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Paul La Rosee et al.
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Genetic predisposition to hemophagocytic lymphohistiocytosis: Report on 500 patients from the Italian registry
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Treosulfan-Based Conditioning and Hematopoietic Cell Transplantation for Nonmalignant Diseases: A Prospective Multicenter Trial
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Treosulfan-based conditioning regimen for children and adolescents with hemophagocytic lymphohistiocytosis
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Reduced-intensity conditioning and HLA-matched haemopoietic stem-cell transplantation in patients with chronic granulomatous disease: a prospective multicentre study
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LANCET (2014)
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Rebecca A. Marsh et al.
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION (2013)
Increased complications and morbidity in children with hemophagocytic lymphohistiocytosis undergoing hematopoietic stem cell transplantation
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Feasibility of reduced-intensity conditioning followed by unrelated cord blood transplantation for primary hemophagocytic lymphohistiocytosis: a nationwide retrospective analysis in Japan
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Risk factors for early death in children with haemophagocytic lymphohistiocytosis
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A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes
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BLOOD (2012)
CNS involvement at the onset of primary hemophagocytic lymphohistiocytosis
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Hyperferritinemia in the critically ill child with secondary hemophagocytic lymphohistiocytosis/sepsis/multiple organ dysfunction syndrome/macrophage activation syndrome: what is the treatment?
Demet Demirkol et al.
CRITICAL CARE (2012)
Chemoimmunotherapy for hemophagocytic lymphohistiocytosis: long-term results of the HLH-94 treatment protocol
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Excellent outcome of allogeneic hematopoietic SCT with reduced-intensity conditioning for the treatment of chronic active EBV infection
K. Kawa et al.
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Reduced-intensity conditioning significantly improves survival of patients with hemophagocytic lymphohistiocytosis undergoing allogeneic hematopoietic cell transplantation
Rebecca A. Marsh et al.
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Using flow cytometry to screen patients for X-linked lymphoproliferative disease due to SAP deficiency and XIAP deficiency
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Molecular mechanisms of biogenesis and exocytosis of cytotoxic granules
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Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL-5) Is Caused by Mutations in Munc18-2 and Impaired Binding to Syntaxin 11
Udo zur Stadt et al.
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Patients with early relapse of primary hemophagocytic syndromes or with persistent CNS involvement may benefit from immediate hematopoietic stem cell transplantation
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BONE MARROW TRANSPLANTATION (2009)
Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells
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The use of reduced-intensity stem cell transplantation in haemophagocytic lymphohistiocytosis and Langerhans cell histiocytosis
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Unrelated donor hematopoietic cell transplantation for hemophagocytic lymphohistiocytosis
K. S. Baker et al.
BONE MARROW TRANSPLANTATION (2008)
Frequency and spectrum of central nervous system involvement in 193 children with haemophagocytic lymphohistiocytosis
AnnaCarin Horne et al.
BRITISH JOURNAL OF HAEMATOLOGY (2008)
Highly elevated ferritin levels and the diagnosis of hemophagocytic lymphohistiocytosis
Carl E. Allen et al.
PEDIATRIC BLOOD & CANCER (2008)
Familial and acquired hemophagocytic lymphohistiocytosis
Gritta E. Janka
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HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis
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PEDIATRIC BLOOD & CANCER (2007)
Analysis of natural killer-cell function in familial hemophagocytic lymphohistiocytosis (FHL):: defective CD107a surface expression heralds Munc13-4 defect and discriminates between genetic subtypes of the disease
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BLOOD (2006)
Hematopoietic stem cell transplantation in hemophagocytic lymphohistiocytosis:: A single-center report of 48 patients
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Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11
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HUMAN MOLECULAR GENETICS (2005)
Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3)
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CELL (2003)
Treatment of hemophagocytic lymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation
JI Henter et al.
BLOOD (2002)