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Claudio Bruno

Showing results (161-170 of 302) with videos related to

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Acta Neuropathologica Communications|October 20, 2023
Myopathologic trajectory in Duchenne muscular dystrophy (DMD) reveals lack of regeneration due to senescence in satellite cellsNastasia Cardone, Valentina Taglietti, Serena Baratto, et al.
The American Journal of Pathology|November 19, 2018
The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan-Deficient Muscular DystrophyElisabetta Gazzerro, Serena Baratto, Stefania Assereto, et al.
Neurogenetics|April 25, 2012
TRPV4 mutations in children with congenital distal spinal muscular atrophyChiara Fiorillo, Francesca Moro, Giacomo Brisca, et al.
American Journal of Medical Genetics. Part A|June 7, 2008
Peroxisomal acyl-CoA-oxidase deficiency: two new casesRosalba Carrozzo, Carlo Bellini, Simona Lucioli, et al.
Frontiers in Neurology|October 22, 2021
The Role of Muscle Biopsy in Diagnostic Process of Infant Hypotonia: From Clinical Classification to the Genetic OutcomeMarco Veneruso, Chiara Fiorillo, Paolo Broda, et al.
Neuromuscular Disorders : NMD|February 12, 2013
Centronuclear myopathy related to dynamin 2 mutations: clinical, morphological, muscle imaging and genetic features of an Italian cohortMichela Catteruccia, Fabiana Fattori, Valentina Codemo, et al.
Neurology|July 27, 2018
An observational study of functional abilities in infants, children, and adults with type 1 SMAMarika Pane, Concetta Palermo, Sonia Messina, et al.
Neuromuscular Disorders : NMD|July 2, 2018
Nusinersen in type 1 SMA infants, children and young adults: Preliminary results on motor functionMarika Pane, Concetta Palermo, Sonia Messina, et al.
Plos One|March 24, 2020
Diagnostic journey in Spinal Muscular Atrophy: Is it still an odyssey?Maria Carmela Pera, Giorgia Coratti, Beatrice Berti, et al.
Parkinsonism & Related Disorders|March 9, 2016
Dementia in Parkinson's disease: Is male gender a risk factor?Emanuele Cereda, Roberto Cilia, Catherine Klersy, et al.
Pageof 31

Showing results (161-170 of 302) with videos related to

Sort By:
Pageof 31
Acta Neuropathologica Communications|October 20, 2023
Myopathologic trajectory in Duchenne muscular dystrophy (DMD) reveals lack of regeneration due to senescence in satellite cellsNastasia Cardone, Valentina Taglietti, Serena Baratto, et al.
The American Journal of Pathology|November 19, 2018
The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan-Deficient Muscular DystrophyElisabetta Gazzerro, Serena Baratto, Stefania Assereto, et al.
Neurogenetics|April 25, 2012
TRPV4 mutations in children with congenital distal spinal muscular atrophyChiara Fiorillo, Francesca Moro, Giacomo Brisca, et al.
American Journal of Medical Genetics. Part A|June 7, 2008
Peroxisomal acyl-CoA-oxidase deficiency: two new casesRosalba Carrozzo, Carlo Bellini, Simona Lucioli, et al.
Frontiers in Neurology|October 22, 2021
The Role of Muscle Biopsy in Diagnostic Process of Infant Hypotonia: From Clinical Classification to the Genetic OutcomeMarco Veneruso, Chiara Fiorillo, Paolo Broda, et al.
Neuromuscular Disorders : NMD|February 12, 2013
Centronuclear myopathy related to dynamin 2 mutations: clinical, morphological, muscle imaging and genetic features of an Italian cohortMichela Catteruccia, Fabiana Fattori, Valentina Codemo, et al.
Neurology|July 27, 2018
An observational study of functional abilities in infants, children, and adults with type 1 SMAMarika Pane, Concetta Palermo, Sonia Messina, et al.
Neuromuscular Disorders : NMD|July 2, 2018
Nusinersen in type 1 SMA infants, children and young adults: Preliminary results on motor functionMarika Pane, Concetta Palermo, Sonia Messina, et al.
Plos One|March 24, 2020
Diagnostic journey in Spinal Muscular Atrophy: Is it still an odyssey?Maria Carmela Pera, Giorgia Coratti, Beatrice Berti, et al.
Parkinsonism & Related Disorders|March 9, 2016
Dementia in Parkinson's disease: Is male gender a risk factor?Emanuele Cereda, Roberto Cilia, Catherine Klersy, et al.
Pageof 31