Zobrazeno 1 - 10
of 216
pro vyhledávání: '"Richard Isnard"'
Autor:
Thomas Wallet, Lise Legrand, Richard Isnard, Estelle Gandjbakhch, Françoise Pousset, Julie Proukhnitzky, Marc Dommergues, Jacky Nizard, Philippe Charron
Publikováno v:
ESC Heart Failure, Vol 11, Iss 3, Pp 1506-1514 (2024)
Abstract Aims Inherited cardiomyopathies are relatively rare but carry a high risk of cardiac maternal morbidity and mortality during pregnancy and postpartum. However, data for risk stratification are scarce. The new CARPREG II score improves predic
Externí odkaz:
https://doaj.org/article/79b7af81fbe9461e9004a3bbeba599eb
Autor:
Damien Logeart, Maxime Doublet, Margaux Gouysse, Thibaud Damy, Richard Isnard, François Roubille
Publikováno v:
ESC Heart Failure, Vol 11, Iss 3, Pp 1688-1697 (2024)
Abstract Aims The use of large medical or healthcare claims databases is very useful for population‐based studies on the burden of heart failure (HF). Clinical characteristics and management of HF patients differ according to categories of left ven
Externí odkaz:
https://doaj.org/article/7c71fd25cb99420fb193c353d5bd320a
Autor:
Petros Andrikopoulos, Judith Aron-Wisnewsky, Rima Chakaroun, Antonis Myridakis, Sofia K. Forslund, Trine Nielsen, Solia Adriouch, Bridget Holmes, Julien Chilloux, Sara Vieira-Silva, Gwen Falony, Joe-Elie Salem, Fabrizio Andreelli, Eugeni Belda, Julius Kieswich, Kanta Chechi, Francesc Puig-Castellvi, Mickael Chevalier, Emmanuelle Le Chatelier, Michael T. Olanipekun, Lesley Hoyles, Renato Alves, Gerard Helft, Richard Isnard, Lars Køber, Luis Pedro Coelho, Christine Rouault, Dominique Gauguier, Jens Peter Gøtze, Edi Prifti, Philippe Froguel, The MetaCardis Consortium, Jean-Daniel Zucker, Fredrik Bäckhed, Henrik Vestergaard, Torben Hansen, Jean-Michel Oppert, Matthias Blüher, Jens Nielsen, Jeroen Raes, Peer Bork, Muhammad M. Yaqoob, Michael Stumvoll, Oluf Pedersen, S. Dusko Ehrlich, Karine Clément, Marc-Emmanuel Dumas
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-18 (2023)
Abstract The host-microbiota co-metabolite trimethylamine N-oxide (TMAO) is linked to increased cardiovascular risk but how its circulating levels are regulated remains unclear. We applied “explainable” machine learning, univariate, multivariate
Externí odkaz:
https://doaj.org/article/12ff1d1de8474b4894451345fa26b4ed
Autor:
Josua Vegas, MD, Clélie Van Der Vynckt, MD, Thomas Dietenbeck, PhD, Etienne Charpentier, MD, Samia Boussouar, MD, Nicoletta Pasi, MD, Richard Isnard, MD, PhD, Khaoula Bouazizi, PhD, Nadjia Kachenoura, PhD, Alban Redheuil, MD, PhD
Publikováno v:
Journal of Cardiovascular Magnetic Resonance, Vol 26, Iss , Pp 100775- (2024)
Externí odkaz:
https://doaj.org/article/33992b6accc94c28a07758f1df539165
Autor:
Ulrike Esslinger, Sophie Garnier, Agathe Korniat, Carole Proust, Georgios Kararigas, Martina Müller-Nurasyid, Jean-Philippe Empana, Michael P Morley, Claire Perret, Klaus Stark, Alexander G Bick, Sanjay K Prasad, Jennifer Kriebel, Jin Li, Laurence Tiret, Konstantin Strauch, Declan P O'Regan, Kenneth B Marguiles, Jonathan G Seidman, Pierre Boutouyrie, Patrick Lacolley, Xavier Jouven, Christian Hengstenberg, Michel Komajda, Hakon Hakonarson, Richard Isnard, Eloisa Arbustini, Harald Grallert, Stuart A Cook, Christine E Seidman, Vera Regitz-Zagrosek, Thomas P Cappola, Philippe Charron, François Cambien, Eric Villard
Publikováno v:
PLoS ONE, Vol 15, Iss 2, p e0229472 (2020)
[This corrects the article DOI: 10.1371/journal.pone.0172995.].
