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TITLE: Complex roads from genotype to phenotype in dilated cardiomyopathy: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology  Full Text
AUTHORS: Antoine Bondue; Eloisa Arbustini; Anna Bianco; Michele Ciccarelli; Dana Dawson; Matteo De Rosa; Nazha Hamdani; Denise Hilfiker Kleiner; Benjamin Meder; Adelino F Leite Moreira ; Thomas Thum; Carlo G Tocchetti; Gilda Varricchi; Jolanda Van der Velden; Roddy Walsh; Stephane Heymans;
PUBLISHED: 2018, SOURCE: CARDIOVASCULAR RESEARCH, VOLUME: 114, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef: 84
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TITLE: Expert review document part 2: methodology, terminology and clinical applications of optical coherence tomography for the assessment of interventional procedures
AUTHORS: Francesco Prati; Giulio Guagliumi; Gary S Mintz; Marco Costa; Evelyn Regar; Takashi Akasaka; Peter Barlis; Guillermo J Tearney; Ik Kyung Jang; Elosia Arbustini; Hiram G Bezerra; Yukio Ozaki; Nico Bruining; Darius Dudek; Maria Radu; Andrejs Erglis; Pascale Motreff; Fernando Alfonso; Kostas Toutouzas; Nieves Gonzalo; Corrado Tamburino; Tom Adriaenssens; Fausto Pinto ; Patrick W J Serruys; Carlo Di Mario; ...More
PUBLISHED: 2012, SOURCE: EUROPEAN HEART JOURNAL, VOLUME: 33, ISSUE: 20
INDEXED IN: Scopus WOS CrossRef: 314
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TITLE: Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy
AUTHORS: Felix W Friedrich; Brendan R Wilding; Silke Reischmann; Claudia Crocini; Patrick Lang; Philippe Charron; Oliver J Mueller; Meagan J McGrath; Ingra Vollert; Arne Hansen; Wolfgang A Linke; Christian Hengstenberg; Gisele Bonne; Stellan Morner; Thomas Wichter; Hugo Madeira ; Eloisa Arbustini; Thomas Eschenhagen; Christina A Mitchell; Richard Isnard; Lucie Carrier; ...More
PUBLISHED: 2012, SOURCE: HUMAN MOLECULAR GENETICS, VOLUME: 21, ISSUE: 14
INDEXED IN: Scopus WOS CrossRef
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TITLE: A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy
AUTHORS: Villard, E; Perret, C; Gary, F; Proust, C; Dilanian, G; Hengstenberg, C; Ruppert, V; Arbustini, E; Wichter, T; Germain, M; Dubourg, O; Tavazzi, L; Aumont, MC; De Groote, P; Fauchier, L; Trochu, JN; Gibelin, P; Aupetit, JF; Stark, K; Erdmann, J; Hetzer, R; Roberts, AM; Barton, PJR; Regitz Zagrosek, V; Consortium, C; Aslam, U; Duboscq Bidot, L; Meyborg, M; Maisch, B; Madeira, H ; Waldenstrom, A; Galve, E; Cleland, JG; Dorent, R; Roizes, G; Zeller, T; Blankenberg, S; Goodall, AH; Cook, S; Tregouet, DA; Tiret, L; Isnard, R; Komajda, M; Charron, P; Cambien, F; ...More
PUBLISHED: 2011, SOURCE: EUROPEAN HEART JOURNAL, VOLUME: 32, ISSUE: 9
INDEXED IN: Scopus WOS CrossRef
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TITLE: A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy
AUTHORS: Felix W Friedrich; Pedro Bausero; Yuli L Sun; Andras Treszl; Elisabeth Kraemer; Denise Juhr; Pascale Richard; Karl Wegscheider; Ketty Schwartz; Dulce Brito ; Eloisa Arbustini; Anders Waldenstroem; Richard Isnard; Michel Komajda; Thomas Eschenhagen; Lucie Carrier;
PUBLISHED: 2009, SOURCE: EUROPEAN HEART JOURNAL, VOLUME: 30, ISSUE: 13
INDEXED IN: Scopus WOS CrossRef: 34