Torthaí cuardaigh - Nicola Marziliano

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  1. 1
    When Coronary Artery Disease Meets a Channelopathy: An Unexpected Dangerous Date

    When Coronary Artery Disease Meets a Channelopathy: An Unexpected Dangerous Date de réir Francielle Feitosa Dias-Santos, Nicola Marziliano

    Foilsithe / Cruthaithe 2019
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  2. 2
    Simulated hypogravity impairs the angiogenic response of endothelium by up-regulating apoptotic signals

    Simulated hypogravity impairs the angiogenic response of endothelium by up-regulating apoptotic signals de réir Lucia Morbidelli, Monica Monici, Nicola Marziliano, Augusto Cogoli, Franco Fusi, Johannes Waltenberger, Marina Ziche

    Foilsithe / Cruthaithe 2005
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  3. 3
    The Molecular Basis of Familial Hemolytic Uremic Syndrome

    The Molecular Basis of Familial Hemolytic Uremic Syndrome de réir Jessica Caprioli, Paola Bettinaglio, Peter F. Zipfel, Barbara Amadei, Erica Daina, Sara Gamba, Christine Skerka, Nicola Marziliano, Giuseppe Remuzzi, Marina Noris

    Foilsithe / Cruthaithe 2001
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  4. 4
    Comparison of the human and mouse genes encoding the telomeric protein, TRF1: chromosomal localization, expression and conserved protein domains

    Comparison of the human and mouse genes encoding the telomeric protein, TRF1: chromosomal localization, expression and conserved protein domains de réir Dominique Broccoli, Laura Chong, Stefan Oelmann, Anthony A. Fernald, Nicola Marziliano, Bas van Steensel, David Kipling, Michelle M. Le Beau, Titia de Lange

    Foilsithe / Cruthaithe 1997
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  5. 5
    Calcium release channel RyR2 regulates insulin release and glucose homeostasis

    Calcium release channel RyR2 regulates insulin release and glucose homeostasis de réir Gaetano Santulli, Gennaro Pagano, Celestino Sardu, Wenjun Xie, Steven Reiken, Salvatore Luca D’Ascia, Michele Cannone, Nicola Marziliano, Bruno Trimarco, Theresa A. Guise, Alain Lacampagne, Andrew R. Marks

    Foilsithe / Cruthaithe 2015
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  6. 6
    Two novel and one known mutation of the TGFBR2 gene in Marfan syndrome not associated with FBN1 gene defects

    Two novel and one known mutation of the TGFBR2 gene in Marfan syndrome not associated with FBN1 gene defects de réir Eliana Disabella, Maurizia Grasso, Nicola Marziliano, Silvia Ansaldi, C. Lucchelli, Emanuele Porcu, Marilena Tagliani, Andrea Pilotto, Marta Diegoli, Luca Lanzarini, Clara Malattia, Antonio Pelliccia, Anna Ficcadenti, Orazio Gabrielli, Eloisa Arbustini

    Foilsithe / Cruthaithe 2005
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  7. 7
    Novel α-Actinin 2 Variant Associated With Familial Hypertrophic Cardiomyopathy and Juvenile Atrial Arrhythmias

    Novel α-Actinin 2 Variant Associated With Familial Hypertrophic Cardiomyopathy and Juvenile Atrial Arrhythmias de réir Francesca Girolami, Maria Iascone, Benedetta Tomberli, Sara Bardi, Matteo Benelli, Giuseppina Marseglia, Chiara Pescucci, Laura Pezzoli, Maria Elena Sana, Cristina Basso, Nicola Marziliano, Piera Angelica Merlini, Alessandra Fornaro, Franco Cecchi, Francesca Torricelli, Iacopo Olivotto

    Foilsithe / Cruthaithe 2014
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  8. 8
    Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies

    Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies de réir Michele Pasotti, Catherine Klersy, Andrea Pilotto, Nicola Marziliano, Claudio Rapezzi, Alessandra Serio, Savina Mannarino, Fabiana Isabella Gambarin, Valentina Favalli, Maurizia Grasso, Manuela Agozzino, Carlo Campana, Antonello Gavazzi, Oreste Febo, Massimiliano Marini, Maurizio Landolina, Andrea Mortara, G. Piccolo, Mario Viganò, Luigi Tavazzi, Eloisa Arbustini

    Foilsithe / Cruthaithe 2008
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  9. 9
    Identification of sixty-two novel and twelve known FBN1 mutations in eighty-one unrelated probands with Marfan syndrome and other fibrillinopathies

    Identification of sixty-two novel and twelve known FBN1 mutations in eighty-one unrelated probands with Marfan syndrome and other fibrillinopathies de réir Eloisa Arbustini, Maurizia Grasso, Silvia Ansaldi, Clara Malattia, Andrea Pilotto, Emanuele Porcu, Eliana Disabella, Nicola Marziliano, Angela Pisani, Luca Lanzarini, Savina Mannarino, Daniela Larizza, Mario Mosconi, Elena Antoniazzi, M. C. Zoia, Giulia Meloni, Lorenzo Magrassi, Agnese Brega, Maria Francesca Bedeschi, Isabella Torrente, Francesca Mari, Luigi Tavazzi

    Foilsithe / Cruthaithe 2005
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  10. 10
    Influence of 9p21.3 Genetic Variants on Clinical and Angiographic Outcomes in Early-Onset Myocardial Infarction

    Influence of 9p21.3 Genetic Variants on Clinical and Angiographic Outcomes in Early-Onset Myocardial Infarction de réir Diego Ardissino, Carlo Berzuini, Piera Angelica Merlini, Pier Mannuccio Mannucci, Aarti Surti, Noël P. Burtt, Benjamin F. Voight, Marco Tubaro, Flora Peyvandi, M. Spreafico, Patrizia Celli, Daniela Lina, Maria Francesca Notarangelo, Maurizio Ferrario, Raffaela Fetiveau, Giorgio Casari, Michele Galli, Flavio Ribichini, Marco Rossi, Francesco Bernardi, Nicola Marziliano, Pietro Zonzin, Francesco Mauri, Alberto Piazza, Luisa Foco, Luisa Bernardinelli, David Altshuler, Sekar Kathiresan

    Foilsithe / Cruthaithe 2011
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  11. 11
    Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands

    Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands de réir Laurence Faivre, Gwenaëlle Collod‐Béroud, Anne H. Child, Bert Callewaert, Bart Loeys, Christine Binquet, Élodie Gautier, Eloisa Arbustini, Karin Mayer, Mine Arslan‐Kirchner, Chantal Stheneur, Anatoli Kiotsekoglou, Paolo Comeglio, Nicola Marziliano, Dorothy Halliday, Christophe Béroud, Claire Bonithon‐Kopp, Mireille Claustres, H Plauchu, Peter N. Robinson, Lesley C. Adès, Julie De Backer, Paul Coucke, Uta Francke, Anne De Paepe, Cathérine Boileau, Guillaume Jondeau

    Foilsithe / Cruthaithe 2008
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  12. 12
    Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24–32 mutation

    Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24–32 mutation de réir Laurence Faivre, Gwenaëlle Collod‐Béroud, Bert Callewaert, A. H. Child, Christine Binquet, Élodie Gautier, Bart Loeys, Eloisa Arbustini, Karin Mayer, Mine Arslan‐Kirchner, C. Stheneur, Anatoli Kiotsekoglou, Paolo Comeglio, Nicola Marziliano, J. E. Wolf, O. Bouchot, Philippe Khau Van Kien, Christophe Béroud, Mireille Claustres, C. Bonithon-Kopp, Peter N. Robinson, Lesley C. Adès, Julie De Backer, Paul Coucke, Uta Francke, Anne De Paepe, Guillaume Jondeau, Cathérine Boileau

