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Rivista Di Patologia Nervosa E Mentale|August 1, 1976
The syndrome of carnitine deficiencyS Di Donato, F CornelioNeurology|November 1, 1978
Mitochondria-lipid-glycogen myopathy, hyperlactacidemia, and carnitine deficiencyS Di Donato, F Cornelio, M R Balestrini, 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.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.Journal of the Neurological Sciences|May 1, 1981
Heterogeneity of carnitine-palmitoyltransferase deficiencyS Di Donato, A Castiglione, M Rimoldi, et al.Italian Journal of Neurological Sciences|March 1, 1980
"Carnitine deficient" myopathy and cardiomyopathy with fatal outcomeF Cornelio, S Di Donato, D Testa, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1977
Fatal cases of lipid storage myopathy with carnitine deficiencyF Cornelio, S Di Donato, D Peluchetti, et al.Italian Journal of Neurological Sciences|February 1, 1988
Mitochondrial encephalo-neuro-myopathy with myoclonus epilepsy, basal nuclei calcification and hyperlactacidemiaA Federico, F Cornelio, S Di Donato, et al.Italian Journal of Neurological Sciences|August 10, 2000
The complex clinical and genetic classification of inherited ataxias. I. Dominant ataxiasS Di DonatoPageof 16