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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 16 AL 30

PUBMED

A Chinese pedigree with an individual homozygous for CAG repeats of Huntington's disease.

Shi SS, Lin Y, Zhao GX, Gan SR, Wu ZY.

Psychiatr Genet. 2012 Feb;22(1):53-4. doi: 10.1097/YPG.0b013e328347c203. No abstract available.

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Histone deacetylase (HDAC) inhibitors targeting HDAC3 and HDAC1 ameliorate polyglutamine-elicited phenotypes in model systems of Huntington's disease.

Jia H, Pallos J, Jacques V, Lau A, Tang B, Cooper A, Syed A, Purcell J, Chen Y, Sharma S, Sangrey GR, Darnell SB, Plasterer H, Sadri-Vakili G, Gottesfeld JM, Thompson LM, Rusche JR, Marsh JL, Thomas E

Neurobiol Dis. 2012 May;46(2):351-61.

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Genetic knock-down of HDAC3 does not modify disease-related phenotypes in a mouse model of Huntington's disease.

Moumné L, Campbell K, Howland D, Ouyang Y, Bates GP.

PLoS One. 2012;7(2):e31080. doi: 10.1371/journal.pone.0031080.

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Deficits in spermatogenesis but not neurogenesis are alleviated by chronic testosterone therapy in R6/1 Huntington's disease mice.

Hannan AJ, Ransome MI.

J Neuroendocrinol. 2012 Feb;24(2):341-56. doi: 10.1111/j.1365-2826.2011.02238.x.

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Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset.

Ramos EM, Latourelle JC, Lee JH, Gillis T, Mysore JS, Squitieri F, Di Pardo A, Di Donato S, Hayden MR, Morrison PJ, Nance M, Ross CA, Margolis RL, Gomez-Tortosa E, Ayuso C, Suchowersky O, Trent RJ, Mc

Hum Genet. 2012 Dec;131(12):1833-40. doi: 10.1007/s00439-012-1205-z.

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Discrepancies in reporting the CAG repeat lengths for Huntington's disease.

Quarrell OW, Handley O, O'Donovan K, Dumoulin C, Ramos-Arroyo M, Biunno I, Bauer P, Kline M, Landwehrmeyer GB; European Huntington’s Disease Network..

Eur J Hum Genet. 2012 Jan;20(1):20-6. doi: 10.1038/ejhg.2011.136.

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Is Huntington's disease associated with deficits in theory of mind?

Eddy CM, Sira Mahalingappa S, Rickards HE.

Acta Neurol Scand. 2012 Dec;126(6):376-83. doi: 10.1111/j.1600-0404.2012.01659.x.

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Home or Residential Care? The Role of Behavioral and Psychosocial Factors in Determining Discharge Outcomes for Inpatients with Huntington's Disease.

Fisher F, Andrews S, Churchyard A, Mathers S.

J Huntingtons Dis. 2012;1(2):187-93. doi: 10.3233/JHD-120022.

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A novel nonsense mutation in the TITF-1 gene in a Japanese family with benign hereditary chorea.

Nakamura K, Sekijima Y, Nagamatsu K, Yoshida K, Ikeda S.

J Neurol Sci. 2012 Feb 15;313(1-2):189-92. doi: 10.1016/j.jns.2011.09.013. Review.

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Direct Visualisation of Abnormal Dendritic Spine Morphology in the Hippocampus of the R6/2 Transgenic Mouse Model of Huntington's Disease.

Bulley SJ, Drew CJ, Morton AJ.

J Huntingtons Dis. 2012;1(2):267-73. doi: 10.3233/JHD-120024.

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8OHdG as a marker for Huntington disease progression.

Long JD, Matson WR, Juhl AR, Leavitt BR, Paulsen JS; PREDICT-HD Investigators and Coordinators of the Huntington Study Group..

Neurobiol Dis. 2012 Jun;46(3):625-34. doi: 10.1016/j.nbd.2012.02.012.

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Bone marrow transplantation confers modest benefits in mouse models of Huntington's disease.

Kwan W, Magnusson A, Chou A, Adame A, Carson MJ, Kohsaka S, Masliah E, Möller T, Ransohoff R, Tabrizi SJ, Björkqvist M, Muchowski PJ.

J Neurosci. 2012 Jan 4;32(1):133-42. doi: 10.1523/JNEUROSCI.4846-11.2012.

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Huntington's disease: fighting on many fronts.

Andre R, Wild EJ, Tabrizi SJ.

Brain. 2012 Apr;135(Pt 4):998-1001. doi: 10.1093/brain/aws060. No abstract available.

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Comparative analysis of pathology and behavioural phenotypes in mouse models of Huntington's disease.

Brooks SP, Jones L, Dunnett SB.

Brain Res Bull. 2012 Jun 1;88(2-3):81-93. doi: 10.1016/j.brainresbull.2011.10.002. Review.

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