Treffer 1 - 20 von 136 für Suche 'Clements, Richard O.', Suchdauer: 2,25s Treffer weiter einschränken
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    Global variation in postoperative mortality and complications after cancer surgery: a multicentre, prospective cohort study in 82 countries von Adisa, Adewale O, McLean, Kenneth A, West, Malcolm, Whitaker, John, Kuncarová, Kamila, Adamou, Harissou, Allen Ingabire, JC, Homeida, Anmar, Lee, Yi Jia, Wells, Anna, Drane, Andrew, Jin, Ivan, Jones, Elgan, Nigo Samuel, Lemery, He, Haitian, Osman, Fahima, Karanicolas, Paul, Isaza-Restrepo, Andres, Abdallah, Aya, Elghareeb, Nourhan, Al-Dhufri, Ali, Elmeslemany, Nehal, Sobhy, Mohamed, Elshatby, Bassant, Mahmoud, Rokia, Ainoa, Eppu, Sulpice, Laurent, Gkiokas, Georgios, Prodromidou, Anastasia, Loutzidou, Lydia, Campo, Veronica, Rivera Lara, Verónica, Illes, Kristof, Gupta, Ashish, Jain, Urvashi, Raghavendra, Abhishek, Adidharma, Peter, Pilkington, Isobel, Ridgway, Paul, Tahir, Abd al-Rahman, Picciariello, Arcangelo, Gaudiello, Maria, Pace, Ugo, Sena, Giuseppe, Cicuttin, Enrico, Fontana, Tommaso, Campanelli, Michela, Qwaider, Yasmeen Z., Bani Hani, Farah, Abusalem, Lana, Ngotho, Omar, Gobbi, Abdel Aziz, Cutajar, Ruth, Barrera López, Francisco Javier, Martínez Maldonado, Mónica, van Berge Henegouwen, Mark, Choi, Seung il, Malam Sani, Laminou, Mohammad, Bayan, Elqadi, Muawiyah, Abu Jamie, Najlaa, Fuentes, Joseph Roy, Salazar, Anna Leah, Fernandes, Cristina, Oliveira, Mariline, Velez, Cristina, Ribeiro, João, Alves, Daniela Macedo, Lui, Su Ann, Noor, Fazlin, Garrido López, Lucía, García Bernardo, Carmen, Beltrán de Heredia, Juan, Artigau, Eva, Prieto-Nieto, Maria Isabel, Jimeno Fraile, Jaime, Siso Raber, Christian, Wiberg, Rebecca, Grochola, Lukasz Filip, Atakul, Onur, Gündogdu, Yasemin, Tayar, Serkan, Basarab, Maksym, Rupani, Shamil, Henderson, Scott, Rathore, Munir, Carrington, Emma Victoria, Srivastava, Prakhar, Ali, Shabina, Krastev, Panche, Truncíková, Vendula, Perivoliotis, Konstantinos, Salem, Malik, Reia, Marta, Shakhmatov, Dmitry, Rayya, Fadi, Kannas, Israa, Gnintedeme Olivier, Tchianze, Hammani, Aamr, Nkoronko, Mugisha

    Veröffentlicht in The Lancet (British edition)

