Faranaz Atschekzei

Hannover, NI, Germany

Last Updated: 09/26/2026

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Found 50 publications

Expanding the clinical spectrum of CD3γ deficiency: comprehensive characterization of adult-onset disease and integrated reevaluation of all reported patients.

Expanding the clinical spectrum of CD3γ deficiency: comprehensive characterization of adult-onset disease and integrated reevaluation of all reported patients.

Journal: Frontiers in immunology

Published: May 23, 2026

Rare variants in genes related to inborn errors of immunity in patients with rheumatoid arthritis and secondary immunodeficiency.

Rare variants in genes related to inborn errors of immunity in patients with rheumatoid arthritis and secondary immunodeficiency.

Journal: RMD open

Published: April 10, 2026

Clinical and immunological differentiation of isolated IgG and combined IgG & IgM deficiencies from common variable immunodeficiency.

Clinical and immunological differentiation of isolated IgG and combined IgG & IgM deficiencies from common variable immunodeficiency.

Journal: Frontiers in immunology

Published: December 29, 2025

A germline IκBα mutation outside the signal reception domain blocks nuclear translocation of NFκB1 and associates with autoinflammation-like features.

A germline IκBα mutation outside the signal reception domain blocks nuclear translocation of NFκB1 and associates with autoinflammation-like features.

Journal: Annals of the rheumatic diseases

Published: April 24, 2025

A novel hemizygous nonsense variant in DOCK11 causes systemic inflammation and immunodeficiency.

A novel hemizygous nonsense variant in DOCK11 causes systemic inflammation and immunodeficiency.

Journal: Clinical immunology (Orlando, Fla.)

Published: February 05, 2025

Reappraisal of IgG subclass deficiencies: a retrospective comparative cohort study.

Reappraisal of IgG subclass deficiencies: a retrospective comparative cohort study.

Journal: Frontiers in immunology

Published: December 28, 2024

Novel hypermorphic variants in IRF2BP2 identified in patients with common variable immunodeficiency and autoimmunity.

Novel hypermorphic variants in IRF2BP2 identified in patients with common variable immunodeficiency and autoimmunity.

Journal: Clinical immunology (Orlando, Fla.)

Published: June 03, 2024

JAK inhibitors to treat STAT3 gain-of-function: a single-center report and literature review.

JAK inhibitors to treat STAT3 gain-of-function: a single-center report and literature review.

Journal: Frontiers in immunology

Published: March 13, 2024

Phenotypic and pathomechanistic overlap between tapasin and TAP deficiencies.

Phenotypic and pathomechanistic overlap between tapasin and TAP deficiencies.

Journal: The Journal of allergy and clinical immunology

Published: March 01, 2024

Rituximab to treat prolidase deficiency due to a novel pathogenic copy number variation in PEPD.

Rituximab to treat prolidase deficiency due to a novel pathogenic copy number variation in PEPD.

Journal: RMD open

Published: July 17, 2023

Corrigendum: Vulnerability to meningococcal disease in immunodeficiency due to a novel pathogenic missense variant in NFKB1.

Corrigendum: Vulnerability to meningococcal disease in immunodeficiency due to a novel pathogenic missense variant in NFKB1.

Journal: Frontiers in immunology

Published: April 25, 2023

The GAIN Registry - a New Prospective Study for Patients with Multi-organ Autoimmunity and Autoinflammation.

The GAIN Registry - a New Prospective Study for Patients with Multi-organ Autoimmunity and Autoinflammation.

Journal: Journal of clinical immunology

Published: February 22, 2023

Showing 1-12 of 50

Last Updated: 09/26/2026