Does CVID exist in children? A genetic architecture and manifestation map derived from 7,525 patients
Antonios Gkantaras, ESID Registry Working Party, Dalia Abd Elaziz, Sohilla Lofty M. Abdelkader et autres
0 citationsJournal of Human Immunity
Andrea Hönscheid
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20Publications signalées
778Citations signalées
0Affiliations récentes
Domaines associés
Immunodeficiency and Autoimmune DisordersTrace Elements in HealthImmune Cell Function and InteractionChronic Lymphocytic Leukemia ResearchDNA Repair Mechanisms
Publications récentes
Inborn errors of immunity: Manifestation, treatment, and outcome—an ESID registry 1994–2024 report on 30,628 patients
Gerhard Kindle, Mickaël Alligon, Michael H. Albert, Matthew Buckland et autres
32 citationsJournal of Human Immunity
EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency
Cyrill Schipp, David Schlütermann, Andrea Hönscheid, Schafiq Nabhani et autres
55 citationsFrontiers in Immunology
Human RAD52 – a novel player in DNA repair in cancer and immunodeficiency
Sujal Ghosh, Andrea Hönscheid, Gregor Dückers, Sebastian Ginzel et autres
8 citationsHaematologica
Fatal Lymphoproliferative Disease in Two Siblings Lacking Functional FAAP24
Svenja Daschkey, K. Bienemann, Volker Schuster, Hans Wolfgang Kreth et autres
21 citationsJournal of Clinical Immunology
Specific antibody deficiency and autoinflammatory disease extend the clinical and immunological spectrum of heterozygous NFKB1 loss-of-function mutations in humans
Cyrill Schipp, Schafiq Nabhani, K. Bienemann, Natalia Simanovsky et autres
42 citationsHaematologica
A novel homozygous mutation in UNC13D presenting as Epstein–Barr-virus-associated lymphoproliferative disease at 9 years of age
K. Bienemann, Svenja Daschkey, Jan Sørensen, Dirk Schwabe et autres
2 citationsLeukemia & lymphoma/Leukemia and lymphoma
Hodgkin lymphoma as a novel presentation of familial DICER1 syndrome
Michaela Kuhlen, Andrea Hönscheid, Janina Schemme, Hartmut Merz et autres
17 citationsEuropean Journal of Pediatrics
De novo PIK3R1 gain-of-function with recurrent sinopulmonary infections, long-lasting chronic CMV-lymphadenitis and microcephaly
Michaela Kuhlen, Andrea Hönscheid, Loizos Loizou, Schafiq Nabhani et autres
38 citationsClinical Immunology
Deregulation of Fas ligand expression as a novel cause of autoimmune lymphoproliferative syndrome-like disease
Schafiq Nabhani, Sebastian Ginzel, Hagit Miskin, Shoshana Revel‐Vilk et autres
15 citationsHaematologica
Autoimmune lymphoproliferative syndrome-like disease in patients with LRBA mutation
Shoshana Revel‐Vilk, Ute Fischer, Bärbel Keller, Schafiq Nabhani et autres
96 citationsClinical Immunology
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
Schafiq Nabhani, Andrea Hönscheid, Prasad T. Oommen, Bernhard Fleckenstein et autres
26 citationsClinical Immunology
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