Magnetic Resonance Imaging in Movement Disorders: Ataxia

A.-S. Lebre, A. Brice, Spinocerebellar ataxia 7 (SCA7). Cytogenetic and Genome Research. ,vol. 100, pp. 154- 163 ,(2003) , 10.1159/000072850

Kathrin Reetz, Ana S. Costa, Shahram Mirzazade, Anna Lehmann, Agnes Juzek, Maria Rakowicz, Romana Boguslawska, Ludger Schöls, Christoph Linnemann, Caterina Mariotti, Marina Grisoli, Alexandra Dürr, Bart P. van de Warrenburg, Dagmar Timmann, Massimo Pandolfo, Peter Bauer, Heike Jacobi, Till-Karsten Hauser, Thomas Klockgether, Jörg B. Schulz, , Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6 Brain. ,vol. 136, pp. 905- 917 ,(2013) , 10.1093/BRAIN/AWS369

I E Ormerod, A E Harding, D H Miller, G Johnson, D MacManus, E P du Boulay, B E Kendall, I F Moseley, W I McDonald, Magnetic resonance imaging in degenerative ataxic disorders. Journal of Neurology, Neurosurgery, and Psychiatry. ,vol. 57, pp. 51- 57 ,(1994) , 10.1136/JNNP.57.1.51

Carsten Lukas, Ludger Schöls, Barbara Bellenberg, Udo Rüb, Horst Przuntek, Gebhard Schmid, Odo Köster, Boris Suchan, Dissociation of grey and white matter reduction in spinocerebellar ataxia type 3 and 6: A voxel-based morphometry study Neuroscience Letters. ,vol. 408, pp. 230- 235 ,(2006) , 10.1016/J.NEULET.2006.09.007

F. Maltecca, A. Filla, I. Castaldo, G. Coppola, N.A. Fragassi, M. Carella, A. Bruni, S. Cocozza, G. Casari, A. Servadio, G. De Michele, Intergenerational instability and marked anticipation in SCA-17. Neurology. ,vol. 61, pp. 1441- 1443 ,(2003) , 10.1212/01.WNL.0000094123.09098.A0

S. H. Ying, S. I. Choi, S. L. Perlman, R. W. Baloh, D. S. Zee, A. W. Toga, Pontine and cerebellar atrophy correlate with clinical disability in SCA2. Neurology. ,vol. 66, pp. 424- 426 ,(2006) , 10.1212/01.WNL.0000196464.47508.00

Ana Solodkin, Eitan Peri, E. Elinor Chen, Eshel Ben-Jacob, Christopher M. Gomez, Loss of Intrinsic Organization of Cerebellar Networks in Spinocerebellar Ataxia Type 1: Correlates with Disease Severity and Duration The Cerebellum. ,vol. 10, pp. 218- 232 ,(2011) , 10.1007/S12311-010-0214-5

Ina Klinke, Martina Minnerop, Tanja Schmitz-Hübsch, Marc Hendriks, Thomas Klockgether, Ullrich Wüllner, Christoph Helmstaedter, Neuropsychological Features of Patients with Spinocerebellar Ataxia (SCA) Types 1, 2, 3, and 6 The Cerebellum. ,vol. 9, pp. 433- 442 ,(2010) , 10.1007/S12311-010-0183-8

Gilles David, Nacer Abbas, Giovanni Stevanin, Alexandra Dürr, Gaël Yvert, Géraldine Cancel, Chantal Weber, Georges Imbert, Frédéric Saudou, Eric Antoniou, Harry Drabkin, Robert Gemmill, Paola Giunti, Ali Benomar, Nick Wood, Merle Ruberg, Yves Agid, Jean-Louis Mandel, Alexis Brice, None, Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion Nature Genetics. ,vol. 17, pp. 65- 70 ,(1997) , 10.1038/NG0997-65

Hamed Akhlaghi, Louise Corben, Nellie Georgiou-Karistianis, John Bradshaw, Elsdon Storey, Martin B. Delatycki, Gary F. Egan, Superior Cerebellar Peduncle Atrophy in Friedreich's Ataxia Correlates with Disease Symptoms The Cerebellum. ,vol. 10, pp. 81- 87 ,(2011) , 10.1007/S12311-010-0232-3