C. Fieschi

发表

Low Penetrance, Broad Resistance, and Favorable Outcome of Interleukin 12 Receptor β1 Deficiency

Sami Al-Hajjar, A. Fischer, J. Casanova, 2003, The Journal of Experimental Medicine.

Low penetrance, broad resistance, and favorable outcome of interleukin 12 receptor beta1 deficiency: medical and immunological implications.

Sami Al-Hajjar, A. Fischer, J. Casanova, 2003, The Journal of experimental medicine.

Bacillus Calmette Guérin triggers the IL‐12/IFN‐γ axis by an IRAK‐4‐ and NEMO‐dependent, non‐cognate interaction between monocytes, NK, and T lymphocytes

J. Casanova, C. Picard, M. Feinberg, 2004, European journal of immunology.

Human RHOH deficiency causes T cell defects and susceptibility to EV-HPV infections.

David A. Williams, J. Casanova, C. Picard, 2012, The Journal of clinical investigation.

Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations

Guillaume Vogt, David N Cooper, Mehdi Mirsaeidi, 2005, Nature Genetics.

Effect of amantadine on drug-induced parkisonism: relationship between plasma levels and effect.

R. Latini, M. Nardini, P. Morselli, 1976, British journal of clinical pharmacology.

T Cells Signaling in γ Cells Requires IL-12 and IFN-T Cell-Dependent Activation of Dendritic

F. Deist, J. Casanova, F. Miró, 2006 .

A novel missense mutation (C30S) in the gene encoding tumor necrosis factor receptor 1 linked to autosomal-dominant recurrent fever with localized myositis in a French family.

J. Piette, F. Picard, C. Dodé, 2000, Arthritis and rheumatism.

Strains Responsible for Invasive Meningococcal Disease in Patients With Terminal Complement Pathway Deficiencies

C. Picard, D. Moshous, F. Suarez, 2017, The Journal of infectious diseases.

From idiopathic infectious diseases to novel primary immunodeficiencies.

J. Casanova, C. Picard, H. von Bernuth, 2005, The Journal of allergy and clinical immunology.

Granulomatous Disease in CVID: Retrospective Analysis of Clinical Characteristics and Treatment Efficacy in a Cohort of 59 Patients

É. Oksenhendler, R. Borie, E. Hachulla, 2012, Journal of Clinical Immunology.

Common variable immunodeficiency disorders: division into distinct clinical phenotypes.

Lennart Hammarstrom, B. Grimbacher, M. Abedi, 2008, Blood.

Late-onset combined immune deficiency: a subset of common variable immunodeficiency with severe T cell defect.

É. Oksenhendler, B. Bonnotte, J. Viallard, 2009, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

reliable markers of ALPS associated with FAS loss of function FAS-L, IL-10, and double-negative CD4-CD8-TCR alpha/beta+ T cells are

F. Rieux-Laucat, A. Fischer, J. Casanova, 2011 .

Brief report FAS-L, IL-10, and double-negative CD4 (cid:1) CD8 (cid:1) TCR (cid:2) / (cid:3) (cid:4) T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function

F. Rieux-Laucat, A. Fischer, F. Deist, 2009 .

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

F. Rieux-Laucat, A. Fischer, J. Casanova, 2009, Blood.

Defects in the CD19 complex predispose to glomerulonephritis, as well as IgG1 subclass deficiency.

J. Casanova, É. Oksenhendler, M. Conley, 2011, The Journal of allergy and clinical immunology.

Interleukin (IL)-12 and IL-23 are key cytokines for immunity against Salmonella in humans.

S. Dorman, J. Casanova, C. Picard, 2004, The Journal of infectious diseases.

Oesophageal squamous cell carcinoma in a young adult with IL-12Rβ1 deficiency

J. Casanova, C. Rodríguez-Gallego, C. Fieschi, 2010, Journal of Medical Genetics.

« Les mutations "gain de glycosylation" / Gains of glycosylation mutations »

D. Cooper, N. Chuzhanova, L. Abel, 2015 .

CD56+ T cells in vivo A role for interleukin-12/23 in the maturation of human natural killer and

Sami Al-Hajjar, J. Casanova, L. Abel, 2013 .

A role for interleukin-12/23 in the maturation of human natural killer and CD56+ T cells in vivo.

