Treosulfan-based conditioning in DOCK8 deficiency: Complete lympho-hematopoietic reconstitution with minimal toxicity
Author:
Publisher
Elsevier BV
Subject
Immunology,Immunology and Allergy
Reference11 articles.
1. Combined immunodeficiency associated with DOCK8 mutations;Zhang;N. Engl. J. Med.,2009
2. Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome;Engelhardt;J. Allergy Clin. Immunol.,2009
3. Successful allogeneic hematopoietic stem cell transplantation for DOCK8 deficiency;Barlogis;The Journal of allergy and clinical immunology,2011
4. Successful long-term correction of autosomal recessive hyper-IgE syndrome due to DOCK8 deficiency by hematopoietic stem cell transplantation;Bittner;Klinische Padiatrie.,2010
5. Curative treatment of autosomal-recessive hyper-IgE syndrome by hematopoietic cell transplantation;Gatz;Bone marrow transplantation.,2010
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1. Hematopoietic stem cell transplantation in an infant with dedicator of cytokinesis 8 (DOCK8) deficiency associated with systemic lupus erythematosus;Medicine;2021-04-02
2. Hematopoietic Stem Cell Transplantation in Primary Immunodeficiency Diseases: Current Status and Future Perspectives;Frontiers in Pediatrics;2019-08-08
3. Skewed B cell receptor repertoire and reduced antibody avidity in patients with DOCK8 deficiency;Scandinavian Journal of Immunology;2019-03-18
4. Hematopoietic cell transplantation in primary immunodeficiency – conventional and emerging indications;Expert Review of Clinical Immunology;2018-01-16
5. Hematopoietic stem cell transplantation in children with Griscelli syndrome: A single-center experience;Pediatric Transplantation;2017-08-23
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