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International Consensus Document (ICON): Common Variable Immunodeficiency DisordersPredictors of shingles reports at diagnosis of common variable immunodeficiency and selective immunoglobulin G subclass deficiency in 212 Alabama adultsComparison of diagnostic criteria for common variable immunodeficiency disorderCommon variable immunodeficiency, immune thrombocytopenia, rituximab and splenectomy: important considerations.Comparisons of CVID and IgGSD: referring physicians, autoimmune conditions, pneumovax reactivity, immunoglobulin levels, blood lymphocyte subsets, and HLA-A and -B typing in 432 adult index patients.Interferon signature in the blood in inflammatory common variable immune deficiencyFertility, pregnancies and outcomes reported by females with common variable immune deficiency and hypogammaglobulinemia: results from an internet-based surveyManagement of a pregnant woman with common variable immunodeficiency and previous reactions to intravenous IgG administration.Common variable immunodeficiency associated with microdeletion of chromosome 1q42.1-q42.3 and inositol 1,4,5-trisphosphate kinase B (ITPKB) deficiencyLPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiencyExome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease.Posterior Cord Syndrome and Trace Elements Deficiency as an Uncommon Presentation of Common Variable Immunodeficiency.New diagnostic criteria for common variable immune deficiency (CVID), which may assist with decisions to treat with intravenous or subcutaneous immunoglobulin.Genetic defects and the role of helper T-cells in the pathogenesis of common variable immunodeficiency.Genetics of common variable immunodeficiency: role of transmembrane activator and calcium modulator and cyclophilin ligand interactor.Humoral Primary Immunodeficiencies in Chronic Rhinosinusitis.Role of Calcium Signaling in B Cell Activation and Biology.Chronic lung disease in common variable immune deficiency (CVID): A pathophysiological role for microbial and non-B cell immune factors.Myeloid glycosylation defects lead to a spontaneous common variable immunodeficiency-like condition with associated hemolytic anemia and antilymphocyte autoimmunity.A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferation.Monozygotic twins discordant for common variable immunodeficiency reveal impaired DNA demethylation during naïve-to-memory B-cell transition.Good's syndrome, CVID, and selective antibody deficiency in patients with chronic rhinosinusitis.Immunophenotypic Analysis of B Lymphocytes in Patients with Common Variable Immunodeficiency: Identification of CD23 as a Useful Marker in the Definition of the Disease
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Perspectives on common variable immune deficiency.
@ast
Perspectives on common variable immune deficiency.
@en
type
label
Perspectives on common variable immune deficiency.
@ast
Perspectives on common variable immune deficiency.
@en
prefLabel
Perspectives on common variable immune deficiency.
@ast
Perspectives on common variable immune deficiency.
@en
P2860
P1476
Perspectives on common variable immune deficiency.
@en
P2093
Elena S Resnick
Joon H Park
P2860
P356
10.1111/J.1749-6632.2011.06338.X
P407
P577
2011-12-01T00:00:00Z