    Foilsithe / Cruthaithe 2008
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  13. 13
    Effect of Mutation Type and Location on Clinical Outcome in 1,013 Probands with Marfan Syndrome or Related Phenotypes and FBN1 Mutations: An International Study

    Effect of Mutation Type and Location on Clinical Outcome in 1,013 Probands with Marfan Syndrome or Related Phenotypes and FBN1 Mutations: An International Study de réir Laurence Faivre, Gwenaëlle Collod‐Béroud, Bart Loeys, Anne H. Child, Christine Binquet, Élodie Gautier, Bert Callewaert, Eloisa Arbustini, Karin Mayer, Mine Arslan‐Kirchner, Anatoli Kiotsekoglou, Paolo Comeglio, Nicola Marziliano, Harry C. Dietz, Dorothy Halliday, Christophe Béroud, Claire Bonithon‐Kopp, Mireille Claustres, Christine Muti, Henri Plauchu, Peter N. Robinson, Lesley C. Adès, Andrew Biggin, B. Benetts, Maggie Brett, Katherine Holman, Julie De Backer, Paul Coucke, Uta Francke, Anne De Paepe, Guillaume Jondeau, Cathérine Boileau

    Foilsithe / Cruthaithe 2007
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  14. 14
    Coding Variation in<i>ANGPTL4,</i><i>LPL,</i>and<i>SVEP1</i>and the Risk of Coronary Disease

    Coding Variation in<i>ANGPTL4,</i><i>LPL,</i>and<i>SVEP1</i>and the Risk of Coronary Disease de réir Nathan O. Stitziel, Kathleen Stirrups, Nicholas G. D. Masca, Jeanette Erdmann, Paola G. Ferrario, Inke R. König, Peter Weeke, Tom R. Webb, Paul L. Auer, Ursula M. Schick, Yingchang Lu, He Zhang, Marie‐Pierre Dubé, Anuj Goel, Martin Farrall, Gina M. Peloso, Hong‐Hee Won, Ron Do, Erik P.A. van Iperen, Stavroula Kanoni, Jochen Kruppa, Anubha Mahajan, Robert A. Scott, Christina Willenberg, Peter S. Braund, Julian C. van Capelleveen, Alex S. F. Doney, Louise A. Donnelly, Rosanna Asselta, Piera Angelica Merlini, Stefano Duga, Nicola Marziliano, Joshua C. Denny, Christian M. Shaffer, Nour Eddine El Mokhtari, Andre Franke, Omri Gottesman, Stefanie Heilmann‐Heimbach, Christian Hengstenberg, Per Hoffman, Oddgeir L. Holmen, Kristian Hveem, Jan‐Håkan Jansson, Karl‐Heinz Jöckel, Thorsten Kessler, Jennifer Kriebel, Karl‐Ludwig Laugwitz, Eirini Marouli, Nicola Martinelli, Børge G. Nordestgaard, Tibor V. Varga

    Foilsithe / Cruthaithe 2016
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  15. 15
    Inactivating Mutations in <i>NPC1L1</i> and Protection from Coronary Heart Disease