Externí odkaz:
https://doaj.org/article/8972f4d73bdb419c948a6bd6736188a5
Autor:
Lise Legrand, Carole Maupain, Marie-Lorraine Monin, Claire Ewenczyk, Richard Isnard, Rana Alkouri, Alexandra Durr, Francoise Pousset
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 6, p 1630 (2020)
Background: Friedreich’s ataxia (FA) is a rare autosomal recessive mitochondrial disease resulting of a triplet repeat expansion guanine-adenine-adenine (GAA) in the frataxin (FXN) gene, exhibiting progressive cerebellar ataxia, diabetes and cardio
Externí odkaz:
https://doaj.org/article/6de9290f16c440d3b67334a6c998b3f3
Autor:
Ulrike Esslinger, Sophie Garnier, Agathe Korniat, Carole Proust, Georgios Kararigas, Martina Müller-Nurasyid, Jean-Philippe Empana, Michael P Morley, Claire Perret, Klaus Stark, Alexander G Bick, Sanjay K Prasad, Jennifer Kriebel, Jin Li, Laurence Tiret, Konstantin Strauch, Declan P O'Regan, Kenneth B Marguiles, Jonathan G Seidman, Pierre Boutouyrie, Patrick Lacolley, Xavier Jouven, Christian Hengstenberg, Michel Komajda, Hakon Hakonarson, Richard Isnard, Eloisa Arbustini, Harald Grallert, Stuart A Cook, Christine E Seidman, Vera Regitz-Zagrosek, Thomas P Cappola, Philippe Charron, François Cambien, Eric Villard
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0172995 (2017)
AimsDilated cardiomyopathy (DCM) is an important cause of heart failure with a strong familial component. We performed an exome-wide array-based association study (EWAS) to assess the contribution of missense variants to sporadic DCM.Methods and resu
Externí odkaz:
https://doaj.org/article/57cc136b5b6b488385fb35ea7dfd896e
Autor:
Klaus Stark, Ulrike B Esslinger, Wibke Reinhard, George Petrov, Thomas Winkler, Michel Komajda, Richard Isnard, Philippe Charron, Eric Villard, François Cambien, Laurence Tiret, Marie-Claude Aumont, Olivier Dubourg, Jean-Noël Trochu, Laurent Fauchier, Pascal Degroote, Anette Richter, Bernhard Maisch, Thomas Wichter, Christa Zollbrecht, Martina Grassl, Heribert Schunkert, Patrick Linsel-Nitschke, Jeanette Erdmann, Jens Baumert, Thomas Illig, Norman Klopp, H-Erich Wichmann, Christa Meisinger, Wolfgang Koenig, Peter Lichtner, Thomas Meitinger, Arne Schillert, Inke R König, Roland Hetzer, Iris M Heid, Vera Regitz-Zagrosek, Christian Hengstenberg
Publikováno v:
PLoS Genetics, Vol 6, Iss 10, p e1001167 (2010)
Dilated cardiomyopathy (DCM) is a structural heart disease with strong genetic background. Monogenic forms of DCM are observed in families with mutations located mostly in genes encoding structural and sarcomeric proteins. However, strong evidence su
Externí odkaz:
https://doaj.org/article/56e0d4b0c2df4726aa00ecb1f26bdf14
Autor:
Attali, Valérie, Maria-Anna, Balice, Laurent, Barthel, Rosa, Buendia, Bertien, Buyse, Laurent, Boyer, Marie-Pierre, Cadars, Pascal, Cornec, Thibaud, Damy, Jean-Marc, Davy, Geoffroy, De Faverges, Toufik, Didi, Marie-Pia, d'ortho, Frédéric, Gagnadoux, Thibaud, Gentina, François, Goupil, Frédéric, Goutorbe, Jean-Maurice, Guillemot, Carmen, Iamandi, Richard, Isnard, François, Jounieaux, Christian, Koltes, Alain, Le Coz, Benoit, Lequeux, René, Lerest, Lionel, Lerousseau, Jean-Pierre, Mallet, Francis, Martin, Jean-Claude, Meurice, Ala, Noroc, Frédéric, Ortuno, Alain, Palot, Philippe, Papola, Audrey, Paris, Hélène, Pastinelli, Jean-Louis, Pepin, Christophe, Perrin, Carole, Philippe, Sandrine, Pontier, Arnaud, Prigent, Pascaline, Priou, Vincent, Puel, Claudio, Rabec, Benjamin, Richard, Claude, Richard, Marijke, Rutten, Manuel, Sastry, Murielle, Salvat, Kamila, Sedkaoui, Bharati, Shivalkar, Renaud, Tamisier, Dries, Testelmans, Johan, Verbraecken, Tamisier, Renaud, Damy, Thibaud, Bailly, Sébastien, Goutorbe, Frédéric, Davy, Jean-Marc, Lavergne, Florent, Palot, Alain, Verbraecken, Johan A., d’Ortho, Marie-Pia, Pépin, Jean-Louis
Publikováno v:
In Sleep Medicine January 2024 113:412-421
Autor:
Antonio Molinaro, Ina Nemet, Pierre Bel Lassen, Rima Chakaroun, Trine Nielsen, Judith Aron-Wisnewsky, Per-Olof Bergh, Lin Li, Marcus Henricsson, Lars Køber, Richard Isnard, Gerard Helft, Michael Stumvoll, Oluf Pedersen, J. Gustav Smith, W.H. Wilson Tang, Karine Clément, Stanley L. Hazen, Fredrik Bäckhed
Publikováno v:
JACC: Heart Failure.