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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 106 AL 120

PUBMED

Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational data.

Tabrizi SJ, Reilmann R, Roos RA, Durr A, Leavitt B, Owen G, Jones R, Johnson H, Craufurd D, Hicks SL, Kennard C, Landwehrmeyer B, Stout JC, Borowsky B, Scahill RI, Frost C, Langbehn DR; TRACK-HD inves

Lancet Neurol. 2012 Jan;11(1):42-53. doi: 10.1016/S1474-4422(11)70263-0.

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PUBMED

Assessing the analytic validity of molecular testing for Huntington disease using data from an external proficiency testing survey.

Palomaki GE, Richards CS.

Genet Med. 2012 Jan;14(1):69-75. doi: 10.1038/gim.0b013e3182310bb5.

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PUBMED

Intermediate CAG Repeats in Huntington's Disease: Analysis of COHORT.

Ha AD, Beck CA, Jankovic J.

Tremor Other Hyperkinet Mov (N Y). 2012;2. pii: tre-02-64-287-4. doi: 10.7916/D8FF3R2P.

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PUBMED

Antiphospholipid-related chorea.

Peluso S, Antenora A, De Rosa A, Roca A, Maddaluno G, Brescia Morra V, De Michele G.

Front Neurol. 2012 Oct 22;3:150. doi: 10.3389/fneur.2012.00150.

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PUBMED

Aspiration pneumonia and death in Huntington's disease.

Heemskerk AW, Roos RA.

Version 2. PLoS Curr. 2012 Jan 30 [revised 2012 Jan 1];4:RRN1293.

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PUBMED

'All the burden on all the carers': exploring quality of life with family caregivers of Huntington's disease patients.

Aubeeluck AV, Buchanan H, Stupple EJ.

Qual Life Res. 2012 Oct;21(8):1425-35. doi: 10.1007/s11136-011-0062-x.

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PUBMED

CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion.

Lee JM, Ramos EM, Lee JH, Gillis T, Mysore JS, Hayden MR, Warby SC, Morrison P, Nance M, Ross CA, Margolis RL, Squitieri F, Orobello S, Di Donato S, Gomez-Tortosa E, Ayuso C, Suchowersky O, Trent RJ,

Neurology. 2012 Mar 6;78(10):690-5. doi: 10.1212/WNL.0b013e318249f683.

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PUBMED

Huntington's disease knock-in male mice show specific anxiety-like behaviour and altered neuronal maturation.

Orvoen S, Pla P, Gardier AM, Saudou F, David DJ.

Neurosci Lett. 2012 Jan 24;507(2):127-32. doi: 10.1016/j.neulet.2011.11.063.

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PUBMED

Serum levels of N-acetylaspartate in Huntington's disease: preliminary results.

Ruggieri M, Serpino C, Ceci E, Sciruicchio V, Franco G, Pica C, Trojano M, Livrea P, de Tommaso M.

Mov Disord. 2012 Feb;27(2):329-30. doi: 10.1002/mds.23974. No abstract available.

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PUBMED

Sleep and circadian dysfunction in neurodegenerative disorders: insights from a mouse model of Huntington's disease.

Kuljis D, Schroeder AM, Kudo T, Loh DH, Willison DL, Colwell CS.

Minerva Pneumol. 2012 Sep;51(3):93-106.

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PUBMED

Deep brain stimulation in Huntington's disease: A 4-year follow-up case report.

Spielberger S, Hotter A, Wolf E, Eisner W, Müller J, Poewe W, Seppi K.

Mov Disord. 2012 May;27(6):806-7; author reply 807-8. doi: 10.1002/mds.24959. No abstract available.

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PUBMED

α-Synuclein accumulates in huntingtin inclusions but forms independent filaments and its deficiency attenuates early phenotype in a mouse model of Huntington's disease.

Tomás-Zapico C, Díez-Zaera M, Ferrer I, Gómez-Ramos P, Morán MA, Miras-Portugal MT, Díaz-Hernández M, Lucas JJ.

Hum Mol Genet. 2012 Feb 1;21(3):495-510. doi: 10.1093/hmg/ddr507.

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PUBMED

Longitudinal analysis of the behavioural phenotype in R6/1 (C57BL/6J) Huntington's disease transgenic mice.

Brooks SP, Janghra N, Workman VL, Bayram-Weston Z, Jones L, Dunnett SB.

Brain Res Bull. 2012 Jun 1;88(2-3):94-103. doi: 10.1016/j.brainresbull.2011.01.010.

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