    Inactivating Mutations in <i>NPC1L1</i> and Protection from Coronary Heart Disease de réir Nathan O. Stitziel, Hong‐Hee Won, Alanna C. Morrison, Gina M. Peloso, Ron Do, Leslie A. Lange, Pierre Fontanillas, Namrata Gupta, Stefano Duga, Anuj Goel, Martin Farrall, Danish Saleheen, Paola G. Ferrario, Inke R. König, Rosanna Asselta, Piera Angelica Merlini, Nicola Marziliano, Maria Francesca Notarangelo, Ursula M. Schick, Paul L. Auer, Themistocles L. Assimes, Muredach P. Reilly, Robert Wilensky, Daniel J. Rader, G. Kees Hovingh, Thomas Meitinger, Thorsten Kessler, Adnan Kastrati, Karl‐Ludwig Laugwitz, David S. Siscovick, Jerome I. Rotter, Stanely L Hazen, Russell P. Tracy, Sharon Cresci, John A. Spertus, Rebecca D. Jackson, Stephen M. Schwartz, Pradeep Natarajan, Jacy R. Crosby, Donna M. Muzny, Christie M. Ballantyne, Stephen S. Rich, Christopher J. O’Donnell, Gonçalo R. Abecasis, Shamil Sunaev, Deborah A. Nickerson, Julie E. Buring, Paul M. Ridker, Daniel I. Chasman, Erin Austin, Iftikhar Kullo, Peter Weeke, Christian M. Shaffer, Lisa A. Bastarache, Joshua C. Denny, Dan M. Roden, Colin N. A. Palmer, Panos Deloukas, D. Y. Lin, Zheng-Zheng Tang, Jeanette Erdmann, Heribert Schunkert, John Danesh, Jaume Marrugat, Roberto Elosúa, Diego Ardissino, Ruth McPherson, Hugh Watkins, Alex P. Reiner, James G. Wilson, David Altshuler, Richard A. Gibbs, Eric S. Lander, Eric Boerwinkle, Stacey Gabriel, Sekar Kathiresan

    Foilsithe / Cruthaithe 2014
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  16. 16
    Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

    Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants de réir Sekar Kathiresan, Benjamin F. Voight, Shaun Purcell, Kiran Musunuru, Diego Ardissino, Pier M Mannucci, Sonia Anand, James C. Engert, Nilesh J Samani, Heribert Schunkert, Jeanette Erdmann, Muredach P. Reilly, Daniel J. Rader, Thomas Morgan, John A. Spertus, Monika Stoll, Domenico Girelli, Pascal McKeown, Chris C Patterson, David S Siscovick, Christopher J O'Donnell, Roberto Elosúa, Leena Peltonen, Veikko Salomaa, Stephen M Schwartz, Olle Melander, David Altshuler, Pier Angelica Merlini, Carlo Berzuini, Luisa Bernardinelli, Flora Peyvandi, Marco Tubaro, Patrizia Celli, Maurizio Ferrario, Raffaela Fetiveau, Nicola Marziliano, Giorgio Casari, Michele Galli, Flavio Ribichini, Marco Rossi, Francesco Bernardi, Pietro Zonzin, Alberto Piazza, Jean Yee, Yechiel Friedlander, Jaume Marrugat, Gavin Lucas, Isaac Subirana, Joan Sala, Rafel Ramos, James B Meigs, Gordon Williams, David M Nathan, Calum A. MacRae, Aki S Havulinna, Göran Berglund, Joel N. Hirschhorn, Rosanna Asselta, Stefano Duga, Marta Spreafico, Mark Daly, James Nemesh, Joshua M. Korn, Steven A. McCarroll, Aarti Surti, Candace Guiducci, Lauren Gianniny, Daniel B. Mirel, Melissa Parkin, Noël P. Burtt, Stacey B. Gabriel, John R Thompson, Peter S. Braund, Benjamin J. Wright, Anthony J Balmforth, Stephen G. Ball, Alistair S. Hall, Patrick Linsel‐Nitschke, Wolfgang Lieb, Andreas Ziegler, Inke R. König, Christian Hengstenberg, Marcus Fischer, Klaus Stark, Anika Grosshennig, Michael Preuß, H‐Erich Wichmann, Stefan Schreiber, Willem H. Ouwehand, Panos Deloukas, Michael Scholz, Francois Cambien, Mingyao Li, Zhen Chen, Robert Wilensky, William Matthai, Atif Qasim, Hákon Hákonarson, Joe Devaney, Mary-Susan Burnett

    Foilsithe / Cruthaithe 2009
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  17. 17
    Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease

    Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease de réir Tom R. Webb, Jeanette Erdmann, Kathleen Stirrups, Nathan O. Stitziel, Nicholas G. D. Masca, Henning Jansen, Stavroula Kanoni, Christopher P. Nelson, Paola G. Ferrario, Inke R. König, John D. Eicher, Andrew D. Johnson, Stephen E. Hamby, Christer Betsholtz, Arno Ruusalepp, Oscar Franzén, Eric E. Schadt, Johan Björkegren, Peter Weeke, Paul L. Auer, Ursula M. Schick, Yingchang Lu, He Zhang, Marie‐Pierre Dubé, Anuj Goel, Martin Farrall, Gina M. Peloso, Hong‐Hee Won, Ron Do, Erik Van Iperen, Jochen Kruppa, Anubha Mahajan, Robert A. Scott, Christina Willenborg, Peter S. Braund, Julian C. van Capelleveen, Alex S. F. Doney, Louise A. Donnelly, Rosanna Asselta, Pier Angelica Merlini, Stefano Duga, Nicola Marziliano, Joshua C. Denny, Christian M. Shaffer, Nour Eddine El-Mokhtari, André Franke, Stefanie Heilmann‐Heimbach, Christian Hengstenberg, Per Hoffmann, Oddgeir L. Holmen, Kristian Hveem, Jan-Håkan Jansson, Karl‐Heinz Jöckel, Thorsten Kessler, Jennifer Kriebel, Karl‐Ludwig Laugwitz, Eirini Marouli, Nicola Martinelli, Mark I. McCarthy, Natalie R. van Zuydam, Christa Meisinger, Tõnu Esko, Evelin Mihailov, Stefan Andersson Escher, Maris Alver, Susanne Moebus, Andrew D. Morris, Jarma Virtamo, Majid Nikpay, Oliviero Olivieri, Sylvie Provost, Alaa AlQarawi, Neil R. Robertson, Karen O. Akinsansya, Dermot F. Reilly, Thomas Vogt, Yin Wu, Folkert W. Asselbergs, Charles Kooperberg, Rebecca D. Jackson, Eli A. Stahl, Martina Müller‐Nurasyid, Konstantin Strauch, Tibor V. Varga, Mélanie Waldenberger, Lingyao Zeng, Rajiv Chowdhury, Veikko Salomaa, Ian Ford, J. Wouter Jukema, Philippe Amouyel, Jukka Kontto, Børge G. Nordestgaard, Jean Ferrières, Danish Saleheen, Naveed Sattar, Praveen Surendran, Aline Wagner, Robin Young, Joanna M. M. Howson

    Foilsithe / Cruthaithe 2017
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  18. 18
    Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events

    Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events de réir Riyaz Patel, Amand F. Schmidt, Vinicius Tragante, Raymond O. McCubrey, Michael V. Holmes, Laurence J Howe, Kenan Direk, Axel Åkerblom, Karin Leander, Salim S. Virani, Karol Kamiński, Jochen D. Muehlschlegel, Marie‐Pierre Dubé, Hooman Allayee, Peter Almgren, Maris Alver, E.V. Baranova, Hassan Behlouli, Bram Boeckx, Peter S. Braund, Lutz Philipp Breitling, Graciela Delgado, Núbia E. Duarte, Line Dufresne, Niclas Eriksson, Luisa Foco, Crystel M. Gijsberts, Yan Gong, Jaana Hartiala, Mahyar Heydarpour, Jaroslav A. Hubáček, Marcus E. Kleber, Daniel Kofink, Pekka Kuukasjärvi, Vei‐Vei Lee, Andreas Leiherer, Petra Lenzini, Daniel L. Levin, Leo‐Pekka Lyytikäinen, Nicola Martinelli, Ute Mons, Christopher P. Nelson, Kjell Nikus, Anna P. Pilbrow, Rafał Płoski, Yan V. Sun, Michael W.T. Tanck, W.H. Wilson Tang, Stella Trompet, Sander W. van der Laan, Jessica van Setten, Ragnar O. Vilmundarson, Chiara Viviani Anselmi, Efthymia Vlachopoulou, Eric Boerwinkle, Carlo Briguori, John F. Carlquist, Kathryn Carruthers, Gavino Casu, John Deanfield, Panos Deloukas, Frank Dudbridge, Natalie Fitzpatrick, Bruna Gigante, Stefan James, Marja‐Liisa Lokki, Paulo A. Lotufo, Nicola Marziliano, Ify Mordi, Joseph B. Muhlestein, Chris Newton Cheh, Jan Piťha, Christoph H. Saely, Ayman Samman‐Tahhan, Pratik B. Sandesara, Andrej Teren, Adam Timmis, Frans Van de Werf, Els Wauters, Arthur A.M. Wilde, Ian Ford, David J. Stott, Ale Algra, Maria Grazia Andreassi, Diego Ardissino, Benoît J. Arsenault, Christie M. Ballantyne, Thomas O. Bergmeijer, Connie R. Bezzina, Simon C. Body, Peter Bogaty, Gert J. de Borst, Hermann Brenner, Ralph Burkhardt, Clara Carpeggiani, Gianluigi Condorelli, Rhonda M. Cooper‐DeHoff, Sharon Cresci, Ulf dé Fairé, Robert N. Doughty

