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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2013 | 1 |
2014 | 2 |
2015 | 3 |
2016 | 1 |
2024 | 0 |
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7 results
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Page 1
Clinical Spectrum of PRKAG2 Syndrome.
Circ Arrhythm Electrophysiol. 2016 Jan;9(1):e003121. doi: 10.1161/CIRCEP.115.003121.
Circ Arrhythm Electrophysiol. 2016.
PMID: 26729852
Free PMC article.
Review.
No abstract available.
Arrhythmogenic Phenotype in Dilated Cardiomyopathy: Natural History and Predictors of Life-Threatening Arrhythmias.
Spezzacatene A, Sinagra G, Merlo M, Barbati G, Graw SL, Brun F, Slavov D, Di Lenarda A, Salcedo EE, Towbin JA, Saffitz JE, Marcus FI, Zareba W, Taylor MR, Mestroni L; Familial Cardiomyopathy Registry.
Spezzacatene A, et al.
J Am Heart Assoc. 2015 Oct 16;4(10):e002149. doi: 10.1161/JAHA.115.002149.
J Am Heart Assoc. 2015.
PMID: 26475296
Free PMC article.
Item in Clipboard
The Cardiomyopathy Lamin A/C D192G Mutation Disrupts Whole-Cell Biomechanics in Cardiomyocytes as Measured by Atomic Force Microscopy Loading-Unloading Curve Analysis.
Lanzicher T, Martinelli V, Puzzi L, Del Favero G, Codan B, Long CS, Mestroni L, Taylor MR, Sbaizero O.
Lanzicher T, et al.
Sci Rep. 2015 Sep 1;5:13388. doi: 10.1038/srep13388.
Sci Rep. 2015.
PMID: 26323789
Free PMC article.
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AFM single-cell force spectroscopy links altered nuclear and cytoskeletal mechanics to defective cell adhesion in cardiac myocytes with a nuclear lamin mutation.
Lanzicher T, Martinelli V, Long CS, Del Favero G, Puzzi L, Borelli M, Mestroni L, Taylor MR, Sbaizero O.
Lanzicher T, et al.
Nucleus. 2015;6(5):394-407. doi: 10.1080/19491034.2015.1084453.
Nucleus. 2015.
PMID: 26309016
Free PMC article.
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Danon disease: clinical features, evaluation, and management.
D'souza RS, Levandowski C, Slavov D, Graw SL, Allen LA, Adler E, Mestroni L, Taylor MR.
D'souza RS, et al.
Circ Heart Fail. 2014 Sep;7(5):843-9. doi: 10.1161/CIRCHEARTFAILURE.114.001105.
Circ Heart Fail. 2014.
PMID: 25228319
Free PMC article.
Review.
No abstract available.
Item in Clipboard
Decreased levels of BAG3 in a family with a rare variant and in idiopathic dilated cardiomyopathy.
Feldman AM, Begay RL, Knezevic T, Myers VD, Slavov DB, Zhu W, Gowan K, Graw SL, Jones KL, Tilley DG, Coleman RC, Walinsky P, Cheung JY, Mestroni L, Khalili K, Taylor MR.
Feldman AM, et al.
J Cell Physiol. 2014 Nov;229(11):1697-702. doi: 10.1002/jcp.24615.
J Cell Physiol. 2014.
PMID: 24623017
Free PMC article.
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Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.
Merlo M, Sinagra G, Carniel E, Slavov D, Zhu X, Barbati G, Spezzacatene A, Ramani F, Salcedo E, Di Lenarda A, Mestroni L, Taylor MR; Familial Cardiomyopathy Registry.
Merlo M, et al.
Clin Transl Sci. 2013 Dec;6(6):424-8. doi: 10.1111/cts.12116. Epub 2013 Oct 3.
Clin Transl Sci. 2013.
PMID: 24119082
Free PMC article.
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