Sami Al-Hajjar, J. Casanova, L. Abel, 2008, Blood.

Les mutations « gain de glycosylation »

J. Casanova, D. Cooper, N. Chuzhanova, 2006 .

T Cell-Dependent Activation of Dendritic Cells Requires IL-12 and IFN-γ Signaling in T Cells1

J. Casanova, F. Miró, A. Chapgier, 2006, The Journal of Immunology.

T Cell-Dependent Activation of Dendritic Cells Requires IL-12 and IFN- Signaling in T Cells

F. Deist, J. Casanova, F. Miró, 2006 .

Cutaneous leukocytoclastic vasculitis in a child with interleukin-12 receptor beta-1 deficiency.

J. Casanova, C. Çavuşoğlu, B. Karapinar, 2006, The Journal of pediatrics.

Disseminated Disease in a Patient with Inherited Deficiency in the b 1 Subunit of the Interleukin ( IL ) – 12 / IL-23 Receptor

J. Casanova, C. Fieschi, A. Duarte, 2005 .

Tuberculosis in children and adults: two distinct genetic diseases

J. Casanova, L. Abel, A. Alcaïs, 2005 .

Interleukin-12 receptor beta 1 chain deficiency in a child with disseminated tuberculosis.

J. Casanova, C. Fieschi, J. Feinberg, 2005, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Inherited defects in the interferon-gamma receptor or interleukin-12 signalling pathways are not sufficient to cause allergic disease in children

J. Casanova, C. Picard, T. Ottenhoff, 2005, European Journal of Pediatrics.

Paracoccidioides brasiliensis disseminated disease in a patient with inherited deficiency in the beta1 subunit of the interleukin (IL)-12/IL-23 receptor.

J. Casanova, C. Fieschi, Ludovic de Beaucoudrey, 2005, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Variable outcome of experimental interferon-γ therapy of disseminated Bacillus Calmette-Guerin infection in two unrelated interleukin-12Rβ1-deficient Slovakian children

J. Casanova, S. Kaufmann, H. Hahn, 2005, European Journal of Pediatrics.

Retroviral-mediated gene transfer restores IL-12 and IL-23 signaling pathways in T cells from IL-12 receptor beta1-deficient patients.

J. Casanova, F. Candotti, M. Bosticardo, 2004, Molecular therapy : the journal of the American Society of Gene Therapy.

Human Interleukin-12—Interferon-γ Axis in Protective Immunity to Mycobacteria

J. Casanova, C. Picard, C. Fieschi, 2003 .

Interleukin-12 receptor beta1 deficiency presenting as recurrent Salmonella infection.

J. Casanova, N. Porat, R. Melamed, 2003, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Clinical tuberculosis in 2 of 3 siblings with interleukin-12 receptor beta1 deficiency.

J. Casanova, I. Caragol, C. Fieschi, 2003, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

INHERITED DISORDERS OF THE INTERLEUKIN-12-LNTERFERON GAMMA AXIS: MENDELIAN PREDISPOSITION TO MYCOBACTERIAL DISEASE IN MAN

J. Casanova, C. Picard, C. Fieschi, 2002 .

High Levels of Interferon Gamma in the Plasma of Children With Complete Interferon Gamma Receptor Deficiency

J. Casanova, C. Picard, C. Fieschi, 2001, Pediatrics.

DIAGNOSIS AND MANAGEMENT OF INHERITABLE DISORDERS OF INTERFERON-γ-MEDIATED IMMUNITY

J. Casanova, C. Picard, O. Baud, 2000, Radiologic Clinics of North America.

Natural history of GATA2 deficiency in a survey of 79 French and Belgian patients

H. Cavé, P. Rohrlich, E. W. Van Den Neste, 2018, Haematologica.

Classification of vasculitis.

J. Piette, Z. Amoura, C. Fieschi, 1999, The New England journal of medicine.

Low Circulating Natural Killer Cell Counts are Associated With Severe Disease in Patients With Common Variable Immunodeficiency

É. Oksenhendler, F. Vély, C. Farnarier, 2016, EBioMedicine.

Human IgA binds a diverse array of commensal bacteria

R. Cummings, H. Wardemann, H. Yssel, 2019, The Journal of experimental medicine.

specific memory B cells - The human spleen is a major reservoir for long-lived vaccinia virus

J. Weill, C. Reynaud, C. Staib, 2013 .

Improving the diagnostic efficiency of primary immunodeficiencies with targeted next-generation sequencing.

