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Arquivos Brasileiros De Endocrinologia E Metabologia|March 18, 2006
[Turner syndrome: psychosocial aspects]Lígia Zuppi C Suzigan, Roberto B de Paiva e Silva, Andréa T Maciel-GuerraArquivos Brasileiros De Endocrinologia E Metabologia|March 18, 2006
[Cryptorchidism: diagnosis and treatment]Carlos Alberto LonguiArquivos Brasileiros De Endocrinologia E Metabologia|April 7, 2011
[Evaluation of clinical, laboratorial and ultrasonographic predicting factors of malignancy in thyroid nodules]Ana Luiza Silva Rio, Rosa Paula Mello Biscolla, Danielle Macellaro Andreoni, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|April 7, 2011
[Growth hormone therapy and hypersensitivity type III reaction: a contraindication for desensitization]Wilma Carvalho Neves Forte, Cristiane Kochi, Claudia Dutra Costantin Faria, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|May 18, 2011
[Recommendations of Neuroendocrinology Department from Brazilian Society of Endocrinology and Metabolism for diagnosis and treatment of acromegaly in Brazil]Leonardo Vieira Neto, Julio Abucham, Luiz Antônio de Araujo, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|May 18, 2011
[Body mass index to the cardiovascular disease risk screening in infancy]Gabriel Gustavo Bergmann, Adroaldo Gaya, Ricardo Halpern, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|May 18, 2011
Prevalence of metabolic syndrome and of its specific components among adolescents from Niterói City, Rio de Janeiro State, BrazilMarlene M Alvarez, Ana Carolina R E Vieira, Rosely Sichieri, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|February 23, 2011
Application of genetic testing to define the surgical approach in a sporadic case of multiple endocrine neoplasia type 1Cesar Luiz Boguszewski, Leila Caroline Bianchet, Salmo Raskin, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|February 23, 2011
Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defectSolange Caires Neves, Paola Rossi Mezalira, Vera M A Dias, et al.Arquivos Brasileiros De Endocrinologia E Metabologia|February 23, 2011
Combined 17α-hydroxylase/17,20-lyase deficiency due to p.R96W mutation in the CYP17 gene in a Brazilian patientFabíola Costenaro, Ticiana C Rodrigues, Claudio E Kater, et al.Pageof 141