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

Luciano Merlini

Showing results (31-40 of 117) with videos related to

Pageof 12
Sort By:
Biochemical and Biophysical Research Communications|April 3, 2003
Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblastsGiovanna Lattanzi, Vittoria Cenni, Sandra Marmiroli, et al.
Frontiers in Aging Neuroscience|July 5, 2016
Tendon Extracellular Matrix Alterations in Ullrich Congenital Muscular DystrophyFrancesca Sardone, Francesco Traina, Alice Bondi, et al.
Journal of Child Neurology|September 19, 2003
Role of gabapentin in spinal muscular atrophy: results of a multicenter, randomized Italian studyLuciano Merlini, Alessandra Solari, Giuseppe Vita, et al.
American Journal of Medical Genetics. Part A|January 11, 2005
Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutationPaola Rimessi, Francesca Gualandi, Laurence Duprez, et al.
Muscle & Nerve|April 14, 2011
Macrophages: a minimally invasive tool for monitoring collagen VI myopathiesFrancesca Gualandi, Rosa Curci, Patrizia Sabatelli, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1)Eugenio Mercuri, Beril Talim, Behzad Moghadaszadeh, et al.
International Journal of Molecular Sciences|June 13, 2025
Myopathic Ehlers-Danlos Syndrome (mEDS) Related to <i>COL12A1</i>: Two Novel Families and Literature ReviewLuciano Merlini, Patrizia Sabatelli, Vittoria Cenni, et al.
Thescientificworldjournal|October 29, 2013
Body composition, muscle strength, and physical function of patients with Bethlem myopathy and Ullrich congenital muscular dystrophyMaria Teresa Miscione, Francesca Bruno, Claudio Ripamonti, et al.
Molecular Genetics and Metabolism|March 29, 2011
Pompe disease: design, methodology, and early findings from the Pompe RegistryBarry J Byrne, Priya S Kishnani, Laura E Case, et al.
Muscle & Nerve|May 15, 2012
Early corticosteroid treatment in 4 Duchenne muscular dystrophy patients: 14-year follow-upLuciano Merlini, Monia Gennari, Elisabetta Malaspina, et al.
Pageof 12

Showing results (31-40 of 117) with videos related to

Sort By:
Pageof 12
Biochemical and Biophysical Research Communications|April 3, 2003
Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblastsGiovanna Lattanzi, Vittoria Cenni, Sandra Marmiroli, et al.
Frontiers in Aging Neuroscience|July 5, 2016
Tendon Extracellular Matrix Alterations in Ullrich Congenital Muscular DystrophyFrancesca Sardone, Francesco Traina, Alice Bondi, et al.
Journal of Child Neurology|September 19, 2003
Role of gabapentin in spinal muscular atrophy: results of a multicenter, randomized Italian studyLuciano Merlini, Alessandra Solari, Giuseppe Vita, et al.
American Journal of Medical Genetics. Part A|January 11, 2005
Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutationPaola Rimessi, Francesca Gualandi, Laurence Duprez, et al.
Muscle & Nerve|April 14, 2011
Macrophages: a minimally invasive tool for monitoring collagen VI myopathiesFrancesca Gualandi, Rosa Curci, Patrizia Sabatelli, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1)Eugenio Mercuri, Beril Talim, Behzad Moghadaszadeh, et al.
International Journal of Molecular Sciences|June 13, 2025
Myopathic Ehlers-Danlos Syndrome (mEDS) Related to <i>COL12A1</i>: Two Novel Families and Literature ReviewLuciano Merlini, Patrizia Sabatelli, Vittoria Cenni, et al.
Thescientificworldjournal|October 29, 2013
Body composition, muscle strength, and physical function of patients with Bethlem myopathy and Ullrich congenital muscular dystrophyMaria Teresa Miscione, Francesca Bruno, Claudio Ripamonti, et al.
Molecular Genetics and Metabolism|March 29, 2011
Pompe disease: design, methodology, and early findings from the Pompe RegistryBarry J Byrne, Priya S Kishnani, Laura E Case, et al.
Muscle & Nerve|May 15, 2012
Early corticosteroid treatment in 4 Duchenne muscular dystrophy patients: 14-year follow-upLuciano Merlini, Monia Gennari, Elisabetta Malaspina, et al.
Pageof 12