Tolerance and autoimmunity: lessons at the bedside of primary immunodeficiencies (Q36942513)

17 August 2017

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title

Tolerance and autoimmunity: lessons at the bedside of primary immunodeficiencies (English)

1 reference

17 August 2017

Magda Carneiro-Sampaio

series ordinal

1

1 reference

PubMed ID

17869610

17 August 2017

Antonio Coutinho

series ordinal

2

1 reference

17 August 2017

1 January 2007

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17 August 2017

Advances in Immunology

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17 August 2017

95

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17 August 2017

51-82

1 reference

Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients.

17 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Projection of an immunological self shadow within the thymus by the aire protein

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Autoimmunity in human primary immunodeficiency diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Prospective immunological profiling in a case of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX).

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

IPEX is a unique X-linked syndrome characterized by immune dysfunction, polyendocrinopathy, enteropathy, and a variety of autoimmune phenomena

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Genetic disorders of programmed cell death in the immune system

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Autoimmune lymphoproliferative syndrome. A human disorder of abnormal lymphocyte survival

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

C1q, autoimmunity and apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

B cells and B cell products-helping to restore cellular immunity?

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

TACI is mutant in common variable immunodeficiency and IgA deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

AIRE deficiency in thymus of 2 patients with Omenn syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Clinical findings leading to the diagnosis of X-linked agammaglobulinemia

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Childhood common variable immunodeficiency with autoimmune disease

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Thymic commitment of regulatory T cells is a pathway of TCR-dependent selection that isolates repertoires undergoing positive or negative selection.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Physiology of IgA and IgA deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Hematologic complications of primary immune deficiencies

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Common variable immunodeficiency: clinical and immunological features of 248 patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Molecular defects in T- and B-cell primary immunodeficiency diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Severe chronic neutropenia: treatment and follow-up of patients in the Severe Chronic Neutropenia International Registry

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

1 reference

7 January 2021

Homozygous human TAP peptide transporter mutation in HLA class I deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Promiscuous gene expression in thymic epithelial cells is regulated at multiple levels

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

CXCR4 mutations in WHIM syndrome: a misguided immune system?

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Association of HLA class I antigen deficiency related to a TAP2 gene mutation with familial bronchiectasis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Clinical features of dominant and recessive interferon γ receptor 1 deficiencies

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Fas gene mutations in the Canale-Smith syndrome, an inherited lymphoproliferative disorder associated with autoimmunity

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Autoimmunity in Wiskott-Aldrich syndrome: risk factors, clinical features, and outcome in a single-center cohort of 55 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Hyper-immunoglobulin M syndromes caused by intrinsic B-lymphocyte defects

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Henoch-Schönlein purpura in Wiskott-Aldrich syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Omenn syndrome due to ARTEMIS mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Autoimmune polyendocrine syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Immune deficiency and autoimmunity

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Infectious diseases associated with complement deficiencies

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Human primary immunodeficiency diseases: a perspective

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Complement deficiencies

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

TAP deficiency syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Immune dysregulation, polyendocrinopathy, enteropathy, and X-linked inheritance (IPEX), a syndrome of systemic autoimmunity caused by mutations of FOXP3, a critical regulator of T-cell homeostasis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Omenn's syndrome occurring in patients without mutations in recombination activating genes

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Familial isolated congenital asplenia: a rare, frequently hereditary dominant condition, often detected too late as a cause of overwhelming pneumococcal sepsis. Report of a new case and review of 31 others

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Omenn syndrome in an infant with IL7RA gene mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Tackling the heterogeneity of CVID.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Chorioretinal lesions in patients and carriers of chronic granulomatous disease

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Medullary epithelial cells of the human thymus express a highly diverse selection of tissue-specific genes colocalized in chromosomal clusters

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

1 reference

7 January 2021

WHIM syndrome: a genetic disorder of leukocyte trafficking

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Altered leukocyte response to CXCL12 in patients with warts hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Selective IgA deficiency (SIgAD) and common variable immunodeficiency (CVID)

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Competition of 19S and 7S antigen receptors in the regulation of the primary immune response

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Incidence in Sweden and clinical features of familial hemophagocytic lymphohistiocytosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Omenn syndrome: a lack of tolerance on the background of deficient lymphocyte development and maturation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

The health status and quality of life of adults with X-linked agammaglobulinemia

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

WASP (Wiskott-Aldrich syndrome protein) gene mutations and phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

An animal model of hemophagocytic lymphohistiocytosis (HLH): CD8+ T cells and interferon gamma are essential for the disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Autoimmune lymphoproliferative syndrome presenting with glomerulonephritis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Activation of human CD4+ cells with CD3 and CD46 induces a T-regulatory cell 1 phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Major histocompatibility complex class II deficiency: clinical manifestations, immunologic features, and outcome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Long-term follow-up of health in blood donors with primary selective IgA deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Autoimmunity in systemic lupus erythematosus: integrating genes and biology

