Nerve growth factor for the treatment of spinocerebellar ataxia type 3: an open-label study.

Tan S, Wang RH, Niu HX, Shi CH, Mao CY, Zhang R, Song B, Sun SL, Liu XJ, Hou HM, Liu YT, Gao Y, Fang H, Kong XD, Xu YM.

Chin Med J (Engl). 2015 Feb 5;128(3):291-4. doi: 10.4103/0366-6999.150087.

SCA27 is a cause of early-onset ataxia and developmental delay.

Planes M, Rooryck C, Vuillaume ML, Besnard L, Bouron J, Lacombe D, Arveiler B, Goizet C.

Eur J Paediatr Neurol. 2015 Mar;19(2):271-3. doi: 10.1016/j.ejpn.2014.11.013. No abstract available.

Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion.

Obayashi M, Stevanin G, Synofzik M, Monin ML, Duyckaerts C, Sato N, Streichenberger N, Vighetto A, Desestret V, Tesson C, Wichmann HE, Illig T, Huttenlocher J, Kita Y, Izumi Y, Mizusawa H, Schöls L, K

J Neurol Neurosurg Psychiatry. 2015 Sep;86(9):986-95. doi: 10.1136/jnnp-2014-309153.

Clonal expansion of secondary mitochondrial DNA deletions associated with spinocerebellar ataxia type 28.

Gorman GS, Pfeffer G, Griffin H, Blakely EL, Kurzawa-Akanbi M, Gabriel J, Sitarz K, Roberts M, Schoser B, Pyle A, Schaefer AM, McFarland R, Turnbull DM, Horvath R, Chinnery PF, Taylor RW.

JAMA Neurol. 2015 Jan;72(1):106-11. doi: 10.1001/jamaneurol.2014.1753.

Integration of modeling with experimental and clinical findings synthesizes and refines the central role of inositol 1,4,5-trisphosphate receptor 1 in spinocerebellar ataxia.

Brown SA, Loew LM.

Front Neurosci. 2015 Jan 21;8:453. doi: 10.3389/fnins.2014.00453. Review.

An open-label trial in Friedreich ataxia suggests clinical benefit with high-dose resveratrol, without effect on frataxin levels.

Yiu EM, Tai G, Peverill RE, Lee KJ, Croft KD, Mori TA, Scheiber-Mojdehkar B, Sturm B, Praschberger M, Vogel AP, Rance G, Stephenson SE, Sarsero JP, Stockley C, Lee CY, Churchyard A, Evans-Galea MV, Ry

J Neurol. 2015 May;262(5):1344-53. doi: 10.1007/s00415-015-7719-2.

Early activation of microglia and astrocytes in mouse models of spinocerebellar ataxia type 1.

Cvetanovic M, Ingram M, Orr H, Opal P.

Neuroscience. 2015 Mar 19;289:289-99. doi: 10.1016/j.neuroscience.2015.01.003.

Class switch recombination process in ataxia telangiectasia patients with elevated serum levels of IgM.

Mohammadinejad P, Abolhassani H, Aghamohammadi A, Pourhamdi S, Ghosh S, Sadeghi B, Nasiri Kalmarzi R, Durandy A, Borkhardt A.

J Immunoassay Immunochem. 2015;36(1):16-26. doi: 10.1080/15321819.2014.891525.

Age-dependent gait abnormalities in mice lacking the Rnf170 gene linked to human autosomal-dominant sensory ataxia.

Kim Y, Kim SH, Kim KH, Chae S, Kim C, Kim J, Shin HS, Lee MS, Kim D.

Hum Mol Genet. 2015 Dec 20;24(25):7196-206. doi: 10.1093/hmg/ddv417.

Opsoclonus-myoclonus-ataxia syndrome associated with dengue virus infection.

Tan AH, Linn K, Sam IC, Tan CT, Lim SY.

Parkinsonism Relat Disord. 2015 Feb;21(2):160-1. doi: 10.1016/j.parkreldis.2014.11.009. No abstract available.

Paraneoplastic cerebellar ataxia and the paraneoplastic syndromes.

Afzal S, Recio M, Shamim S.

Proc (Bayl Univ Med Cent). 2015 Apr;28(2):217-20.

Crystallographic and Computational Analyses of AUUCU Repeating RNA That Causes Spinocerebellar Ataxia Type 10 (SCA10).

Park H, González ÀL, Yildirim I, Tran T, Lohman JR, Fang P, Guo M, Disney MD.

Biochemistry. 2015 Jun 23;54(24):3851-9. doi: 10.1021/acs.biochem.5b00551.

Central auditory processing in patients with spinocerebellar ataxia.

Zeigelboim BS, de Carvalho HA, Teive HA, Liberalesso PB, Jurkiewicz AL, da Silva Abdulmassih EM, Marques JM, Cordeiro ML.

Hear Res. 2015 Sep;327:235-44. doi: 10.1016/j.heares.2015.07.006.

ATDC (Ataxia Telangiectasia Group D Complementing) Promotes Radioresistance through an Interaction with the RNF8 Ubiquitin Ligase.

Yang H, Palmbos PL, Wang L, Kim EH, Ney GM, Liu C, Prasad J, Misek DE, Yu X, Ljungman M, Simeone DM.

J Biol Chem. 2015 Nov 6;290(45):27146-57. doi: 10.1074/jbc.M115.665489.

Vision related quality of life in spinocerebellar ataxia.

Kedar S, Ghate D, Murray EL, Corbett JJ, Subramony SH.

J Neurol Sci. 2015 Nov 15;358(1-2):404-8. doi: 10.1016/j.jns.2015.10.013.