[PDF] Top 20 Arq Bras Endocrinol Metab vol.56 número6

... Recurrent PHPT is ascribable to an ectopic abnor- mal gland that was not detected earlier; occurrence of parathyromatosis (seeding of parathyroid cells along cervical region during sur[r] ... 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

... Ectopic ACTH syndrome is a rare disease often associated with severe hypercortisolism. When feasible, optimal management is surgical excision of the tumor. A 33-year-old male patient was admitted to the hospital in 1993 ... See full document

... Frasier syndrome (FS) is characterized by gonadal dysgenesis and nephropathy. It is caused by speciic mutations in the Wilms’ tumor suppressor gene (WT1) located in 11p23. Patients with the 46,XY karyotype present normal ... See full document

... Ao longo de sua vida colecionou merecidos títulos: Membro Titular da Academia Nacional de Medicina e da Academia de Medicina do Estado do Rio de Janeiro, Livre-Docente da UFRJ, Profes[r] ... See full document

... Maturity-onset diabetes of the young (MODY) is characterized by an autosomal dominant mode of inheritance, early onset of hyperglycemia, and defects of insulin secretion. MODY subtypes described present genetic, ... See full document

... Objetivo: Avaliar a validade da hemoglobina A1C (A1C) como ferramenta para o diagnóstico de diabetes tipo 2 e determinar o ponto de corte mais apropriado para a A1C no diagnóstico de uma amostra de haitianos americanos. ... See full document

... The disposition of anