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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

307 ARTíCULOS , VIENDO DEL 181 AL 195

PUBMED

Abstracts from HSG 2016: Discovering Our Future, the 23rd Annual Meeting of the Huntington Study Group (HSG).

[No authors listed]

Neurotherapeutics. 2017 Jan;14(1):227-251. doi: 10.1007/s13311-016-0482-y. No abstract available.

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PUBMED

Motor phenotype is not associated with vascular dysfunction in symptomatic Huntington's disease transgenic R6/2 (160 CAG) mice.

Di Pardo A, Carrizzo A, Damato A, Castaldo S, Amico E, Capocci L, Ambrosio M, Pompeo F, De Sanctis C, Spinelli CC, Puca AA, Remondelli P, Maglione V, Vecchione C.

Sci Rep. 2017 Feb 17;7:42797. doi: 10.1038/srep42797.

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Safety and Exploratory Efficacy at 36 Months in Open-HART, an Open-Label Extension Study of Pridopidine in Huntington's Disease.

McGarry A, Kieburtz K, Abler V, Grachev ID, Gandhi S, Auinger P, Papapetropoulos S, Hayden M.

J Huntingtons Dis. 2017 Aug 12. doi: 10.3233/JHD-170241. [Epub ahead of print]

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Grey matter volume loss is associated with specific clinical motor signs in Huntington's disease.

Coppen EM, Jacobs M, van den Berg-Huysmans AA, van der Grond J, Roos RAC.

Parkinsonism Relat Disord. 2017 Nov 2. pii: S1353-8020(17)30424-8. doi: 10.1016/j.parkreldis.2017.11.001. [Epub ahead of print]

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[Early Diagnosis of Chorea-Acanthocytosis: Orofacial Dyskinesia, Epileptic Seizures, and HyperCKemia].

Schneider C, Danek A, Hostmann A, Fink GR, Burghaus L.

Fortschr Neurol Psychiatr. 2017 May;85(5):270-273. doi: 10.1055/s-0042-123042. Epub 2017 May 23. German.

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Cognitive decline in Huntington's disease expansion gene carriers.

Baake V, Reijntjes RHAM, Dumas EM, Thompson JC; REGISTRY Investigators of the European Huntington's Disease Network., Roos RAC.

Cortex. 2017 Aug 3;95:51-62. doi: 10.1016/j.cortex.2017.07.017. [Epub ahead of print]

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PUBMED

Suppression of MAPK11 or HIPK3 reduces mutant Huntingtin levels in Huntington's disease models.

Yu M, Fu Y, Liang Y, Song H, Yao Y, Wu P, Yao Y, Pan Y, Wen X, Ma L, Hexige S, Ding Y, Luo S, Lu B.

Cell Res. 2017 Dec;27(12):1441-1465. doi: 10.1038/cr.2017.113. Epub 2017 Oct 13.

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PUBMED

Molecular Imaging Markers to Track Huntington's Disease Pathology.

Wilson H, De Micco R, Niccolini F, Politis M.

Front Neurol. 2017 Jan 30;8:11. doi: 10.3389/fneur.2017.00011. eCollection 2017. Review.

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PUBMED

Sensory processing in Huntington's disease.

Mirallave A, Morales M, Cabib C, Muñoz EJ, Santacruz P, Gasull X, Valls-Sole J.

Clin Neurophysiol. 2017 May;128(5):689-696. doi: 10.1016/j.clinph.2017.01.009. Epub 2017 Feb 14.

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PUBMED

Huntington's disease-like 2 with an expansion mutation of the Junctophilin-3 gene; first reported case from Botswana.

Ocampo C, Daimari R, Oyekunle AA.

J Clin Neurosci. 2017 Oct 21. pii: S0967-5868(17)31493-5. doi: 10.1016/j.jocn.2017.10.025. [Epub ahead of print]

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PUBMED

Palliative Care in Huntington Disease: Personal Reflections and a Review of the Literature.

Tarolli CG, Chesire AM, Biglan KM.

Tremor Other Hyperkinet Mov (N Y). 2017 Apr 11;7:454. doi: 10.7916/D88057C7. eCollection 2017. Review.

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Neurofilament light protein in CSF and blood is associated with neurodegeneration and disease severity in Huntington's disease R6/2 mice.

Soylu-Kucharz R, Sandelius Å, Sjögren M, Blennow K, Wild EJ, Zetterberg H, Björkqvist M.

Sci Rep. 2017 Oct 26;7(1):14114. doi: 10.1038/s41598-017-14179-1.

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PUBMED

A randomized, double-blind, placebo-controlled trial evaluating cysteamine in Huntington's disease.

Verny C, Bachoud-Lévi AC, Durr A, Goizet C, Azulay JP, Simonin C, Tranchant C, Calvas F, Krystkowiak P, Charles P, Youssov K, Scherer C, Prundean A, Olivier A, Reynier P, Saudou F, Maison P, Allain P,

Mov Disord. 2017 Apr 24. doi: 10.1002/mds.27010. [Epub ahead of print]

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Identify Huntington's disease associated genes based on restricted Boltzmann machine with RNA-seq data.

Jiang X, Zhang H, Duan F, Quan X.

BMC Bioinformatics. 2017 Oct 11;18(1):447. doi: 10.1186/s12859-017-1859-6.

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1993-2014: two decades of predictive testing for Huntington's disease at the Medical Genetics Unit of the University of Genoa.

Mandich P, Lamp M, Gotta F, Gulli R, Iacometti A, Marchese R, Bellone E, Abbruzzese G, Ferrandes G.

Mol Genet Genomic Med. 2017 Jun 17;5(5):473-480. doi: 10.1002/mgg3.238. eCollection 2017 Sep.

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