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Neurology|May 29, 2003
Idebenone treatment in Friedreich patients: one-year-long randomized placebo-controlled trialC Mariotti, A Solari, D Torta, et al.AJNR. American Journal of Neuroradiology|May 1, 1983
Computed tomography of olivopontocerebellar degenerationM Savoiardo, M Bracchi, A Passerini, et al.Neurology|October 24, 2001
Pathogenic effect of an intermediate-size SCA-6 allele (CAG)(19) in a homozygous patientC Mariotti, C Gellera, M Grisoli, et al.Clinical Neuropathology|November 1, 1989
Sialidosis type I: pathological study in an adultA Allegranza, G Tredici, P Marmiroli, et al.Italian Journal of Neurological Sciences|October 1, 1980
Friedreich's ataxia II. Biochemical studies in cultured cellsB Bertagnolio, G Uziel, E Bottacchi, et al.Acta Neurologica|October 1, 1989
[Muscle weakness and intolerance to exercise in mitochondrial myopathies]D Peluchetti, C Antozzi, G S Roi, et al.Neurology|October 1, 1983
Congenital myopathy due to phosphorylase deficiencyF Cornelio, N Bresolin, S DiMauro, et al.Italian Journal of Neurological Sciences|December 1, 1982
Pyruvate-dehydrogenase complex in ataxic patients: enzyme deficiency in ataxic encephalopathy plus lactic acidosis and normal activity in Friedreich ataxiaG Uziel, E Bottacchi, G Moschen, et al.Italian Journal of Neurological Sciences|August 10, 2000
Practice guidelines: a more rational approach to diagnosis and treatment and a more effective use of health care resourcesE Beghi, A Citterio, F Cornelio, et al.Archives of Neurology|October 1, 1984
Clinical varieties of neuromuscular disease in debrancher deficiencyF Cornelio, N Bresolin, P A Singer, et al.Pageof 16