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

Luca Bello

Showing results (61-70 of 144) with videos related to

Pageof 15
Sort By:
Neurology|April 12, 2015
Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2EClaudio Semplicini, John Vissing, Julia R Dahlqvist, et al.
Autophagy|July 20, 2022
Lack of COL6/collagen VI causes megakaryocyte dysfunction by impairing autophagy and inducing apoptosisVittorio Abbonante, Alessandro Malara, Martina Chrisam, et al.
Journal of Neurology|March 4, 2025
Deep characterization of females with heterozygous Duchenne muscular dystrophy mutationsPietro Riguzzi, Daniele Sabbatini, Aurora Fusto, et al.
Experimental Physiology|May 8, 2021
Striated muscle activator of Rho signalling (STARS) overexpression in the mdx mouse enhances muscle functional capacity and regulates the actin cytoskeleton and oxidative phosphorylation pathwaysKate J Sadler, Paul A Della Gatta, Timur Naim, et al.
Experimental Physiology|July 26, 2016
OPN-a induces muscle inflammation by increasing recruitment and activation of pro-inflammatory macrophagesGina M Many, Yasuyuki Yokosaki, Kitipong Uaesoontrachoon, et al.
The Yale Journal of Biology and Medicine|September 29, 2017
Changes in Muscle Metabolism are Associated with Phenotypic Variability in Golden Retriever Muscular DystrophyPeter P Nghiem, Luca Bello, William B Stoughton, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|September 9, 2020
Limb girdle muscular dystrophy due to <i>LAMA2</i> gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosisFrancesca Magri, Roberta Brusa, Luca Bello, et al.
Human Mutation|August 14, 2014
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregatesDaniela Rossi, Bianca Vezzani, Lucia Galli, et al.
European Journal of Human Genetics : EJHG|May 3, 2012
Cardiomyopathy in patients with POMT1-related congenital and limb-girdle muscular dystrophyLuca Bello, Paola Melacini, Raffaele Pezzani, et al.
Frontiers in Neurology|March 16, 2019
Lipomatosis Incidence and Characteristics in an Italian Cohort of Mitochondrial PatientsOlimpia Musumeci, Emanuele Barca, Costanza Lamperti, et al.
Pageof 15

Showing results (61-70 of 144) with videos related to

Sort By:
Pageof 15
Neurology|April 12, 2015
Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2EClaudio Semplicini, John Vissing, Julia R Dahlqvist, et al.
Autophagy|July 20, 2022
Lack of COL6/collagen VI causes megakaryocyte dysfunction by impairing autophagy and inducing apoptosisVittorio Abbonante, Alessandro Malara, Martina Chrisam, et al.
Journal of Neurology|March 4, 2025
Deep characterization of females with heterozygous Duchenne muscular dystrophy mutationsPietro Riguzzi, Daniele Sabbatini, Aurora Fusto, et al.
Experimental Physiology|May 8, 2021
Striated muscle activator of Rho signalling (STARS) overexpression in the mdx mouse enhances muscle functional capacity and regulates the actin cytoskeleton and oxidative phosphorylation pathwaysKate J Sadler, Paul A Della Gatta, Timur Naim, et al.
Experimental Physiology|July 26, 2016
OPN-a induces muscle inflammation by increasing recruitment and activation of pro-inflammatory macrophagesGina M Many, Yasuyuki Yokosaki, Kitipong Uaesoontrachoon, et al.
The Yale Journal of Biology and Medicine|September 29, 2017
Changes in Muscle Metabolism are Associated with Phenotypic Variability in Golden Retriever Muscular DystrophyPeter P Nghiem, Luca Bello, William B Stoughton, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|September 9, 2020
Limb girdle muscular dystrophy due to <i>LAMA2</i> gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosisFrancesca Magri, Roberta Brusa, Luca Bello, et al.
Human Mutation|August 14, 2014
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregatesDaniela Rossi, Bianca Vezzani, Lucia Galli, et al.
European Journal of Human Genetics : EJHG|May 3, 2012
Cardiomyopathy in patients with POMT1-related congenital and limb-girdle muscular dystrophyLuca Bello, Paola Melacini, Raffaele Pezzani, et al.
Frontiers in Neurology|March 16, 2019
Lipomatosis Incidence and Characteristics in an Italian Cohort of Mitochondrial PatientsOlimpia Musumeci, Emanuele Barca, Costanza Lamperti, et al.
Pageof 15