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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

443 ARTíCULOS , VIENDO DEL 1 AL 15

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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Early-onset familial Alzheimer's disease related to presenilin 1 mutation resembling autosomal dominant spinocerebellar ataxia.

Braga-Neto P, Pedroso JL, Alessi H, de Souza PV, Bertolucci PH, Barsottini OG.

J Neurol. 2013 Apr;260(4):1177-9. doi: 10.1007/s00415-013-6879-1. No abstract available.

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Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa and cataracts (PHARC) screening in an Italian population.

Criscuolo C, Guacci A, Carbone R, Lieto M, Salsano E, Nanetti L, Michele GD, Filla A.

Eur J Neurol. 2013 Apr;20(4):e60. doi: 10.1111/ene.12056. No abstract available.

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The frequency of spinocerebellar ataxia type 23 in a UK population.

Fawcett K, Mehrabian M, Liu YT, Hamed S, Elahi E, Revesz T, Koutsis G, Herscheson J, Schottlaender L, Wardle M, Morrison PJ, Morris HR, Giunti P, Wood N, Houlden H.

J Neurol. 2013 Mar;260(3):856-9. doi: 10.1007/s00415-012-6721-1. Erratum in: J Neurol. 2013 Mar;260(3):860.

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Pemetrexed induces both intrinsic and extrinsic apoptosis through ataxia telangiectasia mutated/p53-dependent and -independent signaling pathways.

Yang TY, Chang GC, Chen KC, Hung HW, Hsu KH, Wu CH, Sheu GT, Hsu SL.

Mol Carcinog. 2013 Mar;52(3):183-94. doi: 10.1002/mc.21842.

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Infantile neuroaxonal dystrophy: a rare cause of early childhood ataxia with poor prognosis.

El Arbi S, Demant A, Kohlschmidt N, Horneff G.

Klin Padiatr. 2013 Jan;225(1):41-2. doi: 10.1055/s-0032-1323834. No abstract available.

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[Autoantibodies associated with autoimmune-mediated cerebellar ataxia].

Mitoma H, Nanri K.

Brain Nerve. 2013 Apr;65(4):355-64. Review. Japanese.

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Non invasive assessment of lung disease in ataxia telangiectasia by high-field magnetic resonance imaging.

Montella S, Mollica C, Finocchi A, Pession A, Pietrogrande MC, Trizzino A, Ranucci G, Maglione M, Giardino G, Salvatore M, Santamaria F, Pignata C.

J Clin Immunol. 2013 Oct;33(7):1185-91. doi: 10.1007/s10875-013-9933-y.

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PUBMED

Epstein-Barr virus-associated cerebellar ataxia.

Ali K, Lawthom C.

BMJ Case Rep. 2013 Apr 22;2013. pii: bcr2013009171. doi: 10.1136/bcr-2013-009171.

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Case of infantile onset spinocerebellar ataxia type 5.

Jacob FD, Ho ES, Martinez-Ojeda M, Darras BT, Khwaja OS.

J Child Neurol. 2013 Oct;28(10):1292-5. doi: 10.1177/0883073812454331.

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[Epidural anesthesia for femoral head replacement in a spinocerebellar ataxia patient: a case report].

Maeda Y, Yamakawa J, Sakamoto Y, Miyazaki K, Katsuki S, Miyagawa Y.

Masui. 2013 Aug;62(8):979-81. Japanese.

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Insights into the role of oxidative stress in the pathology of Friedreich ataxia using peroxidation resistant polyunsaturated fatty acids.

Cotticelli MG, Crabbe AM, Wilson RB, Shchepinov MS.

Redox Biol. 2013;1:398-404. doi: 10.1016/j.redox.2013.06.004.

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Quantitative evaluation of cerebellar ataxia based on pathological patterns of the muscle activities.

Lee J, Kagamihara Y, Kakei S.

Conf Proc IEEE Eng Med Biol Soc. 2013;2013:902-5. doi: 10.1109/EMBC.2013.6609647.

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Early onset of ataxia in moonwalker mice is accompanied by complete ablation of type II unipolar brush cells and Purkinje cell dysfunction.

Sekerková G, Kim JA, Nigro MJ, Becker EB, Hartmann J, Birnbaumer L, Mugnaini E, Martina M.

J Neurosci. 2013 Dec 11;33(50):19689-94. doi: 10.1523/JNEUROSCI.2294-13.2013.

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