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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 46 AL 60

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

Bilateral Chorea Associated with Acute Caudate Nucleus Infarctions.

Qu Y, Jin H, Guo ZN, Zhang FL, Liu J, Qin HQ, Yang Y.

Can J Neurol Sci. 2019 Jun 14:1-2. doi: 10.1017/cjn.2019.50. [Epub ahead of print] No abstract available.

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PUBMED

Transcriptional correlates of the pathological phenotype in a Huntington's disease mouse model.

Gallardo-Orihuela A, Hervás-Corpión I, Hierro-Bujalance C, Sanchez-Sotano D, Jiménez-Gómez G, Mora-López F, Campos-Caro A, Garcia-Alloza M, Valor LM.

Sci Rep. 2019 Dec 10;9(1):18696. doi: 10.1038/s41598-019-55177-9.

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PUBMED

Aberrant brain network connectivity in presymptomatic and manifest Huntington's disease: A systematic review.

Pini L, Jacquemot C, Cagnin A, Meneghello F, Semenza C, Mantini D, Vallesi A.

Hum Brain Mapp. 2020 Jan;41(1):256-269. doi: 10.1002/hbm.24790. Epub 2019 Sep 18. Review.

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PUBMED

Alterations in the tyrosine and phenylalanine pathways revealed by biochemical profiling in cerebrospinal fluid of Huntington's disease subjects.

Herman S, Niemelä V, Emami Khoonsari P, Sundblom J, Burman J, Landtblom AM, Spjuth O, Nyholm D, Kultima K.

Sci Rep. 2019 Mar 11;9(1):4129. doi: 10.1038/s41598-019-40186-5.

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PUBMED

[Classification, differential diagnoses and therapy in patients with chorea].

Liu J, Wang LN.

Zhonghua Nei Ke Za Zhi. 2019 Sep 1;58(9):692-695. doi: 10.3760/cma.j.issn.0578-1426.2019.09.012. Chinese.

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PUBMED

Manganese Acts upon Insulin/IGF Receptors to Phosphorylate AKT and Increase Glucose Uptake in Huntington's Disease Cells.

Bryan MR, Nordham KD, Rose DIR, O'Brien MT, Joshi P, Foshage AM, Gonçalves FM, Nitin R, Uhouse MA, Aschner M, Bowman AB.

Mol Neurobiol. 2019 Dec 4. doi: 10.1007/s12035-019-01824-1. [Epub ahead of print]

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PUBMED

Enhanced cerebral branched-chain amino acid metabolism in R6/2 mouse model of Huntington's disease.

Andersen JV, Skotte NH, Aldana BI, Nørremølle A, Waagepetersen HS.

Cell Mol Life Sci. 2019 Mar 4. doi: 10.1007/s00018-019-03051-2. [Epub ahead of print]

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PUBMED

Striatal morphology and neurocognitive dysfunction in Huntington disease: The IMAGE-HD study.

Wilkes FA, Abaryan Z, Ching CRK, Gutman BA, Madsen SK, Walterfang M, Velakoulis D, Stout JC, Chua P, Egan GF, Thompson PM, Looi JCL, Georgiou-Karistianis N.

Psychiatry Res Neuroimaging. 2019 Sep 30;291:1-8. doi: 10.1016/j.pscychresns.2019.07.003. Epub 2019 Jul 12.

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PUBMED

Early epigenomic and transcriptional changes reveal Elk-1 transcription factor as a therapeutic target in Huntington's disease.

Yildirim F, Ng CW, Kappes V, Ehrenberger T, Rigby SK, Stivanello V, Gipson TA, Soltis AR, Vanhoutte P, Caboche J, Housman DE, Fraenkel E.

Proc Natl Acad Sci U S A. 2019 Dec 3;116(49):24840-24851. doi: 10.1073/pnas.1908113116. Epub 2019 Nov 19.

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PUBMED

Cross-Sectional Area Analysis of the Head of the Caudate Nucleus in Huntington's Disease.

Furukawa F, Ishikawa K, Yokota T, Sanjo N.

Eur Neurol. 2019 Apr 23;81(1-2):13-18. doi: 10.1159/000499909. [Epub ahead of print]

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PUBMED

27 years of prenatal diagnosis for Huntington disease in the United Kingdom.

Piña-Aguilar RE, Simpson SA, Alshatti A, Clarke A, Craufurd D, Dorkins H, Doye K, Lahiri N, Lashwood A, Lynch C, Miller C, Morton S, O'Driscoll M, Quarrell OW, Rae D, Strong M, Tomlinson C, Turnpenny

Genet Med. 2019 Jul;21(7):1639-1643. doi: 10.1038/s41436-018-0367-z. Epub 2018 Dec 14.

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PUBMED

Exploration of a Co-Production Approach to Developing a Walking Group with People with Huntington's Disease.

Jones U, Hamana K, Vougioukalou S, Jones M, Busse M.

Med One. 2019;4(5):e190022. doi: 10.20900/mo.20190022. Epub 2019 Oct 31.

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PUBMED

Pervasive autobiographical memory impairments in Huntington's disease.

Carmichael AM, Irish M, Glikmann-Johnston Y, Singh P, Stout JC.

Neuropsychologia. 2019 Apr;127:123-130. doi: 10.1016/j.neuropsychologia.2019.02.017. Epub 2019 Feb 25.

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PUBMED

Astrocyte molecular signatures in Huntington's disease.

Diaz-Castro B, Gangwani MR, Yu X, Coppola G, Khakh BS.

Sci Transl Med. 2019 Oct 16;11(514). pii: eaaw8546. doi: 10.1126/scitranslmed.aaw8546.

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