Publicaciones en colaboración con investigadores/as de Hospital Universitario Pío del Río Hortega (40)

2024

  1. Biological variability of human intraepithelial lymphocytes throughout the human gastrointestinal tract in health and coeliac disease

    European Journal of Clinical Investigation

2023

  1. Influence of HLADQA1*05 Genotype in Adults With Inflammatory Bowel Disease and Anti-TNF Treatment With Proactive Therapeutic Drug Monitoring: A Retrospective Cohort Study

    Inflammatory bowel diseases, Vol. 29, Núm. 10, pp. 1586-1593

  2. Study and isolation of human intestinal dendritic cell and macrophage subsets

    Methods in Cell Biology (Academic Press Inc.), pp. 69-76

2021

  1. Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition)

    European Journal of Immunology, Vol. 51, Núm. 12, pp. 2708-3145

  2. Human intestinal dendritic cell and macrophage subsets in coeliac disease

    International Review of Cell and Molecular Biology (Elsevier Inc.), pp. 85-104

  3. Immunopathogenesis of Celiac Disease

    Advances in Celiac Disease: Improving Paediatric and Adult Care (Springer International Publishing), pp. 35-49

2020

  1. Circulating Dendritic Cells from Celiac Disease Patients Display a Gut-Homing Profile and are Differentially Modulated by Different Gliadin-Derived Peptides

    Molecular Nutrition and Food Research, Vol. 64, Núm. 6

  2. Deletions of specific exons of FHOD3 detected by next-generation sequencing are associated with hypertrophic cardiomyopathy

    Clinical Genetics, Vol. 98, Núm. 1, pp. 86-90

  3. Different Intraepithelial CD3+ Cell Numbers in Crohn's Disease and Ulcerative Colitis

    Inflammatory Bowel Diseases

2019

  1. B12 hipervitaminosis: Reactant and acute biomarker in cancer

    Atencion Primaria Practica, Vol. 1, Núm. 3, pp. 45-49

2018

  1. Celiac disease and sensitivity to non-celiac gluten: the need for use of alternative diagnostic tools. Controlled provocation and new markers

    Revista del Laboratorio Clinico

  2. Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients

    BMC Medical Genomics, Vol. 11, Núm. 1

  3. Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy

    Journal of the American College of Cardiology, Vol. 72, Núm. 20, pp. 2457-2467

  4. Human corneal fibroblast migration and extracellular matrix synthesis during stromal repair: Role played by platelet-derived growth factor-BB, basic fibroblast growth factor, and transforming growth factor-β1

    Journal of Tissue Engineering and Regenerative Medicine, Vol. 12, Núm. 2, pp. e737-e746

  5. Minimización de errores preanalíticos y su repercusión en el control del laboratorio clínico

    Revista del Laboratorio Clinico

2017

  1. Alagille syndrome with atypical phenotype diagnosed by molecular tests: unreported JAG1 mutation

    Medicina Clinica

  2. Association of the IL-15 and IL-15Rα genes with celiac disease

    Cytokine, Vol. 99, pp. 73-79

  3. El virus Zika y los Juegos Olímpicos

    Revista del Laboratorio Clinico

  4. Hipervitaminosis B12 y cáncer de recto

    Revista del Laboratorio Clinico, Vol. 10, Núm. 2, pp. 105-108

  5. New IL-15 receptor-α splicing variants identified in intestinal epithelial Caco-2 cells

    Innate Immunity, Vol. 23, Núm. 1, pp. 44-53