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2. J. B. Schulz, S. Boesch, K. Burk, A. Durr, P. Giunti, C. Mariotti, F. Pousset, L. Schols, P. Vankan, and M. Pandolfo. Diagnosis and treatment of Friedreich ataxia: a European perspective. Nat Rev Neurol, 5(4):222-34, 2009. Note: Journal ArticleReviewEngland. [WWW] Keyword(s): Antioxidants/therapeutic use, Diagnosis, Differential, Diagnostic Imaging, Europe/epidemiology, Friedreich Ataxia/*diagnosis/epidemiology/genetics/*therapy, Humans, Muscle, Skeletal/physiopathology, Neurophysiology/methods.



3. T. Schmitz-Hubsch, S. T. du Montcel, L. Baliko, J. Berciano, S. Boesch, C. Depondt, P. Giunti, C. Globas, J. Infante, J. S. Kang, B. Kremer, C. Mariotti, B. Melegh, M. Pandolfo, M. Rakowicz, P. Ribai, R. Rola, L. Schols, S. Szymanski, B. P. van de Warrenburg, A. Durr, T. Klockgether, and R. Fancellu. Scale for the assessment and rating of ataxia: development of a new clinical scale. Neurology, 66(11):1717-20, 2006. Note: Journal ArticleRandomized Controlled TrialResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adolescent, Adult, Aged, Aged, 80 and over, Female, *Health Status Indicators, Humans, Male, Middle Aged, Neurologic Examination/*methods, Outcome Assessment (Health Care)/*methods, Reproducibility of Results, Sensitivity and Specificity, *Severity of Illness Index, Spinocerebellar Ataxias/*classification/*diagnosis.



4. M. C. Moreira, S. Klur, M. Watanabe, A. H. Nemeth, I. Le Ber, J. C. Moniz, C. Tranchant, P. Aubourg, M. Tazir, L. Schols, M. Pandolfo, J. B. Schulz, J. Pouget, P. Calvas, M. Shizuka-Ikeda, M. Shoji, M. Tanaka, L. Izatt, C. E. Shaw, A. M'Zahem, E. Dunne, P. Bomont, T. Benhassine, N. Bouslam, G. Stevanin, A. Brice, J. Guimaraes, P. Mendonca, C. Barbot, P. Coutinho, J. Sequeiros, A. Durr, J. M. Warter, and M. Koenig. Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2. Nat Genet, 36(3):225-7, 2004. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Cerebellar Ataxia/*genetics, Chromosome Mapping, Chromosomes, Human, Pair 9, Fungal Proteins/*genetics, Humans, Mutation, Ocular Motility Disorders/*genetics, RNA Helicases/*genetics, Saccharomyces cerevisiae Proteins/genetics, alpha-Fetoproteins/metabolism.

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