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Bibliografía Científica

Artículos por temáticas

En este apartado encontrará una actualización mensual de artículos sobre Trastornos del Movimiento clasificados según los 11 tipos establecidos por la International Parkinson & Movement Disorder Society.

Distonía

269 ARTíCULOS , VIENDO DEL 121 AL 135

PUBMED

Variant ataxia-telangiectasia presenting as primary-appearing dystonia in Canadian Mennonites.

Saunders-Pullman R, Raymond D, Stoessl AJ, Hobson D, Nakamura K, Pullman S, Lefton D, Okun MS, Uitti R, Sachdev R, Stanley K, San Luciano M, Hagenah J, Gatti R, Ozelius LJ, Bressman SB.

Neurology. 2012 Feb 28;78(9):649-57. doi: 10.1212/WNL.0b013e3182494d51. Erratum in: Neurology. 2012 Mar 27;78(13):1029. Nakamura, T [corrected to Nakamura, K].

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PUBMED

Toward a network model of dystonia.

Hendrix CM, Vitek JL.

Ann N Y Acad Sci. 2012 Aug;1265:46-55. doi: 10.1111/j.1749-6632.2012.06692.x.

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PUBMED

White matter abnormalities in gene-positive myoclonus-dystonia.

van der Meer JN, Beukers RJ, van der Salm SM, Caan MW, Tijssen MA, Nederveen AJ.

Mov Disord. 2012 Nov;27(13):1666-72. doi: 10.1002/mds.25128.

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Five-year follow-up of 10 patients treated with globus pallidus internus deep brain stimulation for segmental or multisegmental dystonia.

Sarubbo S, Latini F, Quatrale R, Sensi M, Granieri E, Cavallo MA.

Stereotact Funct Neurosurg. 2012;90(2):84-91. doi: 10.1159/000335706.

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PUBMED

Setting realistic expectations for DBS in dystonia.

Okun MS, Foote KD.

Lancet Neurol. 2012 Dec;11(12):1014-5. doi: 10.1016/S1474-4422(12)70263-6. No abstract available.

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PUBMED

Occurrence of GCH1 gene mutations in a group of Indian dystonia patients.

Naiya T, Misra AK, Biswas A, Das SK, Ray K, Ray J.

J Neural Transm (Vienna). 2012 Nov;119(11):1343-50. doi: 10.1007/s00702-012-0777-z.

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PUBMED

A guide to dosing in the treatment of cervical dystonia and blepharospasm with Xeomin®: a new botulinum neurotoxin A.

Pagan FL, Harrison A.

Parkinsonism Relat Disord. 2012 Jun;18(5):441-5. doi: 10.1016/j.parkreldis.2012.02.008. Review.

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ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia.

Brashear A, Mink JW, Hill DF, Boggs N, McCall WV, Stacy MA, Snively B, Light LS, Sweadner KJ, Ozelius LJ, Morrison L.

Dev Med Child Neurol. 2012 Nov;54(11):1065-7. doi: 10.1111/j.1469-8749.2012.04421.x. Review.

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PUBMED

Plasticity of cortical inhibition in dystonia is impaired after motor learning and paired-associative stimulation.

Meunier S, Russmann H, Shamim E, Lamy JC, Hallett M.

Eur J Neurosci. 2012 Mar;35(6):975-86. doi: 10.1111/j.1460-9568.2012.08034.x.

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PUBMED

Painful cervical dystonia triggered by the extension wire of a deep brain stimulator.

Spagnolo F, Picozzi P, Franzin A, Martinelli V, Comi G, Volonte MA.

J Clin Neurosci. 2012 Nov;19(11):1582-3. doi: 10.1016/j.jocn.2011.11.040.

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PUBMED

Dystonia as a presenting feature of alcohol withdrawal.

Bijjal S, Subodh BN, Narayanaswamy JC, Chand P, Benegal V, Murthy P.

J Neuropsychiatry Clin Neurosci. 2012 Winter;24(1):E15-6. doi: 10.1176/appi.neuropsych.11010026. No abstract available.

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PUBMED

New algorithm for the diagnosis of hereditary dystonia.

Camargos S, Cardoso F.

Arq Neuropsiquiatr. 2012 Sep;70(9):715-7.

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Individuated finger control in focal hand dystonia: an fMRI study.

Moore RD, Gallea C, Horovitz SG, Hallett M.

Neuroimage. 2012 Jul 16;61(4):823-31. doi: 10.1016/j.neuroimage.2012.03.066.

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PUBMED

Surgical treatment for secondary dystonia.

Tierney TS, Lozano AM.

Mov Disord. 2012 Nov;27(13):1598-605. doi: 10.1002/mds.25204. Review.

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PUBMED

Abnormal nuclear envelopes in the striatum and motor deficits in DYT11 myoclonus-dystonia mouse models.

Yokoi F, Dang MT, Zhou T, Li Y.

Hum Mol Genet. 2012 Feb 15;21(4):916-25. doi: 10.1093/hmg/ddr528.

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