Exploration of transitional life events in individuals with Friedreich ataxia: implications for genetic counseling.

White VB, Leib JR, Farmer JM, Biesecker BB.

Behav Brain Funct. 2010 Oct 27;6:65. doi: 10.1186/1744-9081-6-65.

Functional significance for a heterogenous ribonucleoprotein A18 signature RNA motif in the 3'-untranslated region of ataxia telangiectasia mutated and Rad3-related (ATR) transcript.

Yang R, Zhan M, Nalabothula NR, Yang Q, Indig FE, Carrier F.

J Biol Chem. 2010 Mar 19;285(12):8887-93. doi: 10.1074/jbc.M109.013128.

Primary bilateral thalamic astrocytoma presenting with head tremor, ataxia, and dementia.

Machado A, Ribeiro M, Rodrigues M, Ferreira C, Almeida R, Santana I, Castro L, Carpenter S.

J Neuropsychiatry Clin Neurosci. 2010 Summer;22(3):352e.e7-352.e8. doi: 10.1176/appi.neuropsych.22.3.352-e.e7. No abstract available.

Functional effects of spinocerebellar ataxia type 13 mutations are conserved in zebrafish Kv3.3 channels.

Mock AF, Richardson JL, Hsieh JY, Rinetti G, Papazian DM.

BMC Neurosci. 2010 Aug 16;11:99. doi: 10.1186/1471-2202-11-99.

Spinocerebellar ataxia type 11 in the Chinese Han population.

Xu Q, Li X, Wang J, Yi J, Lei L, Shen L, Jiang H, Xia K, Pan Q, Tang B.

Neurol Sci. 2010 Feb;31(1):107-9. doi: 10.1007/s10072-009-0129-4.

Congo red, an amyloid-inhibiting compound, alleviates various types of cellular dysfunction triggered by mutant protein kinase cγ that causes spinocerebellar ataxia type 14 (SCA14) by inhibiting oligomerization and aggregation.

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

J Pharmacol Sci. 2010;114(2):206-16.

Ataxia telangiectasia mutated (ATM) inhibition transforms human mammary gland epithelial cells.

Mandriota SJ, Buser R, Lesne L, Stouder C, Favaudon V, Maechler P, Béna F, Clément V, Rüegg C, Montesano R, Sappino AP.

J Biol Chem. 2010 Apr 23;285(17):13092-106. doi: 10.1074/jbc.M109.078360.

Evidence of mitochondrial dysfunction in fragile X-associated tremor/ataxia syndrome.

Ross-Inta C, Omanska-Klusek A, Wong S, Barrow C, Garcia-Arocena D, Iwahashi C, Berry-Kravis E, Hagerman RJ, Hagerman PJ, Giulivi C.

Biochem J. 2010 Aug 1;429(3):545-52. doi: 10.1042/BJ20091960.

Myelodysplasia as a cause of hindlimb ataxia in two beef calves.

Hill BD.

Aust Vet J. 2010 Apr;88(4):151-3. doi: 10.1111/j.1751-0813.2010.00559.x.

Acute cerebellar ataxia in childhood: initial approach in the emergency department.

Salas AA, Nava A.

Emerg Med J. 2010 Dec;27(12):956-7. doi: 10.1136/emj.2009.079376.

[A case of recurrent paraneoplastic cerebellar ataxia with antibodies to GluR epsilon 2 causally related to ganglioneuroma].

Noguchi S, Kaga Y, Takahashi Y, Aoyagi K, Nakamura K, Kamiya Y, Nakane T, Kanemura H, Sugita K, Aihara M.

No To Hattatsu. 2010 Jul;42(4):297-301. Japanese.

Does oxidative stress contribute to the pathology of Friedreich's ataxia? A radical question.

Armstrong JS, Khdour O, Hecht SM.

FASEB J. 2010 Jul;24(7):2152-63. doi: 10.1096/fj.09-143222. Review.

Progression markers of Spinocerebellar ataxia 2. A twenty years neurophysiological follow up study.

Velázquez-Perez L, Rodríguez-Labrada R, Canales-Ochoa N, Sanchez-Cruz G, Fernandez-Ruiz J, Montero JM, Aguilera-Rodríguez R, Diaz R, Almaguer-Mederos LE, Truitz AP.

J Neurol Sci. 2010 Mar 15;290(1-2):22-6. doi: 10.1016/j.jns.2009.12.013.

Role of ataxia telangiectasia mutated in insulin signalling of muscle-derived cell lines and mouse soleus.

Jeong I, Patel AY, Zhang Z, Patil PB, Nadella ST, Nair S, Ralston L, Hoormann JK, Fisher JS.

Acta Physiol (Oxf). 2010 Apr;198(4):465-75. doi: 10.1111/j.1748-1716.2009.02069.x.

[Ataxia secondary to valproate. The importance of the choice of anti-epileptic treatment in the elderly].

Gutiérrez Rodríguez J.

Rev Esp Geriatr Gerontol. 2010 Jan-Feb;45(1):52-3. doi: 10.1016/j.regg.2009.06.015. Spanish. No abstract available.