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N Bresolin

Showing results (171-180 of 206) with videos related to

Pageof 21
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Neurology|July 14, 2004
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardationR Borgatti, C Zucca, A Cavallini, et al.
Rejuvenation Research|August 30, 2008
Preliminary evidence that VEGF genetic variability confers susceptibility to frontotemporal lobar degenerationB Borroni, S Ghezzi, C Agosti, et al.
Muscle & Nerve|July 1, 1996
In vivo biolistic technique in control and mdx dystrophic miceC D Ausenda, N Bresolin, A De Liso, 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.
Human Molecular Genetics|August 1, 2000
Transplacental injection of somite-derived cells in mdx mouse embryos for the correction of dystrophin deficiencyY Torrente, M G D'Angelo, Z Li, et al.
Respiratory Medicine|November 16, 2011
Low abdominal contribution to breathing as daytime predictor of nocturnal desaturation in adolescents and young adults with Duchenne Muscular DystrophyM Romei, M G D'Angelo, A LoMauro, 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.
European Journal of Neurology|November 29, 2007
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degenerationE Venturelli, C Villa, E Scarpini, et al.
Journal of the Neurological Sciences|May 3, 2011
Respiratory pattern in an adult population of dystrophic patientsM G D'Angelo, M Romei, A Lo Mauro, et al.
Neurology|December 10, 2003
A CAV3 microdeletion differentially affects skeletal muscle and myocardiumR Cagliani, N Bresolin, A Prelle, et al.
Pageof 21

Showing results (171-180 of 206) with videos related to

Sort By:
Pageof 21
Neurology|July 14, 2004
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardationR Borgatti, C Zucca, A Cavallini, et al.
Rejuvenation Research|August 30, 2008
Preliminary evidence that VEGF genetic variability confers susceptibility to frontotemporal lobar degenerationB Borroni, S Ghezzi, C Agosti, et al.
Muscle & Nerve|July 1, 1996
In vivo biolistic technique in control and mdx dystrophic miceC D Ausenda, N Bresolin, A De Liso, 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.
Human Molecular Genetics|August 1, 2000
Transplacental injection of somite-derived cells in mdx mouse embryos for the correction of dystrophin deficiencyY Torrente, M G D'Angelo, Z Li, et al.
Respiratory Medicine|November 16, 2011
Low abdominal contribution to breathing as daytime predictor of nocturnal desaturation in adolescents and young adults with Duchenne Muscular DystrophyM Romei, M G D'Angelo, A LoMauro, 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.
European Journal of Neurology|November 29, 2007
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degenerationE Venturelli, C Villa, E Scarpini, et al.
Journal of the Neurological Sciences|May 3, 2011
Respiratory pattern in an adult population of dystrophic patientsM G D'Angelo, M Romei, A Lo Mauro, et al.
Neurology|December 10, 2003
A CAV3 microdeletion differentially affects skeletal muscle and myocardiumR Cagliani, N Bresolin, A Prelle, et al.
Pageof 21