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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

347 ARTíCULOS , VIENDO DEL 76 AL 90

PUBMED

Skeletal Muscle Modulates Huntington's Disease Pathogenesis in Mice: Role of Physical Exercise.

Corrochano S, Blanco G, Acevedo-Arozena A.

J Exp Neurosci. 2018 Oct 30;12:1179069518809059. doi: 10.1177/1179069518809059. eCollection 2018.

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PUBMED

Bilateral quinolinic acid-induced lipid peroxidation, decreased striatal monoamine levels and neurobehavioral deficits are ameliorated by GIP receptor agonist D-Ala(2)GIP in rat model of Huntington's disease.

Verma MK, Goel R, Nandakumar K, Nemmani KVS.

Eur J Pharmacol. 2018 Mar 22;828:31-41. doi: 10.1016/j.ejphar.2018.03.034. [Epub ahead of print]

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PUBMED

Early postnatal behavioral, cellular, and molecular changes in models of Huntington disease are reversible by HDAC inhibition.

Siebzehnrübl FA, Raber KA, Urbach YK, Schulze-Krebs A, Canneva F, Moceri S, Habermeyer J, Achoui D, Gupta B, Steindler DA, Stephan M, Nguyen HP, Bonin M, Riess O, Bauer A, Aigner L, Couillard-Despres

Proc Natl Acad Sci U S A. 2018 Aug 27. pii: 201807962. doi: 10.1073/pnas.1807962115. [Epub ahead of print]

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PUBMED

Risk factors of suicidal ideation in Huntington's disease: literature review and data from Enroll-HD.

Honrath P, Dogan I, Wudarczyk O, Görlich KS, Votinov M, Werner CJ, Schumann B, Overbeck RT, Schulz JB, Landwehrmeyer BG, Gur RE, Habel U, Reetz K; Enroll-HD investigators..

J Neurol. 2018 Aug 27. doi: 10.1007/s00415-018-9013-6. [Epub ahead of print]

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PUBMED

Mutant huntingtin reduction in astrocytes slows disease progression in the bachd conditional huntington's disease mouse model.

Wood TE, Barry J, Yang Z, Cepeda C, Levine MS, Gray M.

Hum Mol Genet. 2018 Oct 12. doi: 10.1093/hmg/ddy363. [Epub ahead of print]

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PUBMED

HttQ111/+ Huntington's Disease Knock-in Mice Exhibit Brain Region-Specific Morphological Changes and Synaptic Dysfunction.

Kovalenko M, Milnerwood A, Giordano J, St Claire J, Guide JR, Stromberg M, Gillis T, Sapp E, DiFiglia M, MacDonald ME, Carroll JB, Lee JM, Tappan S, Raymond L, Wheeler VC.

J Huntingtons Dis. 2018;7(1):17-33. doi: 10.3233/JHD-170282.

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PUBMED

Modulation of AMPA receptor surface diffusion restores hippocampal plasticity and memory in Huntington's disease models.

Zhang H, Zhang C, Vincent J, Zala D, Benstaali C, Sainlos M, Grillo-Bosch D, Daburon S, Coussen F, Cho Y, David DJ, Saudou F, Humeau Y, Choquet D.

Nat Commun. 2018 Oct 15;9(1):4272. doi: 10.1038/s41467-018-06675-3.

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PUBMED

The contribution of gender differences in motor, behavioral and cognitive features to functional capacity, independence and quality of life in patients with Huntington's disease.

Zielonka D, Ren M, De Michele G, Roos RAC, Squitieri F, Bentivoglio AR, Marcinkowski JT, Landwehrmeyer GB.

Parkinsonism Relat Disord. 2018 Jan 5. pii: S1353-8020(18)30006-3. doi: 10.1016/j.parkreldis.2018.01.006. [Epub ahead of print]

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PUBMED

Multiple clinical features of Huntington's disease correlate with mutant HTT gene CAG repeat lengths and neurodegeneration.

Podvin S, Reardon HT, Yin K, Mosier C, Hook V.

J Neurol. 2018 Jun 28. doi: 10.1007/s00415-018-8940-6. [Epub ahead of print] Review.

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PUBMED

Deubiquitinase Usp12 functions noncatalytically to induce autophagy and confer neuroprotection in models of Huntington's disease.

Aron R, Pellegrini P, Green EW, Maddison DC, Opoku-Nsiah K, Wong JS, Daub AC, Giorgini F, Finkbeiner S.

Nat Commun. 2018 Sep 28;9(1):3191. doi: 10.1038/s41467-018-05653-z.

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PUBMED

Structural and metabolic brain correlates of apathy in Huntington's disease.

Martínez-Horta S, Perez-Perez J, Sampedro F, Pagonabarraga J, Horta-Barba A, Carceller-Sindreu M, Gomez-Anson B, Lozano-Martinez GA, Lopez-Mora DA, Camacho V, Fernández-León A, Carrió I, Kulisevsky J.

Mov Disord. 2018 Jul;33(7):1151-1159. doi: 10.1002/mds.27395. Epub 2018 Apr 20.

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PUBMED

Chorea-Acanthocytosis Presenting as Autosomal Recessive Epilepsy in a Family With a Novel VPS13A Mutation.

Weber J, Frings L, Rijntjes M, Urbach H, Fischer J, Weiller C, Meyer PT, Klebe S.

Front Neurol. 2019 Jan 9;9:1168. doi: 10.3389/fneur.2018.01168. eCollection 2018.

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PUBMED

Salivary levels of total huntingtin are elevated in Huntington's disease patients.

Corey-Bloom J, Haque AS, Park S, Nathan AS, Baker RW, Thomas EA.

Sci Rep. 2018 May 9;8(1):7371. doi: 10.1038/s41598-018-25095-3.

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PUBMED

Medication Management Capacity and Its Neurocognitive Correlates in Huntington's Disease.

Sumida CA, Van Etten EJ, Lopez FV, Sheppard DP, Pirogovsky-Turk E, Corey-Bloom J, Filoteo JV, Woods SP, Gilbert PE, Schmitter-Edgecombe M.

Arch Clin Neuropsychol. 2018 Dec 5. doi: 10.1093/arclin/acy093. [Epub ahead of print]

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PUBMED

Correction of Huntington's Disease Phenotype by Genistein-Induced Autophagy in the Cellular Model.

Pierzynowska K, Gaffke L, Hać A, Mantej J, Niedziałek N, Brokowska J, Węgrzyn G.

Neuromolecular Med. 2018 Feb 12. doi: 10.1007/s12017-018-8482-1. [Epub ahead of print]

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