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Thyroid nodules: diagnosis and therapy.
Weiss RE, Lado-Abeal J. Weiss RE, et al. Curr Opin Oncol. 2002 Jan;14(1):46-52. doi: 10.1097/00001622-200201000-00009. Curr Opin Oncol. 2002. PMID: 11790980 Review.
Mutations in SECISBP2 result in abnormal thyroid hormone metabolism.
Dumitrescu AM, Liao XH, Abdullah MS, Lado-Abeal J, Majed FA, Moeller LC, Boran G, Schomburg L, Weiss RE, Refetoff S. Dumitrescu AM, et al. Nat Genet. 2005 Nov;37(11):1247-52. doi: 10.1038/ng1654. Epub 2005 Oct 16. Nat Genet. 2005. PMID: 16228000
Pendred syndrome in two Galician families: insights into clinical phenotypes through cellular, genetic, and molecular studies.
Palos F, García-Rendueles ME, Araujo-Vilar D, Obregon MJ, Calvo RM, Cameselle-Teijeiro J, Bravo SB, Perez-Guerra O, Loidi L, Czarnocka B, Alvarez P, Refetoff S, Dominguez-Gerpe L, Alvarez CV, Lado-Abeal J. Palos F, et al. J Clin Endocrinol Metab. 2008 Jan;93(1):267-77. doi: 10.1210/jc.2007-0539. Epub 2007 Oct 16. J Clin Endocrinol Metab. 2008. PMID: 17940114 Free PMC article.
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 D, Lado-Abeal J, Palos-Paz F, Lattanzi G, Bandín MA, Bellido D, Domínguez-Gerpe L, Calvo C, Pérez O, Ramazanova A, Martínez-Sánchez N, Victoria B, Costa-Freitas AT. Araújo-Vilar D, et al. Clin Endocrinol (Oxf). 2008 Jul;69(1):61-8. doi: 10.1111/j.1365-2265.2007.03146.x. Epub 2008 Jul 1. Clin Endocrinol (Oxf). 2008. PMID: 18031308
[Clinical and molecular study of five families with resistance to thyroid hormones].
Lado Abeal J, Albero Gamboa R, Araujo Vilar D, Barca Mallo O, Bernabeú Moron I, Calvo MT, Castro Piedras I, Martin Calamata J, Palos Paz F, Peinó R, Peteiro D, Victoria B. Lado Abeal J, et al. Med Clin (Barc). 2011 Nov 12;137(12):551-4. doi: 10.1016/j.medcli.2010.11.037. Epub 2011 Jun 23. Med Clin (Barc). 2011. PMID: 21703645 Spanish.
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).
Lago-Lestón R, Iglesias MJ, San-José E, Areal C, Eiras A, Araújo-Vilar D, Lado-Abeal J, Domínguez-Gerpe L. Lago-Lestón R, et al. Clin Endocrinol (Oxf). 2009 Apr;70(4):636-43. doi: 10.1111/j.1365-2265.2008.03377.x. Epub 2008 Aug 15. Clin Endocrinol (Oxf). 2009. PMID: 18710470
71 results