Publicaciones en colaboración con investigadores/as de Centro de Investigación Biomédica en Red sobre Enfermedades Raras (11)

2023

  1. Maternal obesity and gestational diabetes reprogram the methylome of offspring beyond birth by inducing epigenetic signatures in metabolic and developmental pathways

    Cardiovascular Diabetology, Vol. 22, Núm. 1

2022

  1. MicroRNA-132 is overexpressed in fetuses with late-onset fetal growth restriction

    Health Science Reports, Vol. 5, Núm. 2

  2. MicroRNA-185-5p: a marker of brain-sparing in foetuses with late-onset growth restriction

    Epigenetics, Vol. 17, Núm. 11, pp. 1345-1356

  3. Overexpression of microRNAs miR-25-3p, miR-185-5p and miR-132-3p in late onset fetal growth restriction, validation of results and study of the biochemical pathways involved

    International Journal of Molecular Sciences, Vol. 23, Núm. 1

2021

  1. International BEAT-PCD consensus statement for infection prevention and control for primary ciliary dyskinesia in collaboration with ERN-LUNG PCD Core Network and patient representatives

    ERJ Open Research, Vol. 7, Núm. 3

2020

  1. Core outcome set for studies investigating management of selective fetal growth restriction in twins

    Ultrasound in Obstetrics and Gynecology, Vol. 55, Núm. 5, pp. 652-660

  2. Immunofluorescence analysis as a diagnostic tool in a spanish cohort of patients with suspected primary ciliary dyskinesia

    Journal of Clinical Medicine, Vol. 9, Núm. 11, pp. 1-14

  3. MicroRNA-148b-3p and MicroRNA-25-3p Are Overexpressed in Fetuses with Late-Onset Fetal Growth Restriction

    Fetal Diagnosis and Therapy, Vol. 47, Núm. 9, pp. 665-674

  4. Recurrent wheezing during the first 3 years of life in a birth cohort of moderate-to-late preterm infants

    Pediatric Allergy and Immunology, Vol. 31, Núm. 2, pp. 124-132

2015

  1. Assessment of ten trace elements in umbilical cord blood and maternal blood: Association with birth weight

    Journal of Translational Medicine, Vol. 13, Núm. 1

2009

  1. Síndrome de deleción de genes contiguos en Xp21: Una forma inusual de presentación

    Revista de Neurologia, Vol. 49, Núm. 9, pp. 472-474