Inmunobiología linfocitaria
Hospital Universitario La Paz
Madrid, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitario La Paz (57)
2023
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Clinical Profiles and Patterns of Kidney Disease Progression in C3 Glomerulopathy
Kidney360, Vol. 4, Núm. 5, pp. 659-672
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Clinical manifestations and approach to the management of patients with common variable immunodeficiency and liver disease
Frontiers in Immunology, Vol. 14
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Gluten-sensitive enteropathy in recessive dystrophic epidermolysis bullosa
British Journal of Dermatology, Vol. 189, Núm. 6, pp. 774-776
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Novel Loss-of-Function KCNA5 Variants in Pulmonary Arterial Hypertension
American Journal of Respiratory Cell and Molecular Biology, Vol. 69, Núm. 2, pp. 147-158
2022
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Development and validation of a nomogram to predict kidney survival at baseline in patients with C3 glomerulopathy
Clinical Kidney Journal, Vol. 15, Núm. 9, pp. 1737-1746
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Longitudinal change in proteinuria and kidney outcomes in C3 glomerulopathy
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, Vol. 37, Núm. 7, pp. 1270-1280
2021
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Clinical and Immunological Features of Human BCL10 Deficiency
Frontiers in Immunology, Vol. 12
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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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Next Generation Sequencing for Detecting Somatic FAS Mutations in Patients With Autoimmune Lymphoproliferative Syndrome
Frontiers in Immunology, Vol. 12
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Validation of a Histologic Scoring Index for C3 Glomerulopathy
American Journal of Kidney Diseases, Vol. 77, Núm. 5, pp. 684-695.e1
2020
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Autoantibodies against type I IFNs in patients with life-threatening COVID-19
Science, Vol. 370, Núm. 6515
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Circulating CD19+CD24hiCD38hiregulatory B cells as biomarkers of response to methotrexate in early rheumatoid arthritis
Rheumatology (United Kingdom), Vol. 59, Núm. 10, pp. 3081-3091
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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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Human BCL10 Deficiency due to Homozygosity for a Rare Allele
Journal of Clinical Immunology, Vol. 40, Núm. 2, pp. 388-398
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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
Science, Vol. 370, Núm. 6515
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Mycophenolate mofetil in c3 glomerulopathy and pathogenic drivers of the disease
Clinical Journal of the American Society of Nephrology, Vol. 15, Núm. 9, pp. 1287-1298
2019
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Complement as a diagnostic tool in immunopathology
Seminars in Cell and Developmental Biology, Vol. 85, pp. 86-97
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Double-strand break repair through homologous recombination in autosomal-recessive BCL10 deficiency
Journal of Allergy and Clinical Immunology, Vol. 143, Núm. 5, pp. 1931-1934.e1
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Two populations of circulating PD-1hiCD4 T cells with distinct B cell helping capacity are elevated in early rheumatoid arthritis
Rheumatology (United Kingdom), Vol. 58, Núm. 9, pp. 1662-1673