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European Neurology|August 7, 1998
Congenital muscular dystrophy with partial merosin deficiency and late onset epilepsyF Martinello, C Angelini, C P TrevisanNeurology|July 1, 1987
Exercise-induced recurrent myoglobinuria: defective activity of inner carnitine palmitoyltransferase in muscle mitochondria of two patientsC P Trevisan, G Isaya, C AngeliniEuropean Neurology|January 1, 1995
Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy: a clinical and neuroradiological follow-upC P Trevisan, F Martinello, E Ferruzza, et al.Muscle & Nerve|October 1, 1985
Beta-oxidation enzymes in normal human muscle and in muscle from a patient with an unusual form of myopathic carnitine deficiencyC P Trevisan, H Reichmann, D C DeVivo, et al.Journal of Neurology|May 14, 1999
Clinical and neuroimaging study of central nervous system in congenital myotonic dystrophyF Martinello, A Piazza, E Pastorello, et al.Acta Neurologica|June 1, 1994
Superficial hemosiderosis of the central nervous system. A case reportF Maggioni, F Martinello, R Iavicoli, et al.Behavioural Neurology|February 4, 2014
Reversible aphasia in adolescence: A late-onset form of Landau Kleffner syndrome? Report of a single caseG Denes, C Mantovan, E Ferruzza, et al.Neurology|March 1, 1984
Myoglobinuria and carnitine palmityltransferase (CPT) deficiency: studies with malonyl-CoA suggest absence of only CPT-IIC P Trevisan, C Angelini, L Freddo, et al.European Neurology|January 1, 1986
Malonyl-CoA abnormal inhibition of residual enzyme activity in carnitine palmitoyltransferase deficiencyC P Trevisan, C Angelini, L A Fiorellini, et al.Neurology|November 9, 2000
A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophyE Pegoraro, M Fanin, C P Trevisan, et al.Pageof 4