F. Rieux-Laucat, A. Fischer, C. Picard, 2020, The Journal of allergy and clinical immunology.

Efficiency of immunoglobulin G replacement therapy in common variable immunodeficiency: correlations with clinical phenotype and polymorphism of the neonatal Fc receptor

Smita Y. Patel, É. Oksenhendler, S. Chevret, 2013, Clinical and experimental immunology.

TNFA, ANXA11 and BTNL2 Polymorphisms in CVID Patients with Granulomatous Disease

F. T. P. Group, D. Boutboul, J. Bories, 2016, Journal of Clinical Immunology.

[Lung disease in adult common variable immunodeficiency].

É. Oksenhendler, J. Hadjadj, C. Fieschi, 2015, Revue des maladies respiratoires.

B-Cell and T-Cell Phenotypes in CVID Patients Correlate with the Clinical Phenotype of the Disease

É. Oksenhendler, P. Debré, M. Morisset, 2010, Journal of Clinical Immunology.

Synergistic convergence of microbiota‐specific systemic IgG and secretory IgA

K. Clément, É. Oksenhendler, P. Lepage, 2019, The Journal of allergy and clinical immunology.

Mutations in STAT3 and IL12RB1 impair the development of human IL-17–producing T cells

A. Fischer, J. Casanova, C. Picard, 2008, The Journal of experimental medicine.

Campylobacter infection in adult patients with primary antibody deficiency.

F. Mégraud, É. Oksenhendler, L. Galicier, 2019, The journal of allergy and clinical immunology. In practice.

High risk of infectious disease caused by salmonellae and mycobacteria infections in patients with Crohn disease treated with anti-interleukin-12 antibody.

J. Casanova, M. Allez, C. Fieschi, 2005, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Myositis and Neoplasia

J. Piette, C. Fieschi, 2000 .

Clinical and Genetic Spectrum of a Large Cohort With Total and Sub-total Complement Deficiencies

C. Picard, M. Taha, V. Frémeaux-Bacchi, 2019, Front. Immunol..

[Granulomatous disease in common variable immunodeficiency].

É. Oksenhendler, L. Galicier, C. Fieschi, 2008, La Revue de medecine interne.

Autoimmune cytopenias associated with inflammatory bowel diseases: Insights from a multicenter retrospective cohort.

A. Amiot, É. Oksenhendler, L. Galicier, 2017, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

The full spectrum of Castleman disease: 273 patients studied over 20 years

L. Vercellino, É. Oksenhendler, V. Meignin, 2018, British journal of haematology.

Good syndrome: an adult-onset immunodeficiency remarkable for its high incidence of invasive infections and autoimmune complications.

É. Oksenhendler, B. Bonnotte, R. Borie, 2015, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Uterine intravascular lymphoma as a cause of fever of unknown origin

É. Oksenhendler, L. Galicier, D. Boutboul, 2017, Annals of Hematology.

Autoimmune Hemolytic Anemia and Nodular Lymphocyte-Predominant Hodgkin Lymphoma: A Rare Association

T. Molina, P. Brice, C. Fieschi, 2013, Case reports in hematology.

Romidepsin is an effective and well-tolerated therapy in CD3-CD4+ lymphocyte-variant hypereosinophilic syndrome: A case report.

L. Galicier, P. Brice, C. Fieschi, 2019, The journal of allergy and clinical immunology. In practice.

[Rosai-Dorfman disease: Sinusal histiocytosis with massive lymphadenopathy].

É. Oksenhendler, V. Meignin, L. Galicier, 2017, Presse medicale.

Human herpesvirus 8-related Castleman disease in the absence of HIV infection.

É. Oksenhendler, V. Meignin, L. Galicier, 2013, Clinical Infectious Diseases.

Leg‐type form of idiopathic multicentric Castleman disease associated with severe lower extremity chronic venous/lymphatic disease

É. Oksenhendler, V. Meignin, L. Galicier, 2021, eJHaem.

Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond-like syndrome.

É. Oksenhendler, W. Vainchenker, T. Leblanc, 2018, Blood.

