Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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Material Type: Artigo
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Cardiac amyloidosis: An update on pathophysiology, diagnosis, and treatmentSiddiqi, Omar K. ; Ruberg, Frederick L.Trends in cardiovascular medicine, 2018-01, Vol.28 (1), p.10-21 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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Restrictive Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and TherapyMuchtar, Eli ; Blauwet, Lori A ; Gertz, Morie ACirculation research, 2017-09, Vol.121 (7), p.819-837 [Periódico revisado por pares]United States: American Heart Association, IncTexto completo disponível |
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Material Type: Artigo
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Genetic Restrictive Cardiomyopathy: Causes and Consequences-An Integrative ApproachCimiotti, Diana ; Budde, Heidi ; Hassoun, Roua ; Jaquet, KorneliaInternational journal of molecular sciences, 2021-01, Vol.22 (2), p.558 [Periódico revisado por pares]Switzerland: MDPI AGTexto completo disponível |
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Material Type: Artigo
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Mutations in FLNC are Associated with Familial Restrictive CardiomyopathyBrodehl, Andreas ; Ferrier, Raechel A. ; Hamilton, Sara J. ; Greenway, Steven C. ; Brundler, Marie-Anne ; Yu, Weiming ; Gibson, William T. ; McKinnon, Margaret L. ; McGillivray, Barbara ; Alvarez, Nanette ; Giuffre, Michael ; Schwartzentruber, Jeremy ; Gerull, BrendaHuman mutation, 2016-03, Vol.37 (3), p.269-279 [Periódico revisado por pares]United States: Blackwell Publishing LtdTexto completo disponível |
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Material Type: Artigo
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Mutations in Troponin that cause HCM, DCM AND RCM: What can we learn about thin filament function?Willott, Ruth H ; Gomes, Aldrin V ; Chang, Audrey N ; Parvatiyar, Michelle S ; Pinto, Jose Renato ; Potter, James DJournal of molecular and cellular cardiology, 2010-05, Vol.48 (5), p.882-892 [Periódico revisado por pares]England: Elsevier LtdTexto completo disponível |
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Material Type: Artigo
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Molecular mechanisms in cardiomyopathyDadson, Keith ; Hauck, Ludger ; Billia, FilioClinical science (1979), 2017-07, Vol.131 (13), p.1375-1392 [Periódico revisado por pares]EnglandTexto completo disponível |
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Material Type: Artigo
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The novel αB‐crystallin (CRYAB) mutation p.D109G causes restrictive cardiomyopathyBrodehl, Andreas ; Gaertner‐Rommel, Anna ; Klauke, Bärbel ; Grewe, Simon Andre ; Schirmer, Ilona ; Peterschröder, Andreas ; Faber, Lothar ; Vorgerd, Matthias ; Gummert, Jan ; Anselmetti, Dario ; Schulz, Uwe ; Paluszkiewicz, Lech ; Milting, HendrikHuman mutation, 2017-08, Vol.38 (8), p.947-952 [Periódico revisado por pares]United States: Hindawi LimitedTexto completo disponível |
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Material Type: Artigo
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The Amyloidogenic V122I Transthyretin Variant in Elderly Black AmericansQuarta, C. Cristina ; Buxbaum, Joel N ; Shah, Amil M ; Falk, Rodney H ; Claggett, Brian ; Kitzman, Dalane W ; Mosley, Thomas H ; Butler, Kenneth R ; Boerwinkle, Eric ; Solomon, Scott DThe New England journal of medicine, 2015-01, Vol.372 (1), p.21-29 [Periódico revisado por pares]United States: Massachusetts Medical SocietyTexto completo disponível |
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Material Type: Artigo
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Restrictive cardiomyopathy: from genetics and clinical overview to animal modelingChintanaphol, Michelle ; Orgil, Buyan-Ochir ; Alberson, Neely R ; Towbin, Jeffrey A ; Purevjav, EnkhsaikhanReviews in cardiovascular medicine, 2022-03, Vol.23 (3), p.108-108 [Periódico revisado por pares]Singapore: IMR PressTexto completo disponível |
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10 |
Material Type: Artigo
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Hereditary heart disease: pathophysiology, clinical presentation, and animal models of HCM, RCM, and DCM associated with mutations in cardiac myosin light chainsYadav, Sunil ; Sitbon, Yoel H. ; Kazmierczak, Katarzyna ; Szczesna-Cordary, DanutaPflügers Archiv, 2019-05, Vol.471 (5), p.683-699 [Periódico revisado por pares]Berlin/Heidelberg: Springer Berlin HeidelbergTexto completo disponível |