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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 6826 AL 6840

PUBMED

The wide clinical spectrum and nigrostriatal dopaminergic damage in spinocerebellar ataxia type 6.

Kim JM, Lee JY, Kim HJ, Kim JS, Kim YK, Park SS, Kim SE, Jeon BS.

J Neurol Neurosurg Psychiatry. 2010 May;81(5):529-32. doi: 10.1136/jnnp.2008.166728.

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PUBMED

Current and emerging treatment options in the management of Friedreich ataxia.

Mancuso M, Orsucci D, Choub A, Siciliano G.

Neuropsychiatr Dis Treat. 2010 Sep 7;6:491-9.

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PUBMED

A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia.

Coutelier M, Blesneac I, Monteil A, Monin ML, Ando K, Mundwiller E, Brusco A, Le Ber I, Anheim M, Castrioto A, Duyckaerts C, Brice A, Durr A, Lory P, Stevanin G.

Am J Hum Genet. 2015 Nov 5;97(5):726-37. doi: 10.1016/j.ajhg.2015.09.007.

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PUBMED

Spectrin mutations that cause spinocerebellar ataxia type 5 impair axonal transport and induce neurodegeneration in Drosophila.

Lorenzo DN, Li MG, Mische SE, Armbrust KR, Ranum LP, Hays TS.

J Cell Biol. 2010 Apr 5;189(1):143-58. doi: 10.1083/jcb.200905158.

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PUBMED

Does modulation of the endocannabinoid system have potential therapeutic utility in cerebellar ataxia?

Stephens GJ.

J Physiol. 2016 Aug 15;594(16):4631-41. doi: 10.1113/JP271106.

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PUBMED

Ataxia and vertigo due to anomalous origin of the left vertebral artery.

Gabrielli R, Rosati MS.

J Vasc Surg. 2013 Sep;58(3):803. doi: 10.1016/j.jvs.2012.04.045. No abstract available.

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[Molecular genetic diagnosis of Friedreich's ataxia. Ten years experience based on blood sample analysis].

Kisfali P, Melegh B.

Orv Hetil. 2012 Jun 3;153(22):852-5. doi: 10.1556/OH.2012.29372. Hungarian.

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Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion.

Obayashi M, Stevanin G, Synofzik M, Monin ML, Duyckaerts C, Sato N, Streichenberger N, Vighetto A, Desestret V, Tesson C, Wichmann HE, Illig T, Huttenlocher J, Kita Y, Izumi Y, Mizusawa H, Schöls L, K

J Neurol Neurosurg Psychiatry. 2015 Sep;86(9):986-95. doi: 10.1136/jnnp-2014-309153.

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PUBMED

Progressive hearing loss and cerebellar ataxia in anti-Ma2-associated autoimmune encephalitis.

Souza PV, Bortholin T, Pinto WB, Santos AJ.

Arq Neuropsiquiatr. 2017 Jan;75(1):74-75. doi: 10.1590/0004-282X20160169. No abstract available.

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PUBMED

Generation of induced pluripotent stem cell lines from Friedreich ataxia patients.

Liu J, Verma PJ, Evans-Galea MV, Delatycki MB, Michalska A, Leung J, Crombie D, Sarsero JP, Williamson R, Dottori M, Pébay A.

Stem Cell Rev. 2011 Sep;7(3):703-13. doi: 10.1007/s12015-010-9210-x.

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PUBMED

Delayed postnatal loss of P/Q-type calcium channels recapitulates the absence epilepsy, dyskinesia, and ataxia phenotypes of genomic Cacna1a mutations.

Mark MD, Maejima T, Kuckelsberg D, Yoo JW, Hyde RA, Shah V, Gutierrez D, Moreno RL, Kruse W, Noebels JL, Herlitze S.

J Neurosci. 2011 Mar 16;31(11):4311-26. doi: 10.1523/JNEUROSCI.5342-10.2011.

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PUBMED

Early Cerebellar Network Shifting in Spinocerebellar Ataxia Type 6.

Falcon MI, Gomez CM, Chen EE, Shereen A, Solodkin A.

Cereb Cortex. 2016 Jul;26(7):3205-18. doi: 10.1093/cercor/bhv154.

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PUBMED

MicroRNA expression profiling in blood from fragile X-associated tremor/ataxia syndrome patients.

Alvarez-Mora MI, Rodriguez-Revenga L, Madrigal I, Torres-Silva F, Mateu-Huertas E, Lizano E, Friedländer MR, Martí E, Estivill X, Milà M.

Genes Brain Behav. 2013 Aug;12(6):595-603. doi: 10.1111/gbb.12061.

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PUBMED

Fragile X-associated tremor/ataxia syndrome: cognitive presentations.

Connon P, Larner AJ.

Br J Hosp Med (Lond). 2017 Apr 2;78(4):230-231. doi: 10.12968/hmed.2017.78.4.230. No abstract available.

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PUBMED

Interleukin 6 augments lung cancer chemotherapeutic resistance via ataxia-telangiectasia mutated/NF-kappaB pathway activation.

Yan HQ, Huang XB, Ke SZ, Jiang YN, Zhang YH, Wang YN, Li J, Gao FG.

Cancer Sci. 2014 Sep;105(9):1220-7. doi: 10.1111/cas.12478.

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