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Pediatric Blood & Cancer, ISSN 1545-5009, 11/2015, Volume 62, Issue 11, pp. 2047 - 2049
Journal Article
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2010, Volume 126, Issue 5, pp. 1000 - 1005
Background Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome is characterized by severe systemic autoimmunity caused by mutations... 
Allergy and Immunology | regulatory T cells | Hematopoietic cell transplantation | autoimmunity | immune reconstitution | immunodeficiency | nonmyeloablative conditioning regimen | immune dysregulation | Autoimmunity | Immune dysregulation | Immunodeficiency | Immune reconstitution | Nonmyeloablative conditioning regimen | Regulatory T cells | FOXP3 EXPRESSION | DIARRHEA | BONE-MARROW-TRANSPLANTATION | IPEX SYNDROME | IMMUNOLOGY | VERSUS-HOST-DISEASE | ALLERGY | T-CELLS | Graft vs Host Disease - therapy | Myeloablative Agonists - therapeutic use | Whole-Body Irradiation | Humans | Immunosuppressive Agents - therapeutic use | Infant | Male | Flow Cytometry | Hematopoietic Stem Cell Transplantation - adverse effects | Genetic Diseases, X-Linked - genetics | Transplantation Conditioning - methods | Child | Graft vs Host Disease - etiology | Genetic Diseases, X-Linked - physiopathology | Immunologic Deficiency Syndromes - therapy | Cell Separation | Vidarabine - analogs & derivatives | Vidarabine - therapeutic use | Forkhead Transcription Factors - genetics | Reverse Transcriptase Polymerase Chain Reaction | Syndrome | Graft vs Host Disease - pathology | Cyclosporine - therapeutic use | Mycophenolic Acid - analogs & derivatives | Mycophenolic Acid - therapeutic use | Immunologic Deficiency Syndromes - physiopathology | Adolescent | Immunologic Deficiency Syndromes - genetics | Hematopoietic Stem Cell Transplantation - methods | Genetic Diseases, X-Linked - therapy | Medical colleges | Granulocyte colony-stimulating factor | Oncology, Experimental | Transplantation | Research | Macrophage colony stimulating factor | Hematopoietic stem cells | Cancer | Bone marrow | Mutation | Transplants & implants | Mortality | Stem cells | Index Medicus | Abridged Index Medicus | Regulatory T-cells
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2013, Volume 133, Issue 2, pp. 335 - 347.e11
Journal Article
Biology of Blood and Marrow Transplantation, ISSN 1083-8791, 2017, Volume 23, Issue 10, pp. 1669 - 1677
Journal Article
Blood, ISSN 0006-4971, 02/2019, Volume 133, Issue 7, pp. 754 - 762
Despite improvements, mortality after allogeneic hematopoietic cell transplantation (HCT) for nonmalignant diseases remains a significant problem. We evaluated... 
MORTALITY | REDUCED-INTENSITY | SEVERE COMBINED IMMUNODEFICIENCY | MORBIDITY | VALIDATION | MARROW-TRANSPLANTATION | OUTCOMES | HEMATOLOGY | RISK-ASSESSMENT | BLOOD | AGE
Journal Article
Biology of Blood and Marrow Transplantation, ISSN 1083-8791, 2008, Volume 14, Issue 11, pp. 1279 - 1287
Journal Article
Haematologica, ISSN 0390-6078, 10/2018, Volume 103, Issue 11, pp. 1806 - 1814
A hallmark of Fanconi anemia is accelerated decline in hematopoietic stem and progenitor cells (CD34-) leading to bone marrow failure. Long-term treatment... 
PROGENITOR CELLS | CD34(+) CELLS | COLLECTION | ENGRAFTMENT | SAFETY | BONE-MARROW | SOMATIC MOSAICISM | HEMATOLOGY
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 10/2019, Volume 39, Issue 7, pp. 653 - 667
Journal Article
Journal Article
Biology of Blood and Marrow Transplantation, ISSN 1083-8791, 2014, Volume 20, Issue 12, pp. 1996 - 2003
Abstract Hematopoietic cell transplantation is an effective treatment for patients with nonmalignant diseases and for many is the only known cure. Conventional... 
Hematology, Oncology and Palliative Medicine | Conditioning regimen | Clinical results in inherited disorders | Reduced-intensity conditioning | Nonmalignant diseases | Allo-transplantation | BUSULFAN PHARMACOKINETICS | BONE-MARROW-TRANSPLANTATION | CHRONIC GRANULOMATOUS-DISEASE | IMMUNOLOGY | VERSUS-HOST-DISEASE | THALASSEMIA MAJOR | HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS | TRANSPLANTATION | POLYMERASE-CHAIN-REACTION | TERM-FOLLOW-UP | HEMATOLOGY | HEMATOLOGIC MALIGNANCIES | PRIMARY IMMUNODEFICIENCY | Busulfan - analogs & derivatives | Prospective Studies | Humans | Child, Preschool | Infant | Male | Antineoplastic Agents, Alkylating - administration & dosage | Antilymphocyte Serum - administration & dosage | Busulfan - administration & dosage | Anemia, Aplastic - therapy | Fanconi Anemia - mortality | Anemia, Aplastic - mortality | Adult | Female | Unrelated Donors | Child | Graft vs Host Disease - etiology | Immunosuppressive Agents - administration & dosage | Tacrolimus - administration & dosage | Hematopoietic Stem Cell Transplantation | Vidarabine - analogs & derivatives | Myeloablative Agonists | Adolescent | Graft vs Host Disease - prevention & control | Methotrexate - administration & dosage | Fanconi Anemia - therapy | Vidarabine - administration & dosage | Transplantation Conditioning | Medical colleges | Comorbidity | Mortality | Transplantation | Methotrexate | Health aspects | Hematopoietic stem cells
Journal Article