相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Reduced-intensity conditioning significantly improves survival of patients with hemophagocytic lymphohistiocytosis undergoing allogeneic hematopoietic cell transplantation
Rebecca A. Marsh et al.
BLOOD (2010)
Molecular mechanisms of biogenesis and exocytosis of cytotoxic granules
Genevieve de Saint Basile et al.
NATURE REVIEWS IMMUNOLOGY (2010)
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.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells
Marjorie Cote et al.
JOURNAL OF CLINICAL INVESTIGATION (2009)
Treatment of the X-Linked Lymphoproliferative, Griscelli and Chediak-Higashi Syndromes by HLH Directed Therapy
Helena Trottestam et al.
PEDIATRIC BLOOD & CANCER (2009)
Hematopoietic cell transplantation for hemophagocytic lymphohistiocytosis: a journey of a thousand miles begins with a single (big) step
M. B. Jordan 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)
Defective cytotoxic lymphocyte degranulation in syntaxin-11-deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients
Yenan T. Bryceson et al.
BLOOD (2007)
Immunotherapy of familial Hemophagocytic Lymphohistiocytosis with Antithymocyte globulins:: A single-center retrospective report of 38 patients
Nizar Mahlaoui et al.
PEDIATRICS (2007)
Familial and acquired hemophagocytic lymphohistiocytosis
Gritta E. Janka
EUROPEAN JOURNAL OF PEDIATRICS (2007)
HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis
Jan-Inge Henter et al.
PEDIATRIC BLOOD & CANCER (2007)
Late-onset cases of familial hemophagocytic lymphohistiocytosis with missense perforin gene mutations
Ikuyo Ueda et al.
AMERICAN JOURNAL OF HEMATOLOGY (2007)
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
Stephaine Rigaud et al.
NATURE (2006)
Stem cell transplantation with reduced-intensity conditioning for hemophagocytic lymphohistiocytosis
N Cooper et al.
BLOOD (2006)
Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis
A Horne et al.
BRITISH JOURNAL OF HAEMATOLOGY (2005)
Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11
U zur Stadt et al.
HUMAN MOLECULAR GENETICS (2005)
Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3)
J Feldmann et al.
CELL (2003)
Clinical features and treatment strategies of Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis
S Imashuku
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY (2002)
Treatment of hemophagocytic lymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation
JI Henter et al.
BLOOD (2002)
Adult onset and atypical presentation of hemophagocytic lymphohistiocytosis in siblings carrying PRF1 mutations
R Clementi et al.
BLOOD (2002)
Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome
G Ménasché et al.
NATURE GENETICS (2000)
分享论文
