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Transplantation and Cellular Therapy|June 13, 2026
Nationwide Centralized Manufacturing and Fresh Distribution of TCRαβ/CD19-DepletedGrafts: A Real-World French ExperienceUgo Chartral, Mony Fahd, Emma Gasperment, et al.
Blood|April 4, 2019
Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genesJérôme Hadjadj, Nathalie Aladjidi, Helder Fernandes, et al.
Blood|December 2, 2010
Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)Jana Pachlopnik Schmid, Danielle Canioni, Despina Moshous, et al.
American Journal of Hematology|April 23, 2024
Pediatric refractory chronic immune thrombocytopenia: Identification, patients' characteristics, and outcomeThomas Pincez, Helder Fernandes, Mony Fahd, et al.
The Journal of Clinical Investigation|June 12, 2018
Dominant-negative IKZF1 mutations cause a T, B, and myeloid cell combined immunodeficiencyDavid Boutboul, Hye Sun Kuehn, Zoé Van de Wyngaert, et al.
American Journal of Hematology|March 7, 2023
Impact of age at diagnosis, sex, and immunopathological manifestations in 886 patients with pediatric chronic immune thrombocytopeniaThomas Pincez, Helder Fernandes, Marlène Pasquet, et al.
Blood|June 20, 2018
Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond-like syndromeChristine Bellanné-Chantelot, Barbara Schmaltz-Panneau, Caroline Marty, et al.
Journal of Clinical Immunology|November 22, 2024
2q33 Deletions Underlying Syndromic and Non-syndromic CTLA4 DeficiencyCharlyne Brakta, Anne-Claude Tabet, Mathilde Puel, et al.
The Journal of Allergy and Clinical Immunology|December 14, 2011
Protective effect of IgM against colonization of the respiratory tract by nontypeable Haemophilus influenzae in patients with hypogammaglobulinemiaRomain Micol, Samer Kayal, Nizar Mahlaoui, et al.
Blood Advances|October 21, 2025
Childhood isolated C3d-positive AIHA: favorable prognosis but rare relapse or associated immunodeficiencyMarion Blachez, Nathalie Aladjidi, Thomas Modot, et al.
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