Treffer 1 - 20 von 23 für Suche 'Lyons, Amy V', Suchdauer: 1,23s Treffer weiter einschränken
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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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    Clinical exome sequencing of 1000 families with complex immune phenotypes: Toward comprehensive genomic evaluations von Similuk, Morgan N, Yan, Jia, Ghosh, Rajarshi, Oler, Andrew J, Franco, Luis M, Setzer, Michael R, Kamen, Michael, Jodarski, Colleen, DiMaggio, Thomas, Davis, Joie, Gore, Rachel, Jamal, Leila, Borges, Adrienne, Gentile, Nicole, Niemela, Julie, Lowe, Chenery, Jevtich, Kathleen, Yu, Yunting, Hullfish, Haley, Hsu, Amy P, Hong, Celine, Littel, Patricia, Seifert, Bryce A, Milner, Joshua, Johnston, Jennifer J, Cheng, Xi, Li, Zhiwen, Veltri, Daniel, Huang, Ke, Kaladi, Krishnaveni, Barnett, Jason, Zhang, Lingwen, Vlasenko, Nikita, Fan, Yongjie, Karlins, Eric, Ganakammal, Satishkumar Ranganathan, Gilmore, Robert, Tran, Emily, Yun, Alvin, Mackey, Joseph, Yazhuk, Svetlana, Lack, Justin, Kuram, Vasudev, Cao, Wenjia, Huse, Susan, Frank, Karen, Fahle, Gary, Rosenzweig, Sergio, Su, Yan, Hwang, SuJin, Bi, Weimin, Bennett, John, Myles, Ian A, De Ravin, Suk See, Fuss, Ivan, Strober, Warren, Bielekova, Bibiana, Almeida de Jesus, Adriana, Goldbach-Mansky, Raphaela, Williamson, Peter, Kumar, Kelly, Dempsy, Caeden, Frischmeyer-Guerrerio, Pamela, Fisch, Robin, Bolan, Hyejeong, Metcalfe, Dean D, Komarow, Hirsh, Carter, Melody, Druey, Kirk M, Sereti, Irini, Dropulic, Lesia, Klion, Amy D, Khoury, Paneez, O' Connell, Elise M, Holland-Thomas, Nicole C, Brown, Thomas, McDermott, David H, Murphy, Philip M, Bundy, Vanessa, Keller, Michael D, Peng, Christine, Kim, Helen, Norman, Stephanie, Delmonte, Ottavia M, Kang, Elizabeth, Su, Helen C, Malech, Harry, Freeman, Alexandra, Zerbe, Christa, Uzel, Gulbu, Bergerson, Jenna R E, Rao, V Koneti, Olivier, Kenneth N, Lyons, Jonathan J, Lisco, Andrea, Cohen, Jeffrey I, Lionakis, Michail S, Biesecker, Leslie G, Xirasagar, Sandhya, Notarangelo, Luigi D


