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Arquivos Brasileiros De Endocrinologia E Metabologia|December 17, 2008
[Preoperative evaluation of cytologically indeterminate thyroid nodules with 18F-FDG PET]Fernando M Sebastianes, Juliano J Cerci, José Soares Júnior, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|May 26, 2009
Adipose tissue at the crossroads in the development of the metabolic syndrome, inflammation and atherosclerosisBernardo Léo Wajchenberg, Marcia Nery, Maria Rosaria Cunha, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|May 26, 2009
Protective roles of adiponectin in obesity-related fatty liver diseases: mechanisms and therapeutic implicationsYu Wang, Mingyan Zhou, Karen S L Lam, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|May 26, 2009
From bariatric to metabolic surgery in non-obese subjects: time for some cautionMervyn DeitelArquivos Brasileiros De Endocrinologia E Metabologia|May 26, 2009
HOMA1-IR and HOMA2-IR indexes in identifying insulin resistance and metabolic syndrome: Brazilian Metabolic Syndrome Study (BRAMS)Bruno Geloneze, Ana Carolina Junqueira Vasques, Christiane França Camargo Stabe, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|May 26, 2009
The N363S polymorphism in the glucocorticoid receptor gene: effects on visceral fat assessed by abdominal computed tomographyCintia Cercato, Alfredo Halpern, Eliana S T Frazzatto, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
E449X mutation in the thyroid hormone receptor beta associated with autoimmune thyroid disease and severe neuropsychomotor involvementMaria Helane Costa Gurgel, Renan M Montenegro Junior, Rejane Araujo Magalhaes, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
Prevalence of 15 mitochondrial DNA mutations among type 2 diabetic patients with or without clinical characteristics of maternally inherited diabetes and deafnessDaisy Crispim, Aline A F Estivalet, Israel Roisenberg, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant ricketsLuciana Cosentino de Macedo, Fernanda Caroline Soardi, Nayla Ananias, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
[Absence of PRKAR1A loss of heterozygosity in laser-captured microdissected pigmented nodular adrenocortical tissue from a patient with Carney complex caused by the novel nonsense mutation p.Y21X]Madson Q Almeida, Luciana Pinto Brito, Sorahia Domenice, et al.Pageof 141