Publications by authors named "Florence Bellanger"

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Measurement of circulating CD21CD27 B lymphocytes in SLE patients is associated with disease activity independently of conventional serological biomarkers.
Alice Horisberger, Morgane Humbel, Natalia Fluder, Florence Bellanger, Craig Fenwick

Sci Rep· June 2022

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SLAMF Receptor Expression Identifies an Immune Signature That Characterizes Systemic Lupus Erythematosus.
Morgane Humbel, Florence Bellanger, Alice Horisberger, Madeleine Suffiotti, Natalia Fluder

Front Immunol· May 2022

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Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity.
Viviana Marin-Esteban, Jenny Youn, Blandine Beaupain, Agnieszka Jaracz-Ros, Vincent Barlogis, Florence Bellanger

Haematologica· March 2022

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Restoration of NK Cell Cytotoxic Function With Elotuzumab and Daratumumab Promotes Elimination of Circulating Plasma Cells in Patients With SLE.
Morgane Humbel, Florence Bellanger, Natalia Fluder, Alice Horisberger, Madeleine Suffiotti

Front Immunol· September 2021

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Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French Severe Congenital Neutropenia Registry.
Claire Desplantes, Marie Louise Fremond, Blandine Beaupain, Jean Luc Harousseau, Agnès Buzyn, Florence Bellanger

Orphanet J Rare Dis· December 2014

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Exhaustion of bacteria-specific CD4 T cells and microbial translocation in common variable immunodeficiency disorders.
Matthieu Perreau, Selena Vigano, Florence Bellanger, Céline Pellaton, Guillaume Buss

J Exp Med· September 2014

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CD160-associated CD8 T-cell functional impairment is independent of PD-1 expression.
Selena Viganò, Riddhima Banga, Florence Bellanger, Céline Pellaton, Alex Farina

PLoS Pathog· September 2014

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Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome.
Jean Donadieu, Odile Fenneteau, Blandine Beaupain, Sandrine Beaufils, Florence Bellanger

Haematologica· September 2012

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Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders.
Christine Bellanné-Chantelot, Isabelle Chaumarel, Myriam Labopin, Florence Bellanger, Véronique Barbu

Blood· July 2006

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