LUIS IGNACIO
GONZÁLEZ GRANADO
Profesor asociado
University Medical Center Freiburg
Friburgo de Brisgovia, AlemaniaPublicaciones en colaboración con investigadores/as de University Medical Center Freiburg (17)
2024
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JAK inhibitor treatment for inborn errors of JAK/STAT signaling: An ESID/EBMT-IEWP retrospective study
Journal of Allergy and Clinical Immunology, Vol. 153, Núm. 1, pp. 275-286.e18
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Non-apoptotic FAS signaling controls mTOR activation and extrafollicular maturation in human B cells
Science Immunology, Vol. 9, Núm. 91
2023
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Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity
Journal of Allergy and Clinical Immunology, Vol. 152, Núm. 4, pp. 984-996.e10
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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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Revisiting autoimmune lymphoproliferative syndrome caused by Fas ligand mutations
Journal of Allergy and Clinical Immunology, Vol. 151, Núm. 5, pp. 1391-1401.e7
2022
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Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients
Journal of Clinical Immunology, Vol. 42, Núm. 8, pp. 1748-1765
2021
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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
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
2019
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Correction to: Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group (Journal of Clinical Immunology, (2019), 39, 1, (45-54), 10.1007/s10875-018-0577-9)
Journal of Clinical Immunology
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Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group
Journal of Clinical Immunology, Vol. 39, Núm. 1, pp. 45-54
2017
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Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation
Journal of Allergy and Clinical Immunology, Vol. 139, Núm. 4, pp. 1282-1292
2015
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DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients
Journal of Clinical Immunology, Vol. 35, Núm. 2, pp. 189-198
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Spectrum and Management of Complement Immunodeficiencies (Excluding Hereditary Angioedema) Across Europe
Journal of Clinical Immunology, Vol. 35, Núm. 2, pp. 199-205
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The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: Implications for differential diagnosis and pathogenesis
Haematologica, Vol. 100, Núm. 7, pp. 978-988
2013
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Erratum to Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): A survey of 45 patients. [Clin Exp Immunol 172, (2013) 63-72]
Clinical and Experimental Immunology
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Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): A survey of 45 patients
Clinical and Experimental Immunology, Vol. 172, Núm. 1, pp. 63-72
2012
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Patient-centred screening for primary immunodeficiency, a multi-stage diagnostic protocol designed for non-immunologists: 2011 update
Clinical and Experimental Immunology, Vol. 167, Núm. 1, pp. 108-119