Effects of Conditioning Regimens and T Cell Depletion in Hematopoietic Cell Transplantation for Primary Immune Deficiency-Reference-Cited by-同舟云学术

Effects of Conditioning Regimens and T Cell Depletion in Hematopoietic Cell Transplantation for Primary Immune Deficiency

Published:2012-12 Issue:12 Volume:18 Page:1911-1920
ISSN:1083-8791
Container-title:Biology of Blood and Marrow Transplantation
language:en
Short-container-title:Biology of Blood and Marrow Transplantation

Author:

Triplett Brandon M.,Wang Chong,Yang Jie,Dallas Mari,Hartford Christine,Howard Vanessa,Pillai Asha,Shook David,Srinivasan Ashok,Laver Joseph,Leung Wing

Funder

National Institutes of Health Cancer Center Support

State of Tennessee

Assisi Foundation of Memphis

American Lebanese Syrian Associated Charities

Publisher

Elsevier BV

Subject

Transplantation,Hematology

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4. Molecular defects in human severe combined immunodeficiency and approaches to immune reconstitution;Buckley;Annu Rev Immunol,2004

5. Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies: report of the European experience 1968-99;Antoine;Lancet,2003

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1. Considerations in Preparative Regimen Selection to Minimize Rejection in Pediatric Hematopoietic Transplantation in Non-Malignant Diseases;Frontiers in Immunology;2020-10-19

2. Successful Reduced Intensity Conditioning Alternate Donor Stem Cell Transplant for Wiskott-Aldrich Syndrome;Journal of Pediatric Hematology/Oncology;2017-11

3. Haploidentical bone marrow and stem cell transplantation: experience with post-transplantation cyclophosphamide;Seminars in Hematology;2016-04

4. Long-term outcomes of fludarabine, melphalan and antithymocyte globulin as reduced-intensity conditioning regimen for allogeneic hematopoietic stem cell transplantation in children with primary immunodeficiency disorders: a prospective single center study;Bone Marrow Transplantation;2015-11-23

5. Successful Haploidentical Donor Hematopoietic Stem Cell Transplant and Restoration of STAT3 Function in an Adolescent with Autosomal Dominant Hyper-IgE Syndrome;Journal of Clinical Immunology;2015-05-12