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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

440 ARTíCULOS , VIENDO DEL 346 AL 360

PUBMED

Oral and dental health in Huntington's disease - an observational study.

Saft C, Andrich JE, Müller T, Becker J, Jackowski J.

BMC Neurol. 2013 Sep 3;13:114. doi: 10.1186/1471-2377-13-114.

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PUBMED

Refining the diagnosis of Huntington disease: the PREDICT-HD study.

Biglan KM, Zhang Y, Long JD, Geschwind M, Kang GA, Killoran A, Lu W, McCusker E, Mills JA, Raymond LA, Testa C, Wojcieszek J, Paulsen JS; PREDICT-HD Investigators of the Huntington Study Group..

Front Aging Neurosci. 2013 Apr 2;5:12. doi: 10.3389/fnagi.2013.00012.

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PUBMED

Acute rheumatic fever with chorea.

Buonuomo PS, Macchiaiolo M, Toscano A, De Benedetti F, Villani A, Bartuli A.

Arch Dis Child. 2013 Mar;98(3):203. doi: 10.1136/archdischild-2012-302732. No abstract available.

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PUBMED

Translational research in Huntington's disease: opening up for disease modifying treatment.

Burgunder JM.

Transl Neurodegener. 2013 Jan 25;2(1):2. doi: 10.1186/2047-9158-2-2.

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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

DNA repair mechanisms in Huntington's disease.

Jonson I, Ougland R, Larsen E.

Mol Neurobiol. 2013 Jun;47(3):1093-102. doi: 10.1007/s12035-013-8409-7. Review.

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PUBMED

Dendritic spine instability leads to progressive neocortical spine loss in a mouse model of Huntington's disease.

Murmu RP, Li W, Holtmaat A, Li JY.

J Neurosci. 2013 Aug 7;33(32):12997-3009. doi: 10.1523/JNEUROSCI.5284-12.2013.

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PUBMED

A broad phenotypic screen identifies novel phenotypes driven by a single mutant allele in Huntington's disease CAG knock-in mice.

Hölter SM, Stromberg M, Kovalenko M, Garrett L, Glasl L, Lopez E, Guide J, Götz A, Hans W, Becker L, Rathkolb B, Rozman J, Schrewed A, Klingenspor M, Klopstock T, Schulz H, Wolf E, Wursta W, Gillis T,

PLoS One. 2013 Nov 22;8(11):e80923. doi: 10.1371/journal.pone.0080923.

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PUBMED

[Chorea due to TITF1/NKX2-1 mutation: phenotypical description and therapeutic response in a family].

Salvado M, Boronat-Guerrero S, Hernández-Vara J, Álvarez-Sabin J.

Rev Neurol. 2013 May 16;56(10):515-20. Review. Spanish.

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PUBMED

De novo Huntington disease caused by 26-44 CAG repeat expansion on a low-risk haplotype.

Houge G, Bruland O, Bjørnevoll I, Hayden MR, Semaka A.

Neurology. 2013 Sep 17;81(12):1099-100. doi: 10.1212/WNL.0b013e3182a4a4af. No abstract available.

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PUBMED

Ethical issues and Huntington's disease.

Kromberg JG, Wessels TM.

S Afr Med J. 2013 Oct 11;103(12 Suppl 1):1023-6. doi: 10.7196/samj.7146.

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PUBMED

Huntington's disease: the road to progress.

Walker FO.

Lancet Neurol. 2013 Jul;12(7):624-5. doi: 10.1016/S1474-4422(13)70105-4. No abstract available.

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PUBMED

Doing the right thing for one's children: deciding whether to take the genetic test for Huntington's disease as a moral dilemma.

Smith JA, Stephenson M, Jacobs C, Quarrell O.

Clin Genet. 2013 May;83(5):417-21. doi: 10.1111/cge.12124.

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PUBMED

Why psychometrics is important - a response to: Aubeeluck, Buchanan & Stupple (2013) Journal of Huntington's Disease 2(4) 453-454.

Hagell P, Smith S.

J Huntingtons Dis. 2013;2(4):455-7. doi: 10.3233/JHD-139009. No abstract available.

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PUBMED

Small-molecule TrkB receptor agonists improve motor function and extend survival in a mouse model of Huntington's disease.

Jiang M, Peng Q, Liu X, Jin J, Hou Z, Zhang J, Mori S, Ross CA, Ye K, Duan W.

Hum Mol Genet. 2013 Jun 15;22(12):2462-70. doi: 10.1093/hmg/ddt098.

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