Myriam R. Lorenz

Ulm, BW, Germany

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 36 publications

FAS-controlled T cells drive lymphoproliferation through glycolysis without effector differentiation.

FAS-controlled T cells drive lymphoproliferation through glycolysis without effector differentiation.

Journal: Journal of human immunity

Published: November 06, 2025

Somatic STAT5BN642H mutations shape variable immune landscapes resulting in heterogenous immune diseases.

Somatic STAT5BN642H mutations shape variable immune landscapes resulting in heterogenous immune diseases.

Journal: The Journal of allergy and clinical immunology

Published: September 09, 2025

Non-Skewed X-inactivation Results in NF-κB Essential Modulator (NEMO) Δ-exon 5-autoinflammatory Syndrome (NEMO-NDAS) in a Female with Incontinentia Pigmenti.

Non-Skewed X-inactivation Results in NF-κB Essential Modulator (NEMO) Δ-exon 5-autoinflammatory Syndrome (NEMO-NDAS) in a Female with Incontinentia Pigmenti.

Journal: Journal of clinical immunology

Published: February 01, 2024

Abnormal biomarkers predict complex FAS or FADD defects missed by exome sequencing.

Abnormal biomarkers predict complex FAS or FADD defects missed by exome sequencing.

Journal: The Journal of allergy and clinical immunology

Published: September 21, 2023

Diagnostic evaluation of paediatric autoimmune lymphoproliferative immunodeficiencies (ALPID): a prospective cohort study.

Diagnostic evaluation of paediatric autoimmune lymphoproliferative immunodeficiencies (ALPID): a prospective cohort study.

Journal: The Lancet. Haematology

Published: July 08, 2023

A partial human LCK defect causes a T cell immunodeficiency with intestinal inflammation.

A partial human LCK defect causes a T cell immunodeficiency with intestinal inflammation.

Journal: The Journal of experimental medicine

Published: May 29, 2023

Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndrome.

Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndrome.

Journal: The Journal of allergy and clinical immunology

Published: March 23, 2023

Hematologically important mutations: Leukocyte adhesion deficiency (second update).

Hematologically important mutations: Leukocyte adhesion deficiency (second update).

Journal: Blood cells, molecules & diseases

Published: October 29, 2022

Chronic Active Epstein-Barr Virus (EBV) Infection Controlled by Allogeneic Stem Cell Transplantation and EBV-Specific T Cells.

Chronic Active Epstein-Barr Virus (EBV) Infection Controlled by Allogeneic Stem Cell Transplantation and EBV-Specific T Cells.

Journal: Clinical infectious diseases : an official publication of the Infectious Diseases Society of America

Published: October 15, 2022

Revisiting autoimmune lymphoproliferative syndrome caused by Fas ligand mutations.

Revisiting autoimmune lymphoproliferative syndrome caused by Fas ligand mutations.

Journal: The Journal of allergy and clinical immunology

Published: August 11, 2022

The Growing Spectrum of DADA2 Manifestations-Diagnostic and Therapeutic Challenges Revisited.

The Growing Spectrum of DADA2 Manifestations-Diagnostic and Therapeutic Challenges Revisited.

Journal: Frontiers in pediatrics

Published: February 28, 2022

Compound heterozygous variants in OTULIN are associated with fulminant atypical late-onset ORAS.

Compound heterozygous variants in OTULIN are associated with fulminant atypical late-onset ORAS.

Journal: EMBO molecular medicine

Published: July 26, 2021

Showing 1-12 of 36

Last Updated: 09/26/2026