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Inherited disorders of human Toll-like receptor signaling: immunological implications.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Neutrophil and platelet antibodies in autoimmune lymphoproliferative syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

CD4(+) regulatory T cells in autoimmunity and allergy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Cutting edge: the Wiskott-Aldrich syndrome protein is required for efficient phagocytosis of apoptotic cells

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Clinical spectrum of X-linked hyper-IgM syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Selective IgA deficiency and autoimmunity

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

The role of complement in the development of systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Gastrointestinal involvement in chronic granulomatous disease

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Primary hemophagocytic syndromes point to a direct link between lymphocyte cytotoxicity and homeostasis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Establishment of tissue-specific tolerance is driven by regulatory T cells selected by thymic epithelium

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Association of a syndrome resembling Wegener's granulomatosis with low surface expression of HLA class-I molecules

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Genetics of autoimmune diseases in humans and in animal models

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Clinical and molecular findings in IPEX syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

The combination of polymorphisms within interferon-gamma receptor 1 and receptor 2 associated with the risk of systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Genetics of human systemic lupus erythematosus: the emerging picture

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Systemic lupus erythematosus and complement deficiency: clues to a novel role for the classical complement pathway in the maintenance of immune tolerance

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

AIRE and immunological tolerance: insights from the study of autoimmune polyendocrinopathy candidiasis and ectodermal dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee Meeting in Budapest, 2005

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Immunodeficiency and infections in ataxia-telangiectasia.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Primary immunodeficiencies and the rheumatologist

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

FOXP3 acts as a rheostat of the immune response

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Tolerance induced by thymic epithelial grafts in birds

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Autoimmune lymphoproliferative syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

The presentation and natural history of immunodeficiency caused by nuclear factor kappaB essential modulator mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Human disease resulting from gene mutations that interfere with appropriate nuclear factor-kappaB activation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Mutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

V-region connectivity in T cell repertoires

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes).

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

The Wiskott-Aldrich syndrome in the United States and Canada (1892-1979).

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED): a model disease to study molecular aspects of endocrine autoimmunity

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Systemic lupus erythematosus, complement deficiency, and apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Clinical heterogeneity and reversibility of selective immunoglobulin A deficiency in 80 children

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

An X-linked syndrome of diarrhea, polyendocrinopathy, and fatal infection in infancy.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Paths to understanding the genetic basis of autoimmune disease

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Mutations in the RNA component of RNase mitochondrial RNA processing might cause Omenn syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Defects in the interferon-gamma and interleukin-12 pathways

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Defective cytotoxic granule-mediated cell death pathway impairs T lymphocyte homeostasis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Thymus and autoimmunity: capacity of the normal thymus to produce pathogenic self-reactive T cells and conditions required for their induction of autoimmune disease

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

ICOS deficiency in patients with common variable immunodeficiency.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Invasive pneumococcal infections in children with asplenia

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Autoimmunity in Wiskott-Aldrich syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Genetic, biochemical, and clinical features of chronic granulomatous disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Autoimmune regulator induced changes in the gene expression profile of human monocyte-dendritic cell-lineage

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Complement deficiency and disease: an update

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Autoimmune lymphoproliferative syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Perforin gene defects in familial hemophagocytic lymphohistiocytosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

A history of pediatric immunology

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

The clinical, immunological, and molecular spectrum of chromosome 22q11.2 deletion syndrome and DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

A multiinstitutional survey of the Wiskott-Aldrich syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Defective natural killer cell function in patients with hemophagocytic lymphohistiocytosis and in first degree relatives

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Association of the interferon-gamma receptor variant (Val14Met) with systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Clonal persistence of B lymphocytes in normal mice is determined by variable region-dependent selection.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Update on human systemic lupus erythematosus genetics

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Monogenic autoimmune diseases - lessons of self-tolerance

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

The range of defects associated with nuclear factor kappaB essential modulator

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

The thymus selects the useful, neglects the useless and destroys the harmful

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1-deficient severe combined immunodeficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

The genetics of complex autoimmune diseases: non-MHC susceptibility genes

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Treatment and outcome of autoimmune hematologic disease in common variable immunodeficiency (CVID).

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Type 1 diabetes genes and pathways shared by humans and NOD mice

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Chronic granulomatous disease. Report on a national registry of 368 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

The X-linked hyper-IgM syndrome: clinical and immunologic features of 79 patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Autoimmune lymphoproliferative syndrome: molecular basis of disease and clinical phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Genetic alterations in caspase-10 may be causative or protective in autoimmune lymphoproliferative syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

Clinical and immunological aspects of HLA class I deficiency.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2995002-6

7 January 2021

10.1016/S0065-2776(07)95002-6

Identifiers

DOI

1 reference

17 August 2017

1 reference

PubMed ID

17869610