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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
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 140, Issue 1, pp. 232 - 241
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2016, Volume 113, Issue 51, pp. E8277 - E8285
Journal Article
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 05/2019, Volume 143, Issue 5, pp. 1952 - 1956.e6
Journal Article
Nature Genetics, ISSN 1061-4036, 08/2017, Volume 49, Issue 8, pp. 1192 - 1201
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 12/2015, Volume 62, Issue 12, pp. 2101 - 2107
Aim We analyzed data from 71 patients with chronic granulomatous disease (CGD) with a confirmed genetic diagnosis, registered in the online Latin American... 
infections | registry | mutations | bacillus Calmette‐Guérin vaccine | chronic granulomatous disease | NADPH oxidase | Mutations | Chronic granulomatous disease | Infections | Bacillus Calmette-Guérin vaccine | Registry | SUSCEPTIBILITY | CYBB | FEATURES | PRIMARY IMMUNODEFICIENCY DISEASES | ONCOLOGY | TERM-FOLLOW-UP | PEDIATRICS | COMPLICATIONS | HEMATOLOGICALLY IMPORTANT MUTATIONS | HEMATOLOGY | BCG VACCINATION | 2ND UPDATE | bacillus Calmette-Guerin vaccine | Sepsis - etiology | Skin Diseases - genetics | Humans | Osteomyelitis - genetics | Granulomatous Disease, Chronic - genetics | Hispanic Americans | Abscess - epidemiology | Child, Preschool | Diarrhea - epidemiology | Infant | Male | Abscess - genetics | Granulomatous Disease, Chronic - complications | Granulomatous Disease, Chronic - epidemiology | Lymphatic Diseases - epidemiology | Lymphatic Diseases - genetics | Otitis - genetics | Osteomyelitis - etiology | NADPH Oxidases - genetics | Female | Registries | Skin Diseases - epidemiology | Osteomyelitis - epidemiology | Otitis - etiology | Child | Infant, Newborn | Pneumonia - genetics | Urinary Tract Infections - genetics | Pneumonia - etiology | Pneumonia - epidemiology | Abscess - etiology | Sepsis - epidemiology | NADPH Oxidase 2 | Sepsis - genetics | Membrane Glycoproteins - genetics | Skin Diseases - etiology | Urinary Tract Infections - epidemiology | Diarrhea - genetics | Urinary Tract Infections - etiology | Adolescent | Age of Onset | Diarrhea - etiology | Otitis - epidemiology | Lymphatic Diseases - etiology | Mutation | Pneumonia | Bacterial pneumonia | Vaccination | Immunodeficiency | Mycoses | Urinary tract infections
Journal Article
Journal of Experimental Medicine, ISSN 0022-1007, 08/2011, Volume 208, Issue 18, pp. 1635 - 1648
Chronic mucocutaneous candidiasis disease (CMCD) may be caused by autosomal dominant (AD) IL-17F deficiency or autosomal recessive (AR) IL-17RA deficiency.... 
HYPER-IGE SYNDROME | MEDICINE, RESEARCH & EXPERIMENTAL | SEQUENCING-BASED DISCOVERY | IFN-GAMMA | DISEASE | TH17-ASSOCIATED CYTOKINES | IL-27 | CD4(+) T-CELLS | IMMUNOLOGY | DEFICIENCY | TH17 CELLS | INBORN-ERRORS
Journal Article
European Journal of Immunology, ISSN 0014-2980, 03/2013, Volume 43, Issue 3, pp. 805 - 814
Journal Article
Journal Article
Blood, ISSN 0006-4971, 2016, Volume 127, Issue 25, pp. 3154 - 3164
Journal Article