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    Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans von Tuijnenburg, Paul, Jansen, Machiel H., Carss, Keren J., Baxendale, Helen, Chandra, Anita, Seneviratne, Suranjith L., Oksenhendler, Eric, Tool, Anton T.J., Whitehorn, Deborah, Turro, Ernest, Thaventhiran, James E., Kuijpers, Taco W., Adhya, Zoe, Anantharachagan, Ariharan, Arumugakani, Gururaj, Bacchelli, Chiara, Baxendale, Helen, Bibi, Shahnaz, Booth, Claire, Browning, Michael, Burns, Siobhan, Clifford, Hayley, Cooper, Nichola, Davies, Sophie, Devlin, Lisa, Edgar, David, Egner, William, Ghurye, Rohit, Gilmour, Kimberley, Goddard, Sarah, Gordins, Pavel, Hackett, Scott, Hague, Rosie, Hayman, Grant, Jolles, Stephen, Jones, Julie, Kelleher, Peter, Klein, Nigel, Kuijpers, Taco, Kumararatne, Dinakantha, Laffan, James, Lango Allen, Hana, Lear, Sara, Longhurst, Hilary, Maimaris, Jesmeen, McDermott, Elizabeth, Morrisson, Valerie, Nasir, Iman, Noorani, Sadia, Oksenhendler, Eric, Ponsford, Mark, Qasim, Waseem, Quinn, Ellen, Quinti, Isabella, Samarghitean, Crina, Savic, Sinisa, Seneviratne, Suranjith, Simeoni, Ilenia, Staples, Emily, Steele, Cathal, Thaventhiran, James, Thomas, Moira, Thrasher, Adrian, Worth, Austen, Yong, Patrick, Bradley, John, Hammerton, Tracey, Ouwehand, Willem, Raymond, F Lucy, Veltman, Marijke, Clements-Brod, Naomi, Davis, John, Dewhurst, Eleanor, Erwood, Marie, Frary, Amy, Linger, Rachel, Papadia, Sofia, Rehnstrom, Karola, Astle, William, Attwood, Antony, Bleda, Marta, Carss, Keren, Daugherty, Louise, Deevi, Sri, Graf, Stefan, Greene, Daniel, Halmagyi, Csaba, Matser, Vera, Meacham, Stuart, Megy, Karyn, Shamardina, Olga, Titterton, Catherine, Tuna, Salih, Turro, Ernest, von Ziegenweldt, Julie, Furnell, Abigail, Staines, Simon, Stephens, Jonathan, Whitehorn, Deborah, Watt, Christopher


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    Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations von Lorenzini, Tiziana, Fliegauf, Manfred, Klammer, Nils, Proietti, Michele, Bulashevska, Alla, Schejter, Yael D., Atschekzei, Faranaz, Stepensky, Polina, Pedroza, Luis A., van der Flier, Michiel, Martínez-Gallo, Mónica, Svec, Peter, Fischer, Ute, Ip, Winnie, Geha, Raif, Chou, Janet, Alosaimi, Mohammed, Weintraub, Lauren, Dos Santos Vilela, Maria Marluce, Holzinger, Dirk, Seidl, Maximilian, Lougaris, Vassilios, Plebani, Alessandro, Abolhassani, Hassan, Thaventhiran, James E., Warnatz, Klaus, Grimbacher, Bodo, Ashford, Sofie, Bacchelli, Chiara, Batista, Joana, Bibi, Shahnaz, Boardman, Barbara, Booth, Claire, Breen, Gerome, Burns, Siobhan O., Burren, Oliver S., Carss, Keren, Chambers, John, Cooper, Nichola, Davies, E.G., Dempster, John, Dewhurst, Eleanor F., Drewe, Elizabeth, Duarte, Daniel, Edgar, J. David M., Egner, William, El-Shanawany, Tariq, Erwood, Marie, Fox, James, Frontini, Mattia, Furnell, Abigail, Gaspar, H. Bobby, Gleadall, Nicholas S., Grigoriadou, Sofia, Hackett, Scott, Hague, Rosie, Haimel, Matthias, Hayman, Grant, Hu, Fengyuan, Huissoon, Aarnoud P., Jolles, Stephen, Kasanicki, Mary A., Kelleher, Peter, Klein, Nigel, Kreuzhuber, Roman, Kuijpers, Taco W., Kumararatne, Dinakantha, Allen, Hana Lango, Linger, Rachel, Lorenzo, Lorena E., Maimaris, Jesmeen, Martin, Jennifer, McDermott, Elizabeth M., Meacham, Stuart, Morrisson, Valerie, Nasir, Iman, Nejentsev, Sergey, Papadia, Sofia, Ponsford, Mark J., Quinn, Ellen, Quinti, Isabella, Rayner-Matthews, Paula J., Samani, Nilesh, Sanchis-Juan, Alba, Savic, Sinisa, Simpson, Michael A., Smith, Kenneth G.C., Thaventhiran, James E., Tilly, Tobias, Titterton, Catherine, Tuna, Salih, Urniaz, Rafal, von Ziegenweidt, Julie, Watt, Christopher, Welch, Steven B., Whitehorn, Deborah, Wood, Yvette, Workman, Sarita, Worth, Austen, Young, Timothy


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