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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.

Ataxia

408 ARTíCULOS , VIENDO DEL 16 AL 30

PUBMED

Functional connectivity changes related to cognitive and motor performance in spinocerebellar ataxia type 2.

Hernandez-Castillo CR, Galvez V, Mercadillo RE, Díaz R, Yescas P, Martinez L, Ochoa A, Velazquez-Perez L, Fernandez-Ruiz J.

Mov Disord. 2015 Sep;30(10):1391-9. doi: 10.1002/mds.26320.

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Strategy use, planning, and rule acquisition deficits in spinocerebellar ataxia type 2 patients.

Vaca-Palomares I, Díaz R, Rodríguez-Labrada R, Medrano-Montero J, Aguilera-Rodríguez R, Vázquez-Mojena Y, Fernandez-Ruiz J, Velázquez-Pérez L.

J Int Neuropsychol Soc. 2015 Mar;21(3):214-20. doi: 10.1017/S1355617715000132.

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Balance outcome measures in cerebellar ataxia: a Delphi survey.

Winser SJ, Smith C, Hale LA, Claydon LS, Whitney SL.

Disabil Rehabil. 2015;37(2):165-70. doi: 10.3109/09638288.2014.913709.

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Novel SACS mutation in autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Sánchez MG, Pérez JE, Pérez MR, Redondo AG.

J Neurol Sci. 2015 Nov 15;358(1-2):475-6. doi: 10.1016/j.jns.2015.08.032. No abstract available.

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Abnormalities in synaptic dynamics during development in a mouse model of spinocerebellar ataxia type 1.

Hatanaka Y, Watase K, Wada K, Nagai Y.

Sci Rep. 2015 Nov 4;5:16102. doi: 10.1038/srep16102.

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Loss of the neuron-specific F-box protein FBXO41 models an ataxia-like phenotype in mice with neuronal migration defects and degeneration in the cerebellum.

Mukherjee C, Holubowska A, Schwedhelm-Domeyer N, Mitkovski M, Lee SJ, Kannan M, Matz A, Vadhvani M, Stegmüller J.

J Neurosci. 2015 Jun 10;35(23):8701-17. doi: 10.1523/JNEUROSCI.2133-14.2015.

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The Yield of Neuroimaging in Children Presenting to the Emergency Department With Acute Ataxia in the Post-Varicella Vaccine Era.

Rudloe T, Prabhu SP, Gorman MP, Nigrovic LE, Harper MB, Landschaft A, Kimia AA.

J Child Neurol. 2015 Sep;30(10):1333-9. doi: 10.1177/0883073814561300.

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PUBMED

The 3-second rule in hereditary pure cerebellar ataxia: a synchronized tapping study.

Matsuda S, Matsumoto H, Furubayashi T, Hanajima R, Tsuji S, Ugawa Y, Terao Y.

PLoS One. 2015 Feb 23;10(2):e0118592. doi: 10.1371/journal.pone.0118592.

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PUBMED

Ataxia.

Akbar U, Ashizawa T.

Neurol Clin. 2015 Feb;33(1):225-48. doi: 10.1016/j.ncl.2014.09.004. Review.

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First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy.

Smets K, Duarri A, Deconinck T, Ceulemans B, van de Warrenburg BP, Züchner S, Gonzalez MA, Schüle R, Synofzik M, Van der Aa N, De Jonghe P, Verbeek DS, Baets J.

BMC Med Genet. 2015 Jul 21;16:51. doi: 10.1186/s12881-015-0200-3.

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Broad distribution of ataxin 1 silencing in rhesus cerebella for spinocerebellar ataxia type 1 therapy.

Keiser MS, Kordower JH, Gonzalez-Alegre P, Davidson BL.

Brain. 2015 Dec;138(Pt 12):3555-66. doi: 10.1093/brain/awv292.

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'You don't get told anything, they don't do anything and nothing changes'. Medicine as a resource and constraint in progressive ataxia.

Daker-White G, Kingston H, Payne K, Greenfield J, Ealing J, Sanders C.

Health Expect. 2015 Apr;18(2):177-87. doi: 10.1111/hex.12016.

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Miller-Fisher Syndrome: Is the ataxia central or peripheral?

Sandler RD, Hoggard N, Hadjivassiliou M.

Cerebellum Ataxias. 2015 Mar 1;2:3. doi: 10.1186/s40673-015-0021-3.

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PUBMED

Risk of Atherosclerosis in Patients with Ataxia Telangiectasia.

Andrade IG, Costa-Carvalho BT, da Silva R, Hix S, Kochi C, Suano-Souza FI, Sarni RO.

Ann Nutr Metab. 2015;66(4):196-201. doi: 10.1159/000430790.

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Cycling regimen induces spinal circuitry plasticity and improves leg muscle coordination in individuals with spinocerebellar ataxia.

Chang YJ, Chou CC, Huang WT, Lu CS, Wong AM, Hsu MJ.

Arch Phys Med Rehabil. 2015 Jun;96(6):1006-13. doi: 10.1016/j.apmr.2015.01.021.

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