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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 1 AL 15

PUBMED

Xeroderma pigmentosum complementation group F: A rare cause of cerebellar ataxia with chorea.

Carré G, Marelli C, Anheim M, Geny C, Renaud M, Rezvani HR, Koenig M, Guissart C, Tranchant C.

J Neurol Sci. 2017 May 15;376:198-201. doi: 10.1016/j.jns.2017.03.021. Epub 2017 Mar 16.

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PUBMED

Selective Sparing of Striatal Interneurons after Poly (ADP-Ribose) Polymerase 1 Inhibition in the R6/2 Mouse Model of Huntington's Disease.

Paldino E, Cardinale A, D'Angelo V, Sauve I, Giampà C, Fusco FR.

Front Neuroanat. 2017 Aug 2;11:61. doi: 10.3389/fnana.2017.00061. eCollection 2017.

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Molecular insights into cortico-striatal miscommunications in Huntington's disease.

Veldman MB, Yang XW.

Curr Opin Neurobiol. 2017 Nov 7;48:79-89. doi: 10.1016/j.conb.2017.10.019. [Epub ahead of print] Review.

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Novel VPS13A Gene Mutations Identified in Patients Diagnosed with Chorea-acanthocytosis (ChAc): Case Presentation and Literature Review.

Shen Y, Liu X, Long X, Han C, Wan F, Fan W, Guo X, Ma K, Guo S, Wang L, Xia Y, Liu L, Huang J, Lin Z, Xiong N, Wang T.

Front Aging Neurosci. 2017 Apr 12;9:95. doi: 10.3389/fnagi.2017.00095. eCollection 2017.

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[Hope for Huntington's disease patients: first clinical gene silencing study in progress].

Rollnik JD.

Fortschr Neurol Psychiatr. 2017 Aug;85(8):463-466. doi: 10.1055/s-0043-108061. Epub 2017 Aug 25. German.

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PUBMED

The views of adults with Huntington's disease on assisted dying: A qualitative exploration.

Regan L, Preston NJ, Eccles FJR, Simpson J.

Palliat Med. 2017 Nov 1:269216317741850. doi: 10.1177/0269216317741850. [Epub ahead of print]

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PUBMED

Co-occurring frontal variant Alzheimer's dementia and carrier of Huntington's disease allele with reduced penetrance.

Rawtaer I, Krishnamoorthy A.

Psychogeriatrics. 2017 Jan 27. doi: 10.1111/psyg.12246. [Epub ahead of print] No abstract available.

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PUBMED

Striatal synaptic dysfunction and altered calcium regulation in Huntington disease.

Raymond LA.

Biochem Biophys Res Commun. 2017 Feb 19;483(4):1051-1062. doi: 10.1016/j.bbrc.2016.07.058. Review.

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PUBMED

Functional neuroimaging and chorea: a systematic review.

Ehrlich DJ, Walker RH.

J Clin Mov Disord. 2017 Jun 21;4:8. doi: 10.1186/s40734-017-0056-0. eCollection 2017. Review.

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PUBMED

Treatment of Agitation in Huntington's Disease With Electroconvulsive Therapy.

Shah RP, Alluri V, Sharma S.

J Neuropsychiatry Clin Neurosci. 2017 Jan 25:appineuropsych16080161. doi: 10.1176/appi.neuropsych.16080161. [Epub ahead of print] No abstract available.

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PUBMED

Pramipexole reduces soluble mutant huntingtin and protects striatal neurons through dopamine D3 receptors in a genetic model of Huntington's disease.

Luis-Ravelo D, Estévez-Silva H, Barroso-Chinea P, Afonso-Oramas D, Salas-Hernández J, Rodríguez-Núñez J, Acevedo-Arozena A, Marcellino D, González-Hernández T.

Exp Neurol. 2017 Oct 19. pii: S0014-4886(17)30279-0. doi: 10.1016/j.expneurol.2017.10.019. [Epub ahead of print]

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PUBMED

Huntington's Disease like 2 presenting with isolated Parkinsonism.

Vasconcellos LF, Macêdo PJ, Franck JB, Tumas V, Marques Júnior W, Spitz M.

J Neurol Sci. 2017 Feb 15;373:105-106. doi: 10.1016/j.jns.2016.11.050. No abstract available.

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PUBMED

The pathogenic exon 1 HTT protein is produced by incomplete splicing in Huntington's disease patients.

Neueder A, Landles C, Ghosh R, Howland D, Myers RH, Faull RLM, Tabrizi SJ, Bates GP.

Sci Rep. 2017 May 2;7(1):1307. doi: 10.1038/s41598-017-01510-z.

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PUBMED

Recommendations for the Use of Automated Gray Matter Segmentation Tools: Evidence from Huntington's Disease.

Johnson EB, Gregory S, Johnson HJ, Durr A, Leavitt BR, Roos RA, Rees G, Tabrizi SJ, Scahill RI.

Front Neurol. 2017 Oct 10;8:519. doi: 10.3389/fneur.2017.00519. eCollection 2017.

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