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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

295 ARTíCULOS , VIENDO DEL 1 AL 15

PUBMED

Beta-III spectrin mutation L253P associated with spinocerebellar ataxia type 5 interferes with binding to Arp1 and protein trafficking from the Golgi.

Clarkson YL, Gillespie T, Perkins EM, Lyndon AR, Jackson M.

Hum Mol Genet. 2010 Sep 15;19(18):3634-41. doi: 10.1093/hmg/ddq279.

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PUBMED

Neurochemical alterations in spinocerebellar ataxia type 1 and their correlations with clinical status.

Oz G, Hutter D, Tkác I, Clark HB, Gross MD, Jiang H, Eberly LE, Bushara KO, Gomez CM.

Mov Disord. 2010 Jul 15;25(9):1253-61. doi: 10.1002/mds.23067.

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PUBMED

Sensory neuronopathy in ataxia with oculomotor apraxia type 2.

Gazulla J, Benavente I, López-Fraile IP, Tordesillas C, Modrego P, Alonso I, Pinto-Basto J.

J Neurol Sci. 2010 Nov 15;298(1-2):118-20. doi: 10.1016/j.jns.2010.09.004.

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PUBMED

Acute cerebellar ataxia in childhood: initial approach in the emergency department.

Salas AA, Nava A.

Emerg Med J. 2010 Dec;27(12):956-7. doi: 10.1136/emj.2009.079376.

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PUBMED

Role of ataxia telangiectasia mutated in insulin signalling of muscle-derived cell lines and mouse soleus.

Jeong I, Patel AY, Zhang Z, Patil PB, Nadella ST, Nair S, Ralston L, Hoormann JK, Fisher JS.

Acta Physiol (Oxf). 2010 Apr;198(4):465-75. doi: 10.1111/j.1748-1716.2009.02069.x.

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PUBMED

[Spinocerebellar ataxia type 31].

Ishikawa K, Sato N, Niimi Y, Amino T, Mizusawa H.

Rinsho Shinkeigaku. 2010 Nov;50(11):985-7. Review. Japanese.

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PUBMED

Assessment of patient and caregiver needs in fragile X-associated tremor/ataxia syndrome by utilizing Q-sort methodology.

Gane LW, Iosif AM, Flynn-Wilson L, Venturino M, Hagerman RJ, Seritan AL.

Aging Ment Health. 2010 Nov;14(8):1000-7. doi: 10.1080/13607863.2010.501066.

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PUBMED

[A case of recurrent paraneoplastic cerebellar ataxia with antibodies to GluR epsilon 2 causally related to ganglioneuroma].

Noguchi S, Kaga Y, Takahashi Y, Aoyagi K, Nakamura K, Kamiya Y, Nakane T, Kanemura H, Sugita K, Aihara M.

No To Hattatsu. 2010 Jul;42(4):297-301. Japanese.

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PUBMED

Inactivation of hnRNP K by expanded intronic AUUCU repeat induces apoptosis via translocation of PKCdelta to mitochondria in spinocerebellar ataxia 10.

White MC, Gao R, Xu W, Mandal SM, Lim JG, Hazra TK, Wakamiya M, Edwards SF, Raskin S, Teive HA, Zoghbi HY, Sarkar PS, Ashizawa T.

PLoS Genet. 2010 Jun 10;6(6):e1000984. doi: 10.1371/journal.pgen.1000984.

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PUBMED

A syndrome of the dentate nucleus mimicking psychogenic ataxia.

Salih F, Breuer E, Harnack D, Hoffmann KT, Ploner CJ.

J Neurol Sci. 2010 Mar 15;290(1-2):183-5. doi: 10.1016/j.jns.2009.10.017.

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PUBMED

Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.

Schulz JB, Borkert J, Wolf S, Schmitz-Hübsch T, Rakowicz M, Mariotti C, Schöls L, Timmann D, van de Warrenburg B, Dürr A, Pandolfo M, Kang JS, Mandly AG, Nägele T, Grisoli M, Boguslawska R, Bauer P, K

Neuroimage. 2010 Jan 1;49(1):158-68. doi: 10.1016/j.neuroimage.2009.07.027. Erratum in: Neuroimage. 2010 May 1;50(4):1712. Schoels, Ludger [corrected to Schöls, Ludger].

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PUBMED

Evidence of mitochondrial dysfunction in fragile X-associated tremor/ataxia syndrome.

Ross-Inta C, Omanska-Klusek A, Wong S, Barrow C, Garcia-Arocena D, Iwahashi C, Berry-Kravis E, Hagerman RJ, Hagerman PJ, Giulivi C.

Biochem J. 2010 Aug 1;429(3):545-52. doi: 10.1042/BJ20091960.

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PUBMED

Spinocerebellar ataxia type 11 in the Chinese Han population.

Xu Q, Li X, Wang J, Yi J, Lei L, Shen L, Jiang H, Xia K, Pan Q, Tang B.

Neurol Sci. 2010 Feb;31(1):107-9. doi: 10.1007/s10072-009-0129-4.

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