Factor substitution, technical change, and returns to scale in Canadian forest industriesMARTINELLO, F.Canadian journal of forest research (Print). 1985, Vol 15, Num 6, pp 1116-1124, issn 0045-5067Article

Congenital muscular dystrophy with partial merosin deficiency and late onset epilepsyMARTINELLO, F; ANGELINI, C; TREVISAN, C. P et al.European neurology. 1998, Vol 40, Num 1, pp 37-45, issn 0014-3022Article

Brain alterations in the classical form of congenital muscular dystrophy : Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscleTREVISAN, C. P; MARTINELLO, F; FERRUZZA, E et al.Child's nervous system (Print). 1996, Vol 12, Num 10, pp 604-610, issn 0256-7040Article

Myocardial involvement is very frequent among patients affected with subclinical Becker's muscular dystrophyMELACINI, P; FANIN, M; ANGELINI, C et al.Circulation (New York, N.Y.). 1996, Vol 94, Num 12, pp 3168-3175, issn 0009-7322Article

Clinical and neuroimaging study of central nervous system in congenital myotonic dystrophyMARTINELLO, F; PIAZZA, A; PASTORELLO, E et al.Journal of neurology. 1999, Vol 246, Num 3, pp 186-192, issn 0340-5354Article

Laminin α2 muscular dystrophy: Genotype/phenotype studies of 22 patientsPEGORARO, E; MARKS, H; STELLA, A et al.Neurology. 1998, Vol 51, Num 1, pp 101-110, issn 0028-3878Article

Prognostic factors in mild dystrophinopathiesANGELINI, C; FANIN, M; FREDA, M. P et al.Journal of the neurological sciences. 1996, Vol 142, Num 1-2, pp 70-78, issn 0022-510XArticle

Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy : a clinical and neuroradiological follow-upTREVISAN, C. P; MARTINELLO, F; FERRUZZA, E et al.European neurology. 1995, Vol 35, Num 4, pp 230-235, issn 0014-3022Article

Supplemental therapy in isolated vitamin E deficiency improves the peripheral neuropathy and prevents the progression of ataxiaMARTINELLO, F; FARDIN, P; OTTIN, M et al.Journal of the neurological sciences. 1998, Vol 156, Num 2, pp 177-179, issn 0022-510XArticle

Valutazione clinica, strumentale e citogenetica di un gruppo di pazienti affetti da atassia telangiectasia = Psychopathologic, neuroimaging and cytogenetic data in a group of patients with ataxia telangiectasiaTREVISAN, C. P; MARTINELLO, F; NUNEZ-GUDINO, G. F et al.Nuova rivista di neurologia. 1994, Vol 4, Num 3, pp 75-78, issn 1122-035XConference Paper

Hypolipemic and antioxidant activities from Tamarindus indica L. pulp fruit extract in hypercholesterolemic hamstersMARTINELLO, F; SOARES, S. M; FRANCO, J. J et al.Food and chemical toxicology. 2006, Vol 44, Num 6, pp 810-818, issn 0278-6915, 9 p.Article

Alterations of the retino-cortical conduction in patients affected by classical Congenital Muscular Dystrophy (Cl-CMD) with merosin deficiencyTORMENE, A. P; TREVISAN, C; MARTINELLO, F et al.Documenta ophthalmologica. 1999, Vol 98, Num 2, pp 127-138, issn 0012-4486Article

Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutationsFANIN, M; DUGGAN, D. J; MOSTACCIUOLO, M. L et al.Journal of medical genetics. 1997, Vol 34, Num 12, pp 973-977, issn 0022-2593Article

Genetic epidemiology of congenital muscular dystrophy in a sample from north-east ItalyMOSTACCIUOLO, M. L; MIORIN, M; MARTINELLO, F et al.Human genetics. 1996, Vol 97, Num 3, pp 277-279, issn 0340-6717Article