Andrea Honscheid
Overview
Explore the profile of Andrea Honscheid including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
287
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Recent Articles
1.
Schipp C, Schlutermann D, Honscheid A, Nabhani S, Holl J, Oommen P, et al.
Front Immunol
. 2018 Nov;
9:2400.
PMID: 30386345
Serine/threonine kinase 4 (STK4) deficiency is an autosomal recessive genetic condition that leads to primary immunodeficiency (PID) typically characterized by lymphopenia, recurrent infections and induced lymphoproliferation and -lymphoma. State-of-the-art treatment...
2.
Ghosh S, Honscheid A, Duckers G, Ginzel S, Gohlke H, Gombert M, et al.
Haematologica
. 2016 Dec;
102(2):e69-e72.
PMID: 27979922
No abstract available.
3.
Daschkey S, Bienemann K, Schuster V, Kreth H, Linka R, Honscheid A, et al.
J Clin Immunol
. 2016 Jul;
36(7):684-92.
PMID: 27473539
Hereditary defects in several genes have been shown to disturb the normal immune response to EBV and to give rise to severe EBV-induced lymphoproliferation in the recent years. Nevertheless, in...
4.
Schipp C, Nabhani S, Bienemann K, Simanovsky N, Kfir-Erenfeld S, Assayag-Asherie N, et al.
Haematologica
. 2016 Jul;
101(10):e392-e396.
PMID: 27365489
No abstract available.
5.
Bienemann K, Daschkey S, Sorensen J, Schwabe D, Klingebiel T, Honscheid A, et al.
Leuk Lymphoma
. 2016 Apr;
57(12):2949-2951.
PMID: 27123661
No abstract available.
6.
Kuhlen M, Honscheid A, Loizou L, Nabhani S, Fischer U, Stepensky P, et al.
Clin Immunol
. 2015 Nov;
162:27-30.
PMID: 26529633
PIK3R1 (phosphoinositide-3-kinase, regulatory subunit 1) gain-of-function has recently been described in patients with recurrent sinopulmonary infections, chronic CMV-/EBV-infections, lymphoproliferation, and hypogammaglobulinemia. Here we report a 15-year-old boy with treatment refractory...
7.
Kuhlen M, Honscheid A, Schemme J, Merz H, Mauz-Korholz C, Borkhardt A, et al.
Eur J Pediatr
. 2015 Nov;
175(4):593-7.
PMID: 26526666
Unlabelled: DICER1 germline mutations are associated with an inherited cancer syndrome, most commonly presenting with pleuropulmonary blastoma (PPB), ovarian sex cord tumors, thyroid cysts/goitre, and cystic nephroma. We describe the...
8.
Nabhani S, Ginzel S, Miskin H, Revel-Vilk S, Harlev D, Fleckenstein B, et al.
Haematologica
. 2015 Jun;
100(9):1189-98.
PMID: 26113417
Autoimmune lymphoproliferative syndrome is frequently caused by mutations in genes involved in the Fas death receptor pathway, but for 20-30% of patients the genetic defect is unknown. We observed that...
9.
Revel-Vilk S, Fischer U, Keller B, Nabhani S, Gamez-Diaz L, Rensing-Ehl A, et al.
Clin Immunol
. 2015 May;
159(1):84-92.
PMID: 25931386
Mutations in LPS-responsive and beige-like anchor (LRBA) gene were recently described in patients with combined immunodeficiency, enteropathy and autoimmune cytopenia. Here, we extend the clinical and immunological phenotypic spectrum of...
10.
Nabhani S, Honscheid A, Oommen P, Fleckenstein B, Schaper J, Kuhlen M, et al.
Clin Immunol
. 2014 Dec;
155(2):231-7.
PMID: 25451160
We report a novel type of mutation in the death ligand FasL that was associated with a severe phenotype of the autoimmune lymphoproliferative syndrome in two patients. A frameshift mutation...