Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Quarta CC"'
Autor:
Rapezzi C, Merlini G, Quarta CC, Riva L, Longhi S, Leone O, Salvi F, Ciliberti P, Pastorelli F, Biagini E, Coccolo F, Cooke RM, Bacchi-Reggiani L, Sangiorgi D, Ferlini A, Cavo M, Zamagni E, Fonte ML, Palladini G, Salinaro F
Publikováno v:
Circulation; 9/29/2009, Vol. 120 Issue 13, p1203-1212, 10p
Akademický článek
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Publikováno v:
Journal of the American College of Cardiology (JACC). Sep2012, Vol. 60 Issue 12, p1077-1078. 2p.
Publikováno v:
Circulation; 9/18/2012, Vol. 126 Issue 12, pe178-82, 1p
Autor:
Clara Salas, Christian Gagliardi, Cristina Quarta, Pablo García-Pavía, Marta Cobo-Marcos, Agnese Milandri, Luis Alonso-Pulpón, Serena Foffi, Enrique Lara-Pezzi, Massimiliano Lorenzini, Claudio Rapezzi, Mario Cinelli, F. Javier de Haro-del Moral, Fernando Dominguez, Esther Gonzalez-Lopez
Publikováno v:
DDFV: Repositorio Institucional de la Universidad Francisco de Vitoria
Universidad Francisco de Vitoria
DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
instname
Universidad Francisco de Vitoria
DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
instname
Aims Wild-type transthyretin amyloidosis (ATTRwt) is mostly considered a disease predominantly of elderly male, characterized by concentric LV hypertrophy, preserved LVEF, and low QRS voltages. We sought to describe the characteristics of a large coh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f872f2d326bc5196bbca71453e57e62
https://hdl.handle.net/10641/1295
https://hdl.handle.net/10641/1295
Autor:
Ornella Leone, Christian Gagliardi, Claudio Rapezzi, Ilaria Gallelli, Agnese Milandri, Candida Cristina Quarta, Massimiliano Lorenzini, Simone Longhi
Publikováno v:
Amyloid. 19:16-21
Hereditary transthyretin-related amyloidosis remains a widely underdiagnosed condition, owing to its extreme phenotypic variability: the clinical spectrum of the disease ranges from an almost exclusive neurologic involvement to strictly cardiac manif
Autor:
Francesco Fallani, Antonio Russo, Luciano Potena, Antonella Scalone, Fabio Coccolo, Angelo Branzi, Francesco Grigioni, Gaia Magnani, Candida Cristina Quarta
Publikováno v:
The Journal of Heart and Lung Transplantation. 27:685-688
Although statins have proven efficacy in lowering lipids and improving survival in heart transplantation (HT) recipients, potential drug interactions may limit efficacy and reduce tolerability. This observational study explored the efficacy and toler
Autor:
Taro Yamashita, Juris J. Liepnieks, Yukio Ando, Mitsuharu Ueda, Massimiliano Lorenzini, Merrill D. Benson, Masayoshi Tasaki, Giampaolo Merlini, Hirofumi Jono, Per Westermark, Shu-ichi Ikeda, Ole B. Suhr, Francesca Lavatelli, Toshinori Ohshima, Laura Obici, Ornella Leone, Elisabet Ihse, Claudio Rapezzi, Candida Cristina Quarta
Publikováno v:
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis. 20(3)
The clinical phenotype of familial ATTR amyloidosis depends to some extent on the particular mutation, but differences exist also within mutations. We have previously described that two types of amyloid fibril compositions exist among Swedish ATTRV30
Autor:
Pier Luigi Guidalotti, Giampaolo Merlini, Maurizio Pieroni, Laura Obici, Claudio Rapezzi, Laura Verga, Simone Longhi, Stefano Perlini, Candida Cristina Quarta
Amyloidotic cardiomyopathy is still a widely underdiagnosed condition that usually requires endomyocardial biopsy (EMB) for a definite diagnosis. 99mTc-3,3-diphosphono-1,2-propanodicarboxylic acid ( 99mTc-DPD) has proven highly sensitive for detectin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::003a71814561e44644e8a611ba1d8802
http://hdl.handle.net/11392/2415722
http://hdl.handle.net/11392/2415722
Autor:
Simone Longhi, Candida Cristina Quarta, Lucilla Badiali De Giorgi, Ornella Leone, Ferdinando Pasquale, Claudio Rapezzi, Agnese Milandri, Teresa Ragazzini, Giorgio Arpesella, Luigi Lovato, Luciano Potena
Publikováno v:
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis. 19(2)
Background: Knowledge of the patterns of myocardial amyloid accumulation could improve the interpretation of electrocardiographic, echocardiographic and magnetic resonance imaging findings of amyloidosis. We assessed the extent and pattern of myocard