Comprehensive Cardiovascular Management of Myotonic Dystrophy Type 1 Patients: A Report from the Italian Neuro-Cardiology Network
Myotonic dystrophy is a hereditary disorder with systemic involvement. The Italian Neuro-
Cardiology Network-“Rete delle Neurocardiologie”(INCN-RNC) is a unique collaborative …
Cardiology Network-“Rete delle Neurocardiologie”(INCN-RNC) is a unique collaborative …
Overview of the complex relationship between epigenetics markers, CTG repeat instability and symptoms in myotonic dystrophy type 1
L de Pontual, S Tomé - International Journal of Molecular Sciences, 2022 - mdpi.com
Among the trinucleotide repeat disorders, myotonic dystrophy type 1 (DM1) is one of the
most complex neuromuscular diseases caused by an unstable CTG repeat expansion in the …
most complex neuromuscular diseases caused by an unstable CTG repeat expansion in the …
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials
M Garibaldi, T Nicoletti, E Bucci… - European Journal of …, 2022 - Wiley Online Library
Background Only a few studies have reported muscle imaging data on small cohorts of
patients with myotonic dystrophy type 1 (DM1). We aimed to investigate the muscle …
patients with myotonic dystrophy type 1 (DM1). We aimed to investigate the muscle …
New developments in myotonic dystrophies from a multisystemic perspective
F Montagnese, B Schoser - Current Opinion in Neurology, 2021 - journals.lww.com
Extra-muscular manifestations greatly contribute to the overall disease burden. A
multidisciplinary approach is the key for the management of patients. Consensus-based …
multidisciplinary approach is the key for the management of patients. Consensus-based …
Current Treatment Options for Patients with Myotonic Dystrophy Type 2
F Montagnese - Current Treatment Options in Neurology, 2021 - Springer
Purpose of the review Myotonic dystrophy types 1 and 2 are frequent forms of muscular
dystrophies in adulthood. Their clinical differences need to be taken into account for the …
dystrophies in adulthood. Their clinical differences need to be taken into account for the …
Alterações cardiológicas em portadores de distrofia miotônica de steinert
HC França - 2022 - repositorio.bahiana.edu.br
Introdução: As distrofias miotônicas (DTMT) são um conjunto de doenças genéticas
multissistêmicas raras caracterizadas por miotonia, fraqueza progressiva e catarata …
multissistêmicas raras caracterizadas por miotonia, fraqueza progressiva e catarata …