Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Claudio Semplicini

Showing results (31-40 of 47) with videos related to

Pageof 5
Sort By:
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 16, 2015
Psychological and practical difficulties among parents and healthy siblings of children with Duchenne vs. Becker muscular dystrophy: an Italian comparative studyLorenza Magliano, Maria Grazia D'Angelo, Giuseppe Vita, et al.
Journal of Neurology|November 9, 2013
"I have got something positive out of this situation": psychological benefits of caregiving in relatives of young people with muscular dystrophyLorenza Magliano, Melania Patalano, Alessandra Sagliocchi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|August 8, 2017
Integrated care of muscular dystrophies in Italy. Part 2. Psychological treatments, social and welfare support, and financial costsLorenza Magliano, Marianna Scutifero, Melania Patalano, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 11, 2017
Integrated care of muscular dystrophies in Italy. Part 1. Pharmacological treatment and rehabilitative interventionsLuisa Politano, Marianna Scutifero, Melania Patalano, et al.
Muscle & Nerve|November 4, 2014
Burden, professional support, and social network in families of children and young adults with muscular dystrophiesLorenza Magliano, Melania Patalano, Alessandra Sagliocchi, et al.
Advances in Therapy|March 18, 2019
Assessing the Role of Anti rh-GAA in Modulating Response to ERT in a Late-Onset Pompe Disease Cohort from the Italian GSDII Study GroupMassimiliano Filosto, Stefano Cotti Piccinelli, Sabrina Ravaglia, et al.
Neuromuscular Disorders : NMD|June 9, 2018
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe diseaseMarco Savarese, Annalaura Torella, Olimpia Musumeci, et al.
Current Issues in Molecular Biology|May 15, 2023
Distribution of Exonic Variants in Glycogen Synthesis and Catabolism Genes in Late Onset Pompe Disease (LOPD)Paola De Filippi, Edoardo Errichiello, Antonio Toscano, et al.
Muscle & Nerve|May 18, 2016
The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosisFrancesca Magri, Vincenzo Nigro, Corrado Angelini, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 11, 2017
MRI in sarcoglycanopathies: a large international cohort studyGiorgio Tasca, Mauro Monforte, Jordi Díaz-Manera, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 16, 2015
Psychological and practical difficulties among parents and healthy siblings of children with Duchenne vs. Becker muscular dystrophy: an Italian comparative studyLorenza Magliano, Maria Grazia D'Angelo, Giuseppe Vita, et al.
Journal of Neurology|November 9, 2013
"I have got something positive out of this situation": psychological benefits of caregiving in relatives of young people with muscular dystrophyLorenza Magliano, Melania Patalano, Alessandra Sagliocchi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|August 8, 2017
Integrated care of muscular dystrophies in Italy. Part 2. Psychological treatments, social and welfare support, and financial costsLorenza Magliano, Marianna Scutifero, Melania Patalano, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 11, 2017
Integrated care of muscular dystrophies in Italy. Part 1. Pharmacological treatment and rehabilitative interventionsLuisa Politano, Marianna Scutifero, Melania Patalano, et al.
Muscle & Nerve|November 4, 2014
Burden, professional support, and social network in families of children and young adults with muscular dystrophiesLorenza Magliano, Melania Patalano, Alessandra Sagliocchi, et al.
Advances in Therapy|March 18, 2019
Assessing the Role of Anti rh-GAA in Modulating Response to ERT in a Late-Onset Pompe Disease Cohort from the Italian GSDII Study GroupMassimiliano Filosto, Stefano Cotti Piccinelli, Sabrina Ravaglia, et al.
Neuromuscular Disorders : NMD|June 9, 2018
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe diseaseMarco Savarese, Annalaura Torella, Olimpia Musumeci, et al.
Current Issues in Molecular Biology|May 15, 2023
Distribution of Exonic Variants in Glycogen Synthesis and Catabolism Genes in Late Onset Pompe Disease (LOPD)Paola De Filippi, Edoardo Errichiello, Antonio Toscano, et al.
Muscle & Nerve|May 18, 2016
The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosisFrancesca Magri, Vincenzo Nigro, Corrado Angelini, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 11, 2017
MRI in sarcoglycanopathies: a large international cohort studyGiorgio Tasca, Mauro Monforte, Jordi Díaz-Manera, et al.
Pageof 5