Andrea Honscheid

Duesseldorf, NW, Germany

Last Updated: 09/26/2026

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Found 12 publications

EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency.

EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency.

Journal: Frontiers in immunology

Published: June 29, 2018

Human RAD52 - a novel player in DNA repair in cancer and immunodeficiency.

Human RAD52 - a novel player in DNA repair in cancer and immunodeficiency.

Journal: Haematologica

Published: December 17, 2016

Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans.

Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans.

Journal: Haematologica

Published: July 02, 2016

A novel homozygous mutation in UNC13D presenting as Epstein-Barr-virus-associated lymphoproliferative disease at 9 years of age.

A novel homozygous mutation in UNC13D presenting as Epstein-Barr-virus-associated lymphoproliferative disease at 9 years of age.

Journal: Leukemia & lymphoma

Published: April 29, 2016

Fatal Lymphoproliferative Disease in Two Siblings Lacking Functional FAAP24.

Fatal Lymphoproliferative Disease in Two Siblings Lacking Functional FAAP24.

Journal: Journal of clinical immunology

Published: April 05, 2016

De novo PIK3R1 gain-of-function with recurrent sinopulmonary infections, long-lasting chronic CMV-lymphadenitis and microcephaly.

De novo PIK3R1 gain-of-function with recurrent sinopulmonary infections, long-lasting chronic CMV-lymphadenitis and microcephaly.

Journal: Clinical immunology (Orlando, Fla.)

Published: August 21, 2015

Hodgkin lymphoma as a novel presentation of familial DICER1 syndrome.

Hodgkin lymphoma as a novel presentation of familial DICER1 syndrome.

Journal: European journal of pediatrics

Published: August 10, 2015

Autoimmune lymphoproliferative syndrome-like disease in patients with LRBA mutation.

Autoimmune lymphoproliferative syndrome-like disease in patients with LRBA mutation.

Journal: Clinical immunology (Orlando, Fla.)

Published: November 10, 2014

A novel homozygous Fas ligand mutation leads to early protein truncation, abrogation of death receptor and reverse signaling and a severe form of the autoimmune lymphoproliferative syndrome.

A novel homozygous Fas ligand mutation leads to early protein truncation, abrogation of death receptor and reverse signaling and a severe form of the autoimmune lymphoproliferative syndrome.

Journal: Clinical immunology (Orlando, Fla.)

Published: October 07, 2014

Deregulation of Fas ligand expression as a novel cause of autoimmune lymphoproliferative syndrome-like disease.

Deregulation of Fas ligand expression as a novel cause of autoimmune lymphoproliferative syndrome-like disease.

Journal: Haematologica

Published: July 30, 2014

RAG1 deficiency with a shifting B cell phenotype and chromosomal instability.

RAG1 deficiency with a shifting B cell phenotype and chromosomal instability.

Journal: Clinical immunology (Orlando, Fla.)

Published: February 06, 2014

COL2A1 mutation as a cause of premature osteoarthritis in a 13-year-old child.

COL2A1 mutation as a cause of premature osteoarthritis in a 13-year-old child.

Journal: Joint bone spine

Published: January 21, 2013

Showing 1-12 of 12

Last Updated: 09/26/2026