Olfactory dysfunction in fragile X tremor ataxia syndrome.

Juncos JL, Lazarus JT, Rohr J, Allen EG, Shubeck L, Hamilton D, Novak G, Sherman SL.

Mov Disord. 2012 Oct;27(12):1556-9. doi: 10.1002/mds.25043.

Ataxia telangiectasia mutated kinase controls chronic gammaherpesvirus infection.

Kulinski JM, Leonardo SM, Mounce BC, Malherbe L, Gauld SB, Tarakanova VL.

J Virol. 2012 Dec;86(23):12826-37. doi: 10.1128/JVI.00917-12.

A0001 in Friedreich ataxia: biochemical characterization and effects in a clinical trial.

Lynch DR, Willi SM, Wilson RB, Cotticelli MG, Brigatti KW, Deutsch EC, Kucheruk O, Shrader W, Rioux P, Miller G, Hawi A, Sciascia T.

Mov Disord. 2012 Jul;27(8):1026-33. doi: 10.1002/mds.25058.

Otogenic brain abscess presenting with gait ataxia.

Cho SH, Park MK, Lee JD, Hwang SC.

Korean J Audiol. 2012 Apr;16(1):31-4. doi: 10.7874/kja.2012.16.1.31.

Two in one: report of a patient with spinocerebellar ataxia types 2 and 10.

Kapur SS, Goldman JG.

Arch Neurol. 2012 Sep;69(9):1200-3. doi: 10.1001/archneurol.2011.3044.

Limb ataxia originating from peri-central sulcus demyelinating lesion in multiple sclerosis.

Karmon Y, Morrow SA, Weinstock A, Hojnacki D, Weinstock-Guttman B.

J Neurol Sci. 2012 Sep 15;320(1-2):136-40. doi: 10.1016/j.jns.2012.05.039.

Identification and quantification of differentially expressed proteins in plasma of spinocerebellar ataxia type 12.

Swarup V, Srivastava AK, Rajeswari MR.

Neurosci Res. 2012 Jun;73(2):161-7. doi: 10.1016/j.neures.2012.03.002.

[What we can learn from a case of medical malpractice--compensatory damages awarded to a patient with autonomic ataxia on administrative leave for emotional distress arising out of alleged inappropriate remarks made by his industrial physician].

Asada M, Kuwabara H, Honda Y, Sumioka R, Makita S, Okabe M, Kawasaki S, Kobayashi H.

Nihon Geka Gakkai Zasshi. 2012 Jul;113(4):393-4. Japanese. No abstract available.

A compound heterozygous missense mutation and a large deletion in the KCTD7 gene presenting as an opsoclonus-myoclonus ataxia-like syndrome.

Blumkin L, Kivity S, Lev D, Cohen S, Shomrat R, Lerman-Sagie T, Leshinsky-Silver E.

J Neurol. 2012 Dec;259(12):2590-8. doi: 10.1007/s00415-012-6545-z.

[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.

Deep brain stimulation for the treatment of tremor and ataxia associated with abetalipoproteinemia.

Mammis A, Pourfar M, Feigin A, Mogilner AY.

Tremor Other Hyperkinet Mov (N Y). 2012;2. pii: tre-02-45-228-1. doi: 10.7916/D8542M96.

Functional characterization and targeted correction of ATM mutations identified in Japanese patients with ataxia-telangiectasia.

Nakamura K, Du L, Tunuguntla R, Fike F, Cavalieri S, Morio T, Mizutani S, Brusco A, Gatti RA.

Hum Mutat. 2012 Jan;33(1):198-208. doi: 10.1002/humu.21632.

Machado-Joseph disease in Brazil: from the first descriptions to the emergence as the most common spinocerebellar ataxia.

Pedroso JL, Braga-Neto P, Radvany J, Barsottini OG.

Arq Neuropsiquiatr. 2012 Aug;70(8):630-2.

Tremor-spectrum in spinocerebellar ataxia type 3.

Bonnet C, Apartis E, Anheim M, Legrand AP, Baizabal-Carvallo JF, Bonnet AM, Durr A, Vidailhet M.

J Neurol. 2012 Nov;259(11):2460-70. doi: 10.1007/s00415-012-6531-5. Review.

[Anti-thyroid antibodies in two patients with subacute dementia, ataxia, and myoclonus].

Kondziella D, Hansen K, Gonzalez T, Gideon P, Christiansen I, Sellebjerg F.

Ugeskr Laeger. 2012 Feb 27;174(9):577-9. Danish.