Familial segmental spinal myoclonus: a rare clinical feature of Friedreich's ataxia.

Jain RS, Kumar S, Tejwani S.

Springerplus. 2015 Jul 8;4:330. doi: 10.1186/s40064-015-1121-5.

Myoclonic axial jerks for diagnosing atypical evolution of ataxia telangiectasia.

Nakayama T, Sato Y, Uematsu M, Takagi M, Hasegawa S, Kumada S, Kikuchi A, Hino-Fukuyo N, Sasahara Y, Haginoya K, Kure S.

Brain Dev. 2015 Mar;37(3):362-5. doi: 10.1016/j.braindev.2014.06.001.

SNP Analysis and Whole Exome Sequencing: Their Application in the Analysis of a Consanguineous Pedigree Segregating Ataxia.

Nickerson SL, Marquis-Nicholson R, Claxton K, Ashton F, Leong IU, Prosser DO, Love JM, George AM, Taylor G, Wilson C, Gardner RJ, Love DR.

Microarrays (Basel). 2015 Oct 23;4(4):490-502. doi: 10.3390/microarrays4040490.

Excision of Expanded GAA Repeats Alleviates the Molecular Phenotype of Friedreich's Ataxia.

Li Y, Polak U, Bhalla AD, Rozwadowska N, Butler JS, Lynch DR, Dent SY, Napierala M.

Mol Ther. 2015 Jun;23(6):1055-65. doi: 10.1038/mt.2015.41.

An investigation of diffusion imaging techniques in the evaluation of spinocerebellar ataxia and multisystem atrophy.

Rozenfeld MN, Nemeth AJ, Walker MT, Mohan P, Wang X, Parrish TB, Opal P.

J Clin Neurosci. 2015 Jan;22(1):166-72. doi: 10.1016/j.jocn.2014.08.006.

Rehabilitation for a Patient with Hemiplegia, Ataxia, and Cognitive Dysfunction Caused by Pontine Hemorrhage.

Tsunoda T, Maeshima S, Watanabe M, Nagai A, Ueno Y, Ozeki Y, Okamoto S, Mizuno S, Sonoda S.

Case Rep Neurol. 2015 Oct 27;7(3):213-20. doi: 10.1159/000441617.

Deep brain stimulation of the dentate nucleus improves cerebellar ataxia after cerebellar stroke.

Teixeira MJ, Cury RG, Galhardoni R, Barboza VR, Brunoni AR, Alho E, Lepski G, Ciampi de Andrade D.

Neurology. 2015 Dec 8;85(23):2075-6. doi: 10.1212/WNL.0000000000002204. No abstract available.

Mutation of SLC9A1, encoding the major Na⁺/H⁺ exchanger, causes ataxia-deafness Lichtenstein-Knorr syndrome.

Guissart C, Li X, Leheup B, Drouot N, Montaut-Verient B, Raffo E, Jonveaux P, Roux AF, Claustres M, Fliegel L, Koenig M.

Hum Mol Genet. 2015 Jan 15;24(2):463-70. doi: 10.1093/hmg/ddu461.

The first Japanese familial case of spinocerebellar ataxia 23 with a novel mutation in the PDYN gene.

Saigoh K, Mitsui J, Hirano M, Shioyama M, Samukawa M, Ichikawa Y, Goto J, Tsuji S, Kusunoki S.

Parkinsonism Relat Disord. 2015 Mar;21(3):332-4. doi: 10.1016/j.parkreldis.2014.12.028. No abstract available.

Ethanol-Induced Cerebellar Ataxia: Cellular and Molecular Mechanisms.

Dar MS.

Cerebellum. 2015 Aug;14(4):447-65. doi: 10.1007/s12311-014-0638-4.

Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxia.

Damiano JA, Afawi Z, Bahlo M, Mauermann M, Misk A, Arsov T, Oliver KL, Dahl HH, Shearer AE, Smith RJ, Hall NE, Mahmood K, Leventer RJ, Scheffer IE, Muona M, Lehesjoki AE, Korczyn AD, Herrmann H, Berko

Hum Mol Genet. 2015 Aug 15;24(16):4483-90. doi: 10.1093/hmg/ddv171.

Frataxin levels in peripheral tissue in Friedreich ataxia.

Lazaropoulos M, Dong Y, Clark E, Greeley NR, Seyer LA, Brigatti KW, Christie C, Perlman SL, Wilmot GR, Gomez CM, Mathews KD, Yoon G, Zesiewicz T, Hoyle C, Subramony SH, Brocht AF, Farmer JM, Wilson RB

Ann Clin Transl Neurol. 2015 Aug;2(8):831-42. doi: 10.1002/acn3.225.

Spinocerebellar ataxia type 10 in the South of Brazil: the Amerindian-Belgian connection.

Teive HA, Moro A, Moscovich M, Arruda WO, Munhoz RP, Raskin S, Teive GM, Dallabrida N, Ashizawa T.

Arq Neuropsiquiatr. 2015 Aug;73(8):725-7. doi: 10.1590/0004-282X20150086.

Ataxia-Telangiectasia Presenting as Cerebral Palsy and Recurrent Wheezing: A Case Report.

Navratil M, Đuranović V, Nogalo B, Švigir A, Dumbović Dubravčić I, Turkalj M.

Am J Case Rep. 2015 Sep 18;16:631-6. doi: 10.12659/AJCR.893995.

Spectrum of sleep disorders in a patient with spinocerebellar ataxia 13.

Kapoor M, Greenough G.

J Clin Sleep Med. 2015 Jan 15;11(2):177-9. doi: 10.5664/jcsm.4468.