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Revue Francaise des Laboratoires, ISSN 0338-9898, 2006, Volume 2006, Issue 380, pp. 44 - 47
Journal Article
Revue Francophone des Laboratoires, ISSN 1773-035X, 2006, Volume 2006, Issue 380, pp. 44 - 47
Journal Article
Revue Française des Laboratoires, ISSN 0338-9898, 03/2006, Volume 2006, Issue 380, pp. 44 - 47
Journal Article
Revue Francophone des Laboratoires, ISSN 1773-035X, 03/2006, Volume 2006, Issue 380, p. 44
Journal Article
Revue Francaise des Laboratoires, ISSN 0338-9898, 03/2006, Volume 2006, Issue 380, p. 44
Journal Article
Medicine (United States), ISSN 0025-7974, 07/2012, Volume 91, Issue 4, pp. e1 - e19
Autosomal dominant deficiency of signal transducer and activator of transcription 3 (STAT3) is the main genetic etiology of hyper-immunoglobulin (Ig) E... 
MEDICINE, GENERAL & INTERNAL | JOBS-SYNDROME | TRANSCRIPTION 3 | HYPERIMMUNOGLOBULIN-E SYNDROME | INVASIVE FUNGAL DISEASE | RECURRENT INFECTION | ANTIBODY-RESPONSES | CHRONIC MUCOCUTANEOUS CANDIDIASIS | COLD STAPHYLOCOCCAL ABSCESSES | SIGNAL TRANSDUCER | BONE-RESORPTION | Job Syndrome - immunology | Phosphorylation | Age Distribution | Job Syndrome - genetics | Humans | Middle Aged | Pneumonia, Bacterial - etiology | Child, Preschool | Infant | Male | Incidence | Skin Diseases, Bacterial - etiology | Young Adult | Eczema - epidemiology | Skin Diseases, Bacterial - epidemiology | DNA Mutational Analysis | STAT3 Transcription Factor - deficiency | Adult | Female | Respiratory Tract Infections - etiology | Genetic Predisposition to Disease - epidemiology | Child | Infant, Newborn | STAT3 Transcription Factor - genetics | Databases, Factual | Severity of Illness Index | France - epidemiology | Cross-Sectional Studies | Risk Assessment | Signal Transduction | Pneumonia, Bacterial - epidemiology | Eczema - etiology | Job Syndrome - epidemiology | Staphylococcal Infections - epidemiology | Job Syndrome - complications | Adolescent | Immunocompromised Host - genetics | Survival Analysis | Sex Distribution | Heterozygote | Respiratory Tract Infections - epidemiology | Staphylococcal Infections - etiology | Gene mutations | Causes of | Physiological aspects | Immunological deficiency syndromes | ACHOO syndrome | Genetic aspects | Research | Genetic transcription | T cells | Life Sciences | Genetics | Immunology
Journal Article
by Conti, Francesca, MD, PhD and Lugo-Reyes, Saul Oswaldo, MD and Blancas Galicia, Lizbeth, MD and He, Jianxin, MD and Aksu, Güzide, MD and Borges de Oliveira, Edgar, PhD and Deswarte, Caroline, MSc and Hubeau, Marjorie, PhD and Karaca, Neslihan, MD and de Suremain, Maylis, AS and Guérin, Antoine, MSc and Baba, Laila Ait, PhD and Prando, Carolina, MD, PhD and Guerrero, Gloria G., PhD and Emiroglu, Melike, MD and Öz, Fatma Nur, MD and Yamazaki Nakashimada, Marco Antonio, MD and Gonzalez Serrano, Edith, MD and Espinosa, Sara, MD, PhD and Barlan, Isil, MD and Pérez, Nestor, MD, PhD and Regairaz, Lorena, MD and Guidos Morales, Héctor Eduardo, MD and Bezrodnik, Liliana, MD and Di Giovanni, Daniela, MD and Dbaibo, Ghassan, MD and Ailal, Fatima, MD and Galicchio, Miguel, MD and Oleastro, Matias, MD and Chemli, Jalel, MD and Danielian, Silvia, PhD and Perez, Laura, BSc and Ortega, Maria Claudia, MD and Soto Lavin, Susana, MD, PhD and Hertecant, Joseph, MD and Anal, Ozden, MD and Kechout, Nadia, MD and Al-Idrissi, Eman, MD and ElGhazali, Gehad, MD, PhD and Bondarenko, Anastasia, MD and Chernyshova, Liudmyla, MD and Ciznar, Peter, MD and Herbigneaux, Rose-Marie, MD and Diabate, Aminata, AS and Ndaga, Stéphanie, AS and Konte, Barik, AS and Czarna, Ambre, AS and Migaud, Mélanie, AS and Pedraza-Sánchez, Sigifredo, PhD and Zaidi, Mussaret Bano, MD, Msc and Vogt, Guillaume, PhD and Blanche, Stéphane, MD and Benmustapha, Imen, MD and Mansouri, Davood, MD and Abel, Laurent, MD, PhD and Boisson-Dupuis, Stéphanie, PhD and Mahlaoui, Nizar, MD, MSc, MPH and Bousfiha, Ahmed Aziz, MD and Picard, Capucine, MD, PhD and Barbouche, Ridha, MD, PhD and Al-Muhsen, Saleh, MD and Espinosa-Rosales, Francisco J., MD and Kütükçüler, Necil, MD and Condino-Neto, Antonio, MD, PhD and Casanova, Jean-Laurent, MD, PhD and Bustamante, Jacinta, MD, PhD
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 138, Issue 1, pp. 241 - 248.e3
Background Chronic granulomatous disease (CGD) is a rare primary immunodeficiency caused by inborn errors of the phagocyte nicotinamide adenine dinucleotide... 
Allergy and Immunology | primary immunodeficiency | Mycobacteria | chronic granulomatous disease | BCG | tuberculosis | SUSCEPTIBILITY | VACCINATION | 1ST REPORT | CLINICAL-FEATURES | KINDREDS | IMMUNOLOGY | DEFICIENCY | ALLERGY | INFECTION | 2 CHILDREN | MUTATIONS | Granulomatous Disease, Chronic - mortality | Mycoses - epidemiology | Mycobacterium Infections - diagnosis | Bacterial Infections - etiology | Humans | Tuberculosis - etiology | Child, Preschool | Infant | Male | Granulomatous Disease, Chronic - complications | Tuberculosis - diagnosis | Granulomatous Disease, Chronic - epidemiology | Female | Retrospective Studies | Child | Mycobacterium Infections - epidemiology | Mycobacterium Infections - etiology | Mycobacterium Infections - mortality | Granulomatous Disease, Chronic - therapy | Patient Outcome Assessment | Bacterial Infections - epidemiology | Mycoses - diagnosis | Bacterial Infections - diagnosis | Mycoses - mortality | Mycoses - etiology | BCG Vaccine - administration & dosage | Bacterial Infections - mortality | Care and treatment | Chronic granulomatous disease | Bacterial infections | Analysis | Cytochrome | Pathogens | Immunization | Tuberculosis | Infectious diseases | Laboratories | Infections | Mutation | Patients | Mycoses | Mycobacterium Infections | Life Sciences | Granulomatous Disease, Chronic | BCG Vaccine | Bacterial Infections
Journal Article
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