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Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damageHumoral immunodeficiency : awareness for better supportThe signaling role of CD40 ligand in platelet biology and in platelet component transfusionChallenges in the Role of Gammaglobulin Replacement Therapy and Vaccination Strategies for Hematological MalignancyControl of cytokine production by human fc gamma receptors: implications for pathogen defense and autoimmunityCommon Variable Immunodeficiency Caused by FANC Mutations.Long-term Clinical Outcome of Antibody Replacement Therapy in Humoral Immunodeficient Adults With Respiratory Tract InfectionsICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing.Redemption of autoantibodies on anergic B cells by variable-region glycosylation and mutation away from self-reactivity.B-cell subpopulations in children: National reference valuesBiallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity.Failure to detect functional neutrophil B helper cells in the human spleenHarmful somatic amino acid substitutions affect key pathways in cancers.Maintaining intestinal health: the genetics and immunology of very early onset inflammatory bowel disease.A novel mutation in the POLE2 gene causing combined immunodeficiency.Common Variable Immunodeficiency and Circulating TFHA miR-155-Peli1-c-Rel pathway controls the generation and function of T follicular helper cells.Phenotypic and Functional Comparison of Class Switch Recombination Deficiencies with a Subgroup of Common Variable Immunodeficiencies.Immunoglobulin class switch recombination deficiency type 1 or CD40 ligand deficiency: from bedside to bench and back again.Bilateral lung transplantation in a patient with humoral immune deficiency: a case report with review of the literature.Antibody replacement therapy in primary antibody deficiencies and iatrogenic hypogammaglobulinemia.Serial Serum Immunoglobulin G (IgG) Trough Levels in Patients with X-linked Agammaglobulinemia on Replacement Therapy with Intravenous Immunoglobulin: Its Correlation with Infections in Indian Children.Dissecting Epigenetic Dysregulation of Primary Antibody Deficiencies.Indications to Epigenetic Dysfunction in the Pathogenesis of Common Variable Immunodeficiency.Lung Disease in Primary Antibody Deficiencies.Approach to the Management of Autoimmunity in Primary Immunodeficiency.Crosstalk Between T and B Cells in the Germinal Center After Transplantation.Autoimmunity in Primary Antibody Deficiencies.Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patients.The role of monogenic disease in children with very early onset inflammatory bowel disease.Primary immunodeficiencies suggest redundancy within the human immune system.Functional antibodies to Haemophilus influenzae type B, Neisseria meningitidis, and Streptococcus pneumoniae contained in intravenous immunoglobulin products.The immunophenotypic fingerprint of patients with primary antibody deficiencies is partially present in their asymptomatic first-degree relatives.Whole Genome Sequencing Reveals a Chromosome 9p Deletion Causing DOCK8 Deficiency in an Adult Diagnosed with Hyper IgE Syndrome Who Developed Progressive Multifocal Leukoencephalopathy.Antibody blocks acquisition of bacterial colonization through agglutination.Anti-food and anti-microbial IgG subclass antibodies in inflammatory bowel disease.Autoimmunity in a cohort of 471 patients with primary antibody deficiencies.SIAE Rare Variants in Juvenile Idiopathic Arthritis and Primary Antibody Deficiencies.Mutations in Bruton's tyrosine kinase impair IgA responses.Novel NFKB2 mutation in early-onset CVID.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Primary antibody deficiencies.
@en
type
label
Primary antibody deficiencies.
@en
prefLabel
Primary antibody deficiencies.
@en
P2860
P356
P1476
Primary antibody deficiencies.
@en
P2093
Sven Kracker
P2860
P2888
P304
P356
10.1038/NRI3466
P577
2013-06-14T00:00:00Z
P6179
1040097410