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Journal of the Neurological Sciences|March 7, 2001
Charcot-Marie-Tooth disease (CMT): distinctive phenotypic and genotypic features in CMT type 2F Gemignani, A MarbiniFunctional Neurology|July 1, 1988
Polyneuropathy in Sjögren's syndrome. A case of prevalently autonomic neuropathy with tonic pupil and hypohidrosisF Gemignani, P Manganelli, G Pavesi, et al.Journal of Neurology|October 1, 1989
Debrancher deficiency neuromuscular disorder with pseudohypertrophy in two brothersA Marbini, F Gemignani, F Saccardi, et al.European Neurology|January 1, 1984
Pathological study of the sural nerve in Fabry's diseaseF Gemignani, A Marbini, M M Bragaglia, et al.Clinical Neuropathology|January 1, 1987
Mitochondrial paracrystalline inclusions in the peroneus brevis muscle of patients with peripheral neuropathyA Marbini, F Gemignani, M M Bragaglia, et al.Italian Journal of Neurological Sciences|April 1, 1987
Polyneuropathy and systemic vasculitis. An electrophysiological studyG Pavesi, F Gemignani, P Manganelli, et al.Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma|January 1, 1981
[Late myopathy with mitochondrial changes in the muscle]A Marbini, S Calzetti, F Gemignani, et al.Journal of the Neurological Sciences|September 1, 1983
Immunological abnormalities in a family with progressive external ophthalmoplegiaS Calzetti, F Gemignani, A Marbini, et al.Journal of the Neurological Sciences|November 1, 1996
Immunohistochemical localization of utrophin and other cytoskeletal proteins in skin smooth muscle in neuromuscular diseasesA Marbini, F Gemignani, M F Bellanova, et al.Acta Neuropathologica|August 1, 1997
Immunohistochemical study of merosin-negative congenital muscular dystrophy: laminin alpha 2 deficiency in skin biopsyA Marbini, M F Bellanova, A Ferrari, et al.Pageof 9