    Foilsithe / Cruthaithe 2019
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  19. 19
    Subsequent Event Risk in Individuals With Established Coronary Heart Disease

    Subsequent Event Risk in Individuals With Established Coronary Heart Disease de réir Riyaz Patel, Vinicius Tragante, Amand F. Schmidt, Raymond O. McCubrey, Michael V. Holmes, Laurence J Howe, Kenan Direk, Axel Åkerblom, Karin Leander, Salim S. Virani, Karol Kamiński, Jochen D. Muehlschlegel, Hooman Allayee, Peter Almgren, Maris Alver, E.V. Baranova, Hassan Behloui, Bram Boeckx, Peter S. Braund, Lutz Philipp Breitling, Graciela Delgado, Núbia E. Duarte, Marie‐Pierre Dubé, Line Dufresne, Niclas Eriksson, Luisa Foco, Markus Scholz, Crystel M. Gijsberts, Charlotte Glinge, Yan Gong, Jaana Hartiala, Mahyar Heydarpour, Jaroslav A. Hubáček, Marcus E. Kleber, Daniel Kofink, Salma Kotti, Pekka Kuukasjärvi, Vei-Vei Lee, Andreas Leiherer, Petra Lenzini, Daniel L. Levin, Leo‐Pekka Lyytikäinen, Nicola Martinelli, Ute Mons, Christopher P. Nelson, Kjell Nikus, Anna P. Pilbrow, Rafał Płoski, Yan V. Sun, Michael W.T. Tanck, W.H. Wilson Tang, Stella Trompet, Sander W. van der Laan, Jessica van Setten, Ragnar O. Vilmundarson, Chiara Viviani Anselmi, Efthymia Vlachopoulou, Lawien Al Ali, Eric Boerwinkle, Carlo Briguori, John F. Carlquist, Kathryn Carruthers, Gavino Casu, John Deanfield, Panos Deloukas, Frank Dudbridge, Thomas Engstrøm, Natalie Fitzpatrick, Kim Fox, Bruna Gigante, Stefan James, Marja‐Liisa Lokki, Paulo A. Lotufo, Nicola Marziliano, Ify Mordi, Joseph B Muhlestein, Christopher Newton‐Cheh, Jan Piťha, Christoph H. Saely, Ayman Samman‐Tahhan, Pratik B. Sandesara, Andrej Teren, Adam Timmis, Frans Van de Werf, Els Wauters, Arthur A.M. Wilde, Ian Ford, David J. Stott, Ale Algra, Maria Grazia Andreassi, Diego Ardissino, Benoît J. Arsenault, Christie M. Ballantyne, Thomas O. Bergmeijer, Connie R. Bezzina, Simon C. Body, Eric Boersma, Peter Bogaty, Michiel L. Bots, Hermann Brenner

    Foilsithe / Cruthaithe 2019
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