Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The complex genetics of common variable immunodeficiency.

Journal of investigative medicine : the official publication of the American Federation for Clinical Research - 1 Mar 2004

Schroeder Harry W, Schroeder Harry W, Sheikh Sofia M

Abstract excerpt

Immunoglobulin (Ig)A deficiency and common variable immunodeficiency (CVID) are the most common primary immunodeficiency disorders in North America and Europe. These diseases appear to comprise a familial spectrum of immunodeficiency that ranges from partial IgA deficiency to a complete absence of serum immunoglobulin. The CVID phenotype is typically acquired and can spontaneously revert to IgG and IgM...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged, 80 and over
Share to Antibody Formation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Common Variable Immunodeficiency

Share to Europe

Share to Family Health

Share to Infant

Share to Major Histocompatibility Complex

Share to North America

Source

Identifiers

PMID: 15068224
DOI: 10.1136/jim-52-02-17

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The complex genetics of common variable immunodeficiency.PMID 15068224Read ↗

[Genetic basis of common variable immunodeficiency: from common to variable].Semantic proximity Read ↗

Common variable immunodeficiency: an update on etiology and management.Semantic proximity Read ↗

The Rapidly Expanding Genetic Spectrum of Common Variable Immunodeficiency-Like Disorders.Semantic proximity Read ↗

Common Variable Immunodeficiency: More Pathways than Roads to RomeSemantic proximity Read ↗

Common variable immunodeficiency (CVID): new genetic insight and unanswered questions.Semantic proximity Read ↗

Perspectives on common variable immune deficiency.Semantic proximity Read ↗

The many faces of common variable immunodeficiency.Semantic proximity Read ↗

The variable in common variable immunodeficiency: a disease of complex phenotypes.Semantic proximity Read ↗

Recent advances in elucidating the genetics of common variable immunodeficiencySemantic proximity Read ↗

[Common variable immunodeficiency].Semantic proximity Read ↗

Genetics of common variable immunodeficiency: role of transmembrane activator and calcium modulator and cyclophilin ligand interactor.Semantic proximity Read ↗

Common variable immunodeficiency.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.