Genes associated with common variable immunodeficiency: one diagnosis to rule them all?
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Transcriptome analysis of bronchoalveolar lavage fluid from children with severe Mycoplasma pneumoniae pneumonia reveals novel gene expression and immunodeficiencyEarly-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes.Immunopathogenesis of granulomas in chronic autoinflammatory diseases.Follicular T Cells from smB- Common Variable Immunodeficiency Patients Are Skewed Toward a Th1 PhenotypeA Comparison of Clinical and Immunologic Phenotypes in Familial and Sporadic Forms of Common Variable Immunodeficiency.Identifying functional defects in patients with immune dysregulation due to LRBA and CTLA-4 mutations.Chronic norovirus infection and common variable immunodeficiency.Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study.Neutropenia in Patients with Common Variable Immunodeficiency: a Rare Event Associated with Severe Outcome.Common Variable Immunodeficiency and Liver Involvement.Plasma cell deficiency in human subjects with heterozygous mutations in Sec61 translocon alpha 1 subunit (SEC61A1).Novel nonsense gain-of-function NFKB2 mutations associated with a combined immunodeficiency phenotype.The immunophenotypic fingerprint of patients with primary antibody deficiencies is partially present in their asymptomatic first-degree relatives.Functional Evaluation of an IKBKG Variant Suspected to Cause Immunodeficiency Without Ectodermal Dysplasia.B cell autoimmunity at the extremes.Chronic Diarrhea in Common Variable Immunodeficiency: a Case Series and Review of the Literature.Influenza Vaccination in Patients with Common Variable Immunodeficiency (CVID).B-cell receptor repertoire sequencing in patients with primary immunodeficiency: a review.SIAE Rare Variants in Juvenile Idiopathic Arthritis and Primary Antibody Deficiencies.Review: Diagnosing Common Variable Immunodeficiency Disorder in the Era of Genome Sequencing.An Activating Janus Kinase-3 Mutation Is Associated with Cytotoxic T Lymphocyte Antigen-4-Dependent Immune Dysregulation Syndrome.Reference values for B-cell surface markers and co-receptors associated with primary immune deficiencies in healthy Turkish children.Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond.Delayed Diagnosis and Complications of Predominantly Antibody Deficiencies in a Cohort of Australian Adults.LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental IsodisomyCommon Variable Immunodeficiency with Genetic Defects Identified by Whole Exome SequencingLimited Innovations After More Than 65 Years of Immunoglobulin Replacement Therapy: Potential of IgA- and IgM-Enriched Formulations to Prevent Bacterial Respiratory Tract InfectionsThe Lung in Primary Immunodeficiencies: New Concepts in Infection and Inflammation
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Genes associated with common variable immunodeficiency: one diagnosis to rule them all?
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Genes associated with common variable immunodeficiency: one diagnosis to rule them all?
@en
type
label
Genes associated with common variable immunodeficiency: one diagnosis to rule them all?
@en
prefLabel
Genes associated with common variable immunodeficiency: one diagnosis to rule them all?
@en
P2093
P2860
P50
P1476
Genes associated with common variable immunodeficiency: one diagnosis to rule them all?
@en
P2093
Bart N Lambrecht
Filomeen Haerynck
Karim Y Vermaelen
P2860
P304
P356
10.1136/JMEDGENET-2015-103690
P407
P577
2016-06-01T00:00:00Z