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    Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023) von Lin, Angela E., Scimone, Eleanor R., Thom, Robyn P., Balaguru, Duraisamy, Kinane, T. Bernard, Moschovis, Peter P., Cohen, Michael S., Tan, Weizhen, Hague, Cole D., Dannheim, Katelyn, Levitsky, Lynne L., Lilly, Evelyn, DiGiacomo, Daniel V., Masse, Kara M., Kadzielski, Sarah M., Zar‐Kessler, Claire A., Ginns, Leo C., Neumeyer, Ann M., Colvin, Mary K., Elder, Jack S., Learn, Christopher P., Mou, Hongmei, Weagle, Kathryn M., Buch, Karen A., Butler, William E., Alhadid, Kenda, Musolino, Patricia L., Sultana, Sadia, Bandyopadhyay, Dhrubajyoti, Rapalino, Otto, Peacock, Zachary S., Chou, Elizabeth L., Heidary, Gena, Dorfman, Aaron T., Morris, Shaine A., Bergin, James D., Rayment, Jonathan H., Schimmenti, Lisa A., Lindsay, Mark E., Acosta, Luisa Paredes, Bassetti, Jennifer A., Bowdin, Sarah, Bress, Joy A., Camarda, Joseph A., Chiu, Joanne S., Corrales, C. Eduardo, Costain, Gregory, Dinulos, Mary Beth P., Devanagondi, Rajiv, Doherty, Emily S., Dykes, John, Duhaime, Ann‐Christine, English, Robert F., Fieg, Elizabeth, Friedman, Nora D. B., Garabedian, Carl P., Glowacki, Samantha, Gottlieb, Barbara R., Griffin, Mary Hope, Hayes, Frances J., Hicks, Stephanie R., Hinze, Alicia M., Jason, Brigette A., Krier, Joel, Lindgren, Kristen, Lyons, Michael, Majid, Adnan, Mannem, Hannah C., McDonald, Marie, Misra, Vinod, Morgan, Amy, Nath, Barbara J., Ploutz, Michele, Prijoles, Eloise J., Pulsifer, Margaret B., Quesnel, Alicia M., Rajabi, Farrah, Rohanizadegan, Mersedeh, Rosales, Ana Maria, Rothermel, Holly, Schussler, Edith, Sellars, Elizabeth A., Shieh, Joseph, Sherrill, Stephanie, Taska‐Tench, Heidi, Thompson, Matthew, Tiller, George E., Vallee, Stephanie E., Viskochil, David, Ware, Stephanie, Whooten, Rachel C., Yang, Samuel, Zackai, Elaine H., Zakaria, Dala


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    Clinical Exome Sequencing of 1000 Families with Complex Immune Phenotypes: Towards comprehensive genomic evaluations von Similuk, Morgan N., Yan, Jia, Ghosh, Rajarshi, Oler, Andrew J., Franco, Luis M., Setzer, Michael, Kamen, Michael, Jodarski, Colleen, DiMaggio, Thomas, Davis, Joie, Gore, Rachel, Jamal, Leila, Borges, Adrienne, Gentile, Nicole, Niemela, Julie, Lowe, Chenery, Jevtich, Kathleen, Yu, Yunting, Hullfish, Haley, Hsu, Amy P., Hong, Celine, Littel, Patricia, Seifert, Bryce A., Milner, Joshua, Johnston, Jennifer J., Cheng, Xi, Li, Zhiwen, Veltri, Daniel, Huang, Ke, Kaladi, Krishnaveni, Barnett, Jason, Zhang, Lingwen, Vlasenko, Nikita, Fan, Yongjie, Karlins, Eric, Ganakammal, Satishkumar Ranganathan, Gilmore, Robert, Tran, Emily, Yun, Alvin, Mackey, Joseph, Yazhuk, Svetlana, Lack, Justin, Kuram, Vasu, Cao, Wen, Huse, Susan, Frank, Karen, Fahle, Gary, Rosenzweig, Sergio, Su, Yan, Hwang, SuJin, Bi, Weimin, Bennett, John, Myles, Ian A., De Ravin, Suk See, Fuss, Ivan, Strober, Warren, Bielekova, Bibiana, de Jesus, Adriana Almeida, Goldbach-Mansky, Raphaela, Williamson, Peter, Kumar, Kelly, Dempsy, Caeden, Frischmeyer-Guerrerio, Pamela, Eisch, Robin, Bolan, Hyejeong, Metcalfe, Dean D., Komarow, Hirsh, Carter, Melody, Druey, Kirk M., Sereti, Irini, Dropulic, Lesia, Klion, Amy D., Khoury, Paneez, O’ Connell, Elise M., Holland-Thomas, Nicole C., Brown, Thomas, McDermott, David H., Murphy, Philip M., Bundy, Vanessa, Keller, Michael D., Peng, Christine, Kim, Helen, Norman, Stephanie, Delmonte, Ottavia M., Kang, Elizabeth, Su, Helen C., Malech, Harry, Freeman, Alexandra, Zerbe, Christa, Uzel, Gulbu, Bergerson, Jenna R.E., Rao, V. Koneti, Olivier, Kenneth N., Lyons, Jonathan J., Lisco, Andrea, Cohen, Jeffrey I., Lionakis, Michail S., Biesecker, Leslie G., Xirasagar, Sandhya, Notarangelo, Luigi


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