Human herpesvirus 8+ polyclonal IgMλ B‐cell lymphocytosis mimicking plasmablastic leukemia/lymphoma in HIV‐infected patients

É. Oksenhendler, V. Meignin, L. Galicier, 2013, European journal of haematology.

Autoimmune hypoglycemia expands the biological spectrum of HHV8+ multicentric Castleman disease.

É. Oksenhendler, C. Vigouroux, M. Auclair, 2021, Blood advances.

Lymphoma as an Exclusion Criteria for CVID Diagnosis Revisited

F. Rieux-Laucat, C. Picard, É. Oksenhendler, 2022, Journal of Clinical Immunology.

Bortezomib and dexamethasone, an original approach for treating multi‐refractory warm autoimmune haemolytic anaemia

É. Oksenhendler, L. Galicier, M. Michel, 2019, British Journal of Haematology.

Parental Consanguinity is Associated with a Severe Phenotype in Common Variable Immunodeficiency

É. Oksenhendler, I. Durieu, F. T. P. Group, 2011, Journal of Clinical Immunology.

Immunoglobulin Dosage and Switch from Intravenous to Subcutaneous Immunoglobulin Replacement Therapy in Patients with Primary Hypogammaglobulinemia: Decreasing Dosage Does Not Alter Serum IgG Levels

É. Oksenhendler, S. Thépot, L. Galicier, 2010, Journal of Clinical Immunology.

527 Low Penetrance, Broad Resistance, and Favorable Outcome of Interleukin 12 Receptor (cid:2) 1 Deﬁciency: Medical and Immunological

Sami Al-Hajjar, F. Deist, J. Casanova, 2003 .

Altered chemotactic response to CXCL12 in patients carrying GATA2 mutations

L. Faivre, C. Bellanné-Chantelot, F. Bachelerie, 2016, Journal of leukocyte biology.

iNKT and memory B-cell alterations in HHV-8 multicentric Castleman disease.

É. Oksenhendler, G. Carcelain, B. Autran, 2017, Blood.

Inborn errors of IL-12/23- and IFN-gamma-mediated immunity: molecular, cellular, and clinical features.

J. Casanova, C. Picard, E. Jouanguy, 2006, Seminars in immunology.

A novel form of complete IL-12/IL-23 receptor (cid:1) 1 deﬁciency with cell surface–expressed nonfunctional receptors

J. Casanova, F. Candotti, M. Bosticardo, 2004 .

Staphylococcal Infections Patient with Atypical Mycobacterial and Impairment of STAT Activation by IL-12 in a

J. Casanova, J. Mier, D. Frank, 2000 .

Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis

J. Casanova, J. Uitto, L. Abel, 2022, The Journal of experimental medicine.

Inherited GATA2 Deficiency Is Dominant by Haploinsufficiency and Displays Incomplete Clinical Penetrance

J. Casanova, L. F. Jobim, C. Deswarte, 2021, Journal of Clinical Immunology.

Correction

R. Cummings, H. Wardemann, H. Yssel, 2005, Infection Control & Hospital Epidemiology.

Infections Revealing Complement Deficiency in Adults

F. Lucht, B. Fantin, D. Boutboul, 2016, Medicine.

Treatment and outcome of Unicentric Castleman Disease: a retrospective analysis of 71 cases

É. Oksenhendler, P. Mordant, V. Meignin, 2019, British journal of haematology.

Rituximab decreases the risk of lymphoma in patients with HIV-associated multicentric Castleman disease.

É. Oksenhendler, S. Chevret, V. Meignin, 2012, Blood.

Codon 200 mutation in a new family of Chilean origin with Creutzfeldt-Jakob disease.

G. Macchi, C. Colosimo, P. Brown, 1996, Journal of neurology, neurosurgery, and psychiatry.

Immune/microbial interface perturbation in human IgA deficiency

C. Fieschi, G. Gorochov, D. Sterlin, 2018, Gut microbes.

Coronavirus disease 2019 in patients with inborn errors of immunity: An international study

B. Lambrecht, A. Fischer, E. López-Granados, 2020, Journal of Allergy and Clinical Immunology.

Identification of Umbre Orthobunyavirus as a Novel Zoonotic Virus Responsible for Lethal Encephalitis in 2 French Patients with Hypogammaglobulinemia.

