Treffer 1 - 20 von 58 für Suche 'Stevenson, Alexandra R', Suchdauer: 1,65s Treffer weiter einschränken
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    Implications ofTP53allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes von Bernard, Elsa, Nannya, Yasuhito, Hasserjian, Robert P., Devlin, Sean M., Tuechler, Heinz, Medina-Martinez, Juan S., Yoshizato, Tetsuichi, Shiozawa, Yusuke, Saiki, Ryunosuke, Malcovati, Luca, Levine, Max F., Arango, Juan E., Zhou, Yangyu, Sole, Francesc, Cargo, Catherine A., Haase, Detlef, Creignou, Maria, Germing, Ulrich, Zhang, Yanming, Gundem, Gunes, Sarian, Araxe, van de Loosdrecht, Arjan A., Jadersten, Martin, Tobiasson, Magnus, Kosmider, Olivier, Follo, Matilde Y., Thol, Felicitas, Pinheiro, Ronald F., Santini, Valeria, Kotsianidis, Ioannis, Boultwood, Jacqueline, Santos, Fabio P. S., Schanz, Julie, Kasahara, Senji, Ishikawa, Takayuki, Tsurumi, Hisashi, Takaori-Kondo, Akifumi, Kiguchi, Toru, Polprasert, Chantana, Bennett, John M., Klimek, Virginia M., Savona, Michael R., Belickova, Monika, Ganster, Christina, Palomo, Laura, Sanz, Guillermo, Ades, Lionel, Della Porta, Matteo Giovanni, Smith, Alexandra G., Werner, Yesenia, Patel, Minal, Viale, Agnes, Vanness, Katelynd, Neuberg, Donna S., Stevenson, Kristen E., Menghrajani, Kamal, Bolton, Kelly L., Fenaux, Pierre, Pellagatti, Andrea, Platzbecker, Uwe, Heuser, Michael, Valent, Peter, Chiba, Shigeru, Miyazaki, Yasushi, Finelli, Carlo, Voso, Maria Teresa, Shih, Lee-Yung, Fontenay, Michaela, Jansen, Joop H., Cervera, Jose, Atsuta, Yoshiko, Gattermann, Norbert, Ebert, Benjamin L., Bejar, Rafael, Greenberg, Peter L., Cazzola, Mario, Hellstrom-Lindberg, Eva, Ogawa, Seishi, Papaemmanuil, Elli

    Veröffentlicht in Nature medicine

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    Efficacy of levetiracetam, fosphenytoin, and valproate for established status epilepticus by age group (ESETT): a double-blind, responsive-adaptive, randomised controlled trial von Shinnar, Shlomo, Rogers, Alex, Barsan, William, Cloyd, James, Meinzer, Caitlyn, Cock, Hannah, Underwood, Ellen, Silbergleit, Robert, Gray, Emily, Gunter, Sonya, Fansler, Amy, Harney, Deneil, Speers, Mickie, Fisher, Natalie, Palesch, Yuko, Dillon, Catherine R., Riley, Jodie, Sathe, Abhi, Hartman, Adam, Treiman, David, Ratcliff, Jonathan, Hall, Alex, Simon, Harold, Stanley, Nicholas, Humphries, Roger, Short, Joann, Jones, Elizabeth, Ottman, Misty, Gentile, Nina, Isenberg, Derek, Reimer, Hannah, Hemphill, Claude, Yi Madhok, Debbie, Visweswaran, Anita, Adeoye, Opeolu, McMullan, Jason, Biros, Michelle, Hendrickson, Audrey, Warden, Craig, Selman, Antoine, Becker, Lea, Claassen, Jan, Velazquez, Angela, Falo, Cristina, Baren, Jill, Ellison, Angela, Kittick, Marlena, Bonacquisti, Lisa, Levine, Steven, Fromm, Christian, Likourezos, Antonios, Khaliqdina, Salman, Hill, Michael, Terwilliger, Alexia, Pearson, Claire, Kumar, Vijaya Arun, Ayaz, Farhan, Mika, Valerie H., Dishman, Lorraine, Henry, Thomas, Callaway, Clif, Adams, Peter, Baum, Brian, Nomura, Jason, Emmrich, Amanda, Villot-Santiago, Arelis, Goldstein, Joshua, Howell, Melissa, Jaton, Eric, Dahlmeier, Erica, Zehtabchi, Shahriar, Petty, Bryce, Carlson, Margaret, Weingast, Sarah (Zelonis), Stern, Barney, Kuppermann, Nathan, Dean, J. Michael, Okada, Pamela, Lee, Amanda, Truesdale, Natasha, Carlston, Kristi, Harbour, Toni, Lin, Cindy, Merck, Lisa H., Basso, Kristin, D'Urso, Lesley (Wasilewski), Brown, Kathleen, Nauman, Gina, Grant, Vanessa, Vance, Cheryl, Pimenta, Kyle, Hickey, Robert W., Azrak, Rose, Rubalcava, Daniel, Khalil, Maha, Lumba-Brown, Angela, Quayle, Kim, Chinta, Sri, Robinson, Debra, Ochs, Julie

    Veröffentlicht in The Lancet (British edition)

