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Showing results (11-20 of 19) with videos related to

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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.
Journal of Neurology|June 1, 1997
An atypical case of partial merosin deficiency congenital muscular dystrophyA Prelle, G P Comi, C Rigoletto, et al.
Annals of Neurology|August 17, 2001
Beta-enolase deficiency, a new metabolic myopathy of distal glycolysisG P Comi, F Fortunato, S Lucchiari, et al.
Acta Neuropathologica|November 26, 1998
Sarcoglycan deficiency in a large Italian population of myopathic patientsA Prelle, G P Comi, L Tancredi, et al.
Clinical Neuropathology|August 5, 2000
A sporadic, atypical case of desminopathy: morphological and immunological characterizationA Prelle, M Sciacco, G P Comi, et al.
Neurology|December 10, 2003
A CAV3 microdeletion differentially affects skeletal muscle and myocardiumR Cagliani, N Bresolin, A Prelle, et al.
Acta Neuropathologica|May 8, 2003
Clinical, morphological and immunological evaluation of six patients with dysferlin deficiencyA Prelle, M Sciacco, L Tancredi, et al.
Experimental Cell Research|June 14, 2002
A subpopulation of murine bone marrow cells fully differentiates along the myogenic pathway and participates in muscle repair in the mdx dystrophic mouseS Corti, S Strazzer, R Del Bo, et al.
Journal of Neurology|October 13, 2001
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluationM Sciacco, A Prelle, G P Comi, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
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.
Journal of Neurology|June 1, 1997
An atypical case of partial merosin deficiency congenital muscular dystrophyA Prelle, G P Comi, C Rigoletto, et al.
Annals of Neurology|August 17, 2001
Beta-enolase deficiency, a new metabolic myopathy of distal glycolysisG P Comi, F Fortunato, S Lucchiari, et al.
Acta Neuropathologica|November 26, 1998
Sarcoglycan deficiency in a large Italian population of myopathic patientsA Prelle, G P Comi, L Tancredi, et al.
Clinical Neuropathology|August 5, 2000
A sporadic, atypical case of desminopathy: morphological and immunological characterizationA Prelle, M Sciacco, G P Comi, et al.
Neurology|December 10, 2003
A CAV3 microdeletion differentially affects skeletal muscle and myocardiumR Cagliani, N Bresolin, A Prelle, et al.
Acta Neuropathologica|May 8, 2003
Clinical, morphological and immunological evaluation of six patients with dysferlin deficiencyA Prelle, M Sciacco, L Tancredi, et al.
Experimental Cell Research|June 14, 2002
A subpopulation of murine bone marrow cells fully differentiates along the myogenic pathway and participates in muscle repair in the mdx dystrophic mouseS Corti, S Strazzer, R Del Bo, et al.
Journal of Neurology|October 13, 2001
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluationM Sciacco, A Prelle, G P Comi, et al.
Pageof 2