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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

4411 ARTíCULOS , VIENDO DEL 4201 AL 4215

PUBMED

Defective mitochondrial disulfide relay system, altered mitochondrial morphology and function in Huntington's disease.

Napoli E, Wong S, Hung C, Ross-Inta C, Bomdica P, Giulivi C.

Hum Mol Genet. 2013 Mar 1;22(5):989-1004. doi: 10.1093/hmg/dds503.

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PUBMED

Amyotrophic lateral sclerosis and Huntington's disease: neurodegenerative link or coincidence?

Chhetri SK, Dayanandan R, Bindman D, Craufurd D, Majeed T.

Amyotroph Lateral Scler Frontotemporal Degener. 2014 Mar;15(1-2):145-7. doi: 10.3109/21678421.2013.817586. No abstract available.

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PUBMED

Huntington's disease: progress toward effective disease-modifying treatments and a cure.

Johnson CD, Davidson BL.

Hum Mol Genet. 2010 Apr 15;19(R1):R98-R102. doi: 10.1093/hmg/ddq148. Review.

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PUBMED

Anesthetic management of patients with Huntington disease.

Kivela JE, Sprung J, Southorn PA, Watson JC, Weingarten TN.

Anesth Analg. 2010 Feb 1;110(2):515-23. doi: 10.1213/ANE.0b013e3181c88fcd.

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PUBMED

Neuroendocrine evidence of normal hypothalamus-pituitary dopaminergic function in Huntington's disease.

Markianos M, Panas M, Kalfakis N, Hatzimanolis J, Vassilopoulos D.

Neuro Endocrinol Lett. 2010;31(3):359-62.

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PUBMED

Copy-number variation of the neuronal glucose transporter gene SLC2A3 and age of onset in Huntington's disease.

Vittori A, Breda C, Repici M, Orth M, Roos RA, Outeiro TF, Giorgini F, Hollox EJ; REGISTRY investigators of the European Huntington's Disease Network..

Hum Mol Genet. 2014 Jun 15;23(12):3129-37. doi: 10.1093/hmg/ddu022.

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PUBMED

Multiple Aspects of Gene Dysregulation in Huntington's Disease.

Moumné L, Betuing S, Caboche J.

Front Neurol. 2013 Oct 23;4:127. doi: 10.3389/fneur.2013.00127. Review.

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PUBMED

Abnormal mitochondrial dynamics, mitochondrial loss and mutant huntingtin oligomers in Huntington's disease: implications for selective neuronal damage.

Shirendeb U, Reddy AP, Manczak M, Calkins MJ, Mao P, Tagle DA, Reddy PH.

Hum Mol Genet. 2011 Apr 1;20(7):1438-55. doi: 10.1093/hmg/ddr024.

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PUBMED

A futility study of minocycline in Huntington's disease.

Huntington Study Group DOMINO Investigators..

Mov Disord. 2010 Oct 15;25(13):2219-24. doi: 10.1002/mds.23236.

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PUBMED

Stewarding Hope: The Evolving Landscape of Huntington's Disease Science Communications.

Yohrling GJ, Vetter LA.

J Huntingtons Dis. 2017 Jan 24. doi: 10.3233/JHD-160230. [Epub ahead of print]

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PUBMED

[Periodontitis determining the onset and progression of Huntington's disease: review of the literature].

Rodríguez Coyago ML, Sánchez Temiño VE.

Medwave. 2015 Oct 27;15(9):e6293. doi: 10.5867/medwave.2015.09.6293. Review. Spanish.

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PUBMED

Structural and functional brain network correlates of depressive symptoms in premanifest Huntington's disease.

McColgan P, Razi A, Gregory S, Seunarine KK, Durr A, A C Roos R, Leavitt BR, Scahill RI, Clark CA, Langbehn DR, Rees G, Tabrizi SJ; Track On-HD Investigators..

Hum Brain Mapp. 2017 Mar 15. doi: 10.1002/hbm.23527. [Epub ahead of print]

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PUBMED

Is Huntington disease a developmental disorder?

Humbert S.

EMBO Rep. 2010 Dec;11(12):899. doi: 10.1038/embor.2010.182. No abstract available.

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PUBMED

Poor insight into memory impairment in patients with Huntington disease.

Sitek EJ, Sołtan W, Robowski P, Schinwelski M, Wieczorek D, Sławek J.

Neurol Neurochir Pol. 2012 Jul-Aug;46(4):318-25.

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