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au.\*:("ARAUJO-VILAR, David")

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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-LESTON, Ramon; IGLESIAS, Maria-José; SAN-JOSE, Esther et al.Clinical endocrinology (Oxford. Print). 2009, Vol 70, Num 4, pp 636-643, issn 0300-0664, 8 p.Article

Glucose metabolism in lean patients with mild type 2 diabetes mellitus: Evidence for insulin-sensitive and insulin-resistant variantsGARCIA-ESTEVEZ, Daniel A; ARAUJO-VILAR, David; SAAVEDRA-GONZALEZ, Angeles et al.Metabolism, clinical and experimental. 2002, Vol 51, Num 8, pp 1047-1052, issn 0026-0495Article

Analysis of the relationship between body mass index, insulin resistance, and beta-cell function: A cross-sectional study using the minimal modelGARCIA-ESTEVEZ, Daniel A; ARAUJO-VILAR, David; SAAVEDRA-GONZALEZ, Angeles et al.Metabolism, clinical and experimental. 2004, Vol 53, Num 11, pp 1462-1466, issn 0026-0495, 5 p.Article

A novel phenotypic expression associated with a new mutation in LMNA gene, characterized by partial lipodystrophy, insulin resistance, aortic stenosis and hypertrophic cardiomyopathyARAUJO-VILAR, David; LADO-ABEAL, Joaquin; MARTINEZ-SANCHEZ, Noelia et al.Clinical endocrinology (Oxford. Print). 2008, Vol 69, Num 1, pp 61-68, issn 0300-0664, 8 p.Article

Pendred Syndrome in Two Galician Families : Insights into Clinical Phenotypes through Cellular, Genetic, and Molecular StudiesPALOS, Fernando; GARCIA-RENDUELES, Maria E. R; ALVAREZ, Paula et al.The Journal of clinical endocrinology and metabolism. 2008, Vol 93, Num 1, pp 267-277, issn 0021-972X, 11 p.Article

High variability in CYP21A2 mutated alleles in Spanish 21-hydroxylase deficiency patients, six novel mutations and a founder effectLOIDI, Lourdes; QUINTEIRO, Celsa; POMBOT, Manuel et al.Clinical endocrinology (Oxford. Print). 2006, Vol 64, Num 3, pp 330-336, issn 0300-0664, 7 p.Article

AXONAL NEUROPATHY, LONG LIMBS, AND BUMPY TONGUE: THINK OF MEN2BRAMOS-LEVI, Ana M; DIAZ-PEREZ, Angel; SOBRIDO, María-Jesús et al.Muscle & nerve. 2012, Vol 46, Num 6, pp 961-964, issn 0148-639X, 4 p.Article

Functional Consequences of Seven Novel Mutations in the CYP11B1 Gene: Four Mutations Associated with Nonclassic and Three Mutations Causing Classic 11β-Hydroxylase DeficiencyPARAJES, Silvia; LOIDI, Lourdes; POMBO, Manuel et al.The Journal of clinical endocrinology and metabolism. 2010, Vol 95, Num 2, pp 779-788, issn 0021-972X, 10 p.Article

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