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Neurology|June 1, 1979
Hepatic ketogenesis and muscle carnitine deficiencyS DiDonato, F Cornelio, G Storchi, et al.Annals of Neurology|November 1, 1978
Muscle carnitine palmityltransferase deficiency: a case with enzyme deficiency in cultured fibroblastsS DiDonato, F Cornelio, L Pacini, et al.Italian Journal of Neurological Sciences|February 1, 1986
Myoadenylate deaminase deficiency in twins with recessive olivopontocerebellar atrophyG Uziel, F Cornelio, C Gellera, et al.European Neurology|January 1, 1978
Acid maltase deficiency in adults. Clinical, morphological and biochemical study of three patientsB Bertagnolio, S Di Donato, D Peluchetti, et al.Acta Neuropathologica. Supplementum|January 1, 1981
Systemic carnitine deficiency with peripheral nerve involvement morphological and biochemical studyF Cornelio, D Peluchetti, M Rimoldi, et al.Journal of the Neurological Sciences|September 1, 1991
Riboflavin responsive multiple acyl-CoA dehydrogenase deficiency: functional evaluation of recovery after high dose vitamin supplementationD Peluchetti, C Antozzi, S Roi, et al.Neurology|December 1, 1979
Fatal ataxic encephalopathy and carnitine acetyltransferase deficiency: a functional defect of pyruvate oxidation?S DiDonato, M Rimoldi, A Moise, 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.Clinica Chimica Acta; International Journal of Clinical Chemistry|January 31, 1980
Ketogenic response to fasting in human carnitine deficienciesS Di Donato, D Peluchetti, M Rimoldi, et al.Neurology|November 1, 1994
Late-onset riboflavin-responsive myopathy with combined multiple acyl coenzyme A dehydrogenase and respiratory chain deficiencyC Antozzi, B Garavaglia, M Mora, et al.Pageof 37