Langerhans cell histiocytosis, a new clinical phenotype of x-linked lymphoproliferative disease?
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference13 articles.
1. Factors involved in the generation of memory CD8+T cells in patients with X-linked lymphoproliferative disease (XLP);Belmonte;Clin. Exp. Immunol.,2007
2. Successful treatment of acute Epstein-Barr virus infection associated with X-linked lymphoproliferative disorder with rituximab;Bond;Pediatr. Blood Cancer,2007
3. Current therapy for Langerhans cell histiocytosis;Broadbent;Hematol. Oncol. Clin. North. Am.,1998
4. Macrophage activation and hemophagocytic syndrome in langerhans cell histiocytosis: report of 30 cases;Favara;Pediatr. Dev. Pathol.,2002
5. Improved outcome in multisystem Langerhans cell histiocytosis is associated with therapy intensification;Gadner;Blood,2008
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1. Hemophagocytic Lymphohistiocytosis in Langerhans Cell Histiocytosis: A Case Series and Literature Review;Journal of Pediatric Hematology/Oncology;2021-06-16
2. Langerhans cell histiocytosis complicated with hemophagocytic lymphohistiocytosis in a boy with a novel XIAP mutation;Medicine;2018-11
3. Langerhans cell histiocytosis in IPEX syndrome: Possible role for natural regulatory T cells?;Pediatric Allergy and Immunology;2014-03
4. Genetic factors in the development and course of pulmonary diseases;Medicinska istrazivanja;2014
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