Claudia Schroder
Hannover, NI, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 6 publications
A novel NFKBIA variant substituting serine 36 of IκBα causes immunodeficiency with warts, bronchiectasis and juvenile rheumatoid arthritis in the absence of ectodermal dysplasia.
Journal: Clinical immunology (Orlando, Fla.)
Published: July 15, 2019
Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations.
Journal: The Journal of allergy and clinical immunology
Published: July 08, 2019
Late-Onset Antibody Deficiency Due to Monoallelic Alterations in NFKB1.
Journal: Frontiers in immunology
Published: April 17, 2019
A Novel CARMIL2 Mutation Resulting in Combined Immunodeficiency Manifesting with Dermatitis, Fungal, and Viral Skin Infections As Well as Selective Antibody Deficiency.
Journal: Journal of clinical immunology
Published: October 29, 2018
Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency.
Journal: The Journal of allergy and clinical immunology
Published: October 18, 2017
Evaluation of RAG1 mutations in an adult with combined immunodeficiency and progressive multifocal leukoencephalopathy.
Journal: Clinical immunology (Orlando, Fla.)
Published: September 09, 2016
Showing 1-6 of 6
Last Updated: 09/26/2026