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Bibliografía Científica

Artículo Destacado en trastornos del movimiento

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

443 ARTíCULOS , VIENDO DEL 91 AL 105

PUBMED

Ion channel disorders: still a fascinating topic--news on episodic ataxia type 1.

Strupp M.

J Neurol Neurosurg Psychiatry. 2013 Oct;84(10):1063-4. doi: 10.1136/jnnp-2012-304857. No abstract available.

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PUBMED

Altered GABAergic system in the living brain of a patient with spinocerebellar ataxia type 8.

Terada T, Kono S, Konishi T, Miyajima H, Ouchi Y.

J Neurol. 2013 Dec;260(12):3164-6. doi: 10.1007/s00415-013-7167-9. No abstract available.

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PUBMED

Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxia.

Hick A, Wattenhofer-Donzé M, Chintawar S, Tropel P, Simard JP, Vaucamps N, Gall D, Lambot L, André C, Reutenauer L, Rai M, Teletin M, Messaddeq N, Schiffmann SN, Viville S, Pearson CE, Pandolfo M, Puc

Dis Model Mech. 2013 May;6(3):608-21. doi: 10.1242/dmm.010900.

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PUBMED

Reducing mitochondrial ROS improves disease-related pathology in a mouse model of ataxia-telangiectasia.

D'Souza AD, Parish IA, Krause DS, Kaech SM, Shadel GS.

Mol Ther. 2013 Jan;21(1):42-8. doi: 10.1038/mt.2012.203.

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PUBMED

Teaching neuroimages: ataxia and diabetes insipidus.

Lefaucheur R, Maltête D, Haroche J, Borden A, Wallon D, Bourre B.

Neurology. 2013 Jul 16;81(3):e19. doi: 10.1212/WNL.0b013e31829bfe0a. No abstract available.

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PUBMED

Generation and validation of a zebrafish model of EAST (epilepsy, ataxia, sensorineural deafness and tubulopathy) syndrome.

Mahmood F, Mozere M, Zdebik AA, Stanescu HC, Tobin J, Beales PL, Kleta R, Bockenhauer D, Russell C.

Dis Model Mech. 2013 May;6(3):652-60. doi: 10.1242/dmm.009480.

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PUBMED

Speech in spinocerebellar ataxia.

Schalling E, Hartelius L.

Brain Lang. 2013 Dec;127(3):317-22. doi: 10.1016/j.bandl.2013.10.002. Review.

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PUBMED

Marked inhibition of Na+, K(+)- ATPase activity and the respiratory chain by phytanic acid in cerebellum from young rats: possible underlying mechanisms of cerebellar ataxia in Refsum disease.

Busanello EN, Zanatta Â, Tonin AM, Viegas CM, Vargas CR, Leipnitz G, Ribeiro CA, Wajner M.

J Bioenerg Biomembr. 2013 Feb;45(1-2):137-44. doi: 10.1007/s10863-012-9491-7.

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PUBMED

Progressive sensorineural hearing loss, ataxia and anosmia as manifestation of superficial siderosis in post traumatic brain injury.

Vadalà R, Giugni E, Pezzella FR, Sabatini U, Bastianello S.

Neurol Sci. 2013 Jul;34(7):1259-62. doi: 10.1007/s10072-012-1208-5. No abstract available.

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PUBMED

Spinocerebellar ataxia type 7: clinical course, phenotype-genotype correlations, and neuropathology.

Horton LC, Frosch MP, Vangel MG, Weigel-DiFranco C, Berson EL, Schmahmann JD.

Cerebellum. 2013 Apr;12(2):176-93. doi: 10.1007/s12311-012-0412-4.

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PUBMED

Enteric fever presenting as acute ataxia.

Parakh A, Kumar D, Mishra K.

J Paediatr Child Health. 2013 Mar;49(3):E251. doi: 10.1111/jpc.12116. No abstract available.

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PUBMED

Pharmacological enhancement of mGlu1 metabotropic glutamate receptors causes a prolonged symptomatic benefit in a mouse model of spinocerebellar ataxia type 1.

Notartomaso S, Zappulla C, Biagioni F, Cannella M, Bucci D, Mascio G, Scarselli P, Fazio F, Weisz F, Lionetto L, Simmaco M, Gradini R, Battaglia G, Signore M, Puliti A, Nicoletti F.

Mol Brain. 2013 Nov 19;6:48. doi: 10.1186/1756-6606-6-48.

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PUBMED

Fragile X-associated tremor/ataxia syndrome: influence of the FMR1 gene on motor fiber tracts in males with normal and premutation alleles.

Wang JY, Hessl D, Schneider A, Tassone F, Hagerman RJ, Rivera SM.

JAMA Neurol. 2013 Aug;70(8):1022-9. doi: 10.1001/jamaneurol.2013.2934.

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PUBMED

Safety and efficacy of umbilical cord mesenchymal stem cell therapy in hereditary spinocerebellar ataxia.

Jin JL, Liu Z, Lu ZJ, Guan DN, Wang C, Chen ZB, Zhang J, Zhang WY, Wu JY, Xu Y.

Curr Neurovasc Res. 2013 Feb;10(1):11-20.

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PUBMED

Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum.

Synofzik M, Soehn AS, Gburek-Augustat J, Schicks J, Karle KN, Schüle R, Haack TB, Schöning M, Biskup S, Rudnik-Schöneborn S, Senderek J, Hoffmann KT, MacLeod P, Schwarz J, Bender B, Krüger S, Kreuz F,

Orphanet J Rare Dis. 2013 Mar 15;8:41. doi: 10.1186/1750-1172-8-41.

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