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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 1 AL 15

PUBMED

Investigation of mitochondrial DNA variations among Indian Friedreich's ataxia (FRDA) patients.

Singh I, Faruq M, Padma MV, Goyal V, Behari M, Grover A, Mukerji M, Srivastava AK.

Mitochondrion. 2015 Nov;25:1-5. doi: 10.1016/j.mito.2015.08.003.

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PUBMED

A novel porcine model of ataxia telangiectasia reproduces neurological features and motor deficits of human disease.

Beraldi R, Chan CH, Rogers CS, Kovács AD, Meyerholz DK, Trantzas C, Lambertz AM, Darbro BW, Weber KL, White KA, Rheeden RV, Kruer MC, Dacken BA, Wang XJ, Davis BT, Rohret JA, Struzynski JT, Rohret FA,

Hum Mol Genet. 2015 Nov 15;24(22):6473-84. doi: 10.1093/hmg/ddv356.

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PUBMED

Erratum to: The L450F [Corrected] mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together.

Duarri A, Nibbeling E, Fokkens MR, Meijer M, Boddeke E, Lagrange E, Stevanin G, Brice A, Durr A, Verbeek DS.

Neurogenetics. 2015 Jul;16(3):243. doi: 10.1007/s10048-015-0447-z. No abstract available.

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PUBMED

Fragile X Tremor Ataxia Syndrome With Rapidly Progressive Myopathy.

Nirenberg MJ, Bhatt JM, Roda RH.

JAMA Neurol. 2015 Aug;72(8):946-8. doi: 10.1001/jamaneurol.2015.0812. No abstract available.

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PUBMED

Modeling Suggests TRPC3 Hydrogen Bonding and Not Phosphorylation Contributes to the Ataxia Phenotype of the Moonwalker Mouse.

Hanson SM, Sansom MS, Becker EB.

Biochemistry. 2015 Jul 7;54(26):4033-41. doi: 10.1021/acs.biochem.5b00235.

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PUBMED

Adult-onset myoclonus ataxia associated with the mitochondrial m.8993T>C NARP" mutation."

Martikainen MH, Gorman GS, Goldsmith P, Burn DJ, Turnbull DM, Schaefer AM.

Mov Disord. 2015 Sep;30(10):1432-3. doi: 10.1002/mds.26358. No abstract available.

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PUBMED

Ataxia of cortical origin via crossed cerebellar diaschisis.

Kwon YC, Kim JH, Ahn TB.

Neurol Sci. 2015 Jan;36(1):161-3. doi: 10.1007/s10072-014-1846-x. No abstract available.

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PUBMED

Induced pluripotent stem cell technology for modelling and therapy of cerebellar ataxia.

Watson LM, Wong MM, Becker EB.

Open Biol. 2015 Jul;5(7):150056. doi: 10.1098/rsob.150056. Review.

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PUBMED

Two novel mutations of the SETX gene and ataxia with oculomotor apraxia type 2.

Pera J, Lechner S, Biskup S, Strach M, Grodzicki T, Slowik A.

Clin Neurol Neurosurg. 2015 Jan;128:44-6. doi: 10.1016/j.clineuro.2014.10.024. No abstract available.

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PUBMED

Cerebellar ataxia with unilateral high frequency vestibulopathy and caloric disinhibition.

Helmchen C, Livitzis E, Sprenger A, Trillenberg P.

J Neurol Sci. 2015 Nov 15;358(1-2):527-9. doi: 10.1016/j.jns.2015.09.379. No abstract available.

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PUBMED

Macro- and microstructural changes in patients with spinocerebellar ataxia type 6: assessment of phylogenetic subdivisions of the cerebellum and the brain stem.

Sato K, Ishigame K, Ying SH, Oishi K, Miller MI, Mori S.

AJNR Am J Neuroradiol. 2015 Jan;36(1):84-90. doi: 10.3174/ajnr.A4085.

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PUBMED

Myoclonus in ataxia-telangiectasia.

Termsarasab P, Yang AC, Frucht SJ.

Tremor Other Hyperkinet Mov (N Y). 2015 Mar 13;5:298. doi: 10.7916/D88P5Z9X.

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PUBMED

Familial segmental spinal myoclonus: a rare clinical feature of Friedreich's ataxia.

Jain RS, Kumar S, Tejwani S.

Springerplus. 2015 Jul 8;4:330. doi: 10.1186/s40064-015-1121-5.

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PUBMED

Strategy use, planning, and rule acquisition deficits in spinocerebellar ataxia type 2 patients.

Vaca-Palomares I, Díaz R, Rodríguez-Labrada R, Medrano-Montero J, Aguilera-Rodríguez R, Vázquez-Mojena Y, Fernandez-Ruiz J, Velázquez-Pérez L.

J Int Neuropsychol Soc. 2015 Mar;21(3):214-20. doi: 10.1017/S1355617715000132.

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