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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

7060 ARTíCULOS , VIENDO DEL 6856 AL 6870

PUBMED

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): typical clinical and neuroimaging features in a Brazilian family.

Pedroso JL, Braga-Neto P, Abrahão A, Rivero RL, Abdalla C, Abdala N, Barsottini OG.

Arq Neuropsiquiatr. 2011;69(2B):288-91.

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PUBMED

Novel Blood Biomarkers Are Associated with White Matter Lesions in Fragile X- Associated Tremor/Ataxia Syndrome.

Loesch DZ, Annesley SJ, Trost N, Bui MQ, Lay ST, Storey E, De Piazza SW, Sanislav O, Francione LM, Hammersley EM, Tassone F, Francis D, Fisher PR.

Neurodegener Dis. 2017;17(1):22-30.

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PUBMED

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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PUBMED

Sacsin-related spastic ataxia caused by a novel missense mutation p.Arg272His in a patient from Sicily, southern Italy.

Dibilio V, Cavalcanti F, Nicoletti A, Mostile G, Bruno E, Annesi G, Tarantino P, Gagliardi M, Gambardella A, Quattrone A, Zappia M.

Cerebellum. 2013 Aug;12(4):589-92. doi: 10.1007/s12311-013-0451-5. No abstract available.

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PUBMED

Isolated ataxia after pure left insular cortex infarction.

Liou LM, Guo YC, Lai CL, Tsai CL, Khor GT.

Neurol Sci. 2010 Feb;31(1):89-91. doi: 10.1007/s10072-009-0164-1.

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Dramatic response to pyridoxine in a girl with absence epilepsy with ataxia caused by a de novo CACNA1A mutation.

Du X, Chen Y, Zhao Y, Luo W, Cen Z, Hao W.

Seizure. 2017 Jan 3;45:189-191. doi: 10.1016/j.seizure.2016.12.020. [Epub ahead of print] No abstract available.

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PUBMED

Neurological picture. MRI of metronidazole induced cerebellar ataxia.

Moosa AN, Perkins D.

J Neurol Neurosurg Psychiatry. 2010 Jul;81(7):754-5. doi: 10.1136/jnnp.2008.165308. No abstract available.

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PUBMED

Reply to comment Why do patients with cerebellar ataxia not use environmental cues for reducing unpredictability of sudden gait stopping?" on "Sudden stopping in patients with cerebellar ataxia"."

Serrao M, Conte C, Casali C, Ranavolo A, Mari S, Di Fabio R, Perrotta A, Coppola G, Padua L, Monamì S, Sandrini G, Pierelli F.

Cerebellum. 2013 Dec;12(6):958-9. doi: 10.1007/s12311-013-0501-z. No abstract available.

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PUBMED

Postural Tremor and Ataxia Progression in Spinocerebellar Ataxias.

Gan SR, Wang J, Figueroa KP, Pulst SM, Tomishon D, Lee D, Perlman S, Wilmot G, Gomez CM, Schmahmann J, Paulson H, Shakkottai VG, Ying SH, Zesiewicz T, Bushara K, Geschwind MD, Xia G, Subramony SH, Ash

Tremor Other Hyperkinet Mov (N Y). 2017 Oct 9;7:492. doi: 10.7916/D8GM8KRH. eCollection 2017.

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PUBMED

A combined nucleic acid and protein analysis in Friedreich ataxia: implications for diagnosis, pathogenesis and clinical trial design.

Saccà F, Puorro G, Antenora A, Marsili A, Denaro A, Piro R, Sorrentino P, Pane C, Tessa A, Brescia Morra V, Cocozza S, De Michele G, Santorelli FM, Filla A.

PLoS One. 2011 Mar 11;6(3):e17627. doi: 10.1371/journal.pone.0017627.

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PUBMED

The NRF2 Signaling Network Defines Clinical Biomarkers and Therapeutic Opportunity in Friedreich's Ataxia

La Rosa P, Bertini ES, Piemonte F.

Int J Mol Sci. 2020 Jan 30;21(3):916. doi: 10.3390/ijms21030916.

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PUBMED

SC-III3, a novel scopoletin derivative, induces cytotoxicity in hepatocellular cancer cells through oxidative DNA damage and ataxia telangiectasia-mutated nuclear protein kinase activation.

Zhao P, Chen L, Li LH, Wei ZF, Tong B, Jia YG, Kong LY, Xia YF, Dai Y.

BMC Cancer. 2014 Dec 19;14:987. doi: 10.1186/1471-2407-14-987.

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PUBMED

Nystagmus and ataxia associated with antiganglioside antibodies.

Jeong SH, Nam J, Kwon MJ, Kim JK, Kim JS.

J Neuroophthalmol. 2011 Dec;31(4):326-30. doi: 10.1097/WNO.0b013e31822f6707.

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