Barbara H. Barendregt
Rotterdam, ZH, Netherlands
Last Updated: 09/26/2026
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Found 12 publications
Soluble Interleukin-2 Receptor Is a Promising Serum Biomarker for Granulomatous Disease in Common Variable Immune Deficiency.
Journal: Journal of clinical immunology
Published: August 11, 2020
The Clinical and Genetic Spectrum of 82 Patients With RAG Deficiency Including a c.256_257delAA Founder Variant in Slavic Countries.
Journal: Frontiers in immunology
Published: March 04, 2020
EuroFlow Standardized Approach to Diagnostic Immunopheneotyping of Severe PID in Newborns and Young Children.
Journal: Frontiers in immunology
Published: December 23, 2019
Rapid Low-Cost Microarray-Based Genotyping for Genetic Screening in Primary Immunodeficiency.
Journal: Frontiers in immunology
Published: September 12, 2019
Endocrine Disorders Are Prominent Clinical Features in Patients With Primary Antibody Deficiencies.
Journal: Frontiers in immunology
Published: May 13, 2019
The 11q Terminal Deletion Disorder Jacobsen Syndrome is a Syndromic Primary Immunodeficiency.
Journal: Journal of clinical immunology
Published: September 07, 2015
Increased PI3K/Akt activity and deregulated humoral immune response in human PTEN deficiency.
Journal: The Journal of allergy and clinical immunology
Published: March 09, 2015
Common variable immunodeficiency and idiopathic primary hypogammaglobulinemia: two different conditions within the same disease spectrum.
Journal: Haematologica
Published: June 12, 2013
B-cell development and functions and therapeutic options in adenosine deaminase-deficient patients.
Journal: The Journal of allergy and clinical immunology
Published: June 10, 2013
A reversion of an IL2RG mutation in combined immunodeficiency providing competitive advantage to the majority of CD8+ T cells.
Journal: Haematologica
Published: February 14, 2013
Anti-TNF treatment blocks the induction of T cell-dependent humoral responses.
Journal: Annals of the rheumatic diseases
Published: September 13, 2012
B-cell replication history and somatic hypermutation status identify distinct pathophysiologic backgrounds in common variable immunodeficiency.
Journal: Blood
Published: November 02, 2011
Showing 1-12 of 12
Last Updated: 09/26/2026