5

PRNP H187R mutation associated with neuropsychiatric disorders in childhood and dementia.

Hall DA, Leehey MA, Filley CM, Steinbart E, Montine T, Schellenberg GD, Bosque P, Nixon R, Bird T. Hall DA, et al. Neurology. 2005 Apr 12;64(7):1304-6. doi: 10.1212/01.WNL.0000156911.70131.06. Neurology. 2005. PMID: 15824374

6

Initial diagnoses given to persons with the fragile X associated tremor/ataxia syndrome (FXTAS).

Hall DA, Berry-Kravis E, Jacquemont S, Rice CD, Cogswell J, Zhang L, Hagerman RJ, Hagerman PJ, Leehey MA. Hall DA, et al. Neurology. 2005 Jul 26;65(2):299-301. doi: 10.1212/01.wnl.0000168900.86323.9c. Neurology. 2005. PMID: 16043804

7

Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation.

Hessl D, Tassone F, Loesch DZ, Berry-Kravis E, Leehey MA, Gane LW, Barbato I, Rice C, Gould E, Hall DA, Grigsby J, Wegelin JA, Harris S, Lewin F, Weinberg D, Hagerman PJ, Hagerman RJ. Hessl D, et al. Among authors: hall da. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):115-21. doi: 10.1002/ajmg.b.30241. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 16184602

8

Prevalence of FMR1 repeat expansions in movement disorders. A systematic review.

Hall DA, Hagerman RJ, Hagerman PJ, Jacquemont S, Leehey MA. Hall DA, et al. Neuroepidemiology. 2006;26(3):151-5. doi: 10.1159/000091656. Epub 2006 Feb 21. Neuroepidemiology. 2006. PMID: 16493202 Review.

9

Symptomatic treatment in the fragile X-associated tremor/ataxia syndrome.

Hall DA, Berry-Kravis E, Hagerman RJ, Hagerman PJ, Rice CD, Leehey MA. Hall DA, et al. Mov Disord. 2006 Oct;21(10):1741-4. doi: 10.1002/mds.21001. Mov Disord. 2006. PMID: 16773616

10

Progression of tremor and ataxia in male carriers of the FMR1 premutation.

Leehey MA, Berry-Kravis E, Min SJ, Hall DA, Rice CD, Zhang L, Grigsby J, Greco CM, Reynolds A, Lara R, Cogswell J, Jacquemont S, Hessl DR, Tassone F, Hagerman R, Hagerman PJ. Leehey MA, et al. Among authors: hall da. Mov Disord. 2007 Jan 15;22(2):203-6. doi: 10.1002/mds.21252. Mov Disord. 2007. PMID: 17133502

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