Cardiolaminopathies are a heterogeneous group of disorders which are due to mutations in the genes encoding for nuclear lamins or their binding proteins. The whole spectrum of cardiac manifestations encompasses atrial arrhythmias, conduction disturbances, progressive systolic dysfunction, and malignant ventricular arrhythmias. Despite the prognostic significance of cardiac involvement in this setting, the current recommendations lack strong evidence. The aim of our work was to systematically review the current data on the main cardiovascular outcomes in cardiolaminopathies. We searched PubMed/Embase for studies focusing on cardiovascular outcomes in LMNA mutation carriers (atrial arrhythmias, ventricular arrhythmias, sudden cardiac death, c...
Background: Cardiac problems are common and are a major cause of death in both Duchenne muscular dys...
Myotonic dystrophy type 1 (DM1) is the most common adult form of muscular dystrophy, presenting with...
Cardiac disease is a common clinical manifestation of neuromuscular disorders, particularly of muscu...
Cardiolaminopathies are a heterogeneous group of disorders which are due to mutations in the genes e...
Introduction: Cardiac involvement in patients with muscular dystrophy associated with Lamin A/C muta...
Aims Retrospective studies have identified a mutation in the lamin A/C (LMNA) gene in patients selec...
Aims: Retrospective studies have identified a mutation in the lamin A/C (LMNA) gene in patients sele...
Background and Purpose-Emery-Dreifuss muscular dystrophy (EDMD) is a rare inherited disorder associa...
OBJECTIVE: Myotonic dystrophy type 1 (DM1) is the most frequent muscular dystrophy in adults. DM1 is...
Mutations in lamins, which are ubiquitous nuclear intermediate filaments, lead to a variety of disor...
<p>The paper gives the results of a clinical observation of 5 patients with genetically verified X-l...
OBJECTIVE: Myotonic dystrophy type 1 (DM1) is the most frequent muscular dystrophy in adults. DM1 is...
Duchenne muscle dystrophy (DMD) accounts for over 80 percent of muscle dystrophies due to x-linked m...
Objective Myotonic dystrophy type 1 (DM1) is the most frequent muscular dystrophy in adults. DM1 is ...
Background: Myotonic dystrophy (DM) is an inherited progressive muscle disorder caused by defects in...
Background: Cardiac problems are common and are a major cause of death in both Duchenne muscular dys...
Myotonic dystrophy type 1 (DM1) is the most common adult form of muscular dystrophy, presenting with...
Cardiac disease is a common clinical manifestation of neuromuscular disorders, particularly of muscu...
Cardiolaminopathies are a heterogeneous group of disorders which are due to mutations in the genes e...
Introduction: Cardiac involvement in patients with muscular dystrophy associated with Lamin A/C muta...
Aims Retrospective studies have identified a mutation in the lamin A/C (LMNA) gene in patients selec...
Aims: Retrospective studies have identified a mutation in the lamin A/C (LMNA) gene in patients sele...
Background and Purpose-Emery-Dreifuss muscular dystrophy (EDMD) is a rare inherited disorder associa...
OBJECTIVE: Myotonic dystrophy type 1 (DM1) is the most frequent muscular dystrophy in adults. DM1 is...
Mutations in lamins, which are ubiquitous nuclear intermediate filaments, lead to a variety of disor...
<p>The paper gives the results of a clinical observation of 5 patients with genetically verified X-l...
OBJECTIVE: Myotonic dystrophy type 1 (DM1) is the most frequent muscular dystrophy in adults. DM1 is...
Duchenne muscle dystrophy (DMD) accounts for over 80 percent of muscle dystrophies due to x-linked m...
Objective Myotonic dystrophy type 1 (DM1) is the most frequent muscular dystrophy in adults. DM1 is ...
Background: Myotonic dystrophy (DM) is an inherited progressive muscle disorder caused by defects in...
Background: Cardiac problems are common and are a major cause of death in both Duchenne muscular dys...
Myotonic dystrophy type 1 (DM1) is the most common adult form of muscular dystrophy, presenting with...
Cardiac disease is a common clinical manifestation of neuromuscular disorders, particularly of muscu...