A Probable Korean Case of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.

Kwon KY, Huh K, Eun BL, Yoo HW, Kamsteeg EJ, Scheffer H, Koh SB.

Can J Neurol Sci. 2015 Jul;42(4):271-3. doi: 10.1017/cjn.2015.38. No abstract available.

A novel frameshift mutation in FGF14 causes an autosomal dominant episodic ataxia.

Choquet K, La Piana R, Brais B.

Neurogenetics. 2015 Jul;16(3):233-6. doi: 10.1007/s10048-014-0436-7.

Modifications of resting state networks in spinocerebellar ataxia type 2.

Cocozza S, Saccà F, Cervo A, Marsili A, Russo CV, Giorgio SM, De Michele G, Filla A, Brunetti A, Quarantelli M.

Mov Disord. 2015 Sep;30(10):1382-90. doi: 10.1002/mds.26284.

Friedreich's Ataxia (FRDA) is an extremely rare cause of autosomal recessive ataxia in Chinese Han population.

Zeng J, Wang J, Zeng S, He M, Zeng X, Zhou Y, Liu Z, Jiang H, Tang B.

J Neurol Sci. 2015 Apr 15;351(1-2):124-6. doi: 10.1016/j.jns.2015.03.002.

Miller-Fisher Syndrome: Is the ataxia central or peripheral?

Sandler RD, Hoggard N, Hadjivassiliou M.

Cerebellum Ataxias. 2015 Mar 1;2:3. doi: 10.1186/s40673-015-0021-3.

'You don't get told anything, they don't do anything and nothing changes'. Medicine as a resource and constraint in progressive ataxia.

Daker-White G, Kingston H, Payne K, Greenfield J, Ealing J, Sanders C.

Health Expect. 2015 Apr;18(2):177-87. doi: 10.1111/hex.12016.

Relapsing encephalopathy with cerebellar ataxia related to an ATP1A3 mutation.

Dard R, Mignot C, Durr A, Lesca G, Sanlaville D, Roze E, Mochel F.

Dev Med Child Neurol. 2015 Dec;57(12):1183-6. doi: 10.1111/dmcn.12927.

Ataxia.

Akbar U, Ashizawa T.

Neurol Clin. 2015 Feb;33(1):225-48. doi: 10.1016/j.ncl.2014.09.004. Review.

Loss of the neuron-specific F-box protein FBXO41 models an ataxia-like phenotype in mice with neuronal migration defects and degeneration in the cerebellum.

Mukherjee C, Holubowska A, Schwedhelm-Domeyer N, Mitkovski M, Lee SJ, Kannan M, Matz A, Vadhvani M, Stegmüller J.

J Neurosci. 2015 Jun 10;35(23):8701-17. doi: 10.1523/JNEUROSCI.2133-14.2015.

Spinocerebellar ataxia-10 with paranoid schizophrenia.

Trikamji B, Singh P, Mishra S.

Ann Indian Acad Neurol. 2015 Jan-Mar;18(1):93-5. doi: 10.4103/0972-2327.144285.

Stable isotopes and LC-MS for monitoring metabolic disturbances in Friedreich's ataxia platelets.

Worth AJ, Basu SS, Deutsch EC, Hwang WT, Snyder NW, Lynch DR, Blair IA.

Bioanalysis. 2015;7(15):1843-55. doi: 10.4155/bio.15.118.

Tumor suppressor ataxia telangiectasia mutated functions downstream of TGF-β1 in orchestrating profibrotic responses.

Overstreet JM, Samarakoon R, Cardona-Grau D, Goldschmeding R, Higgins PJ.

FASEB J. 2015 Apr;29(4):1258-68. doi: 10.1096/fj.14-262527.

Friedreich Ataxia: From the Eye of a Molecular Biologist.

Muthuswamy S, Agarwal S.

Neurologist. 2015 Sep;20(3):51-5. doi: 10.1097/NRL.0000000000000054. Review.

Reversible Cerebellar Ataxia Related to Extrapontine Myelinolysis without Hyponatremia after Cisplatin-Based Chemotherapy for Cholangiocarcinoma.

Chung JH, Baik SK, Cho SH, Kim SG.

Cancer Res Treat. 2015 Apr;47(2):329-33. doi: 10.4143/crt.2013.145.

Neurophysiological evidence for generalized sensory neuronopathy in cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome.

Szmulewicz DJ, Seiderer L, Halmagyi GM, Storey E, Roberts L.

Muscle Nerve. 2015 Apr;51(4):600-3. doi: 10.1002/mus.24422.