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Lack of interaction between NEMO and SHARPIN impairs linear ubiquitination and NF-κB activation and leads to incontinentia pigmenti.
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Protective effect of IgM against colonization of the respiratory tract by nontypeable Haemophilus influenzae in patients with hypogammaglobulinemia.
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Pachymeningitis after meningococcal infection.
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Inherited human OX40 deficiency underlying classic Kaposi sarcoma of childhood
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Corrigendum: Evidence of innate lymphoid cell redundancy in humans
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A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity
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Cutaneous granulomas with primary immunodeficiency in children: a report of 17 new patients and a review of the literature
S Leclerc-Mercier
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Successful treatment of JAK1 associated inflammatory disease
Antoine Fayand
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Heterozygous RELA mutations cause early-onset systemic lupus erythematosus by hijacking the NF-κB pathway towards transcriptional activation of type-I Interferon genes
Laura Barnabei
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Outcomes following gene therapy in patients with severe Wiskott-Aldrich syndrome
Salima Hacein-Bey Abina
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Long-term outcome after hematopoietic stem cell transplantation of a single-center cohort of 90 patients with severe combined immunodeficiency
Bénédicte Neven
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Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation
Despina Moshous
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Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency
Bertrand Boisson
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Inherited CARD9 deficiency in 2 unrelated patients with invasive Exophiala infection
Fanny Lanternier
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Elisa Barbati
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Clinical and Genetic Spectrum of a Large Cohort With Total and Sub-total Complement Deficiencies
Carine El Sissy
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Classic Kaposi Sarcoma in 3 Unrelated Turkish Children Born to Consanguineous Kindreds.
Gürses Sahin
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Ayse Palanduz
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Gonul Aydogan
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Olivier Cassar
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Inherited CARD9 deficiency in otherwise healthy children and adults with Candida species–induced meningoencephalitis, colitis, or both
Fanny Lanternier
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Evidence of innate lymphoid cell redundancy in humans
Frédéric Vély
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Vincent Barlogis
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Blandine Vallentin
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Imported African Histoplasmosis in an Immunocompetent Patient 40 Years after Staying in a Disease-Endemic Area
Clémence Richaud
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Type I interferon-mediated autoinflammation due to DNase II deficiency
Mathieu Rodéro
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Alessandra Tesser
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Eva Bartok
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Gillian Rice
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Novel STAT1 alleles in otherwise healthy patients with mycobacterial disease.
Ariane Chapgier
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Stéphanie Boisson-Dupuis
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Copy number variations and founder effect underlying complete IL-10Rβ deficiency in Portuguese kindreds.
Fabienne Charbit-Henrion
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Bernadette Bègue
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Sylvain Hanein
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Marie-Claude Stolzenberg
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Aspergillus fumigatus Infection in Humans With STAT3-Deficiency Is Associated With Defective Interferon-Gamma and Th17 Responses
François Danion
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Jagadeesh Bayry
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Amélie Duréault
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Outcome after failure of allogeneic hematopoietic stem cell transplantation in children with acute leukemia: a study by the société Francophone de greffe de moelle et de thérapie cellulaire (SFGM-TC)
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Mathieu Ing
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Yu-Chun Lone
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Human HOIP and LUBAC deficiency underlies autoinflammation, immunodeficiency, amylopectinosis, and lymphangiectasia.
Bertrand Boisson
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Emmanuel Laplantine
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Kerry Dobbs
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Aurélie Cobat
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Nadine Tarantino
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PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator-dependent autoimmunity
Anne-Laure Mathieu
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Estelle Verronese
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Gillian I. Rice
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A polysaccharide virulence factor of a human fungal pathogen induces neutrophil apoptosis via NK cells.
Pauline Robinet
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Florence Baychelier
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Thierry Fontaine
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Capucine Picard
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Patrice Debré
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Progressive Multifocal Leukoencephalopathy in Primary Immunodeficiencies
Jérôme Hadjadj
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Aurélien Guffroy
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Christophe Delavaud
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Guillaume Taieb
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Isabelle Meyts
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Chronic Aichi virus infection as a cause of long-lasting multi-organ involvement in patients with primary immune deficiencies
Jacques Fourgeaud
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Mathilde Lecuit
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Philippe Pérot
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Julie Bruneau
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Béatrice Regnault
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An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation
Tangui Le Guen
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Isabelle André-Schmutz
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Chantal Lagresle-Peyrou
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Benoit France
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