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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 286 AL 300

PUBMED

Ataxia meets chorioretinal dystrophy and hypogonadism: Boucher-Neuhäuser syndrome due to PNPLA6 mutations.

Synofzik M, Kernstock C, Haack TB, Schöls L.

J Neurol Neurosurg Psychiatry. 2015 May;86(5):580-1. doi: 10.1136/jnnp-2014-307793. No abstract available.

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PUBMED

FXN Promoter Silencing in the Humanized Mouse Model of Friedreich Ataxia.

Chutake YK, Costello WN, Lam CC, Parikh AC, Hughes TT, Michalopulos MG, Pook MA, Bidichandani SI.

PLoS One. 2015 Sep 22;10(9):e0138437. doi: 10.1371/journal.pone.0138437.

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PUBMED

Neuro-Ophthalmological Findings in Children and Adolescents with Chronic Ataxia.

Salman MS, Chodirker BN.

Neuroophthalmology. 2015 Jun 17;39(3):125-131.

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PUBMED

A longitudinal study of the Friedreich Ataxia Impact Scale.

Tai G, Yiu EM, Corben LA, Delatycki MB.

J Neurol Sci. 2015 May 15;352(1-2):53-7. doi: 10.1016/j.jns.2015.03.024.

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A 22-Year Follow-up Study of Long-term Cardiac Outcome and Predictors of Survival in Friedreich Ataxia.

Pousset F, Legrand L, Monin ML, Ewenczyk C, Charles P, Komajda M, Brice A, Pandolfo M, Isnard R, Tezenas du Montcel S, Durr A.

JAMA Neurol. 2015 Nov;72(11):1334-41. doi: 10.1001/jamaneurol.2015.1855.

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Mitochondrial recessive ataxia syndrome: A neurological rarity not to be missed.

Mignarri A, Cenciarelli S, Da Pozzo P, Cardaioli E, Malandrini A, Federico A, Dotti MT.

J Neurol Sci. 2015 Feb 15;349(1-2):254-5. doi: 10.1016/j.jns.2014.12.040. No abstract available.

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Parallel fiber to Purkinje cell synaptic impairment in a mouse model of spinocerebellar ataxia type 27.

Tempia F, Hoxha E, Negro G, Alshammari MA, Alshammari TK, Panova-Elektronova N, Laezza F.

Front Cell Neurosci. 2015 Jun 4;9:205. doi: 10.3389/fncel.2015.00205.

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A variant of Nesprin1 giant devoid of KASH domain underlies the molecular etiology of autosomal recessive cerebellar ataxia type I.

Razafsky D, Hodzic D.

Neurobiol Dis. 2015 Jun;78:57-67. doi: 10.1016/j.nbd.2015.03.027.

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Both Sides of the Wheelchair: The Views of Individuals with, and Parents of Individuals with Friedreich Ataxia Regarding Pre-symptomatic Testing of Minors.

Lowe GC, Corben LA, Duncan RE, Yoon G, Delatycki MB.

J Genet Couns. 2015 Oct;24(5):732-43. doi: 10.1007/s10897-014-9801-9.

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PUBMED

Reversible Cerebellar Ataxia Related to Extrapontine Myelinolysis without Hyponatremia after Cisplatin-Based Chemotherapy for Cholangiocarcinoma.

Chung JH, Baik SK, Cho SH, Kim SG.

Cancer Res Treat. 2015 Apr;47(2):329-33. doi: 10.4143/crt.2013.145.

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Abnormalities in synaptic dynamics during development in a mouse model of spinocerebellar ataxia type 1.

Hatanaka Y, Watase K, Wada K, Nagai Y.

Sci Rep. 2015 Nov 4;5:16102. doi: 10.1038/srep16102.

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Spinocerebellar ataxia type 10 in the South of Brazil: the Amerindian-Belgian connection.

Teive HA, Moro A, Moscovich M, Arruda WO, Munhoz RP, Raskin S, Teive GM, Dallabrida N, Ashizawa T.

Arq Neuropsiquiatr. 2015 Aug;73(8):725-7. doi: 10.1590/0004-282X20150086.

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PUBMED

Differential diagnosis of sporadic adult-onset ataxia: The role of REM sleep behavior disorder.

Teive HA, Arruda WO, Moro A, Moscovich M, Munhoz RP.

Parkinsonism Relat Disord. 2015 Jun;21(6):640-3. doi: 10.1016/j.parkreldis.2015.04.001.

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PUBMED

Ataxia telangiectasia.

Nissenkorn A, Ben-Zeev B.

Handb Clin Neurol. 2015;132:199-214. doi: 10.1016/B978-0-444-62702-5.00014-7. Review.

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