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Marina Pedemonte

Showing results (31-40 of 71) with videos related to

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Pediatric Surgery International|December 30, 2015
Long-term outcome and need of re-operation in gastro-esophageal reflux surgery in childrenValentina Rossi, Cinzia Mazzola, Lorenzo Leonelli, et al.
Clinical Nutrition (Edinburgh, Scotland)|March 21, 2021
Predictive fat mass equations for spinal muscular atrophy type I children: Development and internal validationAndrea Foppiani, Ramona De Amicis, Alessandro Leone, et al.
Molecular Neurobiology|May 5, 2025
Exploratory Analysis of Gut Microbiota Profile in Duchenne Muscular Dystrophy (DMD) Patients with Intellectual DisabilityChiara Panicucci, Sara Casalini, Giovanni Fiorito, et al.
European Journal of Medical Genetics|September 5, 2017
Gait disturbance and lower limb pain in a patient with PIK3CA-related disorderGerarda Cappuccio, Marianna Alagia, Mariangela D'Anna, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|February 7, 2008
Caveolin-3 T78M and T78K missense mutations lead to different phenotypes in vivo and in vitroMonica Traverso, Elisabetta Gazzerro, Stefania Assereto, et al.
Journal of Neurology|April 9, 2013
EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvementRoberta Biancheri, Denise Cassandrini, Francesca Pinto, et al.
Archives of Neurology|October 13, 2006
POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrumRoberta Biancheri, Enrico Bertini, Antonio Falace, et al.
Biomedicines|January 20, 2021
Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in <i>KCNA1</i> Impairing the Voltage Sensitivity of Kv1.1 ChannelPaola Imbrici, Andrea Accogli, Rikard Blunck, et al.
The American Journal of Clinical Nutrition|March 8, 2020
Predictive energy equations for spinal muscular atrophy type I childrenSimona Bertoli, Ramona De Amicis, Giorgio Bedogni, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 1, 2007
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progressionMario Pescatori, Aldobrando Broccolini, Carlo Minetti, et al.
Pageof 8

Showing results (31-40 of 71) with videos related to

Sort By:
Pageof 8
Pediatric Surgery International|December 30, 2015
Long-term outcome and need of re-operation in gastro-esophageal reflux surgery in childrenValentina Rossi, Cinzia Mazzola, Lorenzo Leonelli, et al.
Clinical Nutrition (Edinburgh, Scotland)|March 21, 2021
Predictive fat mass equations for spinal muscular atrophy type I children: Development and internal validationAndrea Foppiani, Ramona De Amicis, Alessandro Leone, et al.
Molecular Neurobiology|May 5, 2025
Exploratory Analysis of Gut Microbiota Profile in Duchenne Muscular Dystrophy (DMD) Patients with Intellectual DisabilityChiara Panicucci, Sara Casalini, Giovanni Fiorito, et al.
European Journal of Medical Genetics|September 5, 2017
Gait disturbance and lower limb pain in a patient with PIK3CA-related disorderGerarda Cappuccio, Marianna Alagia, Mariangela D'Anna, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|February 7, 2008
Caveolin-3 T78M and T78K missense mutations lead to different phenotypes in vivo and in vitroMonica Traverso, Elisabetta Gazzerro, Stefania Assereto, et al.
Journal of Neurology|April 9, 2013
EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvementRoberta Biancheri, Denise Cassandrini, Francesca Pinto, et al.
Archives of Neurology|October 13, 2006
POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrumRoberta Biancheri, Enrico Bertini, Antonio Falace, et al.
Biomedicines|January 20, 2021
Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in <i>KCNA1</i> Impairing the Voltage Sensitivity of Kv1.1 ChannelPaola Imbrici, Andrea Accogli, Rikard Blunck, et al.
The American Journal of Clinical Nutrition|March 8, 2020
Predictive energy equations for spinal muscular atrophy type I childrenSimona Bertoli, Ramona De Amicis, Giorgio Bedogni, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 1, 2007
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progressionMario Pescatori, Aldobrando Broccolini, Carlo Minetti, et al.
Pageof 8