E. Menegazzo

Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation

Jianzhou Wang, Elena Pegoraro, E. Menegazzo et al. · Human Molecular Genetics · 1995 · 175 citations

Mechanobiology, Rare Diseases, Muscle Function +14

Correlation between cardiac involvement and CTG trinucleotide repeat length in myotonic dystrophy

Paola Melacini, C Villanova, E. Menegazzo et al. · Journal of the American College of Cardiology · 1995 · 126 citations

Cardiac Muscle, Cardiomyopathy, Medicine +7

Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeats

Massimo Gennarelli, Giuseppe Novelli, Andreasi Bassi et al. · American Journal of Medical Genetics · 1996 · 90 citations

Genetics, Genetic Epidemiology, Pathology +17

Cognitive impairment and (CTG)n expansion in myotonic dystrophy patients

Giulia Perini, E. Menegazzo, Mario Ermani et al. · Biological Psychiatry · 1999 · 72 citations

Myotonic Dystrophy Patients, Neurodegenerative Diseases, Corticobasal Degeneration +4

Homozygous ?-sarcoglycan mutation in two siblings: One asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patient

C. Angelini, E. Menegazzo, M.P. Freda et al. · Muscle & Nerve · 1998 · 70 citations