Publikationen in Zusammenarbeit mit Forschern von Complexo Hospitalario Universitario de Santiago (12)

2020

  1. High prevalence of non-thyroidal illness syndrome in patients at long-term care facilities

    Endocrine, Vol. 70, Núm. 2, pp. 348-355

2018

  1. Lipopolysaccharide (LPS)-induced septic shock causes profound changes in myocardial energy metabolites in pigs

    Metabolomics, Vol. 14, Núm. 10

2010

  1. New insights into thyroglobulin pathophysiology revealed by the study of a family with congenital goiter

    Journal of Clinical Endocrinology and Metabolism, Vol. 95, Núm. 7, pp. 3522-3526

  2. Reduced adipogenic gene expression in fibroblasts from a patient with type 2 congenital generalized lipodystrophy

    Diabetic Medicine, Vol. 27, Núm. 10, pp. 1178-1187

  3. Thyroid hormone receptors are down-regulated in skeletal muscle of patients with non-thyroidal illness syndrome secondary to non-septic shock

    European Journal of Endocrinology, Vol. 163, Núm. 5, pp. 765-773

2009

  1. Prevalence and functional analysis of the S107P polymorphism (rs6647476) of the monocarboxylate transporter 8 (SLC16A2) gene in the male population of north-west Spain (Galicia)

    Clinical Endocrinology, Vol. 70, Núm. 4, pp. 636-643

  2. Site-dependent differences in both prelamin A and adipogenic genes in subcutaneous adipose tissue of patients with type 2 familial partial lipodystrophy

    Journal of Medical Genetics, Vol. 46, Núm. 1, pp. 40-48

2008

  1. A novel phenotypic expression associated with a new mutation in LMNA gene, characterized by partial lipodystrophy, insulin resistance, aortic stenosis and hypertrophic cardiomyopathy

    Clinical Endocrinology, Vol. 69, Núm. 1, pp. 61-68

  2. Identification of molecular mechanisms related to nonthyroidal illness syndrome in skeletal muscle and adipose tissue from patients with septic shock

    Clinical Endocrinology, Vol. 68, Núm. 5, pp. 821-827

  3. 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

  4. Prevalence of mutations in TSHR, GNAS, PRKAR1A and RAS genes in a large series of toxic thyroid adenomas from Galicia, an iodine-deficient area in NW Spain

    European Journal of Endocrinology, Vol. 159, Núm. 5, pp. 623-631

2003

  1. Síndrome de vena cava superior y carcinoma insular de tiroides: El stent como alternativa terapéutica paliativa

    Anales de Medicina Interna, Vol. 20, Núm. 6, pp. 301-303