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Bibliografía Científica

Artículos por temáticas

En este apartado encontrará la selección de artículos sobre Trastornos del Movimiento clasificados según los 11 tipos establecidos por International Parkinson & Movement Disorder Society.

Corea y enfermedad de Huntington

450 ARTíCULOS , VIENDO DEL 91 AL 105

PUBMED

Anxiety in Huntington's Disease.

Dale M, van Duijn E.

J Neuropsychiatry Clin Neurosci. 2015 Fall;27(4):262-71. doi: 10.1176/appi.neuropsych.14100265. Review.

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PUBMED

Brain Cholesterol Synthesis and Metabolism is Progressively Disturbed in the R6/1 Mouse Model of Huntington's Disease: A Targeted GC-MS/MS Sterol Analysis.

Kreilaus F, Spiro AS, Hannan AJ, Garner B, Jenner AM.

J Huntingtons Dis. 2015;4(4):305-18. doi: 10.3233/JHD-150170.

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PUBMED

Sirtuins: double players in Huntington's disease.

Naia L, Rego AC.

Biochim Biophys Acta. 2015 Oct;1852(10 Pt A):2183-94. doi: 10.1016/j.bbadis.2015.07.003. Review.

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PUBMED

HDAC inhibition imparts beneficial transgenerational effects in Huntington's disease mice via altered DNA and histone methylation.

Jia H, Morris CD, Williams RM, Loring JF, Thomas EA.

Proc Natl Acad Sci U S A. 2015 Jan 6;112(1):E56-64. doi: 10.1073/pnas.1415195112.

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PUBMED

Large Animal Models of Huntington's Disease.

Li XJ, Li S.

Curr Top Behav Neurosci. 2015;22:149-60. doi: 10.1007/7854_2013_246. Review.

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PUBMED

RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorder.

Santens P, Van Damme T, Steyaert W, Willaert A, Sablonnière B, De Paepe A, Coucke PJ, Dermaut B.

Neurology. 2015 Apr 28;84(17):1760-6. doi: 10.1212/WNL.0000000000001521.

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PUBMED

Ultrasensitive measurement of huntingtin protein in cerebrospinal fluid demonstrates increase with Huntington disease stage and decrease following brain huntingtin suppression.

Southwell AL, Smith SE, Davis TR, Caron NS, Villanueva EB, Xie Y, Collins JA, Ye ML, Sturrock A, Leavitt BR, Schrum AG, Hayden MR.

Sci Rep. 2015 Jul 15;5:12166. doi: 10.1038/srep12166.

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PUBMED

A role for Kalirin-7 in corticostriatal synaptic dysfunction in Huntington's disease.

Puigdellívol M, Cherubini M, Brito V, Giralt A, Suelves N, Ballesteros J, Zamora-Moratalla A, Martín ED, Eipper BA, Alberch J, Ginés S.

Hum Mol Genet. 2015 Dec 20;24(25):7265-85. doi: 10.1093/hmg/ddv426.

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PUBMED

Assessing impairment of executive function and psychomotor speed in premanifest and manifest Huntington's disease gene-expansion carriers.

Unmack Larsen I, Vinther-Jensen T, Gade A, Nielsen JE, Vogel A.

J Int Neuropsychol Soc. 2015 Mar;21(3):193-202. doi: 10.1017/S1355617715000090.

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PUBMED

Benign Hereditary Chorea: An Update.

Peall KJ, Kurian MA.

Tremor Other Hyperkinet Mov (N Y). 2015 Jul 14;5:314. doi: 10.7916/D8RJ4HM5. Review.

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PUBMED

[Morvan's syndrome (Morvan's fibrillary chorea)].

Arimura K, Watanabe O.

Nihon Rinsho. 2015 Sep;73 Suppl 7:806-10. Japanese. No abstract available.

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PUBMED

First use of creatine hydrochloride in premanifest Huntington disease.

Tuckfield C.

Med J Aust. 2015 Apr 20;202(7):378-80. No abstract available.

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PUBMED

Enhanced GABAergic Inputs Contribute to Functional Alterations of Cholinergic Interneurons in the R6/2 Mouse Model of Huntington's Disease.

Holley SM, Joshi PR, Parievsky A, Galvan L, Chen JY, Fisher YE, Huynh MN, Cepeda C, Levine MS.

eNeuro. 2015 Jan-Feb;2(1). pii: e0008.

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PUBMED

Erratum. Correction to: Dopamine and Huntington's disease.

Schwab LC, Garas SN, Drouin-Ouellet J, Mason SL, Stott SR, Barker RA.

Expert Rev Neurother. 2015;15(11):1367. doi: 10.1586/14737175.2015.1088179. No abstract available.

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PUBMED

Factors influencing the clinical expression of intermediate CAG repeat length mutations of the Huntington's disease gene.

Panegyres PK, Shu CC, Chen HY, Paulsen JS.

J Neurol. 2015 Feb;262(2):277-84. doi: 10.1007/s00415-014-7559-5.

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