| Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations D Schubert, C Bode, R Kenefeck, TZ Hou, JB Wing, A Kennedy, ... Nature medicine 20 (12), 1410-1416, 2014 | 896 | 2014 |
| Antigen localisation regulates immune responses in a dose‐and time‐dependent fashion: a geographical view of immune reactivity RM Zinkernagel, S Ehl, P Aichele, S Oehen, T Kündig, H Hengartner Immunological reviews 156 (1), 199-209, 1997 | 614 | 1997 |
| Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome KR Engelhardt, S McGhee, S Winkler, A Sassi, C Woellner, ... Journal of Allergy and Clinical Immunology 124 (6), 1289-1302. e4, 2009 | 597 | 2009 |
| Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: a large patient cohort study TI Coulter, A Chandra, CM Bacon, J Babar, J Curtis, N Screaton, ... Journal of Allergy and Clinical Immunology 139 (2), 597-606. e4, 2017 | 576 | 2017 |
| The European Society for Immunodeficiencies (ESID) registry working definitions for the clinical diagnosis of inborn errors of immunity MG Seidel, G Kindle, B Gathmann, I Quinti, M Buckland, J van Montfrans, ... The Journal of Allergy and Clinical Immunology: In Practice 7 (6), 1763-1770, 2019 | 522 | 2019 |
| Lambda interferon renders epithelial cells of the respiratory and gastrointestinal tracts resistant to viral infections M Mordstein, E Neugebauer, V Ditt, B Jessen, T Rieger, V Falcone, ... Journal of virology 84 (11), 5670-5677, 2010 | 521 | 2010 |
| Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency C Picard, H Von Bernuth, P Ghandil, M Chrabieh, O Levy, PD Arkwright, ... Medicine 89 (6), 403-425, 2010 | 499 | 2010 |
| Selective predisposition to bacterial infections in IRAK-4–deficient children: IRAK-4–dependent TLRs are otherwise redundant in protective immunity CL Ku, H Von Bernuth, C Picard, SY Zhang, HH Chang, K Yang, ... The Journal of experimental medicine 204 (10), 2407-2422, 2007 | 494 | 2007 |
| Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11 U Zur Stadt, J Rohr, W Seifert, F Koch, S Grieve, J Pagel, J Strauß, ... The American Journal of Human Genetics 85 (4), 482-492, 2009 | 486 | 2009 |
| Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4–insufficient subjects C Schwab, A Gabrysch, P Olbrich, V Patiño, K Warnatz, D Wolff, ... Journal of Allergy and Clinical Immunology 142 (6), 1932-1946, 2018 | 410 | 2018 |
| ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia CA McCarl, C Picard, S Khalil, T Kawasaki, J Röther, A Papolos, J Kutok, ... Journal of Allergy and Clinical Immunology 124 (6), 1311-1318. e7, 2009 | 380 | 2009 |
| Interleukin-18 diagnostically distinguishes and pathogenically promotes human and murine macrophage activation syndrome ES Weiss, C Girard-Guyonvarc’h, D Holzinger, AA de Jesus, Z Tariq, ... Blood, The Journal of the American Society of Hematology 131 (13), 1442-1455, 2018 | 371 | 2018 |
| Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome C Woellner, EM Gertz, AA Schäffer, M Lagos, M Perro, EO Glocker, ... Journal of Allergy and Clinical Immunology 125 (2), 424-432. e8, 2010 | 350 | 2010 |
| A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes YT Bryceson, D Pende, A Maul-Pavicic, KC Gilmour, H Ufheil, T Vraetz, ... Blood, The Journal of the American Society of Hematology 119 (12), 2754-2763, 2012 | 348 | 2012 |
| DOCK8 deficiency: clinical and immunological phenotype and treatment options-a review of 136 patients SE Aydin, SS Kilic, C Aytekin, A Kumar, O Porras, L Kainulainen, ... Journal of clinical immunology 35, 189-198, 2015 | 311 | 2015 |
| Disease evolution and response to rapamycin in activated phosphoinositide 3-kinase δ syndrome: the european society for immunodeficiencies-activated phosphoinositide 3-kinase δ … ME Maccari, H Abolhassani, A Aghamohammadi, A Aiuti, O Aleinikova, ... Frontiers in immunology 9, 543, 2018 | 306 | 2018 |
| Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: an international multicenter retrospective study F Barzaghi, LCA Hernandez, B Neven, S Ricci, ZY Kucuk, JJ Bleesing, ... Journal of Allergy and Clinical Immunology 141 (3), 1036-1049. e5, 2018 | 277 | 2018 |
| C-reactive protein is a useful marker for guiding duration of antibiotic therapy in suspected neonatal bacterial infection S Ehl, B Gering, P Bartmann, J Högel, F Pohlandt Pediatrics 99 (2), 216-221, 1997 | 260 | 1997 |
| A critical role for neutralizing-antibody-producing B cells, CD4+ T cells, and interferons in persistent and acute infections of mice with lymphocytic choriomeningitis … O Planz, S Ehl, E Furrer, E Horvath, MA Bründler, H Hengartner, ... Proceedings of the National Academy of Sciences 94 (13), 6874-6879, 1997 | 252 | 1997 |
| Lethal hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type II A Enders, B Zieger, K Schwarz, A Yoshimi, C Speckmann, EM Knoepfle, ... Blood 108 (1), 81-87, 2006 | 239 | 2006 |
