Allogeneic hematopoietic cell transplantation for XIAP deficiency: an international survey reveals poor outcomes
Published 2012 View Full Article
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Title
Allogeneic hematopoietic cell transplantation for XIAP deficiency: an international survey reveals poor outcomes
Authors
Keywords
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Journal
BLOOD
Volume 121, Issue 6, Pages 877-883
Publisher
American Society of Hematology
Online
2012-11-07
DOI
10.1182/blood-2012-06-432500
References
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Related references
Note: Only part of the references are listed.- Clinical and Genetic Characteristics of XIAP Deficiency in Japan
- (2012) Xi Yang et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Clinical features and outcome of X-linked lymphoproliferative syndrome type 1 (SAP deficiency) in Japan identified by the combination of flow cytometric assay and genetic analysis
- (2012) Hirokazu Kanegane et al. PEDIATRIC ALLERGY AND IMMUNOLOGY
- Reduced-intensity conditioning significantly improves survival of patients with hemophagocytic lymphohistiocytosis undergoing allogeneic hematopoietic cell transplantation
- (2010) R. A. Marsh et al. BLOOD
- Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)
- (2010) J. P. Schmid et al. BLOOD
- XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease
- (2010) R. A. Marsh et al. BLOOD
- X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease
- (2010) C. Booth et al. BLOOD
- The impact of HLA genotyping on survival following unrelated donor haematopoietic stem cell transplantation
- (2010) Bronwen E. Shaw et al. BRITISH JOURNAL OF HAEMATOLOGY
- Making a definitive diagnosis: Successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease
- (2010) Elizabeth A Worthey et al. GENETICS IN MEDICINE
- The outcome of hematopoietic stem cell transplantation in Korean children with hemophagocytic lymphohistiocytosis
- (2010) Hoi Soo Yoon et al. PEDIATRIC TRANSPLANTATION
- Defining the Intensity of Conditioning Regimens: Working Definitions
- (2009) Andrea Bacigalupo et al. BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
- Phenotypic differences between mice deficient in XIAP and SAP, two factors targeted in X-linked lymphoproliferative syndrome (XLP)
- (2009) Julie M. Rumble et al. CELLULAR IMMUNOLOGY
- A rapid flow cytometric screening test for X-linked lymphoproliferative disease due to XIAP deficiency
- (2009) Rebecca A. Marsh et al. CYTOMETRY PART B-CLINICAL CYTOMETRY
- Phase I/II Trial of AEG35156 X-Linked Inhibitor of Apoptosis Protein Antisense Oligonucleotide Combined With Idarubicin and Cytarabine in Patients With Relapsed or Primary Refractory Acute Myeloid Leukemia
- (2009) Aaron D. Schimmer et al. JOURNAL OF CLINICAL ONCOLOGY
- XIAP discriminates between type I and type II FAS-induced apoptosis
- (2009) Philipp J. Jost et al. NATURE
- Diagnosis and manifestations of chronic graft-versus-host disease
- (2008) Alexandra H. Filipovich BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
- Small molecule XIAP inhibitors cooperate with TRAIL to induce apoptosis in childhood acute leukemia cells and overcome Bcl-2-mediated resistance
- (2008) M. Fakler et al. BLOOD
- The use of reduced-intensity stem cell transplantation in haemophagocytic lymphohistiocytosis and Langerhans cell histiocytosis
- (2008) N Cooper et al. BONE MARROW TRANSPLANTATION
- Unrelated donor hematopoietic cell transplantation for hemophagocytic lymphohistiocytosis
- (2008) K S Baker et al. BONE MARROW TRANSPLANTATION
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