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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

Neuroleptic Malignant Syndrome Induced by Olanzapine in a Patient with Huntington's Disease.

Moreno JL, Palau Fayos JM, Díaz de Santiago A, García de Yébenes J.

J Huntingtons Dis. 2012;1(1):31-2. doi: 10.3233/JHD-2012-120008. No abstract available.

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Longitudinal analyses of operant performance on the serial implicit learning task (SILT) in the YAC128 Huntington's disease mouse line.

Brooks SP, Jones L, Dunnett SB.

Brain Res Bull. 2012 Jun 1;88(2-3):130-6. doi: 10.1016/j.brainresbull.2011.06.008.

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Visual Working Memory Impairment in Premanifest Gene-Carriers and Early Huntington's Disease.

Dumas EM, Say MJ, Jones R, Labuschagne I, O'Regan AM, Hart EP, van den Bogaard SJ, Queller S, Justo D, Coleman A, Dar Santos RC, Dürr A, Leavitt BR, Tabrizi SJ, Roos RA, Stout JC.

J Huntingtons Dis. 2012;1(1):97-106. doi: 10.3233/JHD-2012-120010.

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Drosophila eye color mutants as therapeutic tools for Huntington disease.

Green EW, Campesan S, Breda C, Sathyasaikumar KV, Muchowski PJ, Schwarcz R, Kyriacou CP, Giorgini F.

Fly (Austin). 2012 Apr-Jun;6(2):117-20. doi: 10.4161/fly.19999.

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Altered ventral striatal activation during reward and punishment processing in premanifest Huntington's disease: a functional magnetic resonance study.

Enzi B, Edel MA, Lissek S, Peters S, Hoffmann R, Nicolas V, Tegenthoff M, Juckel G, Saft C.

Exp Neurol. 2012 May;235(1):256-64. doi: 10.1016/j.expneurol.2012.02.003.

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Abnormal apocrine secretory cell mitochondria in a Huntington disease patient.

Sidiropoulos C, LeWitt P, Hashimoto K.

J Neurol Sci. 2012 Dec 15;323(1-2):261-3. doi: 10.1016/j.jns.2012.08.034.

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PUBMED

Implicit contextual learning in prodromal and early stage Huntington's disease patients.

van Asselen M, Almeida I, Júlio F, Januário C, Campos EB, Simões M, Castelo-Branco M.

J Int Neuropsychol Soc. 2012 Jul;18(4):689-96. doi: 10.1017/S1355617712000288.

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Indirect inhibition of 26S proteasome activity in a cellular model of Huntington's disease.

Hipp MS, Patel CN, Bersuker K, Riley BE, Kaiser SE, Shaler TA, Brandeis M, Kopito RR.

J Cell Biol. 2012 Mar 5;196(5):573-87. doi: 10.1083/jcb.201110093.

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Pharmacologic approaches to the treatment of Huntington's disease.

Venuto CS, McGarry A, Ma Q, Kieburtz K.

Mov Disord. 2012 Jan;27(1):31-41. doi: 10.1002/mds.23953. Review.

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PUBMED

Development of the Huntington disease work function scale.

Brossman B, Williams JK, Downing N, Mills JA, Paulsen JS; PREDICT-HD Investigators and Coordinators of the Huntington Study Group..

J Occup Environ Med. 2012 Oct;54(10):1300-8. doi: 10.1097/JOM.0b013e31825f30ab.

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PUBMED

Genetic analysis of polymorphisms in the kalirin gene for association with age-at-onset in European Huntington disease patients.

Tsai YC, Metzger S, Riess O, Soehn AS, Nguyen HP.

BMC Med Genet. 2012 Jun 21;13:48. doi: 10.1186/1471-2350-13-48.

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Motor and non-motor behaviour in experimental Huntington's disease.

Zeef DH, Vlamings R, Lim LW, Tan S, Janssen ML, Jahanshahi A, Hoogland G, Prickaerts J, Steinbusch HW, Temel Y.

Behav Brain Res. 2012 Jan 15;226(2):435-9. doi: 10.1016/j.bbr.2011.09.041.

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PUBMED

Shaping the role of mitochondria in the pathogenesis of Huntington's disease.

Costa V, Scorrano L.

EMBO J. 2012 Apr 18;31(8):1853-64. doi: 10.1038/emboj.2012.65. Review.

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PUBMED

Chorea--an unusual manifestation in a woman recovering from myxedema coma.

Yu CH, Stovel R, Fox S.

Endocr Pract. 2012 May-Jun;18(3):e43-8. doi: 10.4158/EP11255.CR.

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PUBMED

WITHDRAWN: Potential role of ubiquitin ligase Ube3a in synaptic pathophysiology of Huntington's disease.

Maheshwari M, Jana NR.

Int J Dev Neurosci. 2012 Mar 31. pii: S0736-5748(12)00278-X. doi: 10.1016/j.ijdevneu.2012.03.239. [Epub ahead of print]

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