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Bibliografía Científica

Artículo Destacado en trastornos del movimiento

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

443 ARTíCULOS , VIENDO DEL 16 AL 30

PUBMED

Spinocerebellar ataxia type 7: Report of an Indian family.

Wali GM.

Ann Indian Acad Neurol. 2013 Oct;16(4):708-11. doi: 10.4103/0972-2327.120455.

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Relationship between proprioception at the knee joint and gait ataxia in HSAN III.

Macefield VG, Norcliffe-Kaufmann LJ, Axelrod FB, Kaufmann H.

Mov Disord. 2013 Jun;28(6):823-7. doi: 10.1002/mds.25482.

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PUBMED

Patients with autosomal dominant spinocerebellar ataxia have more risk of falls, important balance impairment, and decreased ability to function.

Aizawa CY, Pedroso JL, Braga-Neto P, Callegari MR, Barsottini OG.

Arq Neuropsiquiatr. 2013 Aug;71(8):508-11. doi: 10.1590/0004-282X20130094.

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PUBMED

Ten Years' Follow-Up of a Family With Myokymia and Muscle Cramps Without Ataxia.

Moghimi N, Rosen JB, Jabbari B.

J Child Neurol. 2013 Nov;28(11):1493-1495.

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PUBMED

Therapeutic strategies in Friedreich's ataxia.

Richardson TE, Kelly HN, Yu AE, Simpkins JW.

Brain Res. 2013 Jun 13;1514:91-7. doi: 10.1016/j.brainres.2013.04.005. Review.

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PUBMED

Mutant γPKC that causes spinocerebellar ataxia type 14 upregulates Hsp70, which protects cells from the mutant's cytotoxicity.

Ogawa K, Seki T, Onji T, Adachi N, Tanaka S, Hide I, Saito N, Sakai N.

Biochem Biophys Res Commun. 2013 Oct 11;440(1):25-30. doi: 10.1016/j.bbrc.2013.09.013.

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PUBMED

Novel mutation in the ATM gene in a Malian family with ataxia telangiectasia.

Landouré G, Mochel F, Meilleur K, Ly M, Sangaré M, Bocoum N, Bagayoko K, Coulibaly T, Sarr AM, Bâ HO, Coulibaly S, Guinto CO, Touré M, Traoré M, Fischbeck KH.

J Neurol. 2013 Jan;260(1):324-6. doi: 10.1007/s00415-012-6738-5. No abstract available.

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PUBMED

Optical coherence tomography findings in spinocerebellar ataxia-3.

Alvarez G, Rey A, Sanchez-Dalmau FB, Muñoz E, Ríos J, Adán A.

Eye (Lond). 2013 Dec;27(12):1376-81. doi: 10.1038/eye.2013.201.

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PUBMED

The management of hyperleukocytosis in an adult patient with acute lymphoblastic leukemia and ataxia-telangiectasia.

Keklik M, Sivgin S, Kalin BS, Akyol G, Pala C, Solmaz M, Kaynar L, Eser B, Cetin M, Unal A.

Transfus Apher Sci. 2013 Jun;48(3):293-5. doi: 10.1016/j.transci.2013.04.001.

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PUBMED

[Chronic ataxia in childhood].

Erazo Torricelli R.

Medicina (B Aires). 2013;73 Suppl 1:38-48. Review. Spanish.

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PUBMED

Intrathecal injection of P/Q type voltage-gated calcium channel antibodies from paraneoplastic cerebellar degeneration cause ataxia in mice.

Martín-García E, Mannara F, Gutiérrez-Cuesta J, Sabater L, Dalmau J, Maldonado R, Graus F.

J Neuroimmunol. 2013 Aug 15;261(1-2):53-9. doi: 10.1016/j.jneuroim.2013.05.003.

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PUBMED

Magnetic resonance imaging biomarkers in patients with progressive ataxia: current status and future direction.

Currie S, Hadjivassiliou M, Craven IJ, Wilkinson ID, Griffiths PD, Hoggard N.

Cerebellum. 2013 Apr;12(2):245-66. doi: 10.1007/s12311-012-0405-3. Review.

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PUBMED

Clinical course of two Italian siblings with ataxia-telangiectasia-like disorder.

Palmeri S, Rufa A, Pucci B, Santarnecchi E, Malandrini A, Stromillo ML, Mandalà M, Rosini F, De Stefano N, Federico A.

Cerebellum. 2013 Aug;12(4):596-9. doi: 10.1007/s12311-013-0460-4.

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PUBMED

GABA-A receptor impairment in cerebellar ataxia with anti-glutamic acid decarboxylase antibodies.

Hosoi Y, Suzuki-Sakao M, Terada T, Konishi T, Ouchi Y, Miyajima H, Kono S.

J Neurol. 2013 Dec;260(12):3086-92. doi: 10.1007/s00415-013-7092-y.

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PUBMED

Early abnormalities in 123I-ioflupane (DaTSCAN) imaging in the fragile X-associated tremor ataxia syndrome (FXTAS): a case report.

Madeo G, Alemseged F, Di Pietro B, Schillaci O, Pisani A.

Neurol Sci. 2013 Aug;34(8):1475-7. doi: 10.1007/s10072-012-1223-6. No abstract available.

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