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Bibliografía Científica

Artículos por temáticas

En este apartado encontrará una actualización mensual de artículos sobre Trastornos del Movimiento clasificados según los 11 tipos establecidos por la International Parkinson & Movement Disorder Society.

Ataxia

488 ARTíCULOS , VIENDO DEL 61 AL 75

PUBMED

The Pointing Errors in Optic Ataxia Reveal the Role of Peripheral Magnification" of the PPC."

Vindras P, Blangero A, Ota H, Reilly KT, Rossetti Y, Pisella L.

Front Integr Neurosci. 2016 Jul 26;10:27. doi: 10.3389/fnint.2016.00027.

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Infantile onset spinocerebellar ataxia caused by compound heterozygosity for Twinkle mutations and modeling of Twinkle mutations causing recessive disease.

Pierce SB, Gulsuner S, Stapleton GA, Walsh T, Lee MK, Mandell JB, Morales A, Klevit RE, King MC, Rogers RC.

Cold Spring Harb Mol Case Stud. 2016 Jul;2(4):a001107. doi: 10.1101/mcs.a001107.

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Phenotypic consequences of somatic mutations in the ataxia-telangiectasia mutated gene in non-small cell lung cancer.

Weber AM, Drobnitzky N, Devery AM, Bokobza SM, Adams RA, Maughan TS, Ryan AJ.

Oncotarget. 2016 Sep 20;7(38):60807-60822. doi: 10.18632/oncotarget.11845.

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PUBMED

Clinical Reasoning: A 52-year-old man with diplopia and ataxia.

Bradshaw MJ, Pawate S, Bloch KC, Moots P, Reddy NM.

Neurology. 2016 Sep 27;87(13):e140-3. doi: 10.1212/WNL.0000000000003150. No abstract available.

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NAD(+) Replenishment Improves Lifespan and Healthspan in Ataxia Telangiectasia Models via Mitophagy and DNA Repair.

Fang EF, Kassahun H, Croteau DL, Scheibye-Knudsen M, Marosi K, Lu H, Shamanna RA, Kalyanasundaram S, Bollineni RC, Wilson MA, Iser WB, Wollman BN, Morevati M, Li J, Kerr JS, Lu Q, Waltz TB, Tian J, Si

Cell Metab. 2016 Oct 11;24(4):566-581. doi: 10.1016/j.cmet.2016.09.004.

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PUBMED

Robust reprogramming of Ataxia-Telangiectasia patient and carrier erythroid cells to induced pluripotent stem cells.

Bhatt N, Ghosh R, Roy S, Gao Y, Armanios M, Cheng L, Franco S.

Stem Cell Res. 2016 Sep;17(2):296-305. doi: 10.1016/j.scr.2016.08.006.

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Cerebellar ataxia and autoantibodies restricted to glutamic acid decarboxylase 67 (GAD67).

Guasp M, Solà-Valls N, Martínez-Hernández E, Gil MP, González C, Brieva L, Saiz A, Dalmau J, Graus F, Ariño H.

J Neuroimmunol. 2016 Nov 15;300:15-17. doi: 10.1016/j.jneuroim.2016.09.019.

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PUBMED

Peripheral nerve ultrasound in cerebellar ataxia neuropathy vestibular areflexia syndrome (CANVAS).

Pelosi L, Leadbetter R, Mulroy E, Chancellor AM, Mossman S, Roxburgh R.

Muscle Nerve. 2016 Nov 15. doi: 10.1002/mus.25476. [Epub ahead of print]

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PUBMED

[Pathophysiology of Ataxia in Fisher Syndrome].

Kuwabara S.

Brain Nerve. 2016 Dec;68(12):1411-1414. Japanese.

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PUBMED

Cerebellar ataxia due to Leptospirosis- a case report.

Singh R, Khurana D, Mehta S, Choudhary A, Petluri G, Lal V.

BMC Infect Dis. 2016 Dec 12;16(1):748.

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PUBMED

Specific cerebellar and cortical degeneration correlates with ataxia severity in spinocerebellar ataxia type 7.

Hernandez-Castillo CR, Galvez V, Diaz R, Fernandez-Ruiz J.

Brain Imaging Behav. 2016 Mar;10(1):252-7. doi: 10.1007/s11682-015-9389-1.

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PUBMED

Cytokine therapy-mediated neuroprotection in a Friedreich's ataxia mouse model.

Kemp KC, Cerminara N, Hares K, Redondo J, Cook AJ, Haynes HR, Burton BR, Pook M, Apps R, Scolding NJ, Wilkins A.

Ann Neurol. 2016 Dec 23. doi: 10.1002/ana.24846. [Epub ahead of print]

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PUBMED

Genetic and clinical analysis of spinocerebellar ataxia type 36 in Mainland China.

Zeng S, Zeng J, He M, Zeng X, Zhou Y, Liu Z, Xia K, Pan Q, Jiang H, Shen L, Yan X, Tang B, Wang J.

Clin Genet. 2016 Aug;90(2):141-8. doi: 10.1111/cge.12706.

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PUBMED

A homozygous mutation of VWA3B causes cerebellar ataxia with intellectual disability.

Kawarai T, Tajima A, Kuroda Y, Saji N, Orlacchio A, Terasawa H, Shimizu H, Kita Y, Izumi Y, Mitsui T, Imoto I, Kaji R.

J Neurol Neurosurg Psychiatry. 2016 Jun;87(6):656-62. doi: 10.1136/jnnp-2014-309828.

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Bilateral maculopathy in a patient with ataxia telangiectasia.

Gioia LV, Bonsall D, Moffett K, Leys M.

J AAPOS. 2016 Feb;20(1):85-8. doi: 10.1016/j.jaapos.2015.10.005.

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