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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

440 ARTíCULOS , VIENDO DEL 91 AL 105

PUBMED

Large genetic animal models of Huntington's Disease.

Morton AJ, Howland DS.

J Huntingtons Dis. 2013;2(1):3-19. doi: 10.3233/JHD-130050. Review.

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Functional and connectivity changes during working memory in Huntington's disease: 18 month longitudinal data from the IMAGE-HD study.

Georgiou-Karistianis N, Poudel GR, Domínguez D JF, Langmaid R, Gray MA, Churchyard A, Chua P, Borowsky B, Egan GF, Stout JC.

Brain Cogn. 2013 Oct;83(1):80-91. doi: 10.1016/j.bandc.2013.07.004.

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PUBMED

Regulation of feedback between protein kinase A and the proteasome system worsens Huntington's disease.

Lin JT, Chang WC, Chen HM, Lai HL, Chen CY, Tao MH, Chern Y.

Mol Cell Biol. 2013 Mar;33(5):1073-84. doi: 10.1128/MCB.01434-12.

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PUBMED

Dominant effects of the Huntington's disease HTT CAG repeat length are captured in gene-expression data sets by a continuous analysis mathematical modeling strategy.

Lee JM, Galkina EI, Levantovsky RM, Fossale E, Anne Anderson M, Gillis T, Srinidhi Mysore J, Coser KR, Shioda T, Zhang B, Furia MD, Derry J, Kohane IS, Seong IS, Wheeler VC, Gusella JF, MacDonald ME.

Hum Mol Genet. 2013 Aug 15;22(16):3227-38. doi: 10.1093/hmg/ddt176.

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PUBMED

Association between caffeine intake and age at onset in Huntington's disease.

Simonin C, Duru C, Salleron J, Hincker P, Charles P, Delval A, Youssov K, Burnouf S, Azulay JP, Verny C, Scherer C, Tranchant C, Goizet C, Debruxelles S, Defebvre L, Sablonnière B, Romon-Rousseaux M,

Neurobiol Dis. 2013 Oct;58:179-82. doi: 10.1016/j.nbd.2013.05.013.

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Refining the diagnosis of Huntington disease: the PREDICT-HD study.

Biglan KM, Zhang Y, Long JD, Geschwind M, Kang GA, Killoran A, Lu W, McCusker E, Mills JA, Raymond LA, Testa C, Wojcieszek J, Paulsen JS; PREDICT-HD Investigators of the Huntington Study Group..

Front Aging Neurosci. 2013 Apr 2;5:12. doi: 10.3389/fnagi.2013.00012.

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PUBMED

β-Defensin Genomic Copy Number Does Not Influence the Age of Onset in Huntington's Disease.

Vittori A, Orth M, Roos RA, Outeiro TF, Giorgini F, Hollox EJ; REGISTRY investigators of the European Huntington’s Disease Network..

J Huntingtons Dis. 2013 Mar 27;2(1):107-124.

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PUBMED

Effects of the Pimelic Diphenylamide Histone Deacetylase Inhibitor HDACi 4b on the R6/2 and N171-82Q Mouse Models of Huntington's Disease.

Chen JY, Wang E, Galvan L, Huynh M, Joshi P, Cepeda C, Levine MS.

PLoS Curr. 2013 Feb 5;5. pii: ecurrents.hd.ec3547da1c2a520ba959ee7bf8bdd202. doi: 10.1371/currents.hd.ec3547da1c2a520ba959ee7bf8bdd202.

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PUBMED

Relationship between BDNF expression in major striatal afferents, striatum morphology and motor behavior in the R6/2 mouse model of Huntington's disease.

Samadi P, Boutet A, Rymar VV, Rawal K, Maheux J, Kvann JC, Tomaszewski M, Beaubien F, Cloutier JF, Levesque D, Sadikot AF.

Genes Brain Behav. 2013 Feb;12(1):108-24. doi: 10.1111/j.1601-183X.2012.00858.x.

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PUBMED

The role of iron imaging in Huntington's disease.

van den Bogaard SJ, Dumas EM, Roos RA.

Int Rev Neurobiol. 2013;110:241-50. doi: 10.1016/B978-0-12-410502-7.00011-9. Review.

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PUBMED

How do partners find out about the risk of Huntington's disease in couple relationships?

Forrest Keenan K, Simpson SA, Miedzybrodzka Z, Alexander DA, Semper J.

J Genet Couns. 2013 Jun;22(3):336-44. doi: 10.1007/s10897-012-9562-2.

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PUBMED

Diadochokinetic movements differ between patients with Huntington's disease and controls.

Müller T, Saft C, Andrich J, Harati A.

NeuroRehabilitation. 2013;33(4):649-55. doi: 10.3233/NRE-130992.

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PUBMED

A treatable new cause of chorea: beta-ketothiolase deficiency.

Buhaş D, Bernard G, Fukao T, Décarie JC, Chouinard S, Mitchell GA.

Mov Disord. 2013 Jul;28(8):1054-6. doi: 10.1002/mds.25538. No abstract available.

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PUBMED

Benign hereditary chorea: dopaminergic brain imaging in patients with a novel intronic NKX2.1 gene mutation.

Konishi T, Kono S, Fujimoto M, Terada T, Matsushita K, Ouchi Y, Miyajima H.

J Neurol. 2013 Jan;260(1):207-13. doi: 10.1007/s00415-012-6618-z.

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