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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 391 AL 405

PUBMED

A Case of Spinocerebellar Ataxia With a Reversible Splenium Lesion Due to Malnutrition and Vitamin Deficiency.

Trikamji B, Rexach J, Mishra SK.

J Clin Neuromuscul Dis. 2015 Dec;17(2):95-7. doi: 10.1097/CND.0000000000000092. No abstract available.

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Spontaneous downbeat nystagmus as a clue for the diagnosis of ataxia associated with anti-GAD antibodies.

Vale TC, Pedroso JL, Alquéres RA, Dutra LA, Barsottini OG.

J Neurol Sci. 2015 Dec 15;359(1-2):21-3. doi: 10.1016/j.jns.2015.10.024.

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PUBMED

Low-dose Methylphenidate Monotherapy for Features of Attention-Deficit/Hyperactivity Disorder Secondary to Hereditary Cerebellar Ataxia.

Hu LY, Lin YL, Chang HS, Lu T, Lin WS.

CNS Neurosci Ther. 2015 Aug;21(8):672-3. doi: 10.1111/cns.12403. No abstract available.

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PUBMED

Exome sequencing & homozygosity mapping for identification of genetic aetiology for spastic ataxia in a consanguineous family.

Dalal A, Bhowmik AD, Agarwal D, Phadke SR.

Indian J Med Res. 2015 Aug;142(2):220-4. doi: 10.4103/0971-5916.164262. No abstract available.

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PUBMED

Multi-drugs resistant acne rosacea in a child affected by Ataxia-Telangiectasia: successful treatment with Isotretinoin.

Cantarutti N, Claps A, Angelino G, Chessa L, Callea F, El Hachem M, Diociaiuti A, Finocchi A.

Ital J Pediatr. 2015 Mar 28;41:23. doi: 10.1186/s13052-015-0125-7.

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PUBMED

The mechanism of ipsilateral ataxia in lacunar hemiparesis: SPECT perfusion imaging.

Yamamoto R, Johkura K, Nakae Y, Tanaka F.

Eur Neurol. 2015;73(1-2):106-11. doi: 10.1159/000369009.

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PUBMED

Vision related quality of life in spinocerebellar ataxia.

Kedar S, Ghate D, Murray EL, Corbett JJ, Subramony SH.

J Neurol Sci. 2015 Nov 15;358(1-2):404-8. doi: 10.1016/j.jns.2015.10.013.

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PUBMED

Genome-Engineering Tools to Establish Accurate Reporter Cell Lines That Enable Identification of Therapeutic Strategies to Treat Friedreich's Ataxia.

Villaseñor R, Miraglia L, Romero A, Tu B, Punga T, Knuckles P, Duss S, Orth T, Bühler M.

J Biomol Screen. 2015 Jul;20(6):760-7. doi: 10.1177/1087057114568071.

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PUBMED

Genetic analysis of ten common degenerative hereditary ataxia loci in patients with essential tremor.

Clark LN, Ye X, Liu X, Mirzozoda K, Louis ED.

Parkinsonism Relat Disord. 2015 Aug;21(8):943-7. doi: 10.1016/j.parkreldis.2015.06.004.

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PUBMED

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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PUBMED

The role of the mammalian DNA end-processing enzyme polynucleotide kinase 3'-phosphatase in spinocerebellar ataxia type 3 pathogenesis.

Chatterjee A, Saha S, Chakraborty A, Silva-Fernandes A, Mandal SM, Neves-Carvalho A, Liu Y, Pandita RK, Hegde ML, Hegde PM, Boldogh I, Ashizawa T, Koeppen AH, Pandita TK, Maciel P, Sarkar PS, Hazra TK

PLoS Genet. 2015 Jan 29;11(1):e1004749. doi: 10.1371/journal.pgen.1004749.

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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

Autosomal recessive cerebellar ataxia 3 due to homozygote c.132dupA mutation within the ANO10 gene.

Minnerop M, Bauer P.

JAMA Neurol. 2015 Feb;72(2):238-9. doi: 10.1001/jamaneurol.2014.3918. No abstract available.

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PUBMED

Stable isotopes and LC-MS for monitoring metabolic disturbances in Friedreich's ataxia platelets.

Worth AJ, Basu SS, Deutsch EC, Hwang WT, Snyder NW, Lynch DR, Blair IA.

Bioanalysis. 2015;7(15):1843-55. doi: 10.4155/bio.15.118.

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PUBMED

Health-related quality of life in patients with spinocerebellar ataxia.

Sánchez-López CR, Perestelo-Pérez L, Escobar A, López-Bastida J, Serrano-Aguilar P.

Neurologia. 2015 Nov 2. pii: S0213-4853(15)00213-3. doi: 10.1016/j.nrl.2015.09.002. [Epub ahead of print] English, Spanish.

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