Inmunología, Oftalmología y ORL
Departamento
LUIS IGNACIO
GONZÁLEZ GRANADO
Profesor asociado de Ciencias de la Salud
Publicaciones en las que colabora con LUIS IGNACIO GONZÁLEZ GRANADO (44)
2024
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Enrichment of Immune Dysregulation Disorders in Adult Patients with Human Inborn Errors of Immunity
Journal of Clinical Immunology, Vol. 44, Núm. 3
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Non-apoptotic FAS signaling controls mTOR activation and extrafollicular maturation in human B cells
Science Immunology, Vol. 9, Núm. 91
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The lack of either IRF9, or STAT2, has surprisingly little effect on human natural killer cell development and function
Immunology
2023
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Inborn Error of STAT2-Dependent IFN-I Immunity in a Patient Presented with Hemophagocytic Lymphohistiocytosis and Multisystem Inflammatory Syndrome in Children
Journal of Clinical Immunology, Vol. 43, Núm. 6, pp. 1278-1288
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Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome
Journal of Allergy and Clinical Immunology, Vol. 151, Núm. 4, pp. 1081-1095
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Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
Genome Medicine, Vol. 15, Núm. 1
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TCF3 haploinsufficiency defined by immune, clinical, gene-dosage, and murine studies
Journal of Allergy and Clinical Immunology, Vol. 152, Núm. 3, pp. 736-747
2022
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Altered CXCR4 dynamics at the cell membrane impairs directed cell migration in WHIM syndrome patients
Proceedings of the National Academy of Sciences of the United States of America, Vol. 119, Núm. 21
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Cost-minimization analysis of immunoglobulin treatment of primary immunodeficiency diseases in Spain
European Journal of Health Economics, Vol. 23, Núm. 3, pp. 551-558
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Eczematous dermatitis and thrombocytopenia in a 10-month-old boy
JEADV Clinical Practice, Vol. 1, Núm. 1, pp. 62-65
2021
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Coronavirus disease 2019 in patients with inborn errors of immunity: An international study
Journal of Allergy and Clinical Immunology, Vol. 147, Núm. 2, pp. 520-531
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Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations
Journal of Allergy and Clinical Immunology, Vol. 148, Núm. 5, pp. 1332-1341.e5
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Primary Immune Regulatory Disorders With an Autoimmune Lymphoproliferative Syndrome-Like Phenotype: Immunologic Evaluation, Early Diagnosis and Management
Frontiers in Immunology, Vol. 12
2020
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Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations
Journal of Allergy and Clinical Immunology, Vol. 146, Núm. 4, pp. 901-911
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Executive Summary of the Consensus Document on the Diagnosis and Management of Patients with Primary Immunodeficiencies
Journal of Allergy and Clinical Immunology: In Practice, Vol. 8, Núm. 10, pp. 3342-3347
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Executive Summary of the Consensus Document on the Diagnosis and Management of Patients with Primary Immunodeficiencies
Enfermedades Infecciosas y Microbiologia Clinica, Vol. 38, Núm. 9, pp. 438-443
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Generation, establishment and characterization of a pluripotent stem cell line (CVTTHi001-A) from primary fibroblasts isolated from a patient with activated PI3 kinase delta syndrome (APDS2)
Stem Cell Research, Vol. 49
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Newborn Screening for Presymptomatic Diagnosis of Complement and Phagocyte Deficiencies
Frontiers in Immunology, Vol. 11
2019
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Acquired and innate immunity impairment and severe disseminated Mycobacterium genavense infection in a patient with a NF-κB1 deficiency
Frontiers in Immunology, Vol. 10, Núm. JAN
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Extreme phenotypes with identical mutations: Two patients with same non-sense NHEJ1 homozygous mutation
Frontiers in Immunology, Vol. 10, Núm. JAN