Disease: Limb-girdle muscular dystrophy- type 1B
- 2022 HRS expert consensus statement on evaluation and management of arrhythmic risk in neuromuscular disorders
- A family with 2 different hereditary diseases leading to early cardiac involvement
- A family with limb girdle muscular dystrophy type 1B and multiple exostoses
- A new LMNA mutation causing limb girdle muscular dystrophy 1B
- A novel mutation in a large French-Canadian family with LGMD1B
- A synonymous codon change in the LMNA gene alters mRNA splicing and causes limb girdle muscular dystrophy type 1B
- An elderly-onset limb girdle muscular dystrophy type 1B (LGMD1B) with pseudo-hypertrophy of paraspinal muscles
- Arrhythmias in the muscular dystrophies
- Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations
- Blood glutathione decrease in subjects carrying lamin A/C gene mutations is an early marker of cardiac involvement
- Cardiac diseases as a predictor warning of hereditary muscle diseases. The case of laminopathies
- Cardiac dysrhythmias,cardiomyopathy and muscular dystrophy in patients with Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy type 1B
- Characterization of cardiac involvement in children with <em>LMNA</em>-related muscular dystrophy
- Clinical and genetic features of limb-girdle muscular dystrophy type 1B: a case report
- Clinical outcomes of continuous flow left ventricular assist device therapy as bridge to transplant strategy in muscular dystrophy: a single-center study
- Clinical spectrum and genetic variations of <em>LMNA</em>-related muscular dystrophies in a large cohort of Chinese patients
- Clinical, genealogical and molecular genetic study of Emery-Dreifuss muscular dystrophy
- Clinical, pathological, imaging, and genetic characterization in a Taiwanese cohort with limb-girdle muscular dystrophy
- Co-segregation of LMNA and PMP22 gene mutations in the same family
- Defective skeletal muscle growth in lamin A/C-deficient mice is rescued by loss of Lap2α
- Dystrophies and heart disease
- Early-Onset LMNA-Associated Muscular Dystrophy with Later Involvement of Contracture
- Elevated TGF β2 serum levels in Emery-Dreifuss Muscular Dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes
- Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene
- Heart transplantation in 7 patients from a single family with limb-girdle muscular dystrophy caused by lamin A/C mutation
- Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse
- Identification of lamin A/C ( LMNA) gene mutations in Korean patients with autosomal dominant Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy 1B
- Inflammatory myopathy in the context of an unusual overlapping laminopathy
- Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy
- Lamin A/C truncation in dilated cardiomyopathy with conduction disease
- Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth
- Laminopathies affecting skeletal and cardiac muscles: clinical and pathophysiological aspects
- Laminopathies in Russian families
- LMNA-associated myopathies: the Italian experience in a large cohort of patients
- Muscle imaging analogies in a cohort of patients with different clinical phenotypes caused by LMNA gene mutations
- New intronic splicing mutation in the LMNA gene causing progressive cardiac conduction defects and variable myopathy
- Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease
- Novel LMNA mutation presenting as severe congenital muscular dystrophy
- Novel LMNA mutations in patients with Emery-Dreifuss muscular dystrophy and functional characterization of four LMNA mutations
- Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B
- Nuclear envelope alterations in fibroblasts from LGMD1B patients carrying nonsense Y259X heterozygous or homozygous mutation in lamin A/C gene
- Nuclear envelope proteins and associated diseases
- Nuclear envelope proteins and neuromuscular diseases
- Partial epilepsy in an adolescent male with limb-girdle muscular dystrophy 1B
- Pathological changes of the myonuclear fibrous lamina and internal nuclear membrane in two cases of autosomal dominant limb-girdle muscular dystrophy with atrioventricular conduction disturbance (LGMD1B)
- Prevalent cardiac phenotype resulting in heart transplantation in a novel LMNA gene duplication
- Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy
- R25G mutation in exon 1 of LMNA gene is associated with dilated cardiomyopathy and limb-girdle muscular dystrophy 1B
- SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells
- Somatic and germinal mosaicism in a Han Chinese family with laminopathies
- The A-type lamins: nuclear structural proteins as a focus for muscular dystrophy and cardiovascular diseases
- The Influence of a Genetic Variant in <em>CCDC78</em> on <em>LMNA</em>-Associated Skeletal Muscle Disease
- The Myoblast C2C12 Transfected with Mutant Valosin-Containing Protein Exhibits Delayed Stress Granule Resolution on Oxidative Stress
- The nuclear envelope in muscular dystrophy and cardiovascular diseases
- The nuclear muscular dystrophies
- The phenotypic manifestations of autosomal recessive axonal Charcot-Marie-Tooth due to a mutation in Lamin A/C gene
- Three new cases of dilated cardiomyopathy caused by mutations in LMNA gene
- Uncoordinated transcription and compromised muscle function in the lmna-null mouse model of Emery- Emery-Dreyfuss muscular dystrophy
- Up-regulation of Toll-like receptors 7 and 9 and its potential implications in the pathogenic mechanisms of LMNA-related myopathies