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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

Polyglutamine aggregation in Huntington and related diseases.

Polling S, Hill AF, Hatters DM.

Adv Exp Med Biol. 2012;769:125-40. Review.

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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

Chorea as the first and only manifestation of systemic lupus erythematosus.

Poil AR, Yousef Khan F, Lutf A, Hammoudeh M.

Case Rep Rheumatol. 2012;2012:907402.

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PUBMED

Environmental enrichment rescues female-specific hyperactivity of the hypothalamic-pituitary-adrenal axis in a model of Huntington's disease.

Du X, Leang L, Mustafa T, Renoir T, Pang TY, Hannan AJ.

Transl Psychiatry. 2012 Jul 3;2:e133. doi: 10.1038/tp.2012.58. Erratum in: Transl Psychiatry. 2012;2:e144.

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PUBMED

RNAi-based therapies for Huntington's disease: delivery challenges and opportunities.

Mantha N, Das SK, Das NG.

Ther Deliv. 2012 Sep;3(9):1061-76. Review.

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PUBMED

Raft-like microdomains play a key role in mitochondrial impairment in lymphoid cells from patients with Huntington's disease.

Ciarlo L, Manganelli V, Matarrese P, Garofalo T, Tinari A, Gambardella L, Marconi M, Grasso M, Misasi R, Sorice M, Malorni W.

J Lipid Res. 2012 Oct;53(10):2057-68. doi: 10.1194/jlr.M026062.

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PUBMED

AAV-mediated delivery of the transcription factor XBP1s into the striatum reduces mutant Huntingtin aggregation in a mouse model of Huntington's disease.

Zuleta A, Vidal RL, Armentano D, Parsons G, Hetz C.

Biochem Biophys Res Commun. 2012 Apr 13;420(3):558-63. doi: 10.1016/j.bbrc.2012.03.033.

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PUBMED

Beyond the patient: the broader impact of genetic discrimination among individuals at risk of Huntington disease.

Bombard Y, Palin J, Friedman JM, Veenstra G, Creighton S, Bottorff JL, Hayden MR; Canadian Respond-HD Collaborative Research Group..

Am J Med Genet B Neuropsychiatr Genet. 2012 Mar;159B(2):217-26. doi: 10.1002/ajmg.b.32016.

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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

Cognitive domains that predict time to diagnosis in prodromal Huntington disease.

Harrington DL, Smith MM, Zhang Y, Carlozzi NE, Paulsen JS; PREDICT-HD Investigators of the Huntington Study Group..

J Neurol Neurosurg Psychiatry. 2012 Jun;83(6):612-9. doi: 10.1136/jnnp-2011-301732.

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PUBMED

Genetic Deficiency of Complement Component 3 Does Not Alter Disease Progression in a Mouse Model of Huntington's Disease.

Larkin PB, Muchowski PJ.

J Huntingtons Dis. 2012;1(1):107-18. doi: 10.3233/JHD-2012-120021.

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PUBMED

Pregnancy in patients with Sydenham's Chorea.

Maia DP, Fonseca PG, Camargos ST, Pfannes C, Cunningham MC, Cardoso F.

Parkinsonism Relat Disord. 2012 Jun;18(5):458-61. doi: 10.1016/j.parkreldis.2011.12.013.

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PUBMED

Deep brain stimulation in disabling involuntary vocalization associated with Huntington's disease.

Garcia-Ruiz PJ, Ayerbe J, del Val J, Herranz A.

Parkinsonism Relat Disord. 2012 Jul;18(6):803-4. doi: 10.1016/j.parkreldis.2012.03.005. No abstract available.

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PUBMED

Chorea mollis: long-term follow-up of an infantile case.

Balottin U, Calcaterra E, Zambonin F, Veggiotti P, Luoni C, Termine C.

Neurol Sci. 2012 Jun;33(3):643-5. doi: 10.1007/s10072-011-0806-y.

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PUBMED

ATRX induction by mutant huntingtin via Cdx2 modulates heterochromatin condensation and pathology in Huntington's disease.

Lee J, Hong YK, Jeon GS, Hwang YJ, Kim KY, Seong KH, Jung MK, Picketts DJ, Kowall NW, Cho KS, Ryu H.

Cell Death Differ. 2012 Jul;19(7):1109-16. doi: 10.1038/cdd.2011.196.

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