[PDF] Top 20 Arq Bras Endocrinol Metab vol.52 número5

... 3. Consensus guidelines for the diagnosis and treatment of adults with growth hormone deficiency: summary statement of the growth hormone research society workshop on adult growth hormone deficiency. J Clin ... See full document

... Programa de triagem neonatal para hipotireoidismo congênito no nordeste do Brasil: crité- rios diagnósticos e resultados. Arq Bras Endocrinol Metab[r] ... See full document

... A 16 year-old Brazilian girl was referred due to ab- sence of secondary sexual development. She was born at 40 weeks of gestation after an uncomplicated preg- nancy, a single daughter of non consanguineous pa- rents. At ... See full document

... Objetive: To perform a comparative analysis of atherosclerotic lesions and capillaries changes in diabetic and nondiabetic patients. Methods: Leg ar- teries and skin of 57 amputated lower limbs of diabetic (47.3%) and ... See full document

... puberdade. Outros cinco irmãos eram surdos: um irmão tinha fenotipo se- melhante, três também tinham bócio, porém com função tiroideana normal e um irmão tinha apenas um discreto aumento da tiróide. Outros quatro irmãos ... See full document

... É notória a predominância de pacientes do sexo feminino e o aumento no número de casos tem sido registrado mais entre as mulheres do que entre os homens (1-3) (SEER, INCA).. É possível[r] ... See full document

... In addition, expression profi les of the mRNA somatostatin receptor subtypes (SSTR) in tu- mor fragments may serve as a predictive tool of bio- chemical and tumor volume response to SA [r] ... See full document

... A resistência ao hormônio tireoideano (RHT) é uma doença rara, causada por variável hiporresponsividade dos tecidos aos hormônios tireoideanos, usual- mente causada por mutações no receptor beta do hormônio tireoideano ... See full document

... Carcinoma papilífero da tiróide (PTC) é a neoplasia mais comum da tiróide. Geralmente cresce lentamente e é clinicamente indolente, embora raras, as formas agressivas com invasão local ou metástases distantes podem ... See full document

... The apparent mineralocorticoid excess syndrome (AME) is a rare autosomal re- cessive disorder due to the defi ciency of 11β-hydroxysteroid dehydrogenase type 2 enzyme (11beta-HSD2). The 11beta-HSD2 enzyme, encoded by ... See full document

... A interação da doença vascular, da infecção e em especial da neuropatia periférica transforma o pé diabé- tico em um órgão-alvo de altíssimo risco. Quinze por cento de indivídu[r] ... See full document

... Dessa forma, o fator de impacto JCR é o valor obtido pela soma das citações dos artigos publicados no período prévio de dois anos, em que ambas, a revista citada e a que recebe a citaç[r] ... See full document

... 4. Spencer CA, Takeuchi M, Kazarosyan M, Wang CC, Guttler RB, Singer PA, et al. Serum thyroglobulin autoantibodies: preva- lence, infl uence on serum thyroglobulin measurement, and prognostic signifi cance in patients ... See full document

... The present study was carried to develop and analyze the consequences of hypercaloric pellet-diet cycle that promotes obesity in rats. Male Wistar rats were randomly distributed into two groups that received either ... See full document

... linear correlation coefficient (r) and analysis of standard deviations, constant error (CE) which corresponds to the difference between estimated and measured values, total erro[r] ... See full document

... Multiple endocrine neoplasia type 2A (MEN2A) is an autosomal dominant inherited condition that predisposes to the triad of medullary thyroid cancer (MTC), pheochromocytoma (Pheo), and primary hyperparathyroidism (PHT). ... See full document

... Maturity-onset diabetes of the young (MODY) is a monogenic form of diabe- tes mellitus characterized by autosomal dominant inheritance, early age of onset, and pancreatic beta cell dysfunction. Heterozygous mutations in ... See full document

... Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI) is a rare autosomal dominant disorder characterized by polyuria and polydip- sia due to defi ciency of arginine vasopressin (AVP). More than 50 ... See full document

... mia, blood count, albumin, creatinine, TSH, SGOT, SGPT and bilirubin were studied. Serum samples were obtained before and 30,60,90 and 120 min after oral adminis- tration of 75 g glucose. The test was repeated after 4 ... See full document

... A defi ciência combinada de 17 alfa-hidroxilase/17,20 liase é uma doença rara, de herança autossômica recessiva, causa de hiperplasia adrenal congênita caracter- izada pela presença de hipertensão resultante do acúmulo ... See full document