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Neurology
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April 12, 2015
Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E
Claudio 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 apoptosis
Vittorio Abbonante, Alessandro Malara, Martina Chrisam, et al.
Journal of Neurology
|
March 4, 2025
Deep characterization of females with heterozygous Duchenne muscular dystrophy mutations
Pietro 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 pathways
Kate 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 macrophages
Gina 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 Dystrophy
Peter 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 diagnosis
Francesca 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 aggregates
Daniela 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 dystrophy
Luca Bello, Paola Melacini, Raffaele Pezzani, et al.
Frontiers in Neurology
|
March 16, 2019
Lipomatosis Incidence and Characteristics in an Italian Cohort of Mitochondrial Patients
Olimpia Musumeci, Emanuele Barca, Costanza Lamperti, et al.
Page
of 15
Search research articles
Search
Showing results (61-70 of 144) with videos related to
Sort By:
Page
of 15
Neurology
|
April 12, 2015
Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E
Claudio 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 apoptosis
Vittorio Abbonante, Alessandro Malara, Martina Chrisam, et al.
Journal of Neurology
|
March 4, 2025
Deep characterization of females with heterozygous Duchenne muscular dystrophy mutations
Pietro 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 pathways
Kate 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 macrophages
Gina 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 Dystrophy
Peter 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 diagnosis
Francesca 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 aggregates
Daniela 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 dystrophy
Luca Bello, Paola Melacini, Raffaele Pezzani, et al.
Frontiers in Neurology
|
March 16, 2019
Lipomatosis Incidence and Characteristics in an Italian Cohort of Mitochondrial Patients
Olimpia Musumeci, Emanuele Barca, Costanza Lamperti, et al.
Page
of 15