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Marina Pedemonte

Showing results (1-10 of 71) with videos related to

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American Journal of Medical Genetics. Part A|April 15, 2008
The arthrochalasia type of Ehlers-Danlos syndrome (EDS VIIA and VIIB): the diagnostic value of collagen fibril ultrastructureCecilia Giunta, Céline Chambaz, Marina Pedemonte, et al.
Respiratory Medicine|April 9, 2017
Respiratory pattern in a FSDH paediatric populationFederica Trucco, Marina Pedemonte, Chiara Fiorillo, et al.
Respiratory Medicine|October 4, 2016
Respiratory pattern in a FSHD pediatric populationFederica Trucco, Marina Pedemonte, Chiara Fiorillo, et al.
American Journal of Physical Medicine & Rehabilitation|September 30, 2011
Spinal muscular atrophy type 1: avoidance of hospitalization by respiratory muscle supportGiancarlo Ottonello, Chiara Mastella, Alessia Franceschi, et al.
Biochemical and Biophysical Research Communications|June 14, 2005
Chemokine receptor CCR7 is expressed in muscle fibers in juvenile dermatomyositisCarlo Minetti, Marco Gattorno, Silvia Repetto, et al.
Biochemical and Biophysical Research Communications|November 22, 2005
Multiplex real-time PCR for detection of deletions and duplications in dystrophin geneMonica Traverso, Mauro Malnati, Carlo Minetti, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 9, 2022
Congenital myopathy associated with a novel mutation in <i>MEGF10</i> gene, myofibrillar alteration and progressive courseCarolina Croci, Monica Traverso, Serena Baratto, 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.
The Journal of International Medical Research|December 7, 2017
Detection of early nocturnal hypoventilation in neuromuscular disordersFederica Trucco, Marina Pedemonte, Chiara Fiorillo, 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.
Pageof 8

Showing results (1-10 of 71) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics. Part A|April 15, 2008
The arthrochalasia type of Ehlers-Danlos syndrome (EDS VIIA and VIIB): the diagnostic value of collagen fibril ultrastructureCecilia Giunta, Céline Chambaz, Marina Pedemonte, et al.
Respiratory Medicine|April 9, 2017
Respiratory pattern in a FSDH paediatric populationFederica Trucco, Marina Pedemonte, Chiara Fiorillo, et al.
Respiratory Medicine|October 4, 2016
Respiratory pattern in a FSHD pediatric populationFederica Trucco, Marina Pedemonte, Chiara Fiorillo, et al.
American Journal of Physical Medicine & Rehabilitation|September 30, 2011
Spinal muscular atrophy type 1: avoidance of hospitalization by respiratory muscle supportGiancarlo Ottonello, Chiara Mastella, Alessia Franceschi, et al.
Biochemical and Biophysical Research Communications|June 14, 2005
Chemokine receptor CCR7 is expressed in muscle fibers in juvenile dermatomyositisCarlo Minetti, Marco Gattorno, Silvia Repetto, et al.
Biochemical and Biophysical Research Communications|November 22, 2005
Multiplex real-time PCR for detection of deletions and duplications in dystrophin geneMonica Traverso, Mauro Malnati, Carlo Minetti, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 9, 2022
Congenital myopathy associated with a novel mutation in <i>MEGF10</i> gene, myofibrillar alteration and progressive courseCarolina Croci, Monica Traverso, Serena Baratto, 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.
The Journal of International Medical Research|December 7, 2017
Detection of early nocturnal hypoventilation in neuromuscular disordersFederica Trucco, Marina Pedemonte, Chiara Fiorillo, 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.
Pageof 8