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    Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations by Kindle, Gerhard, Rusch, Stephan, Seppänen, Mikko R.J., Mahlaoui, Nizar, Kojić, Marina, Seidel, Markus G., Smet, Julie, Milota, Tomas, Elaziz, Dalia Abd, Alkady, Radwa Salaheldin, Lotfy, Sohilla, Meshaal, Safa S., Sobh, Ali, Courteille, Virginie, Albert, Michael H., Atschekzei, Faranaz, Behrends, Uta, Belohradsky, Bernd H., Biegner, Anika-Kerstin, Boetticher, Benedikt, Dirks, Johannes, Dückers, Gregor, El-Helou, Sabine, Fasshauer, Maria, Fecker, Gisela, Goldacker, Sigune, Graf, Dagmar, Hanitsch, Leif Gunnar, Henes, Joerg C., Holzer, Ursula, Holzinger, Dirk, Joean, Oana, Kobbe, Robin, Körholz, Julia, Liese, Johannes G., Peter, Hans-Hartmut, Rieber, Nikolaus, Ritterbusch, Henrike, Rockstroh, Jürgen Kurt, Roesler, Joachim, Scheible, Raphael, Schmalzing, Marc, Schwarz, Klaus, Tenbrock, Klaus, Wasmuth, Jan-Christian, Wittke, Kirsten, Wittkowski, Helmut, Zeuner, Rainald A., Kanariou, Maria G., Kapousouzi, Androniki, Liatsis, Emmanouil, Goda, Vera, Kriván, Gergely, Abolhassani, Hassan, Feighery, Conleth, Ryan, Paul, Cesaro, Simone, Gambineri, Eleonora, Pignata, Claudio, Ricci, Silvia, Vacca, Angelo, Sitkauskiene, Brigita, Gowin, Ewelina, Heropolitańska-Pliszka, Edyta, Pietrucha, Barbara, Szaflarska, Anna, Esteves, Isabel, Neves, João Farela, Capilna, Brindusa Ruxandra, Jesenak, Milos, Petrovicova, Otilia, Kopač, Peter, Gonzalez-Granado, Luis Ignacio, Parra-Martínez, Alba, Sánchez-Ramón, Silvia, Solanich, Xavier, Ekwall, Olov, Fasth, Anders, Heininger, Ulrich, Holbro, Andreas, Jandus, Peter, Steiner, Urs C., Bredius, Robbert G., Potjewijd, Judith, van Aerde, Koen J., Aydemir, Sezin, Dogu, Figen, Kiykim, Ayca, Kutukculer, Necil, UNAL, Ekrem, Boyarchuk, Oksana, Alachkar, Hana, Baxendale, Helen E., Coulter, Tanya I., Goddard, Sarah, Gompels, Mark M., Grigoriadou, Sofia, Herriot, Richard, Waruiru, Catherine, Bourne, Helen

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    Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease by Stephens, Jonathan, Dewhurst, Eleanor, Malka, Samantha, Plagnol, Vincent, Rizzo, Roberta, Scott, Richard H., Henderson, Robert H.H., MacLaren, Robert E., Paterson, Joan, Aitman, Timothy, Ali, Sonia, Ambegaonkar, Gautum, Arno, Gavin, Astle, William, Attwood, Antony, Bennett, David, Bitner-Glindzicz, Maria, Bleda, Marta, Boggard, Harm, Carss, Keren, Clements-Brod, Naomi, DaCosta, Rosa, De Vries, Minka, Dewhurst, Eleanor, Drewe, Elizabeth, Egner, William, Erber, Wendy N., Everington, Tamara, Fletcher, Debra, Freson, Kathleen, Gale, Daniel, Ghali, Neeti, Ghurye, Rohit, Gräf, Stefan, Greene, Daniel, Grigoriadou, Sofia, Grozeva, Detelina, Hackett, Scott, Hadinnapola, Charaka, Hague, Rosie, Hammerton, Tracey, Heemskerk, Johan W.M., Holder, Muriel, Holder, Susan, Huissoon, Aarnoud, Hurst, Jane, Jolles, Stephen, Keeling, David, Kennedy, Fiona, Kiely, David, Lawrie, Allan, Lear, Sara, Lees, Melissa, Lentaigne, Claire, Lorenzo, Lorena, Mangles, Sarah, Mapeta, Rutendo, Masati, Larahmie, Mathias, Mary, Michaelides, Michel, Millar, Carolyn M., Moledina, Shahin, Moore, Anthony, Murng, Sai, Oksenhendler, Eric, Park, Soo-Mi, Patch, Chris, Paterson, Joan, Penkett, Christopher J., Pepke-Zaba, Joanna, Pollock, Val, Qasim, Waseem, Quinti, Isabella, Reid, Evan, Rondina, Matthew, Rosser, Elisabeth, Santra, Saikat, Sargur, Ravishankar, Savic, Sinisa, Scully, Marie, Sewell, Carrock, Smith, Kenneth, Southgate, Laura, Stauss, Hans, Stein, Penelope, Talks, Kate, Thomas, Ellen, Thrasher, Adrian, Tischkowitz, Marc, Titterton, Catherine, Turro, Ernest, von Ziegenweldt, Julie, Vonk Noordegraaf, Anton, Wakeling, Emma, Wanjiku, Ivy, Welch, Steve, Westbury, Sarah, Woods, Geoffrey, Yong, Patrick, Webster, Andrew R.

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