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A Prelle

Showing results (61-70 of 84) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2008
DPP6 gene variability confers increased risk of developing sporadic amyotrophic lateral sclerosis in Italian patientsR Del Bo, S Ghezzi, S Corti, 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.
Neuromuscular Disorders : NMD|December 7, 2002
Two dystrophin proteins and transcripts in a mild dystrophinopathic patientR Cagliani, A Bardoni, M Sironi, et al.
Neurology|April 26, 2001
Lack of apoptosis in mitochondrial encephalomyopathiesM Sciacco, G Fagiolari, C Lamperti, et al.
Clinical Neuropathology|February 13, 1999
Critically ill patients: immunological evidence of inflammation in muscle biopsyP Bazzi, M Moggio, A Prelle, et al.
Neuromuscular Disorders : NMD|December 18, 2003
Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian populationR Cagliani, F Fortunato, R Giorda, 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.
Minerva Anestesiologica|March 1, 1996
[Respiratory failure caused by myopathy in severe sepsis]G Veschi, G Zanforlin, G Breda, et al.
Pageof 9

Showing results (61-70 of 84) with videos related to

Sort By:
Pageof 9
Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2008
DPP6 gene variability confers increased risk of developing sporadic amyotrophic lateral sclerosis in Italian patientsR Del Bo, S Ghezzi, S Corti, 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.
Neuromuscular Disorders : NMD|December 7, 2002
Two dystrophin proteins and transcripts in a mild dystrophinopathic patientR Cagliani, A Bardoni, M Sironi, et al.
Neurology|April 26, 2001
Lack of apoptosis in mitochondrial encephalomyopathiesM Sciacco, G Fagiolari, C Lamperti, et al.
Clinical Neuropathology|February 13, 1999
Critically ill patients: immunological evidence of inflammation in muscle biopsyP Bazzi, M Moggio, A Prelle, et al.
Neuromuscular Disorders : NMD|December 18, 2003
Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian populationR Cagliani, F Fortunato, R Giorda, 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.
Minerva Anestesiologica|March 1, 1996
[Respiratory failure caused by myopathy in severe sepsis]G Veschi, G Zanforlin, G Breda, et al.
Pageof 9