Sudden Death Associated With Danon Disease in Women
- 1 February 2012
- journal article
- research article
- Published by Elsevier BV in The American Journal of Cardiology
- Vol. 109 (3), 406-411
- https://doi.org/10.1016/j.amjcard.2011.09.024
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- LAMP2 Microdeletions in Patients With Danon DiseaseCirculation: Cardiovascular Genetics, 2010
- Clinical Outcome and Phenotypic Expression in LAMP2 CardiomyopathyJama-Journal Of The American Medical Association, 2009
- Danon disease presenting with dilated cardiomyopathy and a complex phenotypeJournal of Human Genetics, 2007
- LAMP-2 Positive Vacuolar Myopathy with Dilated CardiomyopathyInternal Medicine, 2007
- Generalized Lysosome-Associated Membrane Protein-2 Defect Explains Multisystem Clinical Involvement and Allows Leukocyte Diagnostic Screening in Danon DiseaseThe American Journal of Pathology, 2006
- Danon Disease as an Underrecognized Cause of Hypertrophic Cardiomyopathy in ChildrenCirculation, 2005
- Familial X-linked cardiomyopathy (Danon disease): diagnostic confirmation by mutation analysis of the LAMP2geneEuropean Journal of Pediatrics, 2005
- Glycogen Storage Diseases Presenting as Hypertrophic CardiomyopathyThe New England Journal of Medicine, 2005
- Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)Nature, 2000
- Lysosomal glycogen storage disease with normal acid maltaseNeurology, 1981