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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 391 AL 405

PUBMED

Change in the cortical complexity of spinocerebellar ataxia type 3 appears earlier than clinical symptoms.

Wang TY, Jao CW, Soong BW, Wu HM, Shyu KK, Wang PS, Wu YT.

PLoS One. 2015 Apr 21;10(4):e0118828. doi: 10.1371/journal.pone.0118828.

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PUBMED

Efavirenz as a cause of ataxia in children.

Hauptfleisch MP, Moore DP, Rodda JL.

S Afr Med J. 2015 Nov;105(11):897-8. doi: 10.7196/SAMJ.2015.v105i11.9451.

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PUBMED

Biological and clinical characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline data.

Reetz K, Dogan I, Costa AS, Dafotakis M, Fedosov K, Giunti P, Parkinson MH, Sweeney MG, Mariotti C, Panzeri M, Nanetti L, Arpa J, Sanz-Gallego I, Durr A, Charles P, Boesch S, Nachbauer W, Klopstock T,

Lancet Neurol. 2015 Feb;14(2):174-82. doi: 10.1016/S1474-4422(14)70321-7.

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PUBMED

Small fiber neuropathy in a woman with fragile X-associated tremor/ataxia syndrome (FXTAS).

Chanson JB, Boehm N, Samama B, Echaniz-Laguna A, Anheim M.

J Neurol. 2015 Jan;262(1):226-7. doi: 10.1007/s00415-014-7597-z. No abstract available.

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PUBMED

Ataxia meets chorioretinal dystrophy and hypogonadism: Boucher-Neuhäuser syndrome due to PNPLA6 mutations.

Synofzik M, Kernstock C, Haack TB, Schöls L.

J Neurol Neurosurg Psychiatry. 2015 May;86(5):580-1. doi: 10.1136/jnnp-2014-307793. No abstract available.

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PUBMED

A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndrome.

Johnson JO, Stevanin G, van de Leemput J, Hernandez DG, Arepalli S, Forlani S, Zonozi R, Gibbs JR, Brice A, Durr A, Singleton AB.

Mov Disord. 2015 Feb;30(2):262-6. doi: 10.1002/mds.26059.

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PUBMED

Sensorimotor processing for balance in spinocerebellar ataxia type 6.

Bunn LM, Marsden JF, Voyce DC, Giunti P, Day BL.

Mov Disord. 2015 Aug;30(9):1259-66. doi: 10.1002/mds.26227.

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PUBMED

Diffusion tensor imaging and tract-based spatial statistics analysis in Friedreich's ataxia patients.

Vieira Karuta SC, Raskin S, de Carvalho Neto A, Gasparetto EL, Doring T, Teive HA.

Parkinsonism Relat Disord. 2015 May;21(5):504-8. doi: 10.1016/j.parkreldis.2015.02.021.

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PUBMED

[Diagnosis of Spinocerebellar Ataxia type 3 (Machado-Joseph disease) in Chile].

Miranda C M.

Rev Med Chil. 2015 Jan;143(1):126-7. doi: 10.4067/S0034-98872015000100019. Spanish. No abstract available.

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PUBMED

Friedreich ataxia in Norway - an epidemiological, molecular and clinical study.

Wedding IM, Kroken M, Henriksen SP, Selmer KK, Fiskerstrand T, Knappskog PM, Berge T, Tallaksen CM.

Orphanet J Rare Dis. 2015 Sep 4;10:108. doi: 10.1186/s13023-015-0328-4.

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PUBMED

Paroxysmal dysarthria ataxia syndrome responds to lacosamide.

Lilleker JB, Gall C, Dayanandan R, Chhetri SK, Emsley HC.

Mult Scler. 2015 Feb;21(2):256. doi: 10.1177/1352458514546792. No abstract available.

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PUBMED

From Mice to Men: TRPC3 in Cerebellar Ataxia.

Becker EB.

Cerebellum. 2015 Mar 14. [Epub ahead of print]

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PUBMED

A longitudinal study of the Friedreich Ataxia Impact Scale.

Tai G, Yiu EM, Corben LA, Delatycki MB.

J Neurol Sci. 2015 May 15;352(1-2):53-7. doi: 10.1016/j.jns.2015.03.024.

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PUBMED

Early and severe autonomic failure: broadening the clinical phenotype of type-2 spinocerebellar ataxia. A case report.

Capozzo R, Rizzo G, De Mari M, Tortorella C, Logroscino G.

J Neurol. 2015 Jan;262(1):224-5. doi: 10.1007/s00415-014-7577-3. No abstract available.

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PUBMED

Treatment for dysphagia (swallowing difficulties) in hereditary ataxia.

Vogel AP, Keage MJ, Johansson K, Schalling E.

Cochrane Database Syst Rev. 2015 Nov 13;(11):CD010169. doi: 10.1002/14651858.CD010169.pub2. Review.

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