[PDF] Top 20 Arq Bras Endocrinol Metab vol.52 número9

... Quanto à valorização dos sócios e da SBEM per si , estabelecemos estra- tégias para divulgação de nossa Sociedade e contamos em todo esse período com a competente Comissão de Comunicaç[r] ... See full document

... 2. Biondi B, Palmieri EA, Fazio S, Cosco C, Nocera M, Saccà L, et al. Endogenous subclinical hyperthyroidism affects quality of life and cardiac morphology and function in young and mid- dle-aged patients. J Clin ... See full document

... 1. Bashin S, Cunningham GR, Hayes FJ, Matsumoto AM, Snyder PJ, Swerdloff RS, Montori VM. Testosterone therapy in adult men with androgen defi ciency syndromes: an Endocrine So- ciety Clinical Practice guideline. J Clin ... 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

... Capillary thyroid carcinoma (PTC) is the most common neoplasm of thyroid. It usually grows slowly and is clinically indolent, although rare, its aggressive forms with local invasion or distant metastases can occur. ... See full document

... Microalbuminuria assessment is essential for diagnosing incipient nephropa- thy in diabetic patients. The present study aim to evaluate whether urinary albumin concentration (UAC) and urinary albumin-to-creatinine ratio ... See full document

... Objective: To analyze the relative risk of late-onset hypogonadism in men with osteoporosis and the usefulness of screening questionnaires. Methods: We correlated the Aging Male’s Symptoms (AMS), Androgen Defi ciency in ... See full document

... Objectives: To evaluate which factors infl uence the laboratorial diagnosis of late-onset male hypogonadism (LOH). Methods: Total testosterone (TT), SHBG and albumin were measured in 216 men aged 52-84 years. The ... See full document

... Pistas sobre essa particularidade funcional existem na literatura pertinente em trabalhos da década de 1950-1960, quando Kennedy propôs uma teoria metabólica para explicar o con[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

... Resistance to thyroid hormone (RTH) is a rare disorder characterized by vari- able tissue hyporesponsiveness to thyroid hormone, usually caused by mu- tations in the thyroid hormone receptor beta (TRβ). We describe a ... See full document

... Objetivo: Comparar as lesões ateroscleróticas das extremidades de diabé- ticos e não-diabéticos, estudando a ocorrência de espessamento capilar. Métodos: Examinou-se segmentos arteriais e da derme de 57 membros in- ... See full document

... Pendred Syndrome (PS) is an autossomal recessive disorder characterized by sensorineural deafness, goiter and iodide organifi cation defect. The hearing loss is associated with inner ear abnormalities, ranging from an ... 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 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

... Combined 17alpha-hydroxylase/17,20-lyase defi ciency is a rare, autosomal re- cessive form of congenital adrenal hyperplasia characterized by the coexis- tence of hypertension, caused by the hyperproduction of ... See full document

... 3. Laurenti R, Jorge MHP, Gotlieb SLD. Maternal mortality in Bra- zilian state capitals: some characteristics and estimates for an adjustment factor. Rev Bras Epidemiologia. 2006;7(4):449-60. 4. Report of the ... 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

... grama, glicemia e dosagens séricas de albumina, creatinina, TSH, TGO, TGP e bilirrubinas normais, foram estudados. Amostras de soro foram obtidas antes e 30, 60, 90 e 120 minutos após administração oral de 75 g de ... See full document

... The amplifi cation of thyroglobulin (TG) mRNA in peripheral blood of patients with thyroid cancer has been studied for almost one decade, but its real con- tribution for diagnosis of cancer relapse has not yet been ... See full document