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Arrhythmias in the muscular dystrophies.
Groh WJ. Groh WJ. Heart Rhythm. 2012 Nov;9(11):1890-5. doi: 10.1016/j.hrthm.2012.06.038. Epub 2012 Jun 30. Heart Rhythm. 2012. PMID: 22760083 Review.
Duchenne, Becker, and limb-girdle types 2C-2F and 2I are muscular dystrophies in which the development of a dilated cardiomyopathy is common. Arrhythmias and conduction disease occur after the development of the dilated cardiomyopathy. Patients are con …
Duchenne, Becker, and limb-girdle types 2C-2F and 2I are muscular dystrophies in which the development of a dilated cardiomyopathy
Dystrophies and heart disease.
Cox GF, Kunkel LM. Cox GF, et al. Curr Opin Cardiol. 1997 May;12(3):329-43. Curr Opin Cardiol. 1997. PMID: 9243091 Review.
The muscular dystrophies are a clinically and genetically heterogeneous group of skeletal muscle-wasting diseases that differ widely in their frequency and pattern of cardiac involvement. Myocardial disease manifesting predominantly as cardiomyopathy and congestive heart f …
The muscular dystrophies are a clinically and genetically heterogeneous group of skeletal muscle-wasting diseases that differ widely in thei …
The nuclear muscular dystrophies.
Wehnert MS, Bonne G. Wehnert MS, et al. Semin Pediatr Neurol. 2002 Jun;9(2):100-7. doi: 10.1053/spen.2002.33806. Semin Pediatr Neurol. 2002. PMID: 12138994 Review.
Phenotypically, they present as Emery-Dreifuss muscular dystrophy (EDMD), limb-girdle muscle dystrophy 1B (LGMD1B), or dilated cardiomyopathy with conduction defects (DCM-CD). ...
Phenotypically, they present as Emery-Dreifuss muscular dystrophy (EDMD), limb-girdle muscle dystrophy 1B (LGMD1B), or dilated
The nuclear envelope in muscular dystrophy and cardiovascular diseases.
Burke B, Mounkes LC, Stewart CL. Burke B, et al. Traffic. 2001 Oct;2(10):675-83. doi: 10.1034/j.1600-0854.2001.21001.x. Traffic. 2001. PMID: 11576443 Free article. Review.
These disorders, described as laminopathies or nuclear envelopathies, include both X-linked and autosomal dominant forms of Emery-Dreifuss muscular dystrophy, dilated cardiomyopathy with conduction system defects, limb girdle muscular dystrophy 1B with atriov …
These disorders, described as laminopathies or nuclear envelopathies, include both X-linked and autosomal dominant forms of Emery-Dreifuss m …
Nuclear envelope proteins and neuromuscular diseases.
Ostlund C, Worman HJ. Ostlund C, et al. Muscle Nerve. 2003 Apr;27(4):393-406. doi: 10.1002/mus.10302. Muscle Nerve. 2003. PMID: 12661041 Review.
Mutations in A-type lamins also cause limb-girdle muscular dystrophy type 1B, dilated cardiomyopathy with conduction defect, and Charcot-Marie-Tooth disorder type 2B1. ...
Mutations in A-type lamins also cause limb-girdle muscular dystrophy type 1B, dilated cardiomyopathy with conduction de …
The A-type lamins: nuclear structural proteins as a focus for muscular dystrophy and cardiovascular diseases.
Mounkes LC, Burke B, Stewart CL. Mounkes LC, et al. Trends Cardiovasc Med. 2001 Oct;11(7):280-5. doi: 10.1016/s1050-1738(01)00126-8. Trends Cardiovasc Med. 2001. PMID: 11709282 Review.
Mutations in the lamin A (LMNA) gene are associated with the tissue-specific diseases Emery-Dreifuss muscular dystrophy (EDMD), limb girdle muscular dystrophy (LGMD-1B), dilated cardiomyopathy with conduction system disease (DCM-CD), and Dunnigan's familial p …
Mutations in the lamin A (LMNA) gene are associated with the tissue-specific diseases Emery-Dreifuss muscular dystrophy (EDMD), limb girdle …
Laminopathies affecting skeletal and cardiac muscles: clinical and pathophysiological aspects.
Decostre V, Ben Yaou R, Bonne G. Decostre V, et al. Acta Myol. 2005 Oct;24(2):104-9. Acta Myol. 2005. PMID: 16550926 Review.
This review focuses on laminopathies affecting the striated muscle tissue only, namely Emery-Dreifuss muscular dystrophy (EDMD), limb girdle muscular dystrophy type 1B (LGMD1B) and dilated cardiomyopathy with conduction defects (DCM-CD). ...
This review focuses on laminopathies affecting the striated muscle tissue only, namely Emery-Dreifuss muscular dystrophy (EDMD), limb girdle …