DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients

著者: On behalf of the inborn errors working party of EBMT, Susanne Aydin, Sara Şebnem Kılıç, Caner Aytekin, Ashish Kumar, Óscar Porras, Leena Kainulainen, Larysa Kostyuchenko, Ferah Genel, Necil Kütükçüler, Neslihan Edeer Karaca, Luis Ignacio González‐Granado, Jordan K. Abbott, Daifulah Al-Zahrani, Nima Rezaei, Zeina Baz, Jens Thiel, Stephan Ehl, László Maródi, Jordan S. Orange, Julie Sawalle‐Belohradsky, Sevgi Keleş, Steven M. Holland, Özden Sanal, Deniz Çağdaş, İlhan Tezcan, Hamoud Al‐Mousa, Zobaida Alsum, Abbas Hawwari, Ayşe Metìn, Susanne Matthes‐Martin, Manfred Hönig, Ansgar Schulz, Capucine Pïcard, Vincent Barlogis, Andrew R. Gennery, Marianne Ifversen, Joris van Montfrans, Taco W. Kuijpers, Robbert G. M. Bredius, Gregor Dückers, Waleed Al–Herz, Sung‐Yun Pai, Raif S. Geha, Gundula Notheis, Carl-Philipp Schwarze, Betül Tavil, Fatih Azık, K. Bienemann, Bodo Grimbacher, Valerie Heinz, H. Bobby Gaspar, Roland C. Aydin, Beate Hagl, Benjamin Gathmann, Bernd H. Belohradsky, Hans D. Ochs, Talal A. Chatila, Ellen D. Renner, Helen C. Su, Alexandra F. Freeman, Karin R. Engelhardt, Michael H. Albert - Journal of Clinical Immunology 2015 被引用: 313