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Publications by Catherine Favreau
Expression of a Mutant Lamin a That Causes Emery-Dreifuss Muscular Dystrophy Inhibits in Vitro Differentiation of C2C12 Myoblasts
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Related publications
Cardiac Manifestations in Emery–Dreifuss Muscular Dystrophy
CMAJ
Medicine
Lamin a N-Terminal Phosphorylation Is Associated With Myoblast Activation: Impairment in Emery-Dreifuss Muscular Dystrophy
Journal of Medical Genetics
Genetics
Identification of Lamin a/C ( LMNA ) Gene Mutations in Korean Patients With Autosomal Dominant Emery-Dreifuss Muscular Dystrophy and Limb-Girdle Muscular Dystrophy 1B
Journal of Human Genetics
Genetics
Emery–Dreifuss Muscular Dystrophy: A Test Case for Precision Medicine
The Application of Clinical Genetics
Genetics
Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy
American Journal of Human Genetics
Genetics
Follow Up Study of Cardiac Involvement in Emery-Dreifuss Muscular Dystrophy.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Atrial Arrhythmias in Emery Dreifuss Muscular Dystrophy: Approach to Successful Ablation.
HeartRhythm Case Reports
Cardiovascular Medicine
Cardiology
Clinical Relevance of Atrial Fibrillation/Flutter, Stroke, Pacemaker Implant, and Heart Failure in Emery-Dreifuss Muscular Dystrophy: A Long-Term Longitudinal Study
Stroke
Cardiology
Neurology
Cardiovascular Medicine
Advanced
Medicine
Neuroscience
Specialized Nursing
Emery-Dreifuss Syndrome.
Journal of Medical Genetics
Genetics
