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Biology of Blood and Marrow Transplantation, ISSN 1083-8791, 03/2019, Volume 25, Issue 3, pp. S312 - S313
Patients with primary immunodeficiencies (PIDs) are potentially cured by allogeneic hematopoietic cell transplantation (HCT). The spectrum of PIDs has expanded... 
Medicine, Experimental | Medical research | Transplantation | Hematopoietic stem cells
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 11/2008, Volume 178, Issue 10, pp. 1066 - 1074
Journal Article
Pediatrics, ISSN 0031-4005, 08/2004, Volume 114, Issue 2, pp. 462 - 468
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2008, Volume 122, Issue 6, pp. 1097 - 1103
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 10/2015, Volume 35, Issue 7, pp. 675 - 680
Journal Article
Journal Article
Journal Article
Journal of Cellular and Molecular Medicine, ISSN 1582-1838, 10/2011, Volume 15, Issue 10, pp. 2071 - 2081
WHIM is an acronym for a rare immunodeficiency syndrome (OMIM #193670) caused by autosomal dominant mutations truncating the C‐terminus of the chemokine... 
Human | Warts | Human papillomavirus | Plerixafor | Immunodeficiency | Genetics | Hypogammaglobulinemia | Neutropenia | Regulatory agencies | Bacterial infections | Menopause | Neutrophils | Amino acids | Leukocytes | Patients | CXCR4 protein | Studies | Signaling | Plasmids | Cell lines | Stem cells | Bone marrow | Ligands | Mutation | Chemokines | Deoxyribonucleic acid--DNA | Recombinant
Journal Article
Journal Article
Biology of Blood and Marrow Transplantation, ISSN 1083-8791, 03/2016, Volume 22, Issue 3, p. S327-S328
Journal Article
Blood, ISSN 0006-4971, 12/2015, Volume 126, Issue 23, pp. 5515 - 5515
Abstract Chronic Granulomatous Disease is an inherited immunodeficiency resulting from a defect in one of 5 proteins necessary for the production of NADPH... 
Journal Article
Blood, ISSN 0006-4971, 11/2013, Volume 122, Issue 21, pp. 2157 - 2157
Abstract Chronic Granulomatous Disease (CGD) results from a mutation in the NADPH oxidase complex. As a result, patients are prone to recurrent infections and... 
Journal Article
Respiratory Medicine, ISSN 0954-6111, 2005, Volume 99, Issue 9, pp. 1175 - 1182
Journal Article
Gastroenterology, ISSN 0016-5085, 2008, Volume 134, Issue 7, pp. 1917 - 1926
Background & Aims: Chronic granulomatous disease (CGD) is a rare genetic disorder, predisposing affected individuals to recurrent infectious complications and... 
Gastroenterology and Hepatology | INFECTIONS | NODULAR REGENERATIVE HYPERPLASIA | HYPERDYNAMIC CIRCULATION | INTERFERON-GAMMA | POLYCYSTIC KIDNEY-DISEASE | CIRRHOSIS | ESCHERICHIA-COLI | LIVER | GASTROENTEROLOGY & HEPATOLOGY | BACTERIAL TRANSLOCATION | ESOPHAGEAL-VARICES | Granulomatous Disease, Chronic - mortality | Hypertension, Portal - physiopathology | Prospective Studies | Humans | Middle Aged | Child, Preschool | Male | Granulomatous Disease, Chronic - complications | Granulomatous Disease, Chronic - physiopathology | Microcirculation - physiopathology | Hypertension, Portal - mortality | Hypertension, Portal - etiology | Time Factors | Liver Diseases - etiology | Adult | Female | Retrospective Studies | Odds Ratio | Child | Liver Diseases - blood | Risk Assessment | Risk Factors | Proportional Hazards Models | Granulomatous Disease, Chronic - blood | Liver - blood supply | Platelet Count | Adolescent | Liver Diseases - mortality | Hypertension, Portal - blood | Liver Diseases - physiopathology | Medical research | Chronic granulomatous disease | Phosphatases | Prognosis | Analysis | Mortality | Portal hypertension | Medicine, Experimental | Health aspects | non-cirrhotic portal hypertension | chronic granulomatous disease (CGD) | platelet slope | nodular regenerative hyperplasia (NRH) | thrombocytopenia | venopathy | hepatic venous pressure gradient (HVPG) | mortality
Journal Article