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    Breaking barriers: holistic assessment of ability to work in patients with sarcoidosis von Russell, Anne-Marie, Spagnolo, Paolo, Wells, Athol U, Kock, Selene, Verheyen, Karolien, Cantin, André, Gillson, Ashley, Kolb, Martin, Bendstrup, Elisabeth, Leistiko, Anna, Kaarteenaho, Riitta, Cohen Aubart, Fleur, Nunes, Hilario, Buschulte, Katharina, Costabel, Ulrich, Kortsen, Peter, Kreuter, Michael, Quadder, Bernd, Braune, Renate, Skowasch, Dirk, Bouros, Demosthenes, Margaritopoulos, George A., Manali, Effrosyni D, Tzilas, Vasilios, Unnati, Desai, Abedini, Atefeh, Bargagli, Elena, Cinetto, Francesco, Harari, Sergio, Luppi, Fabrizio, Rottoli, Paola, Salton, Francesco, Tana, Claudio, Tomassetti, Sara, Azuma, Arata, Inui, Naoki, Nakamura, Yutaro, Tanino, Yoshinori, Boomars, Karin, Bresser, Paul, Claessen, Laura, Erckens, Roel, van Helmondt, Sanne, Karakaya, Bekir, Hoitsma, Elske, Jansen, Tim L, Kahlmann, Vivienne, Korenromp, Ingrid, Lenssen, Ton, Maassen vd Brinkdrs, Karen, Mager, Johannes Jurgen, Marcellis, Rik, Möller, Trudeke, Moonen, Linda A.A., Moor, Karen, Mostard, Rémy L.M., Nienhuis, Willemien, Nossent, Esther, Paulus, Michelle, Nossent, George, Rottenberg, Felix, Segers, Ruud, Soechitram, Shalini D., Swaans, Martin, van den Toorn, Leon, Vorselaars, Adriane Dore Marie, Wijnen, Petal A., Wijsenbeek, Marlies, De Vries, Jolanda, Strambu, Irina, Vizel, Alexander, Cano, Rafael, Balcells, Eva, Castillo, Diego, Francesqui, Joel, Molina, Maria, Arkema, Elizabeth, Darlington, Pernilla, Eldhagen, Per, Elfström, Katinka, Grunewald, Johan, Werner, Joanna, Dincer, Irem, Koç, Gülcan, Yucesan, Canan, Birring, Surinder, Boyd, Jeanette, Spencer, Lisa, Barreras, Paula, James, W. Ennis, Maier, Lisa, Morgenthau, Adam, Obi, Ogugua Ndili, Patel, Divya, Rossman, Milton D., Sharma, Maggie, Stern, Barney J., Zank, Daniel, Gavrysyuk, Volodymyr, Merenkova, Levgeniia

    Veröffentlicht in The lancet respiratory medicine

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    Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing von Sifrim, Alejandro, Hitz, Marc-Phillip, Wilsdon, Anna, Breckpot, Jeroen, Turki, Saeed H. Al, Thienpont, Bernard, McRae, Jeremy, Fitzgerald, Tomas W, Singh, Tarjinder, Swaminathan, Ganesh Jawahar, Prigmore, Elena, Rajan, Diana, Abdul-Khaliq, Hashim, Banka, Siddharth, Bauer, Ulrike M.M, Bentham, Jamie, Berger, Felix, Bhattacharya, Shoumo, Bu'Lock, Frances, Canham, Natalie, Colgiu, Irina-Gabriela, Cosgrove, Catherine, Cox, Helen, Daehnert, Ingo, Daly, Allan, Danesh, John, Fryer, Alan, Gewillig, Marc, Hobson, Emma, Hoff, Kirstin, Homfray, Tessa, the INTERVAL Study, Kahlert, Anne-Karin, Ketley, Ami, Kramer, Hans-Heiner, Lachlan, Katherine, Lampe, Anne Katrin, Louw, Jacoba J, Manickara, Ashok Kumar, Manase, Dorin, McCarthy, Karen P, Metcalfe, Kay, Moore, Carmel, Newbury-Ecob, Ruth, Omer, Seham Osman, Ouwehand, Willem H, Park, Soo-Mi, Parker, Michael J, Pickardt, Thomas, Pollard, Martin O, Robert, Leema, Roberts, David J, Sambrook, Jennifer, Setchfield, Kerry, Stiller, Brigitte, Thornborough, Chris, Toka, Okan, Watkins, Hugh, Williams, Denise, Wright, Michael, Mital, Seema, Daubeney, Piers E.F, Keavney, Bernard, Goodship, Judith, the UK10K Consortium, Abu-Sulaiman, Riyadh Mahdi, Klaassen, Sabine, Wright, Caroline F, Firth, Helen V, Barrett, Jeffrey C, Devriendt, Koenraad, FitzPatrick, David R, Brook, J. David, the Deciphering Developmental Disorders Study, Hurles, Matthew E

    Veröffentlicht in Nature Genetics

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