![[höher]](/style/images/multi_up.png)
Eine Ebene höherGruppiert nach:
Dokumententyp
| Veröffentlichungsdatum
Springe zu: Zeitschriftenartikel
Anzahl der Publikationen: 7
Zeitschriftenartikel
Meyts, Isabelle; Bucciol, Giorgia; Quinti, Isabella; Neven, Benedicte; Fischer, Alain; Seoane, Elena; Lopez-Grandos, Eduardo; Gianelli, Carla; Robles-Marhuenda, Angel; Jeandel, Pierre-Yves; Paillard, Catherine; Sankaran, Vijay G.; Demirdag, Yesim Yilmaz; Lougaris, Vassilios; Aiuti, Alessandro; Plebani, Alessandro; Milito, Cinzia; Dalm, Virgil A. S. H.; Guevara-Hoyer, Kissy; Sanchez-Ramon, Silvia; Bezrodnik, Liliana; Barzaghi, Federica; Ignacio Gonzalez-Granado, Luis; Hayman, Grant R.; Uzel, Gulbu; Mendonca, Leonardo Oliveira; Agostini, Carlo; Spadaro, Giuseppe; Badolato, Raffaele; Soresina, Annarosa; Vermeulen, Francois; Bosteels, Cedric; Lambrecht, Bart N.; Keller, Michael; Mustillo, Peter J.; Abraham, Roshini S.; Gupta, Sudhir; Ozen, Ahmet; Karakoc-Aydiner, Elif; Baris, Safa; Freeman, Alexandra F.; Yamazaki-Nakashimada, Marco; Scheffler-Mendoza, Selma; Espinosa-Padilla, Sara; Gennery, Andrew R.; Jolles, Stephen; Espinosa, Yazmin; Poli, M. Cecilia; Fieschi, Claire; Hauck, Fabian; Cunningham-Rundles, Charlotte; Mahlaoui, Nizar; Warnatz, Klaus; Sullivan, Kathleen E. und Tangye, Stuart G.
(2021):
Coronavirus disease 2019 in patients with inborn errors of immunity: An international study.
In: Journal of Allergy and Clinical Immunology, Bd. 147, Nr. 2: S. 520-531
Lorenzini, Tiziana; Fliegauf, Manfred; Klammer, Nils; Frede, Natalie; Proietti, Michele; Bulashevska, Alla; Camacho-Ordonez, Nadezhda; Varjosalo, Markku; Kinnunen, Matias; Vries, Esther de; Meer, Jos W. M. van der; Ameratunga, Rohan; Roifman, Chaim M.; Schejter, Yael D.; Kobbe, Robin; Hautala, Timo; Atschekzei, Faranaz; Schmidt, Reinhold E.; Schroeder, Claudia; Stepensky, Polina; Shadur, Bella; Pedroza, Luis A.; Flier, Michiel van der; Martinez-Gallo, Monica; Ignacio Gonzalez-Granado, Luis; Allende, Luis M.; Shcherbina, Anna; Kuzmenko, Natalia; Zakharova, Victoria; Neves, Joao Farela; Svec, Peter; Fischer, Ute; Ip, Winnie; Bartsch, Oliver; Baris, Safa; Klein, Christoph; Geha, Raif; Chou, Janet; Alosaimi, Mohammed; Weintraub, Lauren; Boztug, Kaan; Hirschmugl, Tatjana; Dos Santos Vilela, Maria Marluce; Holzinger, Dirk; Seidl, Maximilian; Lougaris, Vassilios; Plebani, Alessandro; Alsina, Laia; Piquer-Gibert, Monica; Deya-Martinez, Angela; Slade, Charlotte A.; Aghamohammadi, Asghar; Abolhassani, Hassan; Hammarstrom, Lennart; Kuismin, Outi; Helminen, Merja; Allen, Hana Lango; Thaventhiran, James E.; Freeman, Alexandra F.; Cook, Matthew; Bakhtiar, Shahrzad; Christiansen, Mette; Cunningham-Rundles, Charlotte; Patel, Niraj C.; Rae, William; Niehues, Tim; Brauer, Nina; Syrjanen, Jaana; Seppanen, Mikko R. J.; Burns, Siobhan O.; Tuijnenburg, Paul; Kuijpers, Taco W.; Warnatz, Klaus und Grimbacher, Bodo
(2020):
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations.
In: Journal of Allergy and Clinical Immunology, Bd. 146, Nr. 4: S. 901-911
Albert, Michael H. und Freeman, Alexandra F.
(5. November 2019):
Wiskott-Aldrich Syndrome (WAS) and Dedicator of Cytokinesis 8- (DOCK8) Deficiency.
