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2025

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Year Number of Results
1974 1
1976 1
1979 1
1989 1
1992 1
1993 1
1995 1
1996 1
1997 1
1998 1
1999 1
2000 1
2001 3
2002 2
2003 2
2005 1
2006 2
2007 3
2008 3
2009 3
2010 1
2011 2
2012 4
2013 6
2014 2
2015 4
2016 6
2017 2
2018 4
2019 6
2020 5
2021 5
2022 1
2023 8
2024 5
2025 0

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81 results

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Page 1
International Consensus on Differential Diagnosis and Management of Patients With Danon Disease: JACC State-of-the-Art Review.
Hong KN, Eshraghian EA, Arad M, Argirò A, Brambatti M, Bui Q, Caspi O, de Frutos F, Greenberg B, Ho CY, Kaski JP, Olivotto I, Taylor MRG, Yesso A, Garcia-Pavia P, Adler ED. Hong KN, et al. J Am Coll Cardiol. 2023 Oct 17;82(16):1628-1647. doi: 10.1016/j.jacc.2023.08.014. J Am Coll Cardiol. 2023. PMID: 37821174 Free article. Review.
Danon disease is a rare X-linked autophagic vacuolar cardioskeletal myopathy associated with severe heart failure that can be accompanied with extracardiac neurologic, skeletal, and ophthalmologic manifestations. ...Herein, the authors review the differential diagno
Danon disease is a rare X-linked autophagic vacuolar cardioskeletal myopathy associated with severe heart failure that can be
Applications of Gene Therapy in Cardiomyopathies.
Argiro A, Bui Q, Hong KN, Ammirati E, Olivotto I, Adler E. Argiro A, et al. JACC Heart Fail. 2024 Feb;12(2):248-260. doi: 10.1016/j.jchf.2023.09.015. Epub 2023 Oct 7. JACC Heart Fail. 2024. PMID: 37966402 Review.
Notably, gene therapy for Duchenne muscular dystrophy has recently been approved and pivotal clinical trials are testing gene therapy approaches in rare myocardial conditions such as Danon disease and Fabry disease. Furthermore, promising results have been sh …
Notably, gene therapy for Duchenne muscular dystrophy has recently been approved and pivotal clinical trials are testing gene therapy approa …
Nuts in the Prevention and Management of Type 2 Diabetes.
Nishi SK, Viguiliouk E, Kendall CWC, Jenkins DJA, Hu FB, Sievenpiper JL, Atzeni A, Misra A, Salas-Salvadó J. Nishi SK, et al. Nutrients. 2023 Feb 9;15(4):878. doi: 10.3390/nu15040878. Nutrients. 2023. PMID: 36839236 Free PMC article. Review.
This review considers the epidemiological and clinical evidence to date for the role of nut consumption as a dietary strategy for the prevention and management of type 2 diabetes (T2D) and related complications. Findings suggest nut consumption may have a potential role in …
This review considers the epidemiological and clinical evidence to date for the role of nut consumption as a dietary strategy for the preven …
Roles of LAMP-1 and LAMP-2 in lysosome biogenesis and autophagy.
Eskelinen EL. Eskelinen EL. Mol Aspects Med. 2006 Oct-Dec;27(5-6):495-502. doi: 10.1016/j.mam.2006.08.005. Epub 2006 Sep 14. Mol Aspects Med. 2006. PMID: 16973206 Review.
Mutations in LAMP-2 gene cause a lysosomal glycogen storage disease, Danon disease, in humans. LAMP-2 deficient mice replicate the symptoms found in Danon patients including accumulation of autophagic vacuoles in heart and skeletal muscle …
Mutations in LAMP-2 gene cause a lysosomal glycogen storage disease, Danon disease, in humans. LAMP-2 def …
Genetic causes of heart failure with preserved ejection fraction: emerging pharmacological treatments.
Olivotto I, Udelson JE, Pieroni M, Rapezzi C. Olivotto I, et al. Eur Heart J. 2023 Feb 21;44(8):656-667. doi: 10.1093/eurheartj/ehac764. Eur Heart J. 2023. PMID: 36582184 Review.
Finally, a better understanding of the molecular underpinnings of monogenic myocardial disease may help identify therapeutic targets and develop innovative treatments for selected HFpEF phenotypes of broader epidemiological relevance. ...The present review addressed existi …
Finally, a better understanding of the molecular underpinnings of monogenic myocardial disease may help identify therapeutic targets …
Review: Danon disease: Review of natural history and recent advances.
Cenacchi G, Papa V, Pegoraro V, Marozzo R, Fanin M, Angelini C. Cenacchi G, et al. Neuropathol Appl Neurobiol. 2020 Jun;46(4):303-322. doi: 10.1111/nan.12587. Epub 2019 Nov 25. Neuropathol Appl Neurobiol. 2020. PMID: 31698507 Review.
Danon disease is a severe multisystem disorder clinically characterized by hypertrophic cardiomyopathy, skeletal myopathy and mental retardation in male patients, and by a milder phenotype (predominantly involving cardiac muscle) in female patients. ...We surveyed o
Danon disease is a severe multisystem disorder clinically characterized by hypertrophic cardiomyopathy, skeletal myopathy and
Genetic Infiltrative Cardiomyopathies.
Sweet ME, Mestroni L, Taylor MRG. Sweet ME, et al. Heart Fail Clin. 2018 Apr;14(2):215-224. doi: 10.1016/j.hfc.2017.12.003. Heart Fail Clin. 2018. PMID: 29525649 Free PMC article. Review.
Danon disease: a case report and literature review.
Xu J, Li Z, Liu Y, Zhang X, Niu F, Zheng H, Wang L, Kang L, Wang K, Xu B. Xu J, et al. Diagn Pathol. 2021 May 1;16(1):39. doi: 10.1186/s13000-021-01100-8. Diagn Pathol. 2021. PMID: 33933120 Free PMC article. Review.
BACKGROUND: Danon disease (DD) is a rare x-linked dominant multisystemic disorder with a clinical triad of severe cardiomyopathy, skeletal myopathy, and mental retardation. It is caused by a defect in the lysosomal-associated membrane protein-2 (LAMP2) gene, which l …
BACKGROUND: Danon disease (DD) is a rare x-linked dominant multisystemic disorder with a clinical triad of severe cardiomyopat …
Clinical features of Danon disease and insights gained from LAMP-2 deficiency models.
Zhai Y, Miao J, Peng Y, Wang Y, Dong J, Zhao X. Zhai Y, et al. Trends Cardiovasc Med. 2023 Feb;33(2):81-89. doi: 10.1016/j.tcm.2021.10.012. Epub 2021 Nov 2. Trends Cardiovasc Med. 2023. PMID: 34737089 Review.
Danon disease (DD) is an X-linked multisystem disorder with clinical features characterized by the triad of hypertrophic cardiomyopathy, skeletal muscle weakness, and mental retardation. ...
Danon disease (DD) is an X-linked multisystem disorder with clinical features characterized by the triad of hypertrophic cardi
Autophagic vacuolar myopathies.
Nishino I. Nishino I. Curr Neurol Neurosci Rep. 2003 Jan;3(1):64-9. doi: 10.1007/s11910-003-0040-y. Curr Neurol Neurosci Rep. 2003. PMID: 12507414 Review.
Hereditary myopathies characterized by the development of autophagic vacuoles can be categorized into three groups: rimmed vacuolar myopathies, acid maltase deficiency (glycogen storage disease type II), and myopathies characterized by the autophagic v …
Hereditary myopathies characterized by the development of autophagic vacuoles can be categorized into three groups: rimmed vacuolar myopathi …
81 results