Artículos por temáticas

Congenital ataxia due to cerebellar malformation presenting with unilateral hypoplasia.

Souza PV, Pinto WB, Pedroso JL, Barsottini OG.

Arq Neuropsiquiatr. 2013 Mar;71(3):198. No abstract available.

Perverted head impulse test in cerebellar ataxia.

Jeong SH, Kim JS, Baek IC, Shin JW, Jo H, Lee AY, Kim JM.

Cerebellum. 2013 Oct;12(5):773-5. doi: 10.1007/s12311-013-0480-0. No abstract available.

Cerebellar soluble mutant ataxin-3 level decreases during disease progression in Spinocerebellar Ataxia Type 3 mice.

Nguyen HP, Hübener J, Weber JJ, Grueninger S, Riess O, Weiss A.

PLoS One. 2013 Apr 23;8(4):e62043. doi: 10.1371/journal.pone.0062043.

Couples at risk for spinocerebellar ataxia type 2: the Cuban prenatal diagnosis experience.

Cruz-Mariño T, Velázquez-Pérez L, González-Zaldivar Y, Aguilera-Rodríguez R, Velázquez-Santos M, Vázquez-Mojena Y, Estupiñán-Rodríguez A, Reynaldo-Armiñán R, Almaguer-Mederos LE, Laffita-Mesa JM, Tama

J Community Genet. 2013 Oct;4(4):451-60. doi: 10.1007/s12687-013-0147-z.

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.

Reply to comment Why do patients with cerebellar ataxia not use environmental cues for reducing unpredictability of sudden gait stopping?" on "Sudden stopping in patients with cerebellar ataxia"."

Serrao M, Conte C, Casali C, Ranavolo A, Mari S, Di Fabio R, Perrotta A, Coppola G, Padua L, Monamì S, Sandrini G, Pierelli F.

Cerebellum. 2013 Dec;12(6):958-9. doi: 10.1007/s12311-013-0501-z. No abstract available.

Purkinje cell loss is the major brain pathology of spinocerebellar ataxia type 10.

Xia G, McFarland KN, Wang K, Sarkar PS, Yachnis AT, Ashizawa T.

J Neurol Neurosurg Psychiatry. 2013 Dec;84(12):1409-11. doi: 10.1136/jnnp-2013-305080. No abstract available.

Teaching neuroimages: ataxia and diabetes insipidus.

Lefaucheur R, Maltête D, Haroche J, Borden A, Wallon D, Bourre B.

Neurology. 2013 Jul 16;81(3):e19. doi: 10.1212/WNL.0b013e31829bfe0a. No abstract available.

Clinical features of Friedreich's ataxia: classical and atypical phenotypes.

Parkinson MH, Boesch S, Nachbauer W, Mariotti C, Giunti P.

J Neurochem. 2013 Aug;126 Suppl 1:103-17. doi: 10.1111/jnc.12317. Review.

A novel de novo exon 21 DNMT1 mutation causes cerebellar ataxia, deafness, and narcolepsy in a Brazilian patient.

Pedroso JL, Povoas Barsottini OG, Lin L, Melberg A, Oliveira AS, Mignot E.

Sleep. 2013 Aug 1;36(8):1257-9, 1259A. doi: 10.5665/sleep.2898.

Successful treatment of acute myeloid leukaemia in a patient with ataxia telangiectasia.

Onoda T, Kanno M, Meguro T, Sato H, Takahashi N, Kawakami T, Mitsui T, Hayasaka K.

Eur J Haematol. 2013 Dec;91(6):557-60. doi: 10.1111/ejh.12186.

Effects of ataxia telangiectasia mutated (ATM) genotypes and smoking habits on lung cancer risk in Taiwan.

Hsia TC, Tsai CW, Liang SJ, Chang WS, Lin LY, Chen WC, Tu CY, Tsai CH, Bau DT.

Anticancer Res. 2013 Sep;33(9):4067-71.

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.

Somatostatin receptor positron emission tomography/computed tomography (PET/CT) in the evaluation of opsoclonus-myoclonus ataxia syndrome.

Joshi P, Lele V.

Indian J Nucl Med. 2013 Apr;28(2):108-11. doi: 10.4103/0972-3919.118236.

Friedreich ataxia.

Gibilisco P, Vogel AP.

BMJ. 2013 Dec 3;347:f7062. doi: 10.1136/bmj.f7062. No abstract available.