C. Duyckaerts, S. Demeret, F. Bonneville, 2020, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Autosomal Dominant STAT3 Deficiency and Hyper-IgE Syndrome: Molecular, Cellular, and Clinical Features From a French National Survey

A. Fischer, C. Bodemer, J. Casanova, 2012, Medicine.

Revisiting Human IL-12R&bgr;1 Deficiency: A Survey of 141 Patients From 30 Countries

Smita Y. Patel, A. Al-ghonaium, Sami Al-Hajjar, 2010, Medicine.

Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease

J. Casanova, P. Newburger, C. Picard, 2011, Nature Immunology.

A novel X-linked recessive form of Mendelian susceptibility to mycobaterial disease

J. Casanova, C. Picard, A. Lemainque, 2006, Journal of Medical Genetics.

Inborn errors of IL-12/23- and IFN-γ-mediated immunity: molecular, cellular, and clinical features

J. Casanova, C. Picard, E. Jouanguy, 2006 .

An ACT1 mutation selectively abolishes interleukin-17 responses in humans with chronic mucocutaneous candidiasis.

J. Casanova, C. Picard, B. Boisson, 2013, Immunity.

Impaired response to interferon-alpha/beta and lethal viral disease in human STAT1 deficiency.

Sami Al-Hajjar, H. Al-Rayes, J. Casanova, 2003, Nature genetics.

Human interferon‐g‐mediated immunity is a genetically controlled continuous trait that determines the outcome of mycobacterial invasion

R. Döffinger, J. Casanova, C. Picard, 2000, Immunological reviews.

Impaired response to interferon-α/β and lethal viral disease in human STAT1 deficiency

Sami Al-Hajjar, H. Al-Rayes, J. Casanova, 2003, Nature Genetics.

T cell-dependent activation of dendritic cells requires IL-12 and IFN-gamma signaling in T cells.

J. Casanova, F. Miró, A. Chapgier, 2006, Journal of immunology.

French ENT Society (SFORL) guidelines for the management of immunodeficient patients with head and neck cancer of cutaneous origin.

C. Lebbé, N. Basset-Seguin, F. Faure, 2014, European annals of otorhinolaryngology, head and neck diseases.

Pyogenic Bacterial Infections in Humans with IRAK-4 Deficiency

A. Al-ghonaium, Sami Al-Hajjar, S. Al-Jumaah, 2003, Science.

Microbial ecology perturbation in human IgA deficiency

Mathieu Almeida, E. Le Chatelier, J. Doré, 2018, Science Translational Medicine.

Dramatic efficiency of pegylated interferon in sinus histiocytosis with massive lymphadenopathy

É. Oksenhendler, V. Meignin, L. Galicier, 2011, The British journal of dermatology.

Multicentric Castleman Disease in an HHV8-Infected Child Born to Consanguineous Parents With Systematic Review

A. Fischer, J. Casanova, C. Picard, 2012, Pediatrics.

Genetic screening of male patients with primary hypogammaglobulinemia can guide diagnosis and clinical management.

É. Oksenhendler, P. Debré, P. Gourraud, 2018, Human immunology.

Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

David R. Murdock, J. Rosenfeld, B. Lambrecht, 2020, The Journal of experimental medicine.

Inherited interleukin-12 deficiency: IL12B genotype and clinical phenotype of 13 patients from six kindreds.

A. Al-ghonaium, Sami Al-Hajjar, J. Casanova, 2002, American journal of human genetics.

PROMIDIS&agr;: A T‐cell receptor &agr; signature associated with immunodeficiencies caused by V(D)J recombination defects

A. Fischer, C. Picard, É. Oksenhendler, 2019, The Journal of allergy and clinical immunology.

Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiency

J. Casanova, C. Picard, S. Tangye, 2017, The Journal of clinical investigation.

Inherited GATA2 Deficiency Is Dominant by Haploinsufficiency and Displays Incomplete Clinical Penetrance

J. Casanova, L. F. Jobim, C. Deswarte, 2021, Journal of Clinical Immunology.

Persistent risk of adult T-cell leukemia/lymphoma after neonatal HTLV-1 infection through exchange transfusion

J. Cayuela, É. Oksenhendler, V. Meignin, 2017, International Journal of Hematology.

X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production

C. Bodemer, J. Casanova, A. Israël, 2006, The Journal of experimental medicine.

A novel form of complete IL-12/IL-23 receptor beta1 deficiency with cell surface-expressed nonfunctional receptors.

