Inicia sesión Registrate Mi Biblioteca idioma

Idioma

biblioteca idioma abrir menu

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

405 ARTíCULOS , VIENDO DEL 1 AL 15

PUBMED

Dysregulated Neuronal Activity Patterns Implicate Corticostriatal Circuit Dysfunction in Multiple Rodent Models of Huntington's Disease.

Miller BR, Walker AG, Barton SJ, Rebec GV.

Front Syst Neurosci. 2011 May 9;5:26. doi: 10.3389/fnsys.2011.00026.

0

0

0

PUBMED

Postural deficits in Huntington's disease when performing motor skills involved in daily living.

Panzera R, Salomonczyk D, Pirogovosky E, Simmons R, Goldstein J, Corey-Bloom J, Gilbert PE.

Gait Posture. 2011 Mar;33(3):457-61. doi: 10.1016/j.gaitpost.2010.12.025.

0

0

0

PUBMED

Magnetic resonance perfusion imaging of resting-state cerebral blood flow in preclinical Huntington's disease.

Wolf RC, Grön G, Sambataro F, Vasic N, Wolf ND, Thomann PA, Saft C, Landwehrmeyer GB, Orth M.

J Cereb Blood Flow Metab. 2011 Sep;31(9):1908-18. doi: 10.1038/jcbfm.2011.60.

0

0

0

PUBMED

Exploring the correlates of intermediate CAG repeats in Huntington disease.

Ha AD, Jankovic J.

Postgrad Med. 2011 Sep;123(5):116-21. doi: 10.3810/pgm.2011.09.2466. Review.

0

0

0

PUBMED

Indexing disease progression at study entry with individuals at-risk for Huntington disease.

Zhang Y, Long JD, Mills JA, Warner JH, Lu W, Paulsen JS; PREDICT-HD Investigators and Coordinators of the Huntington Study Group..

Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(7):751-63. doi: 10.1002/ajmg.b.31232.

0

0

0

PUBMED

FK506 ameliorates cell death features in Huntington's disease striatal cell models.

Rosenstock TR, de Brito OM, Lombardi V, Louros S, Ribeiro M, Almeida S, Ferreira IL, Oliveira CR, Rego AC.

Neurochem Int. 2011 Oct;59(5):600-9. doi: 10.1016/j.neuint.2011.04.009.

0

0

0

PUBMED

Healthcare experiences of families affected by Huntington disease: need for improved care.

Etchegary H.

Chronic Illn. 2011 Sep;7(3):225-38. doi: 10.1177/1742395311403637.

0

0

0

PUBMED

Reversible striatal hypermetabolism in a case of rare adult-onset Sydenham chorea on two sequential 18F-FDG PET studies.

Paghera B, Caobelli F, Giubbini R, Premi E, Padovani A.

J Neuroradiol. 2011 Dec;38(5):325-6. doi: 10.1016/j.neurad.2010.10.002. No abstract available.

0

0

0

PUBMED

Parent-of-origin differences of mutant HTT CAG repeat instability in Huntington's disease.

Aziz NA, van Belzen MJ, Coops ID, Belfroid RD, Roos RA.

Eur J Med Genet. 2011 Jul-Aug;54(4):e413-8. doi: 10.1016/j.ejmg.2011.04.002.

0

0

0

PUBMED

Up-regulation of the isoenzymes MAO-A and MAO-B in the human basal ganglia and pons in Huntington's disease revealed by quantitative enzyme radioautography.

Richards G, Messer J, Waldvogel HJ, Gibbons HM, Dragunow M, Faull RL, Saura J.

Brain Res. 2011 Jan 25;1370:204-14. doi: 10.1016/j.brainres.2010.11.020.

0

0

0

PUBMED

Decreased striatal RGS2 expression is neuroprotective in Huntington's disease (HD) and exemplifies a compensatory aspect of HD-induced gene regulation.

Seredenina T, Gokce O, Luthi-Carter R.

PLoS One. 2011;6(7):e22231. doi: 10.1371/journal.pone.0022231.

0

0

0

PUBMED

Huntington's disease: from molecular pathogenesis to clinical treatment.

Ross CA, Tabrizi SJ.

Lancet Neurol. 2011 Jan;10(1):83-98. doi: 10.1016/S1474-4422(10)70245-3. Review.

0

0

0

PUBMED

Hdac6 knock-out increases tubulin acetylation but does not modify disease progression in the R6/2 mouse model of Huntington's disease.

Bobrowska A, Paganetti P, Matthias P, Bates GP.

PLoS One. 2011;6(6):e20696. doi: 10.1371/journal.pone.0020696.

0

0

0

PUBMED

Chorea associated with thyrotoxicosis due to toxic multinodular goiter.

Masannat Y, Gandhy R, Olajide O, Kheetan R, Yaqub A.

Thyroid. 2011 Nov;21(11):1279-80. doi: 10.1089/thy.2011.0018. No abstract available.

0

0

0

PUBMED

Sir2 is induced by oxidative stress in a yeast model of Huntington disease and its activation reduces protein aggregation.

Sorolla MA, Nierga C, Rodríguez-Colman MJ, Reverter-Branchat G, Arenas A, Tamarit J, Ros J, Cabiscol E.

Arch Biochem Biophys. 2011 Jun 1;510(1):27-34. doi: 10.1016/j.abb.2011.04.002.

0

0

0

Comentarios

En ningún caso la información facilitada constituye asesoramiento por parte de Zambon

Con el aval de:

Logo SEN Logo HONcode Logo WIS

En colaboración con:

Zambon Neuroacademy