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Showing results (51-60 of 84) with videos related to

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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.
Journal of the Neurological Sciences|September 1, 1996
Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscleA Prelle, C Rigoletto, M Moggio, et al.
Neurology|October 1, 1988
Immunocytochemical study of nebulin in Duchenne muscular dystrophyE Bonilla, A F Miranda, A Prelle, 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.
Journal of Neurology|May 1, 1995
Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNAC Mariotti, N Savarese, A Suomalainen, et al.
Neurology Research International|December 29, 2010
IgD Multiple Myeloma Paraproteinemia as a Cause of MyositisI Colombo, M E Fruguglietti, L Napoli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 24, 2006
High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithmL Morandi, C Angelini, A Prelle, 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.
Human Molecular Genetics|November 1, 1995
A G+1-->A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patientG P Comi, E Ciafaloni, H A de Silva, et al.
Neurology|March 15, 2006
Coexistence of CMT-2D and distal SMA-V phenotypes in an Italian family with a GARS gene mutationR Del Bo, F Locatelli, S Corti, et al.
Pageof 9

Showing results (51-60 of 84) with videos related to

Sort By:
Pageof 9
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.
Journal of the Neurological Sciences|September 1, 1996
Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscleA Prelle, C Rigoletto, M Moggio, et al.
Neurology|October 1, 1988
Immunocytochemical study of nebulin in Duchenne muscular dystrophyE Bonilla, A F Miranda, A Prelle, 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.
Journal of Neurology|May 1, 1995
Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNAC Mariotti, N Savarese, A Suomalainen, et al.
Neurology Research International|December 29, 2010
IgD Multiple Myeloma Paraproteinemia as a Cause of MyositisI Colombo, M E Fruguglietti, L Napoli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 24, 2006
High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithmL Morandi, C Angelini, A Prelle, 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.
Human Molecular Genetics|November 1, 1995
A G+1-->A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patientG P Comi, E Ciafaloni, H A de Silva, et al.
Neurology|March 15, 2006
Coexistence of CMT-2D and distal SMA-V phenotypes in an Italian family with a GARS gene mutationR Del Bo, F Locatelli, S Corti, et al.
Pageof 9