Co-Occurrence of Familial Hemophagocytic Lymphohistiocytosis Type 2 and Chronic Active Epstein-Barr Virus in Adulthood
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference35 articles.
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2. Late-onset cases of familial hemophagocytic lymphohistiocytosis with missenseperforin gene mutations;Ueda;Am J Hematol,2007
3. Hypomorphic mutations in PRF1, MUNC13-4, and STXBP2 are associated with adult-onset familial HLH;Zhang;Blood,2011
4. Previously undiagnosed fatal familial haemophagocytic lymphohistiocytosis in a 24-year-old woman;Barmettler;BMJ Case Rep,2016
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1. Case report: Ruxolitinib plus dexamethasone as first-line therapy in haemophagocytic lymphohistiocytosis;Frontiers in Oncology;2023-03-02
2. Misdiagnosis of adult primary hemophagocytic lymphohistiocytosis as NK/T‐cell lymphoma: A case report;eJHaem;2022-10-06
3. RF1 Gene Mutation in Familial Hemophagocytic Lymphohistiocytosis 2: A Family Report and Literature Review;Pharmacogenomics and Personalized Medicine;2021-12
4. Multiple-Organ Involvement in Familial Hemophagocytic Lymphohistiocytosis Type 2 Shown on FDG PET/CT;Clinical Nuclear Medicine;2021-05-25
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