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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 91 AL 105

PUBMED

Visual scanning area is abnormally enlarged in hereditary pure cerebellar ataxia.

Matsuda S, Matsumoto H, Furubayashi T, Fukuda H, Hanajima R, Tsuji S, Ugawa Y, Terao Y.

Cerebellum. 2015 Apr;14(2):63-71. doi: 10.1007/s12311-014-0600-5.

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Comparing speech characteristics in spinocerebellar ataxias type 3 and type 6 with Friedreich ataxia.

Brendel B, Synofzik M, Ackermann H, Lindig T, Schölderle T, Schöls L, Ziegler W.

J Neurol. 2015 Jan;262(1):21-6. doi: 10.1007/s00415-014-7511-8.

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PUBMED

Appendicular ataxia without position sense loss in a patient with parietal lobe infarct.

Mowla A, Kamal H, Nabavizadeh SA.

J Neurol Sci. 2015 May 15;352(1-2):107. doi: 10.1016/j.jns.2015.03.015. No abstract available.

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A comprehensive clinical and genetic study of a large Mexican population with spinocerebellar ataxia type 7.

Velázquez-Pérez L, Cerecedo-Zapata CM, Hernández-Hernández O, Martínez-Cruz E, Tapia-Guerrero YS, González-Piña R, Salas-Vargas J, Rodríguez-Labrada R, Gurrola-Betancourth R, Leyva-García N, Cisneros

Neurogenetics. 2015 Jan;16(1):11-21. doi: 10.1007/s10048-014-0424-y.

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Structural and functional MRI abnormalities of cerebellar cortex and nuclei in SCA3, SCA6 and Friedreich's ataxia.

Stefanescu MR, Dohnalek M, Maderwald S, Thürling M, Minnerop M, Beck A, Schlamann M, Diedrichsen J, Ladd ME, Timmann D.

Brain. 2015 May;138(Pt 5):1182-97. doi: 10.1093/brain/awv064.

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PUBMED

New practical definitions for the diagnosis of autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Pilliod J, Moutton S, Lavie J, Maurat E, Hubert C, Bellance N, Anheim M, Forlani S, Mochel F, N'Guyen K, Thauvin-Robinet C, Verny C, Milea D, Lesca G, Koenig M, Rodriguez D, Houcinat N, Van-Gils J, Du

Ann Neurol. 2015 Dec;78(6):871-86. doi: 10.1002/ana.24509.

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PUBMED

Unusual cerebral white matter change in a Chinese family with Spinocerebellar ataxia type 12.

Hu T, Zhao B, Wei QQ, Shang H.

J Neurol Sci. 2015 Feb 15;349(1-2):243-5. doi: 10.1016/j.jns.2014.12.045.

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PUBMED

Ataxia telangiectasia mutated inhibits oxidative stress-induced apoptosis by regulating heme oxygenase-1 expression.

Yu JH, Cho SO, Lim JW, Kim N, Kim H.

Int J Biochem Cell Biol. 2015 Mar;60:147-56. doi: 10.1016/j.biocel.2015.01.002.

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PUBMED

Blood metal levels and related antioxidant enzyme activities in patients with ataxia telangiectasia.

Squadrone S, Brizio P, Mancini C, Pozzi E, Cavalieri S, Abete MC, Brusco A.

Neurobiol Dis. 2015 Sep;81:162-7. doi: 10.1016/j.nbd.2015.04.001.

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PUBMED

Phenotype variability and early onset ataxia symptoms in spinocerebellar ataxia type 7: comparison and correlation with other spinocerebellar ataxias.

Albuquerque MV, Pedroso JL, Braga Neto P, Barsottini OG.

Arq Neuropsiquiatr. 2015 Jan;73(1):18-21. doi: 10.1590/0004-282X20140192.

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PUBMED

Ataxia-Telangiectasia Presenting as Cerebral Palsy and Recurrent Wheezing: A Case Report.

Navratil M, Đuranović V, Nogalo B, Švigir A, Dumbović Dubravčić I, Turkalj M.

Am J Case Rep. 2015 Sep 18;16:631-6. doi: 10.12659/AJCR.893995.

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PUBMED

First Presentation of Diabetes as Diabetic Ketoacidosis in a Case of Friedreich's Ataxia.

Chakraborty PP, Ray S, Bhattacharjee R, Ghosh S, Mukhopadhyay P, Mukhopadhyay S, Chowdhury S.

Clin Diabetes. 2015 Apr;33(2):84-6. doi: 10.2337/diaclin.33.2.84. No abstract available.

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PUBMED

Psychiatric disorders, spinocerebellar ataxia type 3 and CAG expansion.

Silva UC, Marques W Jr, Lourenço CM, Hallak JE, Osório FL.

J Neurol. 2015 Jul;262(7):1777-9. doi: 10.1007/s00415-015-7807-3.

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