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    Characterizing Long COVID in Children and Adolescents von Thaweethai, Tanayott, Snowden, Jessica N, Rosenzweig, Erika B, Milner, Joshua D, Tantisira, Kelan G, Jernigan, Terry L, Kinser, Patricia A, Salisbury, Amy L, Warburton, David, Mohandas, Sindhu, Wood, John C, Newburger, Jane W, Truong, Dongngan T, Flaherman, Valerie J, Karlson, Elizabeth W, Krishnamoorthy, Aparna, Gallagher, Richard, Lamendola-Essel, Michelle F, Hasson, Denise C, Katz, Stuart D, Yin, Shonna, Dreyer, Benard P, Coombs, K, Güthe, Nick, Hornig, Mady, Letts, Rebecca J, Stockwell, Melissa S, Bogie, Amanda, Bukulmez, Hulya, Dozor, Allen J, Farkas, Jonathan S, Faustino, E. Vincent S, Harahsheh, Ashraf S, Hasan, Uzma N, Hsia, Daniel S, Hummel, Kathy D, Kadish, Matt P, Krishnan, Sankaran, Kosut, Jessica S, Larrabee, Jerry, Michelow, Ian C, Oliveira, Carlos R, Raissy, Hengameh, Sato, Alice I, Stevenson, Michelle D, Talavera-Barber, Maria M, Weakley, Kathryn E, Zimmerman, Emily, Bind, Marie-Abele C, Guan, Zoe, Morse, Richard E, Akshoomoff, Natascha, Aschner, Judy L, Bhattacharjee, Rakesh, Cottrell, Lesley A, Cowan, Kelly, D'Sa, Viren A, Fiks, Alexander G, Gennaro, Maria L, Irby, Katherine, Guttierrez, Jeremy Landeo, Ness-Cochinwala, Manette, Nolan, Sheila, Ryu, Julie, Salazar, Juan C, Selvarangan, Rangaraj, Stein, Cheryl R, Werzberger, Alan, Zempsky, William T, Banich, Marie T, Barch, Deanna M, Bjork, James M, Bookheimer, Susan Y, Casey, BJ, Chang, Linda, Clark, Duncan B, Dale, Anders M, Ernst, Thomas M, Fair, Damien A, Feldstein Ewing, Sarah W, Foxe, John J, Friedman, Naomi P, Garavan, Hugh, Gee, Dylan G, Gonzalez, Raul, Gray, Kevin M, Heitzeg, Mary M, Herting, Megan M, Laird, Angela R, Larson, Christine L, Luna, Beatriz, Madden, Pamela A.F, McGlade, Erin C, Müller-Oehring, Eva M, Nagel, Bonnie J, Neale, Michael C, Renshaw, Perry F, Squeglia, Lindsay M, Uddin, Lucina Q, Yurgelun-Todd, Deborah A


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    Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases von Pagnamenta, Alistair T, Camps, Carme, Giacopuzzi, Edoardo, Taylor, John M, Hashim, Mona, Calpena, Eduardo, Kaisaki, Pamela J, Hashimoto, Akiko, Yu, Jing, Sanders, Edward, Schwessinger, Ron, Hughes, Jim R, Lunter, Gerton, Dreau, Helene, Ferla, Matteo, Lange, Lukas, Kesim, Yesim, Ragoussis, Vassilis, Vavoulis, Dimitrios V, Allroggen, Holger, Ansorge, Olaf, Babbs, Christian, Banka, Siddharth, Baños-Piñero, Benito, Beeson, David, Ben-Ami, Tal, Bennett, David L, Bento, Celeste, Blair, Edward, Brasch-Andersen, Charlotte, Bull, Katherine R, Cario, Holger, Cilliers, Deirdre, Conti, Valerio, Davies, E Graham, Dhalla, Fatima, Dacal, Beatriz Diez, Dong, Yin, Dunford, James E, Guerrini, Renzo, Harris, Adrian L, Hartley, Jane, Hollander, Georg, Javaid, Kassim, Kane, Maureen, Kelly, Deirdre, Kelly, Dominic, Knight, Samantha J L, Kreins, Alexandra Y, Kvikstad, Erika M, Langman, Craig B, Lester, Tracy, Lines, Kate E, Lord, Simon R, Lu, Xin, Mansour, Sahar, Manzur, Adnan, Maroofian, Reza, Marsden, Brian, Mason, Joanne, McGowan, Simon J, Mei, Davide, Mlcochova, Hana, Murakami, Yoshiko, Németh, Andrea H, Okoli, Steven, Ormondroyd, Elizabeth, Ousager, Lilian Bomme, Palace, Jacqueline, Patel, Smita Y, Pentony, Melissa M, Pugh, Chris, Rad, Aboulfazl, Ramesh, Archana, Riva, Simone G, Roberts, Irene, Roy, Noémi, Salminen, Outi, Schilling, Kyleen D, Scott, Caroline, Sen, Arjune, Smith, Conrad, Stevenson, Mark, Thakker, Rajesh V, Twigg, Stephen R F, Uhlig, Holm H, van Wijk, Richard, Vona, Barbara, Wall, Steven, Wang, Jing, Watkins, Hugh, Zak, Jaroslav, Schuh, Anna H, Kini, Usha, Wilkie, Andrew O M, Popitsch, Niko, Taylor, Jenny C

    Veröffentlicht in Genome medicine

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