A systematic review and meta-analysis of the prevalence of left ventricular non-compaction in adults
Aims To assess the reported prevalence of left ventricular non-compaction (LVNC) in
different adult cohorts, taking in to consideration the role of diagnostic criteria and imaging …
different adult cohorts, taking in to consideration the role of diagnostic criteria and imaging …
[HTML][HTML] Cardiac pathology in myotonic dystrophy type 1
MS Mahadevan, RS Yadava, M Mandal - International journal of …, 2021 - mdpi.com
Myotonic dystrophy type 1 (DM1), the most common muscular dystrophy affecting adults and
children, is a multi-systemic disorder affecting skeletal, cardiac, and smooth muscles as well …
children, is a multi-systemic disorder affecting skeletal, cardiac, and smooth muscles as well …
Guía clínica para el diagnóstico y seguimiento de la distrofia miotónica tipo 1, DM1 o enfermedad de Steinert
GG Gutiérrez, J Díaz-Manera, M Almendrote, S Azriel… - Medicina Clínica, 2019 - Elsevier
Antecedentes y objetivos La enfermedad de Steinert o distrofia miotónica tipo 1
(DM1),(OMIM 160900) es la miopatía más prevalente en el adulto. Es una enfermedad …
(DM1),(OMIM 160900) es la miopatía más prevalente en el adulto. Es una enfermedad …
Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease
GG Gutiérrez, J Díaz-Manera, M Almendrote… - … Clínica (English Edition), 2019 - Elsevier
Background and objectives Steinert's disease or myotonic dystrophy type 1 (MD1),(OMIM
160900), is the most prevalent myopathy in adults. It is a multisystemic disorder with …
160900), is the most prevalent myopathy in adults. It is a multisystemic disorder with …
Systemic therapy in an RNA toxicity mouse model with an antisense oligonucleotide therapy targeting a non-CUG sequence within the DMPK 3′UTR RNA
Abstract Myotonic dystrophy type 1 (DM1), the most common adult muscular dystrophy, is an
autosomal dominant disorder caused by an expansion of a (CTG) n tract within the 3 …
autosomal dominant disorder caused by an expansion of a (CTG) n tract within the 3 …
[HTML][HTML] Comprehensive transcriptome-wide analysis of spliceopathy correction of myotonic dystrophy using CRISPR-Cas9 in iPSCs-derived cardiomyocytes
CTG repeat expansion (CTG exp) is associated with aberrant alternate splicing that
contributes to cardiac dysfunction in myotonic dystrophy type 1 (DM1). Excision of this CTG …
contributes to cardiac dysfunction in myotonic dystrophy type 1 (DM1). Excision of this CTG …
[HTML][HTML] Echocardiographic features of cardiac involvement in myotonic dystrophy 1: prevalence and prognostic value
V Russo, A Capolongo, R Bottino, A Carbone… - Journal of Clinical …, 2023 - mdpi.com
Myotonic dystrophy type 1 (DM1) is the most common muscular dystrophy in adults. Cardiac
involvement is reported in 80% of cases and includes conduction disturbances, arrhythmias …
involvement is reported in 80% of cases and includes conduction disturbances, arrhythmias …
[HTML][HTML] 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 …
Non-invasive evaluation of the relationship between electrical and structural cardiac abnormalities in patients with myotonic dystrophy type 1
L Chmielewski, M Bietenbeck, A Patrascu… - Clinical Research in …, 2019 - Springer
Background Cardiac involvement in myotonic dystrophy type 1 (MD1) includes conduction
disease, arrhythmias, and left-ventricular (LV) systolic dysfunction leading to an increased …
disease, arrhythmias, and left-ventricular (LV) systolic dysfunction leading to an increased …
The role of multimodality imaging in the diagnosis of left ventricular noncompaction
K Rao, A Bhaskaran, P Choudhary… - European Journal of …, 2020 - Wiley Online Library
Left ventricular noncompaction (LVNC) is a heterogeneous entity and, in reality, a likely
spectrum of disease which is clinically associated with arrhythmia, thromboembolic …
spectrum of disease which is clinically associated with arrhythmia, thromboembolic …