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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

362 ARTíCULOS , VIENDO DEL 1 AL 15

PUBMED

Protein oxidation in Huntington disease affects energy production and vitamin B6 metabolism.

Sorolla MA, Rodríguez-Colman MJ, Tamarit J, Ortega Z, Lucas JJ, Ferrer I, Ros J, Cabiscol E.

Free Radic Biol Med. 2010 Aug 15;49(4):612-21. doi: 10.1016/j.freeradbiomed.2010.05.016.

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Tetrabenazine: the first approved drug for the treatment of chorea in US patients with Huntington disease.

Frank S.

Neuropsychiatr Dis Treat. 2010 Oct 5;6:657-65. doi: 10.2147/NDT.S6430.

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PUBMED

Mitochondrial-dependent apoptosis in Huntington's disease human cybrids.

Ferreira IL, Nascimento MV, Ribeiro M, Almeida S, Cardoso SM, Grazina M, Pratas J, Santos MJ, Januário C, Oliveira CR, Rego AC.

Exp Neurol. 2010 Apr;222(2):243-55. doi: 10.1016/j.expneurol.2010.01.002.

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[Hydrogen magnetic resonance quantitative spectroscopy at 3 T in symptomatic and asymptomatic Huntington's disease patients].

Alcauter-Solórzano S, Pasaye-Alcaraz EH, Alvarado-Alanis P, Fermín-Delgado RO, Alonso-Vilatela ME, Salgado-Lujambio P, Barrios FA.

Rev Neurol. 2010 Aug 16;51(4):208-12. Spanish.

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Impaired TrkB-mediated ERK1/2 activation in huntington disease knock-in striatal cells involves reduced p52/p46 Shc expression.

Ginés S, Paoletti P, Alberch J.

J Biol Chem. 2010 Jul 9;285(28):21537-48. doi: 10.1074/jbc.M109.084202.

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Comprehension of complex discourse in different stages of Huntington's disease.

Saldert C, Fors A, Ströberg S, Hartelius L.

Int J Lang Commun Disord. 2010 Nov-Dec;45(6):656-69. doi: 10.3109/13682820903494742.

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PUBMED

Juvenile Huntington's disease: a case report and literature review.

Reyes Molón L, Yáñez Sáez RM, López-Ibor Alcocer MI.

Actas Esp Psiquiatr. 2010 Sep-Oct;38(5):285-94. Review. English, Spanish.

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PUBMED

Cerebral cortex structure in prodromal Huntington disease.

Nopoulos PC, Aylward EH, Ross CA, Johnson HJ, Magnotta VA, Juhl AR, Pierson RK, Mills J, Langbehn DR, Paulsen JS; PREDICT-HD Investigators Coordinators of Huntington Study Group (HSG)..

Neurobiol Dis. 2010 Dec;40(3):544-54. doi: 10.1016/j.nbd.2010.07.014.

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Huntington's disease: the value of transcranial meganetic stimulation.

Medina FJ, Túnez I.

Curr Med Chem. 2010;17(23):2482-91.

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PUBMED

Central pattern generator: the main cause of Huntington's disease.

Banaie M, Sarbaz Y, Gharibzadeh S, Towhidkhah F.

J Neuropsychiatry Clin Neurosci. 2010 Winter;22(1):123.E34. doi: 10.1176/appi.neuropsych.22.1.123-u.e34. No abstract available.

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PUBMED

Age at onset in Huntington's disease is modified by the autophagy pathway: implication of the V471A polymorphism in Atg7.

Metzger S, Saukko M, Van Che H, Tong L, Puder Y, Riess O, Nguyen HP.

Hum Genet. 2010 Oct;128(4):453-9. doi: 10.1007/s00439-010-0873-9.

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Huntington's disease presenting as amyotrophic lateral sclerosis.

Phukan J, Ali E, Pender NP, Molloy F, Hennessy M, Walsh RJ, Hardiman O.

Amyotroph Lateral Scler. 2010 Aug;11(4):405-7. doi: 10.1080/17482960903055958.

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A Huntington's disease phenocopy characterized by pallido-nigro-luysian degeneration with brain iron accumulation and p62-positive glial inclusions.

Ahmed Z, Tabrizi SJ, Li A, Houlden H, Sailer A, Lees AJ, Revesz T, Holton JL.

Neuropathol Appl Neurobiol. 2010 Oct;36(6):551-7. doi: 10.1111/j.1365-2990.2010.01093.x. No abstract available.

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PUBMED

The role of REST in transcriptional and epigenetic dysregulation in Huntington's disease.

Buckley NJ, Johnson R, Zuccato C, Bithell A, Cattaneo E.

Neurobiol Dis. 2010 Jul;39(1):28-39. doi: 10.1016/j.nbd.2010.02.003. Review.

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