Clinical and molecular aspects of Turkish familial hemophagocytic lymphohistiocytosis patients with perforin mutations
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Oncology,Hematology
Reference24 articles.
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2. Modern management of children with haemophagocytic Iymphohistiocytosis;Janka;Br J Haematol,2004
3. Histiocyte society. Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis;Horne;Br J Haematol,2005
4. Linkage of familial hemophagocytic Iymphohistiocytosis to 10q21-22 and evidence for heterogeneity;Dufourcq-Lagelouse;Am J Hum Genet,1999
5. Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3);Feldmann;Cell,2003
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1. Genetic background of primary and familial HLH in Qatar: registry data and population study;Frontiers in Pediatrics;2024-05-09
2. Hemophagocytic lymphohistiocytosis with a hemizygous PRF1 c.674G>A mutation;The American Journal of the Medical Sciences;2023-11
3. Hemophagocytic Lymphohistiocytosis;Balkan Medical Journal;2022-09-09
4. Unusual Prominent Pulmonary Involvement in a Homozygous PRF1 Gene Variant in a Female Patient;Journal of Clinical Immunology;2020-09-28
5. Type 2 familial hemophagocytic lymphohistiocytosis in half brothers;Medicine;2018-07
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