Publications in collaboration with researchers from Universidad Miguel Hernández de Elche (9)

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

2020

  1. Hereditary leiomyomatosis and renal cell cancer syndrome in spain: Clinical and genetic characterization

    Cancers, Vol. 12, Núm. 11, pp. 1-16

2010

  1. 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

2006

  1. Brain edema and inflammatory activation in bile duct ligated rats with diet-induced hyperammonemia: A model of hepatic encephalopathy in cirrhosis

    Hepatology, Vol. 43, Núm. 6, pp. 1257-1266

  2. Chapter 17 Crossmodal audio-visual interactions in the primary visual cortex of the visually deprived cat: a physiological and anatomical study

    Progress in Brain Research, Vol. 155 B, pp. 287-311

2005

  1. Transient maternal hypothyroxinemia at onset of corticogenesis alters tangential migration of medial ganglionic eminence-derived neurons

    European Journal of Neuroscience, Vol. 22, Núm. 3, pp. 541-551

2004

  1. A moderate and transient deficiency of maternal thyroid function at the beginning of fetal neocorticogenesis alters neuronal migration

    Endocrinology, Vol. 145, Núm. 9, pp. 4037-4047

2001

  1. Protracted expression of serotonin transporter and altered thalamocortical projections in the barrelfield of hypothyroid rats

    European Journal of Neuroscience, Vol. 14, Núm. 12, pp. 1968-1980

  2. Role of thyroid hormones in the maturation and organisation of rat barrel cortex

    Neuroscience, Vol. 107, Núm. 3, pp. 383-394