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

Marco Savarese

Showing results (1-10 of 109) with videos related to

Pageof 11
Sort By:
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 21, 2014
Genetic basis of limb-girdle muscular dystrophies: the 2014 updateVincenzo Nigro, Marco Savarese
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 26, 2024
Long-read sequencing improves diagnostic rate in neuromuscular disordersRafaela Owusu, Marco Savarese
Current Opinion in Neurology|July 26, 2016
Next-generation sequencing approaches for the diagnosis of skeletal muscle disordersVincenzo Nigro, Marco Savarese
Handbook of Clinical Neurology|August 10, 2023
Distal myopathyMarco Savarese, Manu Jokela, Bjarne Udd
Muscle & Nerve|January 23, 2016
Next generation sequencing detection of late onset pompe diseaseCorrado Angelini, Marco Savarese, Marina Fanin, et al.
Journal of Cellular and Molecular Medicine|September 6, 2022
Use of animal models to understand titin physiology and pathologyMatteo Marcello, Viviana Cetrangolo, Marco Savarese, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 8, 2025
Empowering clinicians with artificial intelligence in hereditary neuromuscular disordersAndi Nuredini, Marco Savarese, Filippo Maria Santorelli, et al.
Journal of Neuromuscular Diseases|March 17, 2020
Is Gene-Size an Issue for the Diagnosis of Skeletal Muscle Disorders?Marco Savarese, Salla Välipakka, Mridul Johari, et al.
Journal of Neuromuscular Diseases|November 18, 2016
Increasing Role of Titin Mutations in Neuromuscular DisordersMarco Savarese, Jaakko Sarparanta, Anna Vihola, et al.
Neurology. Genetics|April 12, 2016
GYG1 gene mutations in a family with polyglucosan body myopathyMarina Fanin, Annalaura Torella, Marco Savarese, et al.
Pageof 11

Showing results (1-10 of 109) with videos related to

Sort By:
Pageof 11
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 21, 2014
Genetic basis of limb-girdle muscular dystrophies: the 2014 updateVincenzo Nigro, Marco Savarese
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 26, 2024
Long-read sequencing improves diagnostic rate in neuromuscular disordersRafaela Owusu, Marco Savarese
Current Opinion in Neurology|July 26, 2016
Next-generation sequencing approaches for the diagnosis of skeletal muscle disordersVincenzo Nigro, Marco Savarese
Handbook of Clinical Neurology|August 10, 2023
Distal myopathyMarco Savarese, Manu Jokela, Bjarne Udd
Muscle & Nerve|January 23, 2016
Next generation sequencing detection of late onset pompe diseaseCorrado Angelini, Marco Savarese, Marina Fanin, et al.
Journal of Cellular and Molecular Medicine|September 6, 2022
Use of animal models to understand titin physiology and pathologyMatteo Marcello, Viviana Cetrangolo, Marco Savarese, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 8, 2025
Empowering clinicians with artificial intelligence in hereditary neuromuscular disordersAndi Nuredini, Marco Savarese, Filippo Maria Santorelli, et al.
Journal of Neuromuscular Diseases|March 17, 2020
Is Gene-Size an Issue for the Diagnosis of Skeletal Muscle Disorders?Marco Savarese, Salla Välipakka, Mridul Johari, et al.
Journal of Neuromuscular Diseases|November 18, 2016
Increasing Role of Titin Mutations in Neuromuscular DisordersMarco Savarese, Jaakko Sarparanta, Anna Vihola, et al.
Neurology. Genetics|April 12, 2016
GYG1 gene mutations in a family with polyglucosan body myopathyMarina Fanin, Annalaura Torella, Marco Savarese, et al.
Pageof 11