Publications in collaboration with researchers from Centro de Investigación Biomédica en Red sobre Enfermedades Raras (3)

2024

  1. Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndrome

    Orphanet Journal of Rare Diseases, Vol. 19, Núm. 1

2010

  1. Role of late maternal thyroid hormones in cerebral cortex development: An experimental model for human prematurity

    Cerebral Cortex, Vol. 20, Núm. 6, pp. 1462-1475

  2. Thyroid hormone regulation of gene expression in the developing rat fetal cerebral cortex: Prominent role of the Ca2+/calmodulin-dependent protein kinase IV pathway

    Endocrinology, Vol. 151, Núm. 2, pp. 810-820