Berry-Kravis E - Search Results

1

Language processing skills linked to FMR1 variation: A study of gaze-language coordination during rapid automatized naming among women with the FMR1 premutation.

Nayar K, McKinney W, Hogan AL, Martin GE, La Valle C, Sharp K, Berry-Kravis E, Norton ES, Gordon PC, Losh M. Nayar K, et al. PLoS One. 2019 Jul 26;14(7):e0219924. doi: 10.1371/journal.pone.0219924. eCollection 2019. PLoS One. 2019. PMID: 31348790 Free PMC article.

2

Neuropathic features in fragile X premutation carriers.

Berry-Kravis E, Goetz CG, Leehey MA, Hagerman RJ, Zhang L, Li L, Nguyen D, Hall DA, Tartaglia N, Cogswell J, Tassone F, Hagerman PJ. Berry-Kravis E, et al. Am J Med Genet A. 2007 Jan 1;143A(1):19-26. doi: 10.1002/ajmg.a.31559. Am J Med Genet A. 2007. PMID: 17152065

3

Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype.

Collins SC, Coffee B, Benke PJ, Berry-Kravis E, Gilbert F, Oostra B, Halley D, Zwick ME, Cutler DJ, Warren ST. Collins SC, et al. PLoS One. 2010 Mar 5;5(3):e9476. doi: 10.1371/journal.pone.0009476. PLoS One. 2010. PMID: 20221430 Free PMC article.

4

FMR1 gray-zone alleles: association with Parkinson's disease in women?

Hall DA, Berry-Kravis E, Zhang W, Tassone F, Spector E, Zerbe G, Hagerman PJ, Ouyang B, Leehey MA. Hall DA, et al. Mov Disord. 2011 Aug 15;26(10):1900-6. doi: 10.1002/mds.23755. Epub 2011 May 12. Mov Disord. 2011. PMID: 21567456 Free PMC article.

5

Associated features in females with an FMR1 premutation.

Wheeler AC, Bailey DB Jr, Berry-Kravis E, Greenberg J, Losh M, Mailick M, Milà M, Olichney JM, Rodriguez-Revenga L, Sherman S, Smith L, Summers S, Yang JC, Hagerman R. Wheeler AC, et al. J Neurodev Disord. 2014;6(1):30. doi: 10.1186/1866-1955-6-30. Epub 2014 Jul 30. J Neurodev Disord. 2014. PMID: 25097672 Free PMC article. Review.

6

White matter disease and cognitive impairment in FMR1 premutation carriers.

Filley CM, Brown MS, Onderko K, Ray M, Bennett RE, Berry-Kravis E, Grigsby J. Filley CM, et al. Neurology. 2015 May 26;84(21):2146-52. doi: 10.1212/WNL.0000000000001612. Epub 2015 Apr 29. Neurology. 2015. PMID: 25925982 Free PMC article.

7

Neurological and endocrine phenotypes of fragile X carrier women.

Hall D, Todorova-Koteva K, Pandya S, Bernard B, Ouyang B, Walsh M, Pounardjian T, Deburghraeve C, Zhou L, Losh M, Leehey M, Berry-Kravis E. Hall D, et al. Clin Genet. 2016 Jan;89(1):60-7. doi: 10.1111/cge.12646. Epub 2015 Sep 4. Clin Genet. 2016. PMID: 26212380 Free PMC article.

8

Update on the Clinical, Radiographic, and Neurobehavioral Manifestations in FXTAS and FMR1 Premutation Carriers.

Hall DA, Robertson E, Shelton AL, Losh MC, Mila M, Moreno EG, Gomez-Anson B, Martínez-Cerdeño V, Grigsby J, Lozano R, Hagerman R, Maria LS, Berry-Kravis E, O'Keefe JA. Hall DA, et al. Cerebellum. 2016 Oct;15(5):578-86. doi: 10.1007/s12311-016-0799-4. Cerebellum. 2016. PMID: 27287737 Free PMC article. Review.

9

A developmental, longitudinal investigation of autism phenotypic profiles in fragile X syndrome.

Lee M, Martin GE, Berry-Kravis E, Losh M. Lee M, et al. J Neurodev Disord. 2016 Dec 30;8:47. doi: 10.1186/s11689-016-9179-0. eCollection 2016. J Neurodev Disord. 2016. PMID: 28050218 Free PMC article.

10

Erratum to: A developmental, longitudinal investigation of autism phenotypic profiles in fragile X syndrome.

Lee M, Martin GE, Berry-Kravis E, Losh M. Lee M, et al. J Neurodev Disord. 2017 Mar 6;9:10. doi: 10.1186/s11689-017-9192-y. eCollection 2017. J Neurodev Disord. 2017. PMID: 28286580 Free PMC article.

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