Lista de obras - Marianne Debré - Dominio Público Uruguay

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

artículo científico publicado en 2011

Allogeneic bone marrow transplantation in mevalonic aciduria

artículo científico publicado en 2007

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

artículo científico publicado en 2012

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

artículo científico publicado en 2004

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

artículo científico publicado en 2003

Efficacy of gene therapy for X-linked severe combined immunodeficiency

artículo científico publicado en 2010

Expansion of regulatory T cells in patients with Langerhans cell histiocytosis

artículo científico publicado en 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

artículo científico publicado en 2009

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

artículo científico publicado en 2011

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

artículo científico publicado en 2014

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

artículo científico publicado en 2012

Inherited MST1 deficiency underlies susceptibility to EV-HPV infections

artículo científico publicado en 2012

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

artículo científico

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

artículo científico publicado en 2009

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

artículo científico publicado en 2011

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

artículo científico publicado en 2014

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

artículo científico publicado en 2013

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

artículo científico publicado en 2012

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

artículo científico publicado en 2004

Lista de obras de 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