Publicacións en colaboración con investigadores/as de University of Chicago (6)

2008

  1. Pendred syndrome in two Galician families: Insights into clinical phenotypes through cellular, genetic, and molecular studies

    Journal of Clinical Endocrinology and Metabolism, Vol. 93, Núm. 1, pp. 267-277

2005

  1. A de novo mutation in an already mutant nucleotide of the thyroid hormone receptor β gene perpetuates resistance to thyroid hormone

    Journal of Clinical Endocrinology and Metabolism, Vol. 90, Núm. 3, pp. 1760-1767

  2. Mutations in SECISBP2 result in abnormal thyroid hormone metabolism

    Nature Genetics, Vol. 37, Núm. 11, pp. 1247-1252

  3. Sex differences in the neuroendocrine response to short-term fasting in rhesus macaques

    Journal of Neuroendocrinology, Vol. 17, Núm. 7, pp. 435-444

2003

  1. Partial thyroxine-binding globulin (TBG) deficiency in a family with no detectable mutation of the TBG gene [2]

    Clinical Endocrinology

  2. The effect of short-term treatment with recombinant human thyroid-stimulating hormones on leydig cell function in men

    Thyroid, Vol. 13, Núm. 7, pp. 649-652