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Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|October 1, 1996
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 muscleC P Trevisan, F Martinello, E Ferruzza, et al.Rivista Di Neurologia|January 1, 1991
[A case of polymyositis in autoimmune thyroiditis with hyperthyroidism]F Stevanato, F Martinello, R Pesce, et al.Journal of the Neurological Sciences|May 20, 1998
Supplemental therapy in isolated vitamin E deficiency improves the peripheral neuropathy and prevents the progression of ataxiaF Martinello, P Fardin, M Ottina, et al.Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|December 7, 2005
Hypolipemic and antioxidant activities from Tamarindus indica L. pulp fruit extract in hypercholesterolemic hamstersF Martinello, S M Soares, J J Franco, et al.Journal of the Neurological Sciences|October 1, 1996
Prognostic factors in mild dystrophinopathiesC Angelini, M Fanin, M P Freda, et al.Journal of Medical Genetics|January 16, 1998
Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutationsM Fanin, D J Duggan, M L Mostacciuolo, et al.Die Pharmazie|May 9, 2007
Effect of rutin on polymorphonuclear leukocytes oxidative metabolism in hypercholesterolemic Golden Syrian hamsters: evaluation by chemiluminescence and flow cytometryA Kanashiro, L M Kabeya, F Martinello, et al.Circulation|December 15, 1996
Myocardial involvement is very frequent among patients affected with subclinical Becker's muscular dystrophyP Melacini, M Fanin, G A Danieli, et al.Neurology|July 23, 1998
Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patientsE Pegoraro, H Marks, C A Garcia, et al.Pageof 2