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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
Nature Communications, ISSN 2041-1723, 2014, Volume 5, Issue 1, p. 4746
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 09/2018, Volume 26, Issue 9, pp. 1282 - 1287
Recently, variants in DONSON have been reported to cause different disorders of the microcephalic primordial dwarfism spectrum. Using whole-exome sequencing,... 
PRIMORDIAL DWARFISM | GENETIC-VARIATION | GENOME REPLICATION | MICROMELIA | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | Dwarfism | Phenotypes | Microencephaly | Anemia | Limb malformations | Fanconi syndrome | Siblings
Journal Article
Cytometry Part B: Clinical Cytometry, ISSN 1552-4949, 05/2014, Volume 86, Issue 3, pp. 191 - 206
Background The heterogeneity of primary and secondary immunodeficiencies demands for the development of a comprehensive flow cytometric screening system, based... 
immunodeficiencies | reference values | lymphocytes | NK‐cell | T‐cell | flow cytometry | B‐cell | T-cell | B-cell | NK-cell | DIGEORGE-SYNDROME | RECENT THYMIC EMIGRANTS | SUBSETS | COMMON VARIABLE IMMUNODEFICIENCY | 22Q11.2 DELETION SYNDROME | PATHOLOGY | DEFICIENCY | HYPER-IGE SYNDROME | MEMORY | FLOW-CYTOMETRY | MEDICAL LABORATORY TECHNOLOGY | TH17 CELLS | Chemical properties | T cells | Analysis | Immunodeficiency
Journal Article
Blood, ISSN 0006-4971, 12/2016, Volume 128, Issue 22, pp. 420 - 420
Abstract INTRODUCTION: Cerebral sinovenous thrombosis (CSVT) is a serious disease, that leads to longterm neurological sequaelae in the majority of survivors.... 
Journal Article
Thrombosis and Haemostasis, ISSN 0340-6245, 02/2009, Volume 101, Issue 2, pp. 239 - 247
Journal Article
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 11/2011, Volume 26, Issue 11, pp. 1947 - 1956
Journal Article