Disease: Scapuloperoneal myopathy- MYH7-related
- <em>LMNA</em>-related muscular dystrophy: Identification of variants in alternative genes and personalized clinical translation
- 253rd ENMC international workshop: Striated muscle laminopathies - natural history and clinical trial readiness. 24-26 June 2022, Hoofddorp, the Netherlands
- A Case of Cardiogenic Stroke With a Novel LMNA Variant (c. 1135C>A; p.Leu379Ile)
- Cardiac manifestations and clinical management of X-linked Emery-Dreifuss muscular dystrophy: a case series
- Cardiac Rehabilitation in a Transplanted Person with Emery-Dreifuss Muscular Dystrophy
- Characteristics of nuclear architectural abnormalities of myotubes differentiated from Lmna<sup>H222P/H222P</sup> skeletal muscle cells
- Characterization of cardiac involvement in children with <em>LMNA</em>-related muscular dystrophy
- Clinical and genetic analysis of Emery-Dreifuss muscular dystrophy type 2 caused by LMNA gene mutation
- Clinical and Genetic Heterogeneity of Nuclear Envelopathy Related Muscular Dystrophies in an Indian Cohort
- COMPREHENSIVE CARDIOVASCULAR THERAPY IN EMERY-DREIFUSS MUSCULAR DYSTROPHY: A CASE REPORT
- Desmin and Plectin Recruitment to the Nucleus and Nuclei Orientation Are Lost in Emery-Dreifuss Muscular Dystrophy Myoblasts Subjected to Mechanical Stimulation
- Detection of gonosomal mosaicism by ultra-deep sequencing and droplet digital PCR in patients with Emery-Dreifuss muscular dystrophy
- Drosophila Models Reveal Properties of Mutant Lamins That Give Rise to Distinct Diseases
- Early Muscle MRI Findings in a Pediatric Case of Emery-Dreifuss Muscular Dystrophy Type 1
- Effect of nutritional therapy in Emery-Dreifuss muscular dystrophy: a case report
- Emerin deficiency does not exacerbate cardiomyopathy in a murine model of Emery-Dreifuss muscular dystrophy caused by an LMNA gene mutation
- Emery-Dreifuss Muscular Dystrophy 1 is associated with high risk of malignant ventricular arrhythmias and end-stage heart failure
- Emery-Dreifuss muscular dystrophy Type 1 is associated with a high risk of malignant ventricular arrhythmias and end-stage heart failure
- Emery-Dreifuss muscular dystrophy: a closer look at cardiac complications
- Familial Testicular Germ Cell Tumor in Two Brothers With Emery Dreifuss Muscular Dystrophy Caused by an FHL-1 Mutation: A Case Report
- Genetic Patterns of Selected Muscular Dystrophies in the Muscular Dystrophy Surveillance, Tracking, and Research Network
- Heart transplant anesthetic approach in a patient with Emery Dreyfuss muscular dystrophy: A case report
- Identification of mutations on the <em>EMD</em> and <em>EYA4</em> genes associated with Emery-Dreifuss muscular dystrophy and deafness: a case report
- Identification of mutations on the EMD and EYA4 genes associated with Emery-Dreifuss muscular dystrophy and deafness: a case report
- Metastasis-associated 1 localizes to the sarcomeric Z-disc and is implicated in skeletal muscle pathology
- Native lamin A/C proteomes and novel partners from heart and skeletal muscle in a mouse chronic inflammation model of human frailty
- Nesprin proteins: bridging nuclear envelope dynamics to muscular dysfunction
- Nesprin-1: novel regulator of striated muscle nuclear positioning and mechanotransduction
- Nesprin-2 is a novel scaffold protein for telethonin and FHL-2 in the cardiomyocyte sarcomere
- Net39 protects muscle nuclei from mechanical stress during the pathogenesis of Emery-Dreifuss muscular dystrophy
- Nuclear envelope transmembrane proteins involved in genome organization are misregulated in myotonic dystrophy type 1 muscle
- The bi-directional relationship between sleep and inflammation in muscular dystrophies: A narrative review