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Journal Articles

Antinuclear antibody–associated autoimmune cytopenia in childhood is a risk factor for systemic lupus erythematosus

Blood (2024) 143 (16): 1576–1585.

https://doi.org/10.1182/blood.2023021884

Published: 2024

Includes: Supplemental data

Journal Articles

DOCK11 deficiency in patients with X-linked actinopathy and autoimmunity

Charlotte Boussard, Laure Delage, Tania Gajardo, Alexandre Kauskot, Maxime Batignes, Nicolas Goudin, Marie-Claude Stolzenberg, Camille Brunaud, Patricia Panikulam, Quentin Riller, Maryse Moya-Nilges, Jean Solarz, Christelle Repérant, Béatrice Durel, Jean-Claude Bordet, Olivier Pellé, Corinne Lebreton, Aude Magérus, Vithura Pirabakaran, Pablo Vargas, Sébastien Dupichaud, Marie Jeanpierre, Angélique Vinit, Mohammed Zarhrate, Cécile Masson, Nathalie Aladjidi, Peter D. Arkwright, Brigitte Bader-Meunier, Sandrine Baron Joly, Joy Benadiba, Elise Bernard, Dominique Berrebi, Christine Bodemer, Martin Castelle, Fabienne Charbit-Henrion, Marwa Chbihi, Agathe Debray, Philippe Drabent, Sylvie Fraitag, Miguel Hié, Judith Landman-Parker, Ludovic Lhermitte, Despina Moshous, Pierre Rohrlich, Frank Ruemmele, Anne Welfringer-Morin, Maud Tusseau, Alexandre Belot, Nadine Cerf-Bensussan, Marie Roelens, Capucine Picard, Bénédicte Neven, Alain Fischer, Isabelle Callebaut, Mickaël Ménager, Fernando E. Sepulveda, Frédéric Adam, Frédéric Rieux-Laucat

Blood (2023) 141 (22): 2713–2726.

https://doi.org/10.1182/blood.2022018486

Published: 2023

Includes: Supplemental data

Journal Articles

Therapeutic Plasma Exchange in Pediatrics for Immunologic Disorders; Tolerated and Safe Process for Pediatric Life-Threatening Conditions

Blood (2019) 134 (Supplement_1): 4986.

https://doi.org/10.1182/blood-2019-122106

Published: 2019

Journal Articles

Genetic of Sporadic Hemophagocytic Lymphohistiocytosis

Coralie Bloch, MD PhD, Jean-Philippe Jais, MD PhD, Marine Gil, Marouane Boubaya, PhD, Felipe Suarez, MD PhD, Brigitte Bader-Meunier, MD, Nizar Malhaoui, MD PhD, Alain Fischer, MD PhD, Genevieve de Saint Basile, MD PhD, Olivier Hermine, MD PhD

Blood (2019) 134 (Supplement_1): 82.

https://doi.org/10.1182/blood-2019-129743

Published: 2019

Journal Articles

Germline TIM-3 Mutations Characterize Sub-Cutaneous Panniculitis T-Cell Lymphomas with Hemophagocytic Lymphohistiocytic Syndrome

Blood (2018) 132 (Supplement 1): 1569.

https://doi.org/10.1182/blood-2018-99-120297

Published: 2018

Journal Articles

Defective anti-polysaccharide response and splenic marginal zone disorganization in ALPS patients

Blood (2014) 124 (10): 1597–1609.

https://doi.org/10.1182/blood-2014-02-553834

Published: 2014

Includes: Supplemental data

Journal Articles

Excellent Prognosis of Late Relapses of ETV6/RUNX1 Childhood Acute Lymphoblastic Leukemia: Lessons From the FRALLE 93 Protocol

Virginie Gandemer, MD, PhD, Sylvie Chevret, Arnaud Petit, Christiane Vermylen, MD, PhD, Thierry Leblanc, MD, Gerard Michel, Claudine Schmitt, Odile Lejars, Jean-Pierre Vannier, Francois Demeocq, Brigitte Bader-Meunier, Francoise Bernaudin, Yves Perel, MD, PhD, Marie-Francoise Auclerc, Jean Michel Cayuela, MD, PhD, Guy Leverger, MD, PhD, Andre Baruchel

Blood (2011) 118 (21): 1508.

https://doi.org/10.1182/blood.V118.21.1508.1508

Published: 2011

Journal Articles

A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation

Blood (2011) 118 (18): 4798–4807.

https://doi.org/10.1182/blood-2011-04-347641

Published: 2011

Journal Articles

New Insights Into Autoimmune Hemolytic Anemia of children : A French National Observational study of 268 Children.

Nathalie Aladjidi, MD, Thierry Leblanc, MD, Guy Leverger, MD, PhD, Marie Quitterie Picat, Gerard Michel, MD, PhD, Brigitte Bader-Meunier, MD, Yves Bertrand, MD, PhD, Alain Fischer, MD, PhD, Genevieve Chene, MD, PhD, Yves Perel, MD, PhD

Blood (2009) 114 (22): 3017.

https://doi.org/10.1182/blood.V114.22.3017.3017

Published: 2009

Journal Articles

FAS-L, IL-10, and double-negative CD4 − CD8 − TCR α/β + T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function

Blood (2009) 113 (13): 3027–3030.

https://doi.org/10.1182/blood-2008-09-179630

Published: 2009

Includes: Supplemental data

Journal Articles

Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin A

Ashley M. Toye, Rosalind C. Williamson, Moudji Khanfar, Brigitte Bader-Meunier, Thérèse Cynober, Madeleine Thibault, Gil Tchernia, Michèle Déchaux, Jean Delaunay, Lesley J. Bruce

Blood (2008) 111 (11): 5380–5389.

https://doi.org/10.1182/blood-2007-07-099473

Published: 2008

Includes: Supplemental data

Journal Articles

Band 3 Courcouronne: Homozygous Mutation Ser667Phe Causes Severe Hereditary Spherocytosis and Incomplete Distal Renal Tubular Acidosis.

Jean Delaunay, MD, PhD, Ashley Toye, BSc PhD, Rosalind Williamson, BSc, Moudji Khanfar, MD, Brigitte Bader-Meunier, MD, Thérèse Cynober, MD, Madeleine Thibault, Gilbert Jean Tchernia, MD, Michèle Déchaux, MD, Lesley Bruce, BSc PhD

Blood (2006) 108 (11): 1563.

https://doi.org/10.1182/blood.V108.11.1563.1563

Published: 2006

Journal Articles

Autoimmune Hemolytic Anemia (AIHA) in Children: A French Observational Study of 171 Patients for the French Society of Pediatric Hematology and Immunology (SHIP).

Nathalie Aladjidi, Antoine Pariente, Thierry Leblanc, Brigitte Bader Meunier, Yves Bertrand, Gerard Michel, Francoise Ledeist, Yves Colin, Genevieve Chene, Brigitte Nelken, Guy Leverger, Yves Perel

Blood (2005) 106 (11): 1684.

https://doi.org/10.1182/blood.V106.11.1684.1684

Published: 2005

Journal Articles

Severe and progressive encephalitis as a presenting manifestation of a novel missense perforin mutation and impaired cytolytic activity

Jérôme Feldmann, Gaël Ménasché, Isabelle Callebaut, Véronique Minard-Colin, Brigitte Bader-Meunier, Laurence Le Clainche, Alain Fischer, Françoise Le Deist, Marc Tardieu, Geneviève de Saint Basile

Blood (2005) 105 (7): 2658–2663.

https://doi.org/10.1182/blood-2004-09-3590

Published: 2005

Journal Articles

Molecular Basis of Congenital Dyserythropoietic Anemia Type I in French Patients.

Hannah Tamary, MD, Orly Dgany, PhD, Alexis Proust, MSc, Tanya Krasnov, MSc, Nili Avidan, PhD, Gil Tchernia, MD, David Geneviève, MD, Valérie Comier-Darre, MD, Martine Le Merrer, MD, Brigitte Bader-Meunier, MD, Corinne Ferrero-Vacher, MD, Isaac Yaniv, MD, Jean Delaunay, MD

Blood (2004) 104 (11): 3709.

https://doi.org/10.1182/blood.V104.11.3709.3709

Published: 2004

Journal Articles

Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis

Brigitte Bader-Meunier, Frédéric Gauthier, Frédérique Archambaud, Thérèse Cynober, Francoise Miélot, Jean-Paul Dommergues, Josiane Warszawski, Narla Mohandas, Gil Tchernia

Blood (2001) 97 (2): 399–403.

https://doi.org/10.1182/blood.V97.2.399

Published: 2001

Journal Articles

Lymphoproliferative Syndrome With Autoimmunity: A Possible Genetic Basis for Dominant Expression of the Clinical Manifestations

Frédéric Rieux-Laucat, Séverine Blachère, Sylvia Danielan, Jean Pierre De Villartay, Mathias Oleastro, Eric Solary, Brigitte Bader-Meunier, Peter Arkwright, Corinne Pondaré, Françoise Bernaudin, Helen Chapel, Susan Nielsen, Mohamed Berrah, Alain Fischer, Françoise Le Deist

Blood (1999) 94 (8): 2575–2582.

https://doi.org/10.1182/blood.V94.8.2575.420k17_2575_2582

Published: 1999

NARROW

Antinuclear antibody–associated autoimmune cytopenia in childhood is a risk factor for systemic lupus erythematosus

DOCK11 deficiency in patients with X-linked actinopathy and autoimmunity

Therapeutic Plasma Exchange in Pediatrics for Immunologic Disorders; Tolerated and Safe Process for Pediatric Life-Threatening Conditions

Genetic of Sporadic Hemophagocytic Lymphohistiocytosis

Germline TIM-3 Mutations Characterize Sub-Cutaneous Panniculitis T-Cell Lymphomas with Hemophagocytic Lymphohistiocytic Syndrome

Defective anti-polysaccharide response and splenic marginal zone disorganization in ALPS patients

Excellent Prognosis of Late Relapses of ETV6/RUNX1 Childhood Acute Lymphoblastic Leukemia: Lessons From the FRALLE 93 Protocol

A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation

New Insights Into Autoimmune Hemolytic Anemia of children : A French National Observational study of 268 Children.

FAS-L, IL-10, and double-negative CD4 − CD8 − TCR α/β + T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function

Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin A

Band 3 Courcouronne: Homozygous Mutation Ser667Phe Causes Severe Hereditary Spherocytosis and Incomplete Distal Renal Tubular Acidosis.

Autoimmune Hemolytic Anemia (AIHA) in Children: A French Observational Study of 171 Patients for the French Society of Pediatric Hematology and Immunology (SHIP).

Severe and progressive encephalitis as a presenting manifestation of a novel missense perforin mutation and impaired cytolytic activity

Molecular Basis of Congenital Dyserythropoietic Anemia Type I in French Patients.

Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis

Lymphoproliferative Syndrome With Autoimmunity: A Possible Genetic Basis for Dominant Expression of the Clinical Manifestations

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American Society of Hematology

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American Society of Hematology

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