Arrhythmogenic Left Ventricular Cardiomyopathy: From Diagnosis to Risk Management
A Mauriello, AS Roma, A Ascrizzi, R Molinari… - Journal of Clinical …, 2024 - mdpi.com
Purpose of Review: Left ventricular arrhythmogenic cardiomyopathy (ALVC) is a rare and
poorly characterized cardiomyopathy that has recently been reclassified in the group of non …
poorly characterized cardiomyopathy that has recently been reclassified in the group of non …
Cardiac involvement in patient-specific induced pluripotent stem cells of myotonic dystrophy type 1: unveiling the impact of voltage-gated sodium channels
Myotonic dystrophy type 1 (DM1) is a genetic disorder that causes muscle weakness and
myotonia. In DM1 patients, cardiac electrical manifestations include conduction defects and …
myotonia. In DM1 patients, cardiac electrical manifestations include conduction defects and …
A case of myotonic dystrophy type 1 with severe dilated cardiomyopathy: an unusual presenting manifestation of the most common muscular dystrophy in adults
R Ghosh, M León-Ruiz, AS Mondal, S Dubey… - Neurological …, 2024 - Springer
Myotonic dystrophy type 1 (DM1), recognized as the most prevalent form of muscular
dystrophy in adults, is an autosomal dominant disorder that impacts multiple systems …
dystrophy in adults, is an autosomal dominant disorder that impacts multiple systems …
Left Bundle Branch Optimized Implantable Cardioverter Defibrillator (LOT-ICD) Implantation in a Patient with Myotonic Dystrophy
S KARA, M DOĞAN, U Canpolat - European Journal of …, 2024 - avesis.hacettepe.edu.tr
Left bundle branch (LBB) optimized implantable cardioverter defibrillator (LOT-ICD) is a
recently emerged alternative to the standard biventricular pacing-ICD (BiVp-ICD). The IS-1 …
recently emerged alternative to the standard biventricular pacing-ICD (BiVp-ICD). The IS-1 …
Caracterización clínica y genética de una serie de pacientes con distrofia miotónica tipo 1
M Almendrote Muñoz - tdx.cat
La distrofia miotónica tipo 1 (DM1) es una enfermedad de origen genético causada por la
expansión de tripletes CTG en el gen DMPK. Se caracteriza por una afectación …
expansión de tripletes CTG en el gen DMPK. Se caracteriza por una afectación …
[HTML][HTML] Congenital Myotonic Dystrophy
S Liegel, D Jewell - now.aapmr.org
Myotonic dystrophy (MD) is a form of muscular dystrophy that is classified into two types:
Myotonic Dystrophy type 1 (DM1), and Myotonic Dystrophy type 2 (DM2). DM1 and DM2 …
Myotonic Dystrophy type 1 (DM1), and Myotonic Dystrophy type 2 (DM2). DM1 and DM2 …