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Biology of Blood and Marrow Transplantation, ISSN 1083-8791, 2012, Volume 18, Issue 9, pp. 1368 - 1377
Journal Article
Journal Article
European Journal of Pediatrics, ISSN 0340-6199, 12/2008, Volume 167, Issue 12, pp. 1389 - 1394
In this paper, we examined the details of severe infections, treatment efficacies, and the prognoses of 23 Japanese patients with chronic granulomatous disease... 
Pediatrics | Interferon-gamma | Medicine & Public Health | Antifungal prophylaxis | Severe infection | Survival rate | Colitis | Hematopoietic stem cell transplantation | PROPHYLAXIS | BONE-MARROW TRANSPLANTATION | GASTRIC OUTLET OBSTRUCTION | PEDIATRICS | INFECTION | CHILDHOOD | Granulomatous Disease, Chronic - mortality | Japan - epidemiology | Prognosis | Follow-Up Studies | Thinness - etiology | Humans | Granulomatous Disease, Chronic - genetics | Child, Preschool | Genetic Diseases, X-Linked - complications | Growth Disorders - etiology | Hospitals, Pediatric | Male | Opportunistic Infections - mortality | Granulomatous Disease, Chronic - complications | Opportunistic Infections - prevention & control | Opportunistic Infections - etiology | Stem Cell Transplantation | NADPH Oxidases - deficiency | Aspergillosis - etiology | Aspergillosis - mortality | Adult | Female | Drug Therapy, Combination | Child | Aspergillosis - complications | Biomarkers - metabolism | Trimethoprim, Sulfamethoxazole Drug Combination - administration & dosage | Granulomatous Disease, Chronic - therapy | Antiviral Agents - administration & dosage | NADPH Oxidase 2 | Hospitals, State | Opportunistic Infections - microbiology | Anti-Infective Agents - administration & dosage | Interferon-gamma - administration & dosage | Phosphoproteins - deficiency | Adolescent | Survival Analysis | Body Height | Granulomatous Disease, Chronic - enzymology | Antifungal Agents - administration & dosage | Membrane Glycoproteins - deficiency | Pneumonia | Chronic granulomatous disease | Transplantation | Bacterial pneumonia | Hematopoietic stem cells
Journal Article
Biology of Blood and Marrow Transplantation, ISSN 1083-8791, 03/2013, Volume 19, Issue 3, pp. 338 - 343
Journal Article
Immunologic Research, ISSN 0257-277X, 7/2009, Volume 44, Issue 1, pp. 35 - 41
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 6/2011, Volume 31, Issue 3, pp. 332 - 337
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 5/2006, Volume 26, Issue 3, pp. 291 - 296
Abstract CGD is a rare phagocytic disorder manifesting as recurrent, severe bacterial and fungal infections. We describe an Iranian family with eight children,... 
CGD | familial | pattern of inheritance | outcome | Pattern of inheritance | Familial | Outcome | GASTRIC OUTLET OBSTRUCTION | ADULTS | IMMUNOLOGY | Granulomatous Disease, Chronic - mortality | Lung - pathology | Humans | Middle Aged | Granulomatous Disease, Chronic - genetics | Male | Pedigree | Adolescent | Fatal Outcome | Adult | Female | Child | Granulomatous Disease, Chronic - pathology
Journal Article
Journal of Medical Mycology, ISSN 1156-5233, 03/2012, Volume 22, Issue 1, pp. 52 - 57
Objectives: Fungal infection presents a serious risk to individuals with compromised immune systems. Chronic granulomatous disease is a primary... 
Pathogens | Chronic granulomatous disease | Recurrent infection | Lung | Mortality | Immunodeficiency | X chromosome | Chronic infection | Granulomatosis | Data processing | Heredity | Leukocytes (neutrophilic) | Risk factors | Fungi | Osteomyelitis | Lymphadenopathy | fusariosis | Biopsy | Skin | medical records | Age | Immune system
Journal Article
Current Allergy and Asthma Reports, ISSN 1529-7322, 11/2006, Volume 6, Issue 6, pp. 468 - 474
Primary immunodeficiency disorders (PIDs) continue to illuminate mechanisms of human immunity and hypersensitivity. New discoveries in common variable... 
Allergology | Infectious Diseases | Otorhinolaryngology | Pneumology/Respiratory System | Medicine & Public Health | X-LINKED SYNDROME | INHERITED DISORDERS | DISEASES | ALLERGY | REGULATORY T-CELLS | COMMON VARIABLE IMMUNODEFICIENCY | GENE-THERAPY | IGA DEFICIENCY | FOXP3 GENE | IMMUNOLOGY | SUBCUTANEOUS IMMUNOGLOBULIN REPLACEMENT | NF-KAPPA-B | Forkhead Transcription Factors - immunology | Common Variable Immunodeficiency - immunology | Granulomatous Disease, Chronic - mortality | Humans | Granulomatous Disease, Chronic - genetics | Immunity, Innate - genetics | Severe Combined Immunodeficiency - mortality | Child, Preschool | Interleukin-1 Receptor-Associated Kinases - deficiency | Male | Granulomatous Disease, Chronic - immunology | T-Lymphocytes, Regulatory - immunology | Female | Child | Antibody Formation - immunology | Genetic Therapy - mortality | Severe Combined Immunodeficiency - therapy | Common Variable Immunodeficiency - genetics | Granulomatous Disease, Chronic - therapy | Severe Combined Immunodeficiency - immunology | Forkhead Transcription Factors - genetics | Immunity, Innate - immunology | Severe Combined Immunodeficiency - genetics | Autoantibodies - immunology | Common Variable Immunodeficiency - therapy | Autoantibodies - genetics | Antibody Formation - genetics | Genetic Therapy - methods | Gene therapy | Mortality
Journal Article