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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

5445 ARTíCULOS , VIENDO DEL 5266 AL 5280

PUBMED

[Advances in Neurological Therapeutics for Friedreich Ataxia and Machado-Joseph Disease].

Yabe I, Sasaki H.

Brain Nerve. 2017 Aug;69(8):913-924. doi: 10.11477/mf.1416200842. Japanese.

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Characterization of the Kv1.1 I262T and S342I mutations associated with episodic ataxia 1 with distinct phenotypes.

Zhu J, Alsaber R, Zhao J, Ribeiro-Hurley E, Thornhill WB.

Arch Biochem Biophys. 2012 Aug 15;524(2):99-105. doi: 10.1016/j.abb.2012.05.006.

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PUBMED

Ataxia telangiectasia: Family management.

Seshachalam A, Cyriac S, Reddy N, Gnana ST.

Indian J Hum Genet. 2010 Jan;16(1):39-42. doi: 10.4103/0971-6866.64940.

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PUBMED

Differentially Regulated Cell-Free MicroRNAs in the Plasma of Friedreich's Ataxia Patients and Their Association with Disease Pathology.

Dantham S, Srivastava AK, Gulati S, Rajeswari MR.

Neuropediatrics. 2017 Nov 27. doi: 10.1055/s-0037-1607279. [Epub ahead of print] No abstract available.

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PUBMED

[Anti-GAD antibodies in paraneoplastic cerebellar ataxia associated with limbic encephalitis and autonomic dysfunction].

Carra-Dalliere C, Thouvenot E, Bonafé A, Ducray F, Touchon J, Charif M.

Rev Neurol (Paris). 2012 Apr;168(4):363-6. doi: 10.1016/j.neurol.2011.07.018. French.

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PUBMED

Does the Type of Multisystem Atrophy, Parkinsonism, or Cerebellar Ataxia Impact on the Nature of Sleep Disorders?

Ferini-Strambi L, Marelli S, Combi R.

Curr Neurol Neurosci Rep. 2016 Dec;16(12):105. Review.

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Acetazolamide-responsive Episodic Ataxia Without Baseline Deficits or Seizures Secondary to GLUT1 Deficiency: A Case Report and Review of the Literature.

Tchapyjnikov D, Mikati MA.

Neurologist. 2018 Jan;23(1):17-18. doi: 10.1097/NRL.0000000000000168.

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PUBMED

A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy.

Utine GE, Haliloğlu G, Salanci B, Çetinkaya A, Kiper PÖ, Alanay Y, Aktas D, Boduroğlu K, Alikaşifoğlu M.

J Child Neurol. 2013 Jul;28(7):926-32. doi: 10.1177/0883073813484967.

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PUBMED

Risk Factors for Cognitive Impairment in Fragile X-Associated Tremor/Ataxia Syndrome.

Seritan AL, Kim K, Benjamin I, Seritan I, Hagerman RJ.

J Geriatr Psychiatry Neurol. 2016 Sep 19. pii: 0891988716666379. [Epub ahead of print]

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PUBMED

A novel variant in ATM gene causes ataxia telangiectasia revealed by whole-exome sequencing.

Alonazi NA, Hundallah KJ, Al Hashem AM, Mohamed S.

Neurosciences (Riyadh). 2018 Apr;23(2):162-164. doi: 10.17712/nsj.2018.2.20170463.

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PUBMED

Impact of Friedreich's Ataxia on health-care resource utilization in the United Kingdom and Germany.

Giunti P, Greenfield J, Stevenson AJ, Parkinson MH, Hartmann JL, Sandtmann R, Piercy J, O'Hara J, Casas LR, Smith FM.

Orphanet J Rare Dis. 2013 Feb 28;8:38. doi: 10.1186/1750-1172-8-38.

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PUBMED

Altered redox mitochondrial biology in the neurodegenerative disorder fragile X-tremor/ataxia syndrome: use of antioxidants in precision medicine.

Song G, Napoli E, Wong S, Hagerman R, Liu S, Tassone F, Giulivi C.

Mol Med. 2016 Jun 30;22. doi: 10.2119/molmed.2016.00122. [Epub ahead of print]

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PUBMED

Test-retest reliability of an instrumented electronic walkway system (GAITRite) for the measurement of spatio-temporal gait parameters in young patients with Friedreich's ataxia.

Roche B, Simon AL, Guilmin-Crépon S, Boizeau P, Andriss B, Alberti C, Presedo A, Ilharreborde B, Husson I.

Gait Posture. 2018 Aug 20;66:45-50. doi: 10.1016/j.gaitpost.2018.08.017. [Epub ahead of print]

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PUBMED

Cerebellar Ataxia and CoQ10 Deficiency.

Quinzii CM, Hirano M, Naini A.

J Neurol Disord Stroke. 2013;1(1):1004. No abstract available.

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PUBMED

Cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS) - a case report and review of literature.

Figura M, Gaweł M, Kolasa A, Janik P.

Neurol Neurochir Pol. 2014;48(5):368-72. doi: 10.1016/j.pjnns.2014.08.003. Review.

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