Cardiac manifestations of congenital LMNA-related muscular dystrophy in children: three case reports and recommendations for care

Prevalence of congenital muscular dystrophy in Italy: A population study

(2015) A. Graziano et al.   NEUROLOGY

LMNA-associated myopathies: The Italian experience in a large cohort of patients

(2014) L. Maggi et al.   NEUROLOGY

Diagnostic approach to the congenital muscular dystrophies

(2014) Carsten G. Bönnemann et al.   NEUROMUSCULAR DISORDERS

Implantable cardioverter-defibrillators in lamin A/C mutation carriers with cardiac conduction disorders

(2013) Frédéric Anselme et al.   HEART RHYTHM

Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers

(2012) Ingrid A.W. van Rijsingen et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Rapamycin Reverses Elevated mTORC1 Signaling in Lamin A/C-Deficient Mice, Rescues Cardiac and Skeletal Muscle Function, and Extends Survival

(2012) F. J. Ramos et al.   Science Translational Medicine

Consensus Statement on Standard of Care for Congenital Muscular Dystrophies

(2010) Ching H. Wang et al.   JOURNAL OF CHILD NEUROLOGY

The Gut and Intestinal Bacteria in Chronic Heart Failure

(2009) Anja Sandek et al.   CURRENT DRUG METABOLISM

De novoLMNAmutations cause a new form of congenital muscular dystrophy

(2008) Susana Quijano-Roy et al.   ANNALS OF NEUROLOGY