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Lancet, The, ISSN 0140-6736, 2014, Volume 383, Issue 9915, pp. 436 - 448
Summary Background In chronic granulomatous disease allogeneic haemopoietic stem-cell transplantation (HSCT) in adolescents and young adults and patients with... 
Internal Medicine | NADPH OXIDASE | MEDICINE, GENERAL & INTERNAL | EXCELLENT SURVIVAL | IN-VITRO | UNRELATED DONOR | BONE-MARROW-TRANSPLANTATION | EUROPEAN EXPERIENCE | INTRAVENOUS BUSULFAN | RECONSTITUTION | NONMALIGNANT DISEASES | CHILDREN | Transplantation Chimera - physiology | Prospective Studies | Humans | Child, Preschool | Infant | Treatment Outcome | Granulomatous Disease, Chronic - therapy | Vidarabine - analogs & derivatives | Alemtuzumab | Antilymphocyte Serum - administration & dosage | Busulfan - administration & dosage | Young Adult | Antibodies, Monoclonal, Humanized - administration & dosage | Adolescent | Adult | Graft vs Host Disease - prevention & control | Vidarabine - administration & dosage | HLA Antigens | Hematopoietic Stem Cell Transplantation - methods | Transplantation Conditioning - methods | Drug Therapy, Combination | Graft Survival - drug effects | Child | Immunosuppressive Agents - administration & dosage | Granuloma | Care and treatment | Histocompatibility antigens | Patient outcomes | HLA histocompatibility antigens | Stem cells | Transplantation | Identification and classification | Bone marrow | Teenagers | Transplants & implants | Mortality | Pediatrics | Immunologi inom det medicinska området | Pediatrik | hematopoietisk stamcellstransplantation | chronic granulomatous disease | Immunology in the medical area
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2013, Volume 133, Issue 2, pp. 335 - 347.e11
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 10/2014, Volume 371, Issue 15, pp. 1407 - 1417
Journal Article
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 09/2008, Volume 118, Issue 9, pp. 3143 - 3150
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 10/2017, Volume 377, Issue 17, pp. 1630 - 1638
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2010, Volume 126, Issue 3, pp. 602 - 610.e11
Journal Article
by Slack, James and Albert, Michael H and Balashov, Dmitry and Belohradsky, Bernd H and Bertaina, Alice and Bleesing, Jack and Booth, Claire and Buechner, Jochen and Buckley, Rebecca H and Ouachée-Chardin, Marie and Deripapa, Elena and Drabko, Katarzyna and Eapen, Mary and Feuchtinger, Tobias and Finocchi, Andrea and Gaspar, H. Bobby and Ghosh, Sujal and Gillio, Alfred and Gonzalez-Granado, Luis I and Grunebaum, Eyal and Güngör, Tayfun and Heilmann, Carsten and Helminen, Merja and Higuchi, Kohei and Imai, Kohsuke and Kalwak, Krzysztof and Kanazawa, Nubuo and Karasu, Gülsün and Kucuk, Zeynep Y and Laberko, Alexandra and Lange, Andrzej and Mahlaoui, Nizar and Meisel, Roland and Moshous, D and Muramatsu, Hideki and Parikh, Suhag and Pasic, Srdjan and Schmid, Irene and Schuetz, Catharina and Schulz, Ansgar and Schultz, Kirk R and Shaw, Peter J and Slatter, Mary A and Sykora, Karl-Walter and Tamura, Shinobu and Taskinen, Mervi and Wawer, Angela and Wolska-Kuśnierz, Beata and Cowan, Morton J and Fischer, Alain and Gennery, Andrew R and Center for International Blood and Marrow Transplant Research and Inborn Errors Working Party of the European Society for Blood and Marrow Transplantation and the European Society for Immunodeficiencies and Primary Immunodeficiency Treatment Consortium and Stem Cell Transplant for Immunodeficiencies in Europe (SCETIDE) and Ctr Int Blood Marrow and European Soc Blood Marrow and Primary Immunodeficiency Treatment and European Soc Immunodeficiencies and Stem Cell Transplant
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 01/2018, Volume 141, Issue 1, pp. 322 - 328.e10
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2014, Volume 135, Issue 4, pp. 988 - 997.e6
Background Common variable immunodeficiency (CVID) is usually well controlled with immunoglobulin substitution and immunomodulatory drugs. A subgroup of... 
Allergy and Immunology | Common variable immunodeficiency | immunologic reconstitution | survival | hematopoietic stem cell transplantation | immunoglobulin substitution/replacement | mortality | hypogammaglobulinemia | outcome | BONE-MARROW-TRANSPLANTATION | ACUTE GVHD | DISORDERS | CLASSIFICATION | SEVERE APLASTIC-ANEMIA | EUROPEAN GROUP | VERSUS-HOST-DISEASE | WORKING PARTY | Journal Article | B-CELL | Research Support, Non-U.S. Gov't | Multicenter Study | BLOOD | ABNORMALITIES | BONE-MARROW | IMMUNOLOGY | ALLERGY | Follow-Up Studies | Humans | Middle Aged | Graft Survival | Male | Treatment Outcome | Common Variable Immunodeficiency - complications | Cause of Death | Young Adult | Common Variable Immunodeficiency - mortality | Common Variable Immunodeficiency - therapy | Adolescent | Hematopoietic Stem Cell Transplantation - adverse effects | Adult | Female | Graft vs Host Disease - prevention & control | Retrospective Studies | Transplantation Conditioning | Child | Graft vs Host Disease - etiology | Hematopoietic Stem Cells | Complications and side effects | Hospitals | Mortality | Stem cells | Immunological deficiency syndromes | Transplantation | Hematopoietic stem cells | Cytomegalovirus | Life expectancy | Transplants & implants | Lung diseases | Liver | Values | Infections | Patients | Variables | Cell growth | Software | Lymphomas | Age
Journal Article