Clinical features, genetics, and outcome of pediatric patients with hemophagocytic lymphohistiocytosis in Korea: report of a nationwide survey from Korea Histiocytosis Working Party
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Title
Clinical features, genetics, and outcome of pediatric patients with hemophagocytic lymphohistiocytosis in Korea: report of a nationwide survey from Korea Histiocytosis Working Party
Authors
Keywords
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Journal
EUROPEAN JOURNAL OF HAEMATOLOGY
Volume 94, Issue 1, Pages 51-59
Publisher
Wiley
Online
2014-06-17
DOI
10.1111/ejh.12399
References
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Related references
Note: Only part of the references are listed.- Hemophagocytic Lymphohistiocytosis
- (2013) Flavia G. N. Rosado et al. AMERICAN JOURNAL OF CLINICAL PATHOLOGY
- Advances in understanding the pathogenesis of HLH
- (2013) G. Naheed Usmani et al. BRITISH JOURNAL OF HAEMATOLOGY
- X-linked lymphoproliferative syndromes and related autosomal recessive disorders
- (2013) André Veillette et al. Current Opinion in Allergy and Clinical Immunology
- Fludarabine-based reduced-intensity conditioning regimen for hematopoietic stem cell transplantation in primary hemophagocytic lymphohistiocytosis
- (2013) Amir Ali Hamidieh et al. EUROPEAN JOURNAL OF HAEMATOLOGY
- Familial Hemophagocytic Lymphohistiocytosis Type 3 Diagnosed at School Age
- (2013) Emma C. Manno et al. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
- Hemophagocytic Lymphohistiocytosis: Advances in Pathophysiology, Diagnosis, and Treatment
- (2013) Shanmuganathan Chandrakasan et al. JOURNAL OF PEDIATRICS
- Founder effects in two predominant intronic mutations of UNC13D, c.118-308C>T and c.754-1G>C underlie the unusual predominance of type 3 familial hemophagocytic lymphohistiocytosis (FHL3) in Korea
- (2012) Ja Young Seo et al. ANNALS OF HEMATOLOGY
- Diagnostic evaluation of patients with suspected haemophagocytic lymphohistiocytosis
- (2012) Kai Lehmberg et al. BRITISH JOURNAL OF HAEMATOLOGY
- Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3
- (2011) E. Sieni et al. JOURNAL OF MEDICAL GENETICS
- Screening the PRF1, UNC13D, STX11, SH2D1A, XIAP, and ITK gene mutations in Chinese children with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis
- (2011) Huang Zhizhuo et al. PEDIATRIC BLOOD & CANCER
- Reduced-intensity conditioning significantly improves survival of patients with hemophagocytic lymphohistiocytosis undergoing allogeneic hematopoietic cell transplantation
- (2010) R. A. Marsh et al. BLOOD
- Hemophagocytic syndrome in elderly patients with underlying autoimmune diseases
- (2009) Rie Tabata et al. CLINICAL RHEUMATOLOGY
- UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis
- (2009) H. S. Yoon et al. HAEMATOLOGICA
- Experience With Hemophagocytic Lymphohistiocytosis/Macrophage Activation Syndrome at a Single Institution
- (2009) Abha A. Gupta et al. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
- Hemophagocytic lymphohistiocytosis in Texas: Observations on ethnicity and race
- (2009) J. Allyson Niece et al. PEDIATRIC BLOOD & CANCER
- Frequency and spectrum of central nervous system involvement in 193 children with haemophagocytic lymphohistiocytosis
- (2008) AnnaCarin Horne et al. BRITISH JOURNAL OF HAEMATOLOGY
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