Laminopathies are genetic disorders due to gene mutation encoding for proteins of the nuclear envelope. Patients are at risk of conduction defect, arrhythmia, sudden death and heart failure. The authors summarize predictive factors for cardiac events reported in the literature in this group of disease
ObjectivesThe aim of this study was to analyze the long-term follow-up of dilated cardiolaminopathie...
Laminopathies, a broad class of diseases that primarily impact mechanically active tissues such as c...
Introduction: Cardiac involvement in patients with muscular dystrophy associated with Lamin A/C muta...
Mutations in lamins, which are ubiquitous nuclear intermediate filaments, lead to a variety of disor...
Aims: Retrospective studies have identified a mutation in the lamin A/C (LMNA) gene in patients sele...
Mutations in the LMNA gene are associated with a wide spectrum of disease phenotypes, ranging from n...
International audienceThe nuclear envelopathies, more frequently known as laminopathies are a rapidl...
Aims Retrospective studies have identified a mutation in the lamin A/C (LMNA) gene in patients selec...
Cardiolaminopathies are a heterogeneous group of disorders which are due to mutations in the genes e...
This study evaluated common clinical characteristics of patients with lamin A/C gene mutations that ...
This study evaluated common clinical characteristics of patients with lamin A/C gene mutations that ...
Mutations in the lamin A/C gene are found in Emery-Dreifuss muscular dystrophy, limb girdle muscular...
Patients with a partial reduction of merosin due to mutations in the laminin-α2 chain gene usually p...
International audienceA-type lamins gene (LMNA) mutations cause an autosomal dominant inherited form...
Familial occurrence of sudden cardiac death (SCD) is related to a variety of clinical conditions, wh...
ObjectivesThe aim of this study was to analyze the long-term follow-up of dilated cardiolaminopathie...
Laminopathies, a broad class of diseases that primarily impact mechanically active tissues such as c...
Introduction: Cardiac involvement in patients with muscular dystrophy associated with Lamin A/C muta...
Mutations in lamins, which are ubiquitous nuclear intermediate filaments, lead to a variety of disor...
Aims: Retrospective studies have identified a mutation in the lamin A/C (LMNA) gene in patients sele...
Mutations in the LMNA gene are associated with a wide spectrum of disease phenotypes, ranging from n...
International audienceThe nuclear envelopathies, more frequently known as laminopathies are a rapidl...
Aims Retrospective studies have identified a mutation in the lamin A/C (LMNA) gene in patients selec...
Cardiolaminopathies are a heterogeneous group of disorders which are due to mutations in the genes e...
This study evaluated common clinical characteristics of patients with lamin A/C gene mutations that ...
This study evaluated common clinical characteristics of patients with lamin A/C gene mutations that ...
Mutations in the lamin A/C gene are found in Emery-Dreifuss muscular dystrophy, limb girdle muscular...
Patients with a partial reduction of merosin due to mutations in the laminin-α2 chain gene usually p...
International audienceA-type lamins gene (LMNA) mutations cause an autosomal dominant inherited form...
Familial occurrence of sudden cardiac death (SCD) is related to a variety of clinical conditions, wh...
ObjectivesThe aim of this study was to analyze the long-term follow-up of dilated cardiolaminopathie...
Laminopathies, a broad class of diseases that primarily impact mechanically active tissues such as c...
Introduction: Cardiac involvement in patients with muscular dystrophy associated with Lamin A/C muta...