Publicacións en colaboración con investigadores/as de Hospital Universitario de Salamanca (3)

2024

  1. PTEN hamartoma tumor syndrome: Clinical and genetic characterization in pediatric patients

    Child's Nervous System, Vol. 40, Núm. 6, pp. 1689-1697

2022

  1. Recurrent NOMO1 Gene Deletion Is a Potential Clinical Marker in Early-Onset Colorectal Cancer and Is Involved in the Regulation of Cell Migration

    Cancers, Vol. 14, Núm. 16

2020

  1. A mutation in p62 protein (p. R321C), associated to Paget's disease of bone, causes a blockade of autophagy and an activation of NF-kB pathway

    Bone, Vol. 133