[PDF] Top 20 Arq Bras Endocrinol Metab vol.54 número7

... As mentioned before, while PI3Ks phosphorylate PtdIns at the 3-hydroxyl group of the inositol ring, PTEN is responsible for its dephosphorylation. Thus, changes in the activity of PTEN are expected to dra- matically ... See full document

... Objetivo: Correlacionar o trabalho de turno com índice de massa corporal (IMC), circunferência abdominal, cronotipo e sintomas depressivos. Sujeitos e métodos: Amostra de 14 trabalha- dores de turno e 13 diurnos, com ... See full document

... Spranger J, et al. Growth hormone response during oral glucose tolerance test: the impact of assay method on the estimation of reference values in patients with acromegaly and in healthy con- trols, and the role of ... See full document

... Treatment with rosiglitazone has been associated with severe paradoxical HDL-c reductions. To our knowledge, there are very few reports of this reaction occurring when patients are treated without the combination of a ... See full document

... Spindle epithelial tumor with thymus-like element (SETTLE) is a rare malignant neoplasm of the thyroid, occurring predominantly in children, adolescents, and young adults. SETTLE usually presents itself as a thyroid ... See full document

... Objective: To determine whether previous insulin treatment independently inluences subse- quent outcomes in diabetic patients with ACS (acute coronary syndromes). Subjects and me- thods: 375 diabetic patients with ACS, ... See full document

... Objective: To establish limits of normal serum TSH for the adult (18 to 60 years) Brazilian popula- tion according to recommendations of the National Academy of Clinical Biochemistry. Subjects and methods: Healthy ... See full document

... obesity among students aged 18 to 20 years, smoking and alcohol intake. The probability of hypertension increases if the subject is male, has a waist circumference (WC) ≥ 90, WC ≥ 75 and does not practice physical ... See full document

... Objetivo: O hipotireoidismo congênito (HC) pode ser causado por defeitos na formação da tireoide ou em uma das etapas da síntese dos hormônios tireoidianos. A disgenesia da tireoide pode ser associada a mutações no fator ... See full document

... Embora a maior parte dos pacientes com hipotiroidismo ique bem com um único comprimido diário de tiroxina, aproximadamente 10% não icam satisfeitos e outro importante grupo de pacientes apresenta controle difícil. Foram ... See full document

... bone age was 10 years. Prolactin was 10.560 ng/mL (3-25), FSH and LH were undetectable, IGF-1, TSH, Free T4, ACTH, and cortisol were within normal ranges. MRI showed a pituitary macroadeno- ma, 5.3 X 4.0 X 3.5 cm with ... See full document

... 8. Ranke MB, Lindberg A, Cowell CT, Albertsson-Wikland K, Reiter EO, Wilton P, et al. Prediction of response to growth hormone tre- atment in short children born small for gestational age: analysis of data from KIGS ... See full document

... Objective: The aim of this study was to evaluate the accuracy of the measurement of thyroglo- bulin in washout needle aspiration biopsy (FNAB-Tg) to detect papillary thyroid cancer (PTC) metastases. Subjects and methods: ... See full document

... Objective: To evaluate the frequency of subclinical acromegaly (in the absence of clinical phe- notype but biochemically uncontrolled) in patients with prolactinoma during treatment with dopaminergic agonists. Subjects ... See full document

... 9. Maghnie M, Ghirardello S, De Bellis A, di Iorgi N, Ambrosini L, Secco A, et al. Idiopathic central diabetes insipidus in children and young adults is commonly associated with vasopressin-cell antibodies and markers of ... See full document

... gene, is a key enzyme involved in the biosynthesis of all the classes of steroid hormones. De- leterious mutations in the HSD3B2 gene cause the classical deficiency of 3β-HSD2, which is a rare autosomal recessive disease ... See full document

... 1. Saraiva GL, Cendoroglo MS, Ramos LR, Araújo LMQ, Vieira JGH, Maeda SS, et al. Prevalência da deiciência, insuiciência de vita- mina D e hiperparatireoidismo secundário em idosos institucio- nalizados e moradores na ... See full document

... Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant hereditary cancer syn- drome characterized mostly by parathyroid, enteropancreatic, and anterior pituitary tumors. We present a case of an 8-year-old ... See full document

... Objetivo: Determinar a frequência do polimorismo +1730 G/A do gene do receptor beta de es- trógeno (ERβ) em mulheres inférteis com e sem endometriose e controles. Sujeitos e métodos: Estudo caso-controle que incluiu 136 ... See full document

... Introdução: O diabetes insípido (DI) central, caracterizado por poliúria, polidipsia e inabilida- de em concentrar a urina, apresenta diferentes etiologias, incluindo causas genética, autoi- mune, pós-traumática, entre ... See full document