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Blood|February 23, 2010
X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment optionsMichael H Albert, Tanja C Bittner, Shigeaki Nonoyama, et al.Journal of Clinical Immunology|May 10, 2013
A phenotypic approach for IUIS PID classification and diagnosis: guidelines for clinicians at the bedsideAhmed Aziz Bousfiha, Leïla Jeddane, Fatima Ailal, et al.Clinical Immunology (Orlando, Fla.)|January 14, 2018
Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutationsCaroline Besnard, Eva Levy, Nathalie Aladjidi, et al.Blood Cells, Molecules & Diseases|December 3, 2011
Hematologically important mutations: leukocyte adhesion deficiency (first update)Edith van de Vijver, Anne Maddalena, Özden Sanal, et al.Blood|February 11, 2020
Clonal tracking in gene therapy patients reveals a diversity of human hematopoietic differentiation programsEmmanuelle Six, Agathe Guilloux, Adeline Denis, et al.Transplantation|October 8, 2005
Inolimomab in steroid-refractory acute graft-versus-host disease following allogeneic hematopoietic stem cell transplantation: retrospective analysis and comparison with other interleukin-2 receptor antibodiesJacques-Olivier Bay, Nathalie Dhédin, Martin Goerner, et al.Blood|October 23, 2013
SCID patients with ARTEMIS vs RAG deficiencies following HCT: increased risk of late toxicity in ARTEMIS-deficient SCIDCatharina Schuetz, Benedicte Neven, Christopher C Dvorak, et al.Genome Medicine|September 29, 2018
T cell dynamics and response of the microbiota after gene therapy to treat X-linked severe combined immunodeficiencyErik L Clarke, A Jesse Connell, Emmanuelle Six, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|August 16, 2014
Prevention of infections during primary immunodeficiencyClaire Aguilar, Marion Malphettes, Jean Donadieu, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|April 1, 2017
Chronic Granulomatous Disease in Patients Reaching Adulthood: A Nationwide Study in FranceBertrand Dunogué, Benoit Pilmis, Nizar Mahlaoui, et al.Pageof 44