About: Severe deficiency of switched memory B cells (CD27(+)IgM(-)IgD(-)) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease

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About: Severe deficiency of switched memory B cells (CD27(+)IgM(-)IgD(-)) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease Goto Sponge NotDistinct Permalink

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scientific article published on 01 March 2002

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 2002 (uk) im März 2002 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en marzu de 2002 (ast) scientific article published on 01 March 2002 (en)
publication date	wds:Q77678228-95945FC3-E1A9-4AC8-9745-05A9880E1C25
publication date	2002-03-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q77678228-04B8917F-3F00-463A-BEBF-C173C9CED058 wds:Q77678228-1A6B9BCE-D260-4EB3-A2CD-FBA5554D14ED wds:Q77678228-1A767599-4B90-47F3-982C-A8D2450D948F wds:Q77678228-68917574-09D2-4FD7-9E54-D4C8357BA414 wds:Q77678228-9D795168-75DB-42E8-9943-7B9910A3D188 wds:Q77678228-A4EB6F66-FC6D-418F-8E61-2F98A29D5945 wds:Q77678228-E32C8C01-AF72-4983-87B5-EB4048269A2B wds:Q77678228-ECBF6E5A-0A4C-4EEC-8452-ADFCCBFCC8AC
author name string	Hermann Eibel Hans Hartmut Peter Michael Schlesier Moritz Braun Axel Denz Christoph Groth Guido Wolff-Vorbeck Ruth Dräger
rdfs:label	Severe deficiency of switched memory B cells (CD27(+)IgM(-)IgD(-)) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease (en) Severe deficiency of switched memory B cells (nl)
skos:prefLabel	Severe deficiency of switched memory B cells (CD27(+)IgM(-)IgD(-)) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease (en) Severe deficiency of switched memory B cells (nl)
name	Severe deficiency of switched memory B cells (CD27(+)IgM(-)IgD(-)) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease (en) Severe deficiency of switched memory B cells (nl)
author	wds:Q77678228-068D967B-03E2-4615-A1B2-392EE4F2681F
author	Klaus Warnatz
title	wds:Q77678228-3F55419D-D6BA-4FAC-8687-1F2D4C20DD33
title	Severe deficiency of switched memory B cells (CD27(+)IgM(-)IgD(-)) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease (en)
page(s)	wds:Q77678228-BA3EBFFD-8AFB-4FF8-9737-065FF9A94A84
page(s)	1544-1551
instance of	wds:Q77678228-52975143-D862-4FDE-9415-AF09B5B288AA
instance of	scholarly article
main subject	wds:Q77678228-6ACFB40E-8AD2-4440-9C3A-AF4E83AC6A33 wds:Q77678228-70E1D222-65A2-47DF-8C58-D9CF20DE3D24
main subject	common variable immunodeficiency memory B cell
PubMed ID	wds:Q77678228-00EE8B6B-99FE-4B44-81C2-920A3347C01E
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11861266
PubMed ID	11861266
published in	wds:Q77678228-27E674F3-AE38-4311-BDD5-DE10A02D588E
published in	Blood
issue	wds:Q77678228-251A1945-72E4-40EE-A87B-AE778410CD08
volume	wds:Q77678228-3FA24E66-556C-49CC-B930-67F2A1A40BE1
issue	5
volume	99
DOI	wds:Q77678228-4C066689-BE81-449E-B2FD-D57FAE49F6BD
DOI	http://dx.doi.org/10.1182/BLOOD.V99.5.1544
DOI	10.1182/BLOOD.V99.5.1544
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q77678228
is cites work of	Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency A decreased frequency of regulatory T cells in patients with common variable immunodeficiency The establishment of early B cell tolerance in humans: lessons from primary immunodeficiency diseases Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans. Autoimmunity in common variable immunodeficiency How I treat common variable immune deficiency Defective regulatory B-cell compartment in patients with immune thrombocytopenia Splenectomy associated changes in IgM memory B cells in an adult spleen registry cohort. Complement receptor 2/CD21- human naive B cells contain mostly autoreactive unresponsive clones Circulating phenotypic B-1 cells are decreased in common variable immunodeficiency and correlate with immunoglobulin M levels Immunophenotyping of putative human B1 B cells in healthy controls and common variable immunodeficiency (CVID) patients. The ITP syndrome: pathogenic and clinical diversity Dysfunctional BLK in common variable immunodeficiency perturbs B-cell proliferation and ability to elicit antigen-specific CD4+ T-cell help. Altered dendritic cell distribution in patients with common variable immunodeficiency Granulomatous disease in common variable immunodeficiency TLR-mediated B cell defects and IFN-α in common variable immunodeficiency Age-dependent changes in peripheral blood dendritic cell subsets in normal children and children with specific polysaccharide antibody deficiency (SPAD). Common variable immunodeficiency: an update Regulatory T cell dysfunction in subjects with common variable immunodeficiency complicated by autoimmune disease Decrease in phenotypic regulatory T cells in subsets of patients with common variable immunodeficiency. B-cell and T-cell phenotypes in CVID patients correlate with the clinical phenotype of the disease. Gene expression analysis of peripheral T cells in a subgroup of common variable immunodeficiency shows predominance of CCR7(-) effector-memory T cells. Frequency of Treg cells is reduced in CVID patients with autoimmunity and splenomegaly and is associated with expanded CD21lo B lymphocytes. The molecular pathology of primary immunodeficiencies Toll-like receptor 7 and 9 defects in common variable immunodeficiency Autoimmunity in primary immune deficiency: taking lessons from our patients Autoimmune cytopenias in common variable immunodeficiency Elucidation of seventeen human peripheral blood B-cell subsets and quantification of the tetanus response using a density-based method for the automated identification of cell populations in multidimensional flow cytometry data International Consensus Document (ICON): Common Variable Immunodeficiency Disorders Immune dysregulation in human subjects with heterozygous germline mutations in CTLA4 Morbidity and mortality in common variable immune deficiency over 4 decades Long-term follow-up and outcome of a large cohort of patients with common variable immunodeficiency Ill-defined germinal centers and severely reduced plasma cells are histological hallmarks of lymphadenopathy in patients with common variable immunodeficiency. Novel mutations in a Japanese patient with CD19 deficiency Pathogenesis, diagnosis, and management of primary antibody deficiencies and infections Profiling of polychromatic flow cytometry data on B-cells reveals patients' clusters in common variable immunodeficiency. PID comes full circle: applications of V(D)J recombination excision circles in research, diagnostics and newborn screening of primary immunodeficiency disorders. Thymic and bone marrow output in patients with common variable immunodeficiency. Memory B cells and pneumococcal antibody after splenectomy Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions Autoimmune manifestations in common variable immunodeficiency Common variable immunodeficiency: a new look at an old disease. Impaired humoral immunity in X-linked lymphoproliferative disease is associated with defective IL-10 production by CD4+ T cells Loss of circulating CD27+ memory B cells and CCR4+ T cells occurring in association with elevated EBV loads in XLP patients surviving primary EBV infection

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