Identification of molecular mechanisms related to nonthyroidal illness syndrome in skeletal muscle and adipose tissue from patients with septic shock
Rodriguez-Perez, Alfonso, Palos-Paz, Fernando, Kaptein, Ellen, Visser, Theo J., Dominguez-Gerpe, L., Alvarez-Escudero, Julian, Lado-Abeal, Joaquin
Published in Clinical endocrinology (Oxford) (01.05.2008)
Published in Clinical endocrinology (Oxford) (01.05.2008)
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A novel phenotypic expression associated with a new mutation in LMNA gene, characterized by partial lipodystrophy, insulin resistance, aortic stenosis and hypertrophic cardiomyopathy
Araújo-Vilar, David, Lado-Abeal, Joaquin, Palos-Paz, Fernando, Lattanzi, Giovanna, Bandín, Manuel A., Bellido, Diego, Domínguez-Gerpe, Lourdes, Calvo, Carlos, Pérez, Oscar, Ramazanova, Alia, Martínez-Sánchez, Noelia, Victoria, Berta, Costa-Freitas, Ana Teresa
Published in Clinical endocrinology (Oxford) (01.07.2008)
Published in Clinical endocrinology (Oxford) (01.07.2008)
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A family with congenital hypothyroidism caused by a combination of loss-of-function mutations in the thyrotropin receptor and adenylate cyclase-stimulating G alpha-protein subunit genes
Lado-Abeal, Joaquin, Castro-Piedras, Isabel, Palos-Paz, Fernando, Labarta-Aizpún, Jose Ignacio, Albero-Gamboa, Ramon
Published in Thyroid (New York, N.Y.) (01.02.2011)
Published in Thyroid (New York, N.Y.) (01.02.2011)
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Clinical and molecular study of five families with resistance to thyroid hormones
Lado Abeal, Joaquin, Albero Gamboa, Ramón, Araujo Vilar, David, Barca Mallo, Olga, Bernabeú Moron, Ignacio, Calvo, María Teresa, Castro Piedras, Isabel, Martin Calamata, Jesús, Palos Paz, Fernando, Peinó, Roberto, Peteiro, Diego, Victoria, Berta
Published in Medicina clinica (12.11.2011)
Published in Medicina clinica (12.11.2011)
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