List of works - Marianne Debré

Activation-induced cytidine deaminase (AID) is required for B-cell tolerance in humans

scientific article

Allogeneic bone marrow transplantation in mevalonic aciduria

scientific article

Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey

scientific article published on July 2012

Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency

scientific article

Efficacy of etanercept for the treatment of juvenile idiopathic arthritis according to the onset type

scientific article

Efficacy of gene therapy for X-linked severe combined immunodeficiency

scientific article

Expansion of regulatory T cells in patients with Langerhans cell histiocytosis

scientific article (publication date: August 2007)

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

scientific article

Granulomatous inflammation in cartilage-hair hypoplasia: risks and benefits of anti-TNF-α mAbs

scientific article published on 28 June 2011

Immune deficiency-related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency

scientific article

Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency

scientific article

Inherited MST1 deficiency underlies susceptibility to EV-HPV infections

scientific article

Invasive mold infections in chronic granulomatous disease: a 25-year retrospective survey

scientific article published on December 2011

Long-term outcome after hematopoietic stem cell transplantation of a single-center cohort of 90 patients with severe combined immunodeficiency

scientific article published on 23 January 2009

Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients

scientific article

Natural antibodies sustain differentiation and maturation of human dendritic cells

scholarly article

Occurrence of B-cell lymphomas in patients with activated phosphoinositide 3-kinase δ syndrome

scientific article

Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damage

scientific article

Polymerase ε1 mutation in a human syndrome with facial dysmorphism, immunodeficiency, livedo, and short stature ("FILS syndrome")

scientific article

Severe cutaneous papillomavirus disease after haemopoietic stem-cell transplantation in patients with severe combined immune deficiency caused by common gammac cytokine receptor subunit or JAK-3 deficiency

scientific article published in June 2004

List of works by Marianne Debré

Activation-induced cytidine deaminase (AID) is required for B-cell tolerance in humans

Allogeneic bone marrow transplantation in mevalonic aciduria

Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey

Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency

Efficacy of etanercept for the treatment of juvenile idiopathic arthritis according to the onset type

Efficacy of gene therapy for X-linked severe combined immunodeficiency

Expansion of regulatory T cells in patients with Langerhans cell histiocytosis

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

Granulomatous inflammation in cartilage-hair hypoplasia: risks and benefits of anti-TNF-α mAbs

Immune deficiency-related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency

Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency

Inherited MST1 deficiency underlies susceptibility to EV-HPV infections

Invasive mold infections in chronic granulomatous disease: a 25-year retrospective survey

Long-term outcome after hematopoietic stem cell transplantation of a single-center cohort of 90 patients with severe combined immunodeficiency

Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients

Natural antibodies sustain differentiation and maturation of human dendritic cells

Occurrence of B-cell lymphomas in patients with activated phosphoinositide 3-kinase δ syndrome

Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damage

Polymerase ε1 mutation in a human syndrome with facial dysmorphism, immunodeficiency, livedo, and short stature ("FILS syndrome")

Severe cutaneous papillomavirus disease after haemopoietic stem-cell transplantation in patients with severe combined immune deficiency caused by common gammac cytokine receptor subunit or JAK-3 deficiency