In: Frontiers in Pediatrics, Bd. 7, 451: S. 1-8
[PDF, 581kB]
Aydin, Susanne E.; Freeman, Alexandra F.; Al-Herz, Waleed; Al-Mousa, Hamoud A.; Arnaout, Rand K.; Aydin, Roland C.; Barlogis, Vincent; Belohradsky, Bernd H.; Bonfim, Carmem; Bredius, Robbert G.; Chu, Julia I.; Ciocarlie, Oana C.; Dogu, Figen; Gaspar, Hubert B.; Geha, Raif S.; Gennery, Andrew R.; Hauck, Fabian; Hawwari, Abbas; Hickstein, Dennis D.; Hönig, Manfred; Ikinciogullari, Aydan; Klein, Christoph; Kumar, Ashish; Ifversen, Marianne R. S.; Matthes, Susanne; Metin, Ayse; Neven, Benedicte; Pai, Sung-Yun; Parikh, Suhag H.; Picard, Capucine; Renner, Ellen D.; Sanal, Özden; Schulz, Ansgar S.; Schuster, Friedhelm; Shah, Nirali N.; Shereck, Evan B.; Slatter, Mary A.; Su, Helen C.; Montfrans, Joris van; Woessmann, Wilhelm; Ziegler, John B. und Albert, Michael H.
(2018):
Hematopoietic stem cell transplantation as treatment for patients with DOCK8 deficiency.
In: Journal of Allergy and Clinical Immunology
Schwerd, Tobias; Twigg, Stephen R. F.; Aschenbrenner, Dominik; Manrique, Santiago; Miller, Kerry A.; Taylor, Indira B.; Capitani, Melania; McGowan, Simon J.; Sweeney, Elizabeth; Weber, Astrid; Chen, Liye; Bowness, Paul; Riordan, Andrew; Cant, Andrew; Freeman, Alexandra F.; Milner, Joshua D.; Holland, Steven M.; Frede, Natalie; Müller, Miryam; Schmidt-Arras, Dirk; Grimbacher, Bodo; Wall, Steven A.; Jones, E. Yvonne; Wilkie, Andrew O. M. und Uhlig, Holm H.
(2017):
A biallelic mutation in IL6ST encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis.
In: Journal of Experimental Medicine, Bd. 214, Nr. 9: S. 2547-2562
Rieber, Nikolaus; Gazendam, Roel P.; Freeman, Alexandra F.; Hsu, Amy P.; Collar, Amanda L.; Sugui, Janyce A.; Drummond, Rebecca A.; Rongkavilit, Chokechai; Hoffman, Kevin; Henderson, Carolyn; Clark, Lily; Mezger, Markus; Swamydas, Muthulekha; Engeholm, Maik; Schüle, Rebecca; Neumayer, Bettina; Ebel, Frank; Mikelis, Constantinos M.; Pittaluga, Stefania; Prasad, Vinod K.; Singh, Anurag; Milner, Joshua D.; Williams, Kelli W.; Lim, Jean K.; Kwon-Chung, Kyung J.; Holland, Steven M.; Hartl, Dominik; Kuijpers, Taco W. und Lionakis, Michail S.
(2016):
Extrapulmonary Aspergillus infection in patients with CARD9 deficiency.
In: Jci insight, Bd. 1, Nr. 17, e89890
Aydin, Susanne; Freeman, Alexandra F.; Su, Helen; Hickstein, Dennis; Pai, Sung-Yun; Geha, Raif; Chatila, Talal; Arnaout, Rand K.; Al-Mousa, Hamoud; Al-Dhekri, Hasan; Renner, Ellen D.; Belohradsky, Bernd H.; Notheis, Gundula; Aydin, Roland; Gaspar, Bobby H.; Al-Herz, Waleed; Gennery, Andrew; Slatter, Mary; Metin, Ayse; Isik, Pamir; Azik, Fatih; Ikinciogullari, Aydan; Haskologlu, Sule; Dogu, Figen; Kumar, Ashish; Ifversen, Marianne; Schuster, Friedhelm; Woessmann, Wilhelm; Bredius, Robbert; Barlogis, Vincent; Kainulainen, Leena; Picard, Capucine; Neven, Benedicte; Shereck, Evan; Schulz, Ansgar; Dueckers, Gregor; Montfrans, Joris van; Matthes-Martin, Susanne; Keles, Sevgi; Ochs, Hans und Albert, Michael H.
(2016):
HSCT for DOCK8 Deficiency - an International Study on 74 Patients.
In: Biology of Blood and Marrow Transplantation, Bd. 22, Nr. 3:
S103-S104