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Table representation of search results timeline featuring number of search results per year.

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 1

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77 results

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Page 1
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.
However, LAMP-2 seems to have more specific functions since LAMP-2 single deficiency has more severe consequences than LAMP-1 single deficiency. Mutations in LAMP-2 gene cause a lysosomal glycogen storage disease, Danon disease, in humans. LAMP- …
However, LAMP-2 seems to have more specific functions since LAMP-2 single deficiency has more severe consequences than LAMP-1 single deficie …
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.
While each of these conditions is rare, they collectively represent a relevant subset within HFpEF cohorts, and their prompt recognition has major consequences for clinical practice, as access to dedicated, disease-specific treatments may radically change the quality of li …
While each of these conditions is rare, they collectively represent a relevant subset within HFpEF cohorts, and their prompt recognition has …
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 …
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 …
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 …
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: Gender differences in presentation and outcomes.
Brambatti M, Caspi O, Maolo A, Koshi E, Greenberg B, Taylor MRG, Adler ED. Brambatti M, et al. Int J Cardiol. 2019 Jul 1;286:92-98. doi: 10.1016/j.ijcard.2019.01.020. Epub 2019 Feb 16. Int J Cardiol. 2019. PMID: 30857840 Review.
BACKGROUND: Danon disease (DD) is a rare X-linked autophagic vacuolar myopathy, characterized by high penetrance and severe cardiomyopathy. ...CONCLUSIONS: In this first systematic review of DD, we confirmed the severe morbidity and mortality associated with dise …
BACKGROUND: Danon disease (DD) is a rare X-linked autophagic vacuolar myopathy, characterized by high penetrance and severe ca …
Cardiac MRI of Hereditary Cardiomyopathy.
Fadl SA, Revels JW, Rezai Gharai L, Hanneman K, Dana F, Proffitt EK, Grizzard JD. Fadl SA, et al. Radiographics. 2022 May-Jun;42(3):625-643. doi: 10.1148/rg.210147. Epub 2022 Mar 11. Radiographics. 2022. PMID: 35275782 Review.
Native T1 mapping may similarly allow differentiation between Fabry disease and amyloidosis without the use of contrast material. T2*-weighted MRI is important in the detection and quantification of iron overload cardiomyopathy. Other hereditary entities for which comprehe …
Native T1 mapping may similarly allow differentiation between Fabry disease and amyloidosis without the use of contrast material. T2* …
Lysosomal Abnormalities in Cardiovascular Disease.
Chi C, Riching AS, Song K. Chi C, et al. Int J Mol Sci. 2020 Jan 27;21(3):811. doi: 10.3390/ijms21030811. Int J Mol Sci. 2020. PMID: 32012649 Free PMC article. Review.
77 results