Phenotypic characterization and outcome of paediatric patients affected with haemophagocytic syndrome of unknown genetic cause-Reference-Cited by-同舟云学术

Phenotypic characterization and outcome of paediatric patients affected with haemophagocytic syndrome of unknown genetic cause

Published:2013-06-29 Issue:5 Volume:162 Page:713-717
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Giardino Giuliana¹,Veropalumbo Claudio¹,Ruggiero Giuseppina¹,Naddei Roberta¹,Rubino Valentina¹,Udhayachandran Annapoorani¹,Cirillo Emilia¹,Gallo Vera¹,Poggi Vincenzo²,De Fusco Carmela²,Pignata Claudio¹

Affiliation:

1. Department of Translational Medical Sciences; “Federico II” University; Naples; Italy

2. Paediatric Haematology and Oncology; Pausilipon Hospital; Naples; Italy

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.12421/fullpdf

Reference10 articles.

1. Atypical features of familial hemophagocytic lymphohistiocytosis;Busiello;Blood,2004

2. A91V perforin variation in healthy subjects and FHLH patients;Busiello;International Journal of Immunogenetics,2006

3. Jinx, an MCMV susceptibility phenotype caused by disruption of Unc13d: a mouse model of type 3 familial hemophagocytic lymphohistiocytosis;Crozat;Journal of Experimental Medicine,2007

4. Prognostic factors of hemophagocytic syndrome in adults: analysis of 34 cases;Kaito;European Journal of Haematology,1997

5. Keeping NK cells in highly regulated antiviral warfare;Lee;Trends in Immunology,2007

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2. Familial Hemophagocytic Lymphohistiocytosis secondary to UNC13D mutation: a report of two cases;BMC Pediatrics;2022-11-19

3. Two Brothers with Atypical UNC13D-Related Hemophagocytic Lymphohistiocytosis Characterized by Massive Lung and Brain Involvement;Frontiers in Immunology;2017-12-21