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Claudio Bruno

Showing results (51-60 of 302) with videos related to

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Chirality|June 23, 2009
Synthesis and in vitro sodium channel blocking activity evaluation of novel homochiral mexiletine analogsAlessia Carocci, Alessia Catalano, Claudio Bruno, et al.
Molecular Pharmacology|November 24, 2012
Molecular dissection of lubeluzole use-dependent block of voltage-gated sodium channels discloses new therapeutic potentialsJean-François Desaphy, Roberta Carbonara, Teresa Costanza, et al.
JAMA Neurology|July 10, 2013
Mitochondrial encephalomyopathy due to a novel mutation in ACAD9Caterina Garone, Maria Alice Donati, Michele Sacchini, et al.
The Journal of International Medical Research|December 7, 2017
Detection of early nocturnal hypoventilation in neuromuscular disordersFederica Trucco, Marina Pedemonte, Chiara Fiorillo, et al.
Muscle & Nerve|December 9, 2024
Bone Health Determinants in Ambulant Prepubertal Boys With Duchenne Muscular Dystrophy Treated With Deflazacort: Findings From a 3-Year StudyChiara Panicucci, Sara Casalini, Alessia Angelelli, et al.
Biochemical and Biophysical Research Communications|July 12, 2011
Mitochondrial myopathy in a child with a muscle-restricted mutation in the mitochondrial transfer RNAAsn geneClaudio Bruno, Denise Cassandrini, Fabiana Fattori, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 17, 2015
Paternal germline mosaicism in collagen VI related myopathiesAnnarita Armaroli, Cecilia Trabanelli, Chiara Scotton, et al.
Journal of Microbiological Methods|June 21, 2020
Alternative primers to identify a range of apicomplexan parasitesSthephanie N Pinheiro, Maria Fernanda B de Souza, Claudio Bruno S Oliveira, et al.
Journal of Clinical Medicine|December 23, 2023
Structured Light Plethysmography for Non-Invasive Assessment of Respiratory Pattern in Spinal Muscular Atrophy Type 1Noemi Brolatti, Federica Trucco, Marta Ferretti, et al.
Biochemical and Biophysical Research Communications|October 28, 2008
Novel mutations in the adipose triglyceride lipase gene causing neutral lipid storage disease with myopathyFilomena Campagna, Luisa Nanni, Fabiana Quagliarini, et al.
Pageof 31

Showing results (51-60 of 302) with videos related to

Sort By:
Pageof 31
Chirality|June 23, 2009
Synthesis and in vitro sodium channel blocking activity evaluation of novel homochiral mexiletine analogsAlessia Carocci, Alessia Catalano, Claudio Bruno, et al.
Molecular Pharmacology|November 24, 2012
Molecular dissection of lubeluzole use-dependent block of voltage-gated sodium channels discloses new therapeutic potentialsJean-François Desaphy, Roberta Carbonara, Teresa Costanza, et al.
JAMA Neurology|July 10, 2013
Mitochondrial encephalomyopathy due to a novel mutation in ACAD9Caterina Garone, Maria Alice Donati, Michele Sacchini, et al.
The Journal of International Medical Research|December 7, 2017
Detection of early nocturnal hypoventilation in neuromuscular disordersFederica Trucco, Marina Pedemonte, Chiara Fiorillo, et al.
Muscle & Nerve|December 9, 2024
Bone Health Determinants in Ambulant Prepubertal Boys With Duchenne Muscular Dystrophy Treated With Deflazacort: Findings From a 3-Year StudyChiara Panicucci, Sara Casalini, Alessia Angelelli, et al.
Biochemical and Biophysical Research Communications|July 12, 2011
Mitochondrial myopathy in a child with a muscle-restricted mutation in the mitochondrial transfer RNAAsn geneClaudio Bruno, Denise Cassandrini, Fabiana Fattori, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 17, 2015
Paternal germline mosaicism in collagen VI related myopathiesAnnarita Armaroli, Cecilia Trabanelli, Chiara Scotton, et al.
Journal of Microbiological Methods|June 21, 2020
Alternative primers to identify a range of apicomplexan parasitesSthephanie N Pinheiro, Maria Fernanda B de Souza, Claudio Bruno S Oliveira, et al.
Journal of Clinical Medicine|December 23, 2023
Structured Light Plethysmography for Non-Invasive Assessment of Respiratory Pattern in Spinal Muscular Atrophy Type 1Noemi Brolatti, Federica Trucco, Marta Ferretti, et al.
Biochemical and Biophysical Research Communications|October 28, 2008
Novel mutations in the adipose triglyceride lipase gene causing neutral lipid storage disease with myopathyFilomena Campagna, Luisa Nanni, Fabiana Quagliarini, et al.
Pageof 31