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A Bardoni

Showing results (21-30 of 29) with videos related to

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Cell Biochemistry and Function|September 1, 1992
Modifications of adhesion properties and proteoglycan structure in rat embryo fibroblast cultures with increasing passagesP Pippia, M Formato, L Sciola, et al.
Neuromuscular Disorders : NMD|July 1, 1994
Cognitive impairment in Duchenne muscular dystrophyN Bresolin, E Castelli, G P Comi, et al.
Neuromuscular Disorders : NMD|November 1, 1995
Duplication of dystrophin gene and dissimilar clinical phenotype in the same familyA Toscano, L Vitiello, G P Comi, et al.
Brain : a Journal of Neurology|February 1, 1994
Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlatesG P Comi, A Prelle, N Bresolin, et al.
Neuromuscular Disorders : NMD|May 23, 2001
Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuriaR Cagliani, G P Comi, L Tancredi, et al.
Neurology|August 23, 2000
Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophyG Felisari, F Martinelli Boneschi, A Bardoni, et al.
Clinical and Experimental Rheumatology|July 17, 2007
Validation of a new immunoenzymatic method to detect antibodies to RNA polymerase III in systemic sclerosisV Codullo, G Morozzi, A Bardoni, et al.
Neuromuscular Disorders : NMD|December 7, 2002
Two dystrophin proteins and transcripts in a mild dystrophinopathic patientR Cagliani, A Bardoni, M Sironi, et al.
Clinical and Experimental Rheumatology|February 10, 2006
Localized and systemic forms of scleroderma in adults and children F Atzeni, A Bardoni, M Cutolo, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Cell Biochemistry and Function|September 1, 1992
Modifications of adhesion properties and proteoglycan structure in rat embryo fibroblast cultures with increasing passagesP Pippia, M Formato, L Sciola, et al.
Neuromuscular Disorders : NMD|July 1, 1994
Cognitive impairment in Duchenne muscular dystrophyN Bresolin, E Castelli, G P Comi, et al.
Neuromuscular Disorders : NMD|November 1, 1995
Duplication of dystrophin gene and dissimilar clinical phenotype in the same familyA Toscano, L Vitiello, G P Comi, et al.
Brain : a Journal of Neurology|February 1, 1994
Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlatesG P Comi, A Prelle, N Bresolin, et al.
Neuromuscular Disorders : NMD|May 23, 2001
Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuriaR Cagliani, G P Comi, L Tancredi, et al.
Neurology|August 23, 2000
Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophyG Felisari, F Martinelli Boneschi, A Bardoni, et al.
Clinical and Experimental Rheumatology|July 17, 2007
Validation of a new immunoenzymatic method to detect antibodies to RNA polymerase III in systemic sclerosisV Codullo, G Morozzi, A Bardoni, et al.
Neuromuscular Disorders : NMD|December 7, 2002
Two dystrophin proteins and transcripts in a mild dystrophinopathic patientR Cagliani, A Bardoni, M Sironi, et al.
Clinical and Experimental Rheumatology|February 10, 2006
Localized and systemic forms of scleroderma in adults and children F Atzeni, A Bardoni, M Cutolo, et al.
Pageof 3