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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

5090 ARTíCULOS , VIENDO DEL 4261 AL 4275

PUBMED

Reagents that block neuronal death from Huntington's disease also curb oxidative stress.

Valencia A, Sapp E, Reeves PB, Alexander J, Masso N, Li X, Kegel KB, DiFiglia M.

Neuroreport. 2012 Jan 4;23(1):10-5. doi: 10.1097/WNR.0b013e32834d92e6.

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Altered lipid metabolism in Drosophila model of Huntington's disease.

Aditi K, Shakarad MN, Agrawal N.

Sci Rep. 2016 Aug 10;6:31411. doi: 10.1038/srep31411.

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PUBMED

Mouse Models for Validating Preclinical Candidates for Huntington’s Disease.

William Yang X, Gray M.

In: Lo DC, Hughes RE, editors. Neurobiology of Huntington's Disease: Applications to Drug Discovery. Boca Raton (FL): CRC Press/Taylor & Francis; 2011. Chapter 7.

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PUBMED

Cortical efferents lacking mutant huntingtin improve striatal neuronal activity and behavior in a conditional mouse model of Huntington's disease.

Estrada-Sánchez AM, Burroughs CL, Cavaliere S, Barton SJ, Chen S, Yang XW, Rebec GV.

J Neurosci. 2015 Mar 11;35(10):4440-51. doi: 10.1523/JNEUROSCI.2812-14.2015.

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Transcranial magnetic stimulation as a tool for understanding neurophysiology in Huntington's disease: a review.

Philpott AL, Fitzgerald PB, Cummins TD, Georgiou-Karistianis N.

Neurosci Biobehav Rev. 2013 Sep;37(8):1420-33. doi: 10.1016/j.neubiorev.2013.05.009. Review.

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Adult neural progenitor cells from Huntington's disease mouse brain exhibit increased proliferation and migration due to enhanced calcium and ROS signals.

Xie W, Wang JQ, Wang QC, Wang Y, Yao S, Tang TS.

Cell Prolif. 2015 Oct;48(5):517-31. doi: 10.1111/cpr.12205.

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Huntington's disease patients display progressive deficits in hippocampal-dependent cognition during a task of spatial memory.

Harris KL, Armstrong M, Swain R, Erzinclioglu S, Das T, Burgess N, Barker RA, Mason SL.

Cortex. 2019 Oct;119:417-427. doi: 10.1016/j.cortex.2019.07.014. Epub 2019 Aug 13.

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PUBMED

Genetics of Huntington disease.

Mahalingam S, Levy LM.

AJNR Am J Neuroradiol. 2014 Jun;35(6):1070-2. doi: 10.3174/ajnr.A3772. No abstract available.

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PUBMED

Targeting CAG repeat RNAs reduces Huntington's disease phenotype independently of huntingtin levels.

Rué L, Bañez-Coronel M, Creus-Muncunill J, Giralt A, Alcalá-Vida R, Mentxaka G, Kagerbauer B, Zomeño-Abellán MT, Aranda Z, Venturi V, Pérez-Navarro E, Estivill X, Martí E.

J Clin Invest. 2016 Nov 1;126(11):4319-4330. doi: 10.1172/JCI83185.

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PUBMED

Comparison of mHTT Antibodies in Huntington's Disease Mouse Models Reveal Specific Binding Profiles and Steady-State Ubiquitin Levels with Disease Development.

Bayram-Weston Z, Jones L, Dunnett SB, Brooks SP.

PLoS One. 2016 May 19;11(5):e0155834. doi: 10.1371/journal.pone.0155834.

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PUBMED

Stability of white matter changes related to Huntington's disease in the presence of imaging noise: a DTI study.

Müller HP, Glauche V, Novak MJ, Nguyen-Thanh T, Unrath A, Lahiri N, Read J, Say MJ, Tabrizi SJ, Kassubek J, Kloppel S.

PLoS Curr. 2011 Jun 7;3:RRN1232. doi: 10.1371/currents.RRN1232.

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Sleep-related modifications of EEG connectivity in the sensory-motor networks in Huntington Disease: An eLORETA study and review of the literature.

Piano C, Imperatori C, Losurdo A, Bentivoglio AR, Cortelli P, Della Marca G.

Clin Neurophysiol. 2016 Dec 5. pii: S1388-2457(16)30995-6. doi: 10.1016/j.clinph.2016.11.019. [Epub ahead of print]

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PUBMED

Assessment of Caregiver Burden in Huntington's Disease.

Yu M, Tan K, Koloms K, Bega D.

J Huntingtons Dis. 2018 Dec 24. doi: 10.3233/JHD-180326. [Epub ahead of print]

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PUBMED

Rhes deletion is neuroprotective in the 3-nitropropionic acid model of Huntington's disease.

Mealer RG, Subramaniam S, Snyder SH.

J Neurosci. 2013 Feb 27;33(9):4206-10. doi: 10.1523/JNEUROSCI.3730-12.2013.

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PUBMED

Mutant huntingtin, abnormal mitochondrial dynamics, defective axonal transport of mitochondria, and selective synaptic degeneration in Huntington's disease.

Reddy PH, Shirendeb UP.

Biochim Biophys Acta. 2012 Feb;1822(2):101-10. doi: 10.1016/j.bbadis.2011.10.016. Review.

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