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Neurology|July 6, 2000
Ataxia, deafness, leukodystrophy: inherited disorder of the white matter in three related patientsV Leuzzi, A Rinna, M Gallucci, et al.Neurology|May 11, 2005
The natural history of Aicardi-Goutières syndrome: follow-up of 11 Italian patientsG Lanzi, E Fazzi, S D'Arrigo, et al.Neurology|November 1, 1993
Cardiomyopathy may be the only clinical manifestation in female carriers of Duchenne muscular dystrophyM Mirabella, S Servidei, G Manfredi, et al.Acta Neuropathologica|January 1, 1994
Reducing body myopathy and desmin storage in skeletal muscle: morphological and biochemical findingsE Bertini, G Salviati, F Apollo, et al.Journal of Inherited Metabolic Disease|March 21, 1998
Fulminant Leigh syndrome and sudden unexpected death in a family with the T9176C mutation of the mitochondrial ATPase 6 geneC Dionisi-Vici, S Seneca, M Zeviani, et al.The Journal of Pediatrics|July 1, 1996
Hypoparathyroidism in mitochondrial trifunctional protein deficiencyC Dionisi-Vici, B Garavaglia, A B Burlina, et al.European Review for Medical and Pharmacological Sciences|August 17, 2010
Myocardial ischemia in cocaine-user with anomalous origin of the left circumflex coronary arteryN Alessandri, A Di Matteo, M Petrassi, et al.American Journal of Medical Genetics|December 1, 1988
Late onset scleroatonic familial myopathy (Ullrich disease): a study of two sibsE Ricci, E Bertini, R Boldrini, et al.Italian Journal of Neurological Sciences|August 10, 2000
X-linked adrenoleukodystrophy: first report of the Italian Study GroupA Di Biase, S Salvati, C Avellino, et al.Brain & Development|January 1, 1990
Involvement of respiratory muscles in cytoplasmic body myopathy--a pathology studyE Bertini, E Ricci, R Boldrini, et al.Pageof 29