J. Casanova, F. Candotti, M. Bosticardo, 2004, Blood.

In a novel form of IFN-gamma receptor 1 deficiency, cell surface receptors fail to bind IFN-gamma.

R. Döffinger, J. Casanova, J. Emile, 2000, The Journal of clinical investigation.

The expansion of human T-bethighCD21low B cells is T cell dependent

J. Casanova, M. Boerries, M. van der Burg, 2021, Science Immunology.

Impairment of Mycobacterial But Not Viral Immunity by a Germline Human STAT1 Mutation

Steven M. Holland, Robert D. Schreiber, Catherine Dargemont, 2001, Science.

Novel STAT1 Alleles in Otherwise Healthy Patients with Mycobacterial Disease

J. Casanova, R. Schreiber, C. Picard, 2006, PLoS genetics.

Parental Consanguinity is Associated with a Severe Phenotype in Common Variable Immunodeficiency

É. Oksenhendler, I. Durieu, F. T. P. Group, 2012, Journal of Clinical Immunology.

Recurrent bacterial infections, but not fungal infections, characterise patients with ELANE‐related neutropenia: a French Severe Chronic Neutropenia Registry study

T. Leblanc, C. Bellanné-Chantelot, S. Blanche, 2021, British journal of haematology.

CorrigendumCorrigendum to “Inborn errors of IL-12/23- and IFN-γ-mediated immunity: Molecular, cellular, and clinical features” [Semin. Immunol. 18 (2006) 347–361]

J. Casanova, C. Picard, E. Jouanguy, 2007 .

Tuberculosis in children and adults

J. Casanova, L. Abel, A. Alcaïs, 2005, The Journal of experimental medicine.

Coagulation disorders in patients with severe hemophagocytic lymphohistiocytosis

É. Azoulay, M. Darmon, L. Galicier, 2021, bioRxiv.

Infections in 252 patients with common variable immunodeficiency.

É. Oksenhendler, P. Debré, R. Jaussaud, 2008, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β

J. Casanova, S. Boughorbel, S. Tangye, 2019, Science Immunology.

A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency

F. Rieux-Laucat, A. Fischer, J. Jais, 2019, Journal of Clinical Immunology.

Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies

F. Rieux-Laucat, A. Fischer, J. Jais, 2017, The Journal of allergy and clinical immunology.

Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency

J. Casanova, C. Saunders, C. Cunningham-Rundles, 2021, The Journal of experimental medicine.

Neutropenia in Patients with Common Variable Immunodeficiency: a Rare Event Associated with Severe Outcome

F. Rieux-Laucat, É. Oksenhendler, S. Hanein, 2017, Journal of Clinical Immunology.

Human IL-23 is essential for IFN-γ-dependent immunity to mycobacteria

J. Casanova, S. Tangye, F. Sallusto, 2023, Science Immunology.

The human spleen is a major reservoir for long-lived vaccinia virus-specific memory B cells.

Jacques-Olivier Pers, Olivier Hermine, Antonio Cosma, 2008, Blood.

Talc pleurodesis allows long-term remission in HIV-unrelated Human Herpesvirus 8-associated primary effusion lymphoma

É. Oksenhendler, L. Galicier, D. Boutboul, 2017, Leukemia & lymphoma.

Intensive chemotherapy regimen (LMB86) for St Jude stage IV AIDS-related Burkitt lymphoma/leukemia: a prospective study.

É. Oksenhendler, V. Meignin, R. Borie, 2007, Blood.

Mini‐review The role of interleukin‐12 in human infectious diseases: only a faint signature

J. Casanova, C. Fieschi, 2003, European journal of immunology.

Granulomatous Disease in CVID: Retrospective Analysis of Clinical Characteristics and Treatment Efficacy in a Cohort of 59 Patients

É. Oksenhendler, R. Borie, E. Hachulla, 2012, Journal of Clinical Immunology.

Campylobacter infection in 4 patients treated with ibrutinib

É. Oksenhendler, L. Galicier, C. Fieschi, 2022, European Journal of Clinical Microbiology & Infectious Diseases.

Exclusion of Patients with a Severe T-Cell Defect Improves the Definition of Common Variable Immunodeficiency.

É. Oksenhendler, D. Boutboul, C. Fieschi, 2016, The journal of allergy and clinical immunology. In practice.

Impairment of STAT Activation by IL-12 in a Patient with Atypical Mycobacterial and Staphylococcal Infections1

J. Casanova, J. Mier, D. Frank, 2000, The Journal of Immunology.

High frequency of fatal haemophagocytic lymphohistiocytosis syndrome in enteropathy-associated T cell lymphoma.

A. Amiot, É. Oksenhendler, L. Galicier, 2012, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q

A. Schäffer, A. Plebani, J. Meer, 2006, European Journal of Human Genetics.

Clinical spectrum, evolution, and management of autoimmune cytopenias associated with angioimmunoblastic T‐cell lymphoma

P. Gaulard, O. Casasnovas, L. de Leval, 2019, European journal of haematology.

Rectal Lymphogranuloma Venereum in HIV-infected Patients Can Mimic Lymphoma

É. Oksenhendler, V. Meignin, L. Galicier, 2015, Journal of clinical gastroenterology.

Association of IL12RB1 polymorphisms with pulmonary tuberculosis in adults in Morocco.

J. Casanova, L. Abel, N. Remus, 2004, The Journal of infectious diseases.

Fatal Epstein-Barr Virus Primo Infection in a 25-Year-Old Man Treated with Azathioprine for Crohn's Disease

R. Jaussaud, L. Andréoletti, Y. N'Guyen, 2009, Journal of Clinical Microbiology.

Characteristics of non-Hodgkin lymphoma arising in HIV-infected patients with suppressed HIV replication

É. Oksenhendler, V. Meignin, L. Galicier, 2009, AIDS.

Revisiting human primary immunodeficiencies

J. Casanova, Shen-Ying Zhang, L. Abel, 2008, Journal of internal medicine.

[Rosai-Dorfman disease].

É. Oksenhendler, V. Meignin, L. Galicier, 2007, Presse medicale.

Tuberculosis associated thrombocytopenic purpura: effectiveness of antituberculous therapy

É. Oksenhendler, R. Borie, L. Galicier, 2009, Hematology Reviews.

Efficacy of oral sirolimus as salvage therapy in refractory lichen planus associated with immune deficiency

É. Oksenhendler, M. Battistella, C. Fieschi, 2018, The British journal of dermatology.

[Genetic susceptibility to mycobacterial disease: Mendelian disorders of the interleukin-12 -interferon-gamma axis].

J. Casanova, C. Fieschi, É. Catherinot, 2005, Revue des maladies respiratoires.

Dasatinib-induced lupus

H. Dombret, C. Fieschi, A. Bergeron, 2008, The Lancet.

18F-fluorodeoxyglucose positron emission tomography/computed tomography in AIDS-related Burkitt lymphoma.

É. Oksenhendler, L. Galicier, J. Moretti, 2008, AIDS patient care and STDs.

Inherited human ZNF341 deficiency

A. Puel, V. Béziat, C. Fieschi, 2023, Current opinion in immunology.

Outcome of Immune Thrombocytopenia in Pregnancy: A French Nationwide Prospective Multicenter Observational Case-Control Study

C. Haioun, N. Costedoat-Chalumeau, J. Viallard, 2020 .

Inherited disorders of IL-12- and IFNgamma-mediated immunity: a molecular genetics update.

R. Döffinger, C. Picard, J. Casanova, 2002, Molecular immunology.

Value of the Overall Pneumococcal Polysaccharide Response in the Diagnosis of Primary Humoral Immunodeficiencies

F. Batteux, D. Launay, C. Fieschi, 2017, Front. Immunol..

Characteristics of thrombocytopenia, anasarca, fever, reticulin fibrosis and organomegaly syndrome: a retrospective study from a large Western cohort

É. Oksenhendler, L. Galicier, D. Boutboul, 2021, British Journal of Haematology.

Amantadine versus L-2 dopa and amatadine plus L-dopa.

M. Casacchia, M. Nardini, C. Fieschi, 1970, Lancet.

The efficacy and safety of systemic corticosteroids as first line treatment for granulomatous lymphocytic interstitial lung disease.

É. Oksenhendler, H. Tiddens, A. Korganow, 2022, The Journal of allergy and clinical immunology.

Somatic genetic alterations predict hematological progression in GATA2 deficiency

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