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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.

Ataxia

9265 ARTíCULOS , VIENDO DEL 9121 AL 9135

PUBMED

Generation of induced Pluripotent Stem Cells (UNIBSi008-A, UNIBSi008-B, UNIBSi008-C) from an Ataxia-Telangiectasia (AT) patient carrying a novel homozygous deletion in ATM gene.

Masneri S, Ferraro RM, Lanzi G, Piovani G, Mori L, Barisani C, Moratto D, Plebani A, Badolato R, Soresina A, Giliani S.

Stem Cell Res. 2019 Oct 18;41:101596. doi: 10.1016/j.scr.2019.101596. [Epub ahead of print]

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Curcumin protects purkinje neurons, ameliorates motor function and reduces cerebellar atrophy in rat model of cerebellar ataxia induced by 3-AP.

Mahmoudi M, Bayat AH, Boroujeni ME, Abdollahifar MA, Ebrahimi V, Danyali S, Heidari MH, Aliaghaei A.

J Chem Neuroanat. 2019 Oct 24:101706. doi: 10.1016/j.jchemneu.2019.101706. [Epub ahead of print]

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Definition: Optic ataxia.

Rossetti Y, Pisella L, McIntosh RD.

Cortex. 2019 Sep 26. pii: S0010-9452(19)30322-3. doi: 10.1016/j.cortex.2019.09.004. [Epub ahead of print] No abstract available.

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Neurological Disease Modelling for Spinocerebellar Ataxia Using Zebrafish.

Namikawa K, Dorigo A, Köster RW.

J Exp Neurosci. 2019 Oct 17;13:1179069519880515. doi: 10.1177/1179069519880515. eCollection 2019.

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Potential biomarker identification for Friedreich's ataxia using overlapping gene expression patterns in patient cells and mouse dorsal root ganglion.

McMackin MZ, Durbin-Johnson B, Napierala M, Napierala JS, Ruiz L, Napoli E, Perlman S, Giulivi C, Cortopassi GA.

PLoS One. 2019 Oct 30;14(10):e0223209. doi: 10.1371/journal.pone.0223209. eCollection 2019.

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Neuropathology of RAN translation proteins in fragile X-associated tremor/ataxia syndrome.

Krans A, Skariah G, Zhang Y, Bayly B, Todd PK.

Acta Neuropathol Commun. 2019 Oct 30;7(1):152. doi: 10.1186/s40478-019-0782-7.

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Fragile X-associated tremor ataxia syndrome with co-occurrent progressive supranuclear palsy-like neuropathology.

Sacino AN, Prokop S, Walsh MA, Adamson J, Subramony SH, Krans A, Todd PK, Giasson BI, Yachnis AT.

Acta Neuropathol Commun. 2019 Oct 30;7(1):158. doi: 10.1186/s40478-019-0818-z.

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Recurrent NUS1 canonical splice donor site mutation in two unrelated individuals with epilepsy, myoclonus, ataxia and scoliosis - a case report.

Den K, Kudo Y, Kato M, Watanabe K, Doi H, Tanaka F, Oguni H, Miyatake S, Mizuguchi T, Takata A, Miyake N, Mitsuhashi S, Matsumoto N.

BMC Neurol. 2019 Oct 27;19(1):253. doi: 10.1186/s12883-019-1489-x.

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Predictors of Left Ventricular Dysfunction in Friedreich's Ataxia in a 16-Year Observational Study

Legrand L, Diallo A, Monin ML, Ewenczyk C, Charles P, Isnard R, Vicaut E, Montalescot G, Durr A, Pousset F.

Am J Cardiovasc Drugs. 2020 Apr;20(2):209-216. doi: 10.1007/s40256-019-00375-z.

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Investigating ataxia in childhood

Petley E, Prasad M, Ojha S, Whitehouse WP.

Arch Dis Child Educ Pract Ed. 2020 Aug;105(4):214-221. doi: 10.1136/archdischild-2018-315893. Epub 2019 Oct 23.

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Cerebellum and cognition in Friedreich ataxia: a voxel-based morphometry and volumetric MRI study

Cocozza S, Costabile T, Pontillo G, Lieto M, Russo C, Radice L, Pane C, Filla A, Brunetti A, Saccà F.

J Neurol. 2020 Feb;267(2):350-358. doi: 10.1007/s00415-019-09582-9. Epub 2019 Oct 22.

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Targeting NRF2 for the Treatment of Friedreich's Ataxia: A Comparison among Drugs.

Petrillo S, D'Amico J, La Rosa P, Bertini ES, Piemonte F.

Int J Mol Sci. 2019 Oct 21;20(20). pii: E5211. doi: 10.3390/ijms20205211.

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PUBMED

Quantifying iron deposition in the cerebellar subtype of multiple system atrophy and spinocerebellar ataxia type 6 by quantitative susceptibility mapping.

Sugiyama A, Sato N, Kimura Y, Fujii H, Maikusa N, Shigemoto Y, Suzuki F, Morimoto E, Koide K, Takahashi Y, Matsuda H, Kuwabara S.

J Neurol Sci. 2019 Oct 13;407:116525. doi: 10.1016/j.jns.2019.116525. [Epub ahead of print]

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