Mitochondrial dysfunction in ataxia-telangiectasia.

Valentin-Vega YA, Maclean KH, Tait-Mulder J, Milasta S, Steeves M, Dorsey FC, Cleveland JL, Green DR, Kastan MB.

Blood. 2012 Feb 9;119(6):1490-500. doi: 10.1182/blood-2011-08-373639.

Rare presentation of unilateral weakness, involuntary movements and ataxia with subcortical t2 hypointensity in a diabetic patient: a case report.

Indiran V, Maduraimuthu P.

Case Rep Radiol. 2012;2012:768189. doi: 10.1155/2012/768189.

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.

Freidreich's ataxia with retained reflexes: a phenotype and genotype correlation.

Verma R, Gupta M.

BMJ Case Rep. 2012 Dec 14;2012. pii: bcr2012007496. doi: 10.1136/bcr-2012-007496.

Annual change in Friedreich's ataxia evaluated by the Scale for the Assessment and Rating of Ataxia (SARA) is independent of disease severity.

Marelli C, Figoni J, Charles P, Anheim M, Tchikviladze M, Vincitorio CM, du Montcel ST, Brice A, Golmard JL, Dürr A.

Mov Disord. 2012 Jan;27(1):135-8. doi: 10.1002/mds.23879.

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.

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.

[Recent advance in genetic study of hereditary autosomal recessive cerebellar ataxia].

Guan WJ, Wang JL, Tang BS.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Dec;29(6):673-6. doi: 10.3760/cma.j.issn.1003-9406.2012.06.010. Review. Chinese.

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.

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.

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.

False-positive head-impulse test in cerebellar ataxia.

Kremmyda O, Kirchner H, Glasauer S, Brandt T, Jahn K, Strupp M.

Front Neurol. 2012 Nov 12;3:162. doi: 10.3389/fneur.2012.00162.