| Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency) JP Schmid, D Canioni, D Moshous, F Touzot, N Mahlaoui, F Hauck, ... Blood, The Journal of the American Society of Hematology 117 (5), 1522-1529, 2011 | 395 | 2011 |
| Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels J Albuisson, SE Murthy, M Bandell, B Coste, H Louis-dit-Picard, J Mathur, ... Nature communications 4 (1), 1884, 2013 | 370 | 2013 |
| Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies A Fischer, J Provot, JP Jais, A Alcais, N Mahlaoui, D Adoue, N Aladjidi, ... Journal of Allergy and Clinical Immunology 140 (5), 1388-1393. e8, 2017 | 311 | 2017 |
| New insights into childhood autoimmune hemolytic anemia: a French national observational study of 265 children N Aladjidi, G Leverger, T Leblanc, MQ Picat, G Michel, Y Bertrand, ... haematologica 96 (5), 655, 2011 | 259 | 2011 |
| Safety and efficacy of allogeneic hematopoietic stem cell transplant after PD-1 blockade in relapsed/refractory lymphoma RW Merryman, HT Kim, PL Zinzani, C Carlo-Stella, SM Ansell, ... Blood, The Journal of the American Society of Hematology 129 (10), 1380-1388, 2017 | 258 | 2017 |
| Preexisting autoantibodies to type I IFNs underlie critical COVID-19 pneumonia in patients with APS-1 P Bastard, E Orlova, L Sozaeva, R Lévy, A James, MM Schmitt, S Ochoa, ... The Journal of experimental medicine 218 (7), 2021 | 254 | 2021 |
| High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia M Pasquet, C Bellanné-Chantelot, S Tavitian, N Prade, B Beaupain, ... Blood, The Journal of the American Society of Hematology 121 (5), 822-829, 2013 | 242 | 2013 |
| Live birth after ovarian tissue autograft in a patient with sickle cell disease treated by allogeneic bone marrow transplantation C Roux, C Amiot, G Agnani, Y Aubard, PS Rohrlich, P Piver Fertility and sterility 93 (7), 2413. e15-2413. e19, 2010 | 196 | 2010 |
| Tmevpg1, a Candidate Gene for the Control of Theiler's Virus Persistence, Could Be Implicated in the Regulation of Gamma Interferon S Vigneau, PS Rohrlich, M Brahic, JF Bureau Journal of virology 77 (10), 5632-5638, 2003 | 192 | 2003 |
| Prospective sandwich enzyme-linked immunosorbent assay for serum galactomannan: early predictive value and clinical use in invasive aspergillosis P Rohrlich, J Sarfati, P Mariani, M Duval, A Carol, C Saint-Martin, ... The Pediatric infectious disease journal 15 (3), 232-237, 1996 | 190 | 1996 |
| Role of STAT3 in CD4+ CD25+ FOXP3+ regulatory lymphocyte generation: implications in graft-versus-host disease and antitumor immunity JR Pallandre, E Brillard, G Créhange, A Radlovic, JP Remy-Martin, ... The Journal of Immunology 179 (11), 7593-7604, 2007 | 189 | 2007 |
| Clinical aspects of STAT3 gain-of-function germline mutations: a systematic review A Fabre, S Marchal, V Barlogis, B Mari, P Barbry, PS Rohrlich, LR Forbes, ... The Journal of Allergy and Clinical Immunology: In Practice 7 (6), 1958-1969. e9, 2019 | 179 | 2019 |
| Treatment of Chediak-Higashi syndrome by allogenic bone marrow transplantation: report of 10 cases E Haddad, F Le Deist, S Blanche, M Benkerrou, P Rohrlich, E Vilmer, ... | 177 | 1995 |
| Adjuvant corticosteroid therapy for chronic disseminated candidiasis F Legrand, M Lecuit, B Dupont, E Bellaton, M Huerre, PS Rohrlich, ... Clinical infectious diseases 46 (5), 696-702, 2008 | 175 | 2008 |
| Chimaeric anti‐CD20 monoclonal antibody (rituximab) in post‐transplant B‐lymphoproliferative disorder following stem cell transplantation in children A Faye, P Quartier, Y Reguerre, P Lutz, AS Carret, A Dehée, P Rohrlich, ... British journal of haematology 115 (1), 112-118, 2001 | 175 | 2001 |
| Prospective monitoring and quantitation of residual blasts in childhood acute lymphoblastic leukemia by polymerase chain reaction study of delta and gamma T-cell receptor genes H Cave, C Guidal, P Rohrlich, MH Delfau, A Broyart, B Lescoeur, ... | 169 | 1994 |
| Natural history of GATA2 deficiency in a survey of 79 French and Belgian patients J Donadieu, M Lamant, C Fieschi, FS de Fontbrune, A Caye, M Ouachee, ... haematologica 103 (8), 1278, 2018 | 163 | 2018 |
| Impact of eculizumab treatment on paroxysmal nocturnal hemoglobinuria: a treatment versus no‐treatment study M Loschi, R Porcher, F Barraco, L Terriou, M Mohty, S De Guibert, B Mahe, ... American Journal of Hematology 91 (4), 366-370, 2016 | 162 | 2016 |
| NOTCH1 and FBXW7 mutations have a favorable impact on early response to treatment, but not on outcome, in children with T-cell acute lymphoblastic leukemia (T-ALL) treated on … E Clappier, S Collette, N Grardel, S Girard, L Suarez, G Brunie, ... Leukemia 24 (12), 2023-2031, 2010 | 157 | 2010 |
| Description and outcome of a cohort of 8 patients with WHIM syndrome from the French Severe Chronic Neutropenia Registry S Beaussant Cohen, O Fenneteau, E Plouvier, PS Rohrlich, G Daltroff, ... Orphanet journal of rare diseases 7, 1-14, 2012 | 134 | 2012 |
