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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 1 AL 15

PUBMED

Microtransplantation of whole ganglionic eminence cells ameliorates motor deficit, enlarges the volume of grafts, and prolongs survival in a rat model of Huntington's disease.

Zhu M, Shu K, Wang H, Li X, Xiao Q, Chan W, Emmanuel B, Jiang W, Lei T.

J Neurosci Res. 2013 Dec;91(12):1563-71. doi: 10.1002/jnr.23282.

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PUBMED

Huntington's disease: easing the NMDAR traffic jam.

Daggett A, Yang XW.

Nat Med. 2013 Aug;19(8):971-3. doi: 10.1038/nm.3283. No abstract available.

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PUBMED

Reliability and minimal detectable change of physical performance measures in individuals with pre-manifest and manifest Huntington disease.

Quinn L, Khalil H, Dawes H, Fritz NE, Kegelmeyer D, Kloos AD, Gillard JW, Busse M; Outcome Measures Subgroup of the European Huntington's Disease Network..

Phys Ther. 2013 Jul;93(7):942-56. doi: 10.2522/ptj.20130032.

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PUBMED

Morphometric analysis of Huntington's disease neurodegeneration in Drosophila.

Song W, Smith MR, Syed A, Lukacsovich T, Barbaro BA, Purcell J, Bornemann DJ, Burke J, Marsh JL.

Methods Mol Biol. 2013;1017:41-57. doi: 10.1007/978-1-62703-438-8_3.

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PUBMED

Acetylcholinesterase inhibitors in cognitive impairment in Huntington's disease: A brief review.

Vattakatuchery JJ, Kurien R.

World J Psychiatry. 2013 Sep 22;3(3):62-4. doi: 10.5498/wjp.v3.i3.62.

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PUBMED

Evaluation of exclusion prenatal and exclusion preimplantation genetic diagnosis for Huntington's disease in the Netherlands.

van Rij MC, de Die-Smulders CE, Bijlsma EK, de Wert GM, Geraedts JP, Roos RA, Tibben A.

Clin Genet. 2013 Feb;83(2):118-24. doi: 10.1111/cge.12058.

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PUBMED

Evidence-based guideline: pharmacologic treatment of chorea in Huntington disease: report of the Guideline Development Subcommittee of the American Academy of Neurology.

Suchowersky O, Armstrong MJ, Miyasaki J.

Neurology. 2013 Mar 5;80(10):970. doi: 10.1212/WNL.0b013e3182885eb3. No abstract available.

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PUBMED

Hypothalamic expression of mutant huntingtin contributes to the development of depressive-like behavior in the BAC transgenic mouse model of Huntington's disease.

Hult Lundh S, Nilsson N, Soylu R, Kirik D, Petersén Å.

Hum Mol Genet. 2013 Sep 1;22(17):3485-97. doi: 10.1093/hmg/ddt203.

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PUBMED

A review of cognition in Huntington's disease.

Dumas EM, van den Bogaard SJ, Middelkoop HA, Roos RA.

Front Biosci (Schol Ed). 2013 Jan 1;5:1-18. Review.

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PUBMED

Dysregulation of mitochondrial calcium signaling and superoxide flashes cause mitochondrial genomic DNA damage in Huntington disease.

Wang JQ, Chen Q, Wang X, Wang QC, Wang Y, Cheng HP, Guo C, Sun Q, Chen Q, Tang TS.

J Biol Chem. 2013 Feb 1;288(5):3070-84. doi: 10.1074/jbc.M112.407726.

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PUBMED

Grasping the grey: patient understanding and interpretation of an intermediate allele predictive test result for Huntington disease."

Semaka A, Balneaves LG, Hayden MR.

J Genet Couns. 2013 Apr;22(2):200-17. doi: 10.1007/s10897-012-9533-7.

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PUBMED

The personal experience of parenting a child with juvenile Huntington's disease: perceptions across Europe.

Eatough V, Santini H, Eiser C, Goller ML, Krysa W, de Nicola ', Paduanello M, Petrollini M, Rakowicz M, Squitieri F, Tibben A, Weille KL, Landwehrmeyer B, Quarrell O, Smith JA.

Eur J Hum Genet. 2013 Oct;21(10):1042-8. doi: 10.1038/ejhg.2013.15.

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PUBMED

The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients.

Metzger S, Walter C, Riess O, Roos RA, Nielsen JE, Craufurd D; REGISTRY Investigators of the European Huntington’s Disease Network., Nguyen HP.

PLoS One. 2013 Jul 22;8(7):e68951. doi: 10.1371/journal.pone.0068951.

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