FATAL SIBLING CASES OF FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS (FHL) WITH MUNC13–4 MUTATIONS: Case Reports-Reference-Cited by-同舟云学术

FATAL SIBLING CASES OF FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS (FHL) WITH MUNC13–4 MUTATIONS: Case Reports

Published:2008-01 Issue:3 Volume:25 Page:171-180
ISSN:0888-0018
Container-title:Pediatric Hematology and Oncology
language:en
Short-container-title:Pediatric Hematology and Oncology

Author:

Nakao Tomohei,Shimizu Takashi,Fukushima Takashi,Saito Makoto,Okamoto Miho,Sugiura Masatoshi,Yamamoto Ken,Ueda Ikuyo,Imashuku Shinsaku,Kobayashi Chie,Koike Kazutoshi,Tsuchida Masahiro,Sumazaki Ryo,Matsui Akira

Publisher

Informa UK Limited

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.1080/08880010801938082

Reference37 articles.

1. Modern management of children with haemophagocytic lymphohistiocytosis

2. Correlation between phenotypic heterogeneity and gene mutational characteristics in familial hemophagocytic lymphohistiocytosis (FHL)

3. Treatment of hemophagocytic lymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation

4. Hemophagocytic Syndrome Presenting as Acute Hepatic Failure in Two Infants: Clinical Overlap with Neonatal Hemochromatosis

5. Low natural killer activity and central nervous system disease as a high-risk prognostic indicator in young patients with hemophagocytic lymphohistiocytosis

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1. Neonatal hemophagocytic lymphohistiocytosis: A meta‐analysis of 205 cases;Pediatric Blood & Cancer;2024-01-31

2. A case of fetal‐onset type 3 familial hemophagocytic lymphohistiocytosis surviving without severe complications after early diagnosis and treatment;Pediatric Blood & Cancer;2021-03-26

3. Hemophagocytic lymphohistiocytosis mimicking neonatal hemochromatosis;Pediatric Hematology and Oncology;2019-08-19

4. First characterization of platelet secretion defect in patients with familial hemophagocytic lymphohistiocytosis type 3 (FHL-3);Blood;2015-01-08

5. Association of Nonimmune Hydrops Fetalis With Familial Hemophagocytic Lymphohistiocytosis in Identical Twin Neonates With Perforin His222Arg (c665A>G) Mutation;Journal of Pediatric Hematology/Oncology;2013-11