Resultats de la cerca - Marie‐Christine Morel‐Kopp

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  1. 1
    Heparin‐induced multi‐electrode aggregometry method for heparin‐induced thrombocytopenia testing: communication from the SSC of the ISTH

    Heparin‐induced multi‐electrode aggregometry method for heparin‐induced thrombocytopenia testing: communication from the SSC of the ISTH per Marie‐Christine Morel‐Kopp, François Mullier, Vasiliki Gkalea, Tamam Bakchoul, Valentine Minet, Ismaı̈l Elalamy, Christopher Wård

    Publicat 2016
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  2. 2
    Reduced T helper and B lymphocytes in Parkinson's disease

    Reduced T helper and B lymphocytes in Parkinson's disease per Claire H. Stevens, Dominic B. Rowe, Marie‐Christine Morel‐Kopp, Carolyn Orr, Tonia Russell, Madelaine Ranola, Christopher Wård, Glenda M. Halliday

    Publicat 2012
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  3. 3
    Role of Nongenomic Signaling Pathways Activated by Aldosterone During Cardiac Reperfusion Injury

    Role of Nongenomic Signaling Pathways Activated by Aldosterone During Cardiac Reperfusion Injury per Anthony W. Ashton, Thi Yen Loan Le, Celso E. Gómez-Sánchez, Marie‐Christine Morel‐Kopp, Brett McWhinney, Amanda L. Hudson, Anastasia S. Mihailidou

    Publicat 2015
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  4. 4
    Effects of continuous positive airway pressure on coagulability in obstructive sleep apnoea: a randomised, placebo-controlled crossover study

    Effects of continuous positive airway pressure on coagulability in obstructive sleep apnoea: a randomised, placebo-controlled crossover study per Craig L. Phillips, Bradley McEwen, Marie‐Christine Morel‐Kopp, Brendon J. Yee, David R. Sullivan, Christopher Wård, Geoffrey H. Tofler, Ronald R. Grunstein

    Publicat 2012
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  5. 5
    GFI1B mutation causes a bleeding disorder with abnormal platelet function

    GFI1B mutation causes a bleeding disorder with abnormal platelet function per William Stevenson, Marie‐Christine Morel‐Kopp, Q. Chen, Hai-Yi Liang, C.J. Bromhead, Stephen Wright, Р. И. Туракулов, Ashley P. Ng, Andrew W. Roberts, Melanie Bahlo, Christopher Wård

    Publicat 2013
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  6. 6
    GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis

    GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thr... per Karyn Mégy, Kate Downes, Marie‐Christine Morel‐Kopp, José María Bastida, Shannon Brooks, Loredana Bury, Eva Leinøe, Keith Gomez, Neil V. Morgan, Maha Othman, Willem H. Ouwehand, Juliana Perez Botero, José Rivera, Harald Schulze, David‐Alexandre Trégouët, Kathleen Freson

    Publicat 2021
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  7. 7
    Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis

    Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis per Lisa Ewans, André E. Minoche, Deborah Schofield, Rupendra Shrestha, Clare Puttick, Ying Zhu, Alexander P. Drew, Velimir Gayevskiy, George Elakis, Corrina Walsh, Lesley C. Adès, Alison Colley, Carolyn Ellaway, Carey‐Anne Evans, Mary‐Louise Freckmann, Linda Goodwin, Anna Hackett, Benjamin Kamien, Edwin P. Kirk, Michelle Lipke, David Mowat, Elizabeth E. Palmer, Sulekha Rajagopalan, Anne Ronan, Rani Sachdev, William Stevenson, Anne Turner, Meredith Wilson, Lisa Worgan, Marie‐Christine Morel‐Kopp, Michael Field, Michael F. Buckley, Mark J. Cowley, Marcel E. Dinger, Tony Roscioli

    Publicat 2022
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  8. 8
    Spectrum of the Mutations in Bernard-Soulier Syndrome

    Spectrum of the Mutations in Bernard-Soulier Syndrome per Anna Savoia, Shinji Kunishima, Daniela De Rocco, Barbara Zieger, Margaret L. Rand, Núria Pujol‐Moix, Ümran Çalışkan, Hüseyin Tokgöz, Alessandro Pecci, Patrizia Noris, Alok Srivastava, Christopher Wård, Marie‐Christine Morel‐Kopp, Marie‐Christine Alessi, Sylvia Bellucci, Philippe Beurrier, Emmanuel de Maistre, Rémi Favier, Nathalie Hézard, Marie-Françoise Hurtaud-Roux, Véronique Latger‐Cannard, Cécile Lavenu‐Bombled, Valérie Proulle, Sandrine Meunier, Claude Négrier, Alan T. Nurden, Hanitra Randrianaivo, Fabrizio Fabris, Helen Platokouki, Nurit Rosenberg, Basma HadjKacem, Paula G. Heller, Mehran Karimi, Carlo L. Balduini, Annalisa Pastore, François Lanza

    Publicat 2014
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  9. 9
    Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC

    Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC per Paolo Gresele, Sara Orsini, Patrizia Noris, Emanuela Falcinelli, Marie‐Christine Alessi, Loredana Bury, M. BORHANY, Cristina Santoro, Ana C. Glembotsky, Ana Rosa Cid, Alberto Tosetto, Erica De Candia, Pierre Fontana, Giuseppe Guglielmini, Alessandro Pecci, Paula G. Heller, Giuseppina Rodorigo, Bernhard Lämmle, Alice Trinchero, Paolo Radossi, Silvia Ferrari, Davide Rancitelli, Amy Stolinski, Abinaya Arulselvan, Giuseppe Lassandro, Analía Sánchez‐Luceros, Martine Jandrot‐Perrus, Shinji Kunishima, José Rivera Pozo, Marie Lordkipanidzé, Federica Melazzini, Céline Falaise, Alessandra Casonato, Gian Marco Podda, Meganathan Kannan, Kerstin Jurk, Teresa Sevivas, Giancarlo Castaman, Elvira Grandone, Mathieu Fiore, Pamela Zúñiga, Yvonne Henskens, Kôji Miyazaki, Arnaud Dupuis, Catherine P.M. Hayward, Carlo Zaninetti, Madiha Abid, Grazia Ferrara, Maria Gabriella Mazzucconi, Giuseppe Tagariello, Paula James, Fabrizio Fabris, Alexandra Russo, Nuria Bermejo, Mariasanta Napolitano, Jennifer Curnow, Gkalea Vasiliki, Barbara Zieger, Marián Fedor, Meera Chitlur, Michele P. Lambert, Luca Barcella, Benilde Cosmi, Paola Giordano, Claudia Porri, İbrahim Eker, Marie‐Christine Morel‐Kopp, Hans Deckmyn, Andrew L. Frelinger, Paul Harrison, Diego Mezzano, Andrew Mumford

    Publicat 2019
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