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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

263 ARTíCULOS , VIENDO DEL 31 AL 45

PUBMED

One-year changes in brain microstructure differentiate preclinical Huntington's disease stages.

Pflanz CP, Charquero-Ballester M, Majid DSA, Winkler AM, Vallée E, Aron AR, Jenkinson M, Douaud G.

Neuroimage Clin. 2019 Dec 3;25:102099. doi: 10.1016/j.nicl.2019.102099. [Epub ahead of print]

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PUBMED

Motivational Impairment is Accompanied by Corticoaccumbal Dysfunction in the BACHD-Tg5 Rat Model of Huntington's Disease.

Zlebnik NE, Gildish I, Sesia T, Fitoussi A, Cole EA, Carson BP, Cachope R, Cheer JF.

Cereb Cortex. 2019 Dec 17;29(11):4763-4774. doi: 10.1093/cercor/bhz009.

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PUBMED

HTT haplogroups in Finnish patients with Huntington disease.

Ylönen S, Sipilä JOT, Hietala M, Majamaa K.

Neurol Genet. 2019 Apr 22;5(3):e334. doi: 10.1212/NXG.0000000000000334. eCollection 2019 Jun.

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PUBMED

Bim contributes to the progression of Huntington's disease-associated phenotypes.

Roberts SL, Evans T, Yang Y, Fu Y, Button RW, Sipthorpe RJ, Cowan K, Valionyte E, Anichtchik O, Li H, Lu B, Luo S.

Hum Mol Genet. 2019 Dec 9. pii: ddz275. doi: 10.1093/hmg/ddz275. [Epub ahead of print]

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PUBMED

Hypomorphic mutation of the mouse Huntington's disease gene orthologue.

Murthy V, Tebaldi T, Yoshida T, Erdin S, Calzonetti T, Vijayvargia R, Tripathi T, Kerschbamer E, Seong IS, Quattrone A, Talkowski ME, Gusella JF, Georgopoulos K, MacDonald ME, Biagioli M.

PLoS Genet. 2019 Mar 21;15(3):e1007765. doi: 10.1371/journal.pgen.1007765. [Epub ahead of print]

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PUBMED

Mild cognitive impairment and dementia in motor manifest Huntington's disease: Classification and prevalence.

Julayanont P, McFarland NR, Heilman KM.

J Neurol Sci. 2020 Jan 15;408:116523. doi: 10.1016/j.jns.2019.116523. Epub 2019 Oct 15.

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PUBMED

Validation of Neuro-QoL and PROMIS Mental Health Patient Reported Outcome Measures in Persons with Huntington Disease.

Carlozzi NE, Goodnight S, Kratz AL, Stout JC, McCormack MK, Paulsen JS, Boileau NR, Cella D, Ready RE.

J Huntingtons Dis. 2019 Aug 16. doi: 10.3233/JHD-190364. [Epub ahead of print]

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PUBMED

Coeliac disease presenting with chorea.

Lefter S, Corcoran L, McAuliffe E, Khan R, Burke L, Regan M, Hadjivassiliou M.

Pract Neurol. 2019 Nov 28. pii: practneurol-2019-002396. doi: 10.1136/practneurol-2019-002396. [Epub ahead of print]

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PUBMED

Huntingtin Lowering Strategies for Disease Modification in Huntington's Disease.

Tabrizi SJ, Ghosh R, Leavitt BR.

Neuron. 2019 Mar 6;101(5):801-819. doi: 10.1016/j.neuron.2019.01.039. Review.

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PUBMED

Genetic cooperativity in multi-layer networks implicates cell survival and senescence in the striatum of Huntington's disease mice synchronous to symptoms.

Bigan E, Sasidharan Nair S, Lejeune FX, Fragnaud H, Parmentier F, Mégret L, Verny M, Aaronson J, Rosinski J, Neri C.

Bioinformatics. 2020 Jan 1;36(1):186-196. doi: 10.1093/bioinformatics/btz514.

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PUBMED

Adult-onset Huntington disease: An update.

[No authors listed]

Nursing. 2019 Jul;49(7):43-44. doi: 10.1097/01.NURSE.0000569736.14018.ce. No abstract available.

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PUBMED

A Systematic Review of Rehabilitation for Corticobulbar Symptoms in Adults with Huntington's Disease.

Burnip E, Wallace E, Gozdzikowska K, Huckabee ML.

J Huntingtons Dis. 2019 Nov 11. doi: 10.3233/JHD-190384. [Epub ahead of print]

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PUBMED

'I have a feeling I can't speak to anybody': A thematic analysis of communication perspectives in people with Huntington's disease.

Zarotti N, Simpson J, Fletcher I.

Chronic Illn. 2019 Mar;15(1):61-73. doi: 10.1177/1742395317733793. Epub 2017 Sep 29.

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PUBMED

Cognitive Screening Tests in Huntington Gene Mutation Carriers: Examining the Validity of the Mini-Mental State Examination and the Montreal Cognitive Assessment.

Ringkøbing SP, Larsen IU, Jørgensen K, Vinther-Jensen T, Vogel A.

J Huntingtons Dis. 2019 Oct 21. doi: 10.3233/JHD-190350. [Epub ahead of print]

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PUBMED

Treatment with JQ1, a BET bromodomain inhibitor, is selectively detrimental to R6/2 Huntington's disease mice.

Kedaigle AJ, Reidling JC, Lim RG, Adam M, Wu J, Wassie B, Stocksdale JT, Casale MS, Fraenkel E, Thompson LM.

Hum Mol Genet. 2019 Nov 7. pii: ddz264. doi: 10.1093/hmg/ddz264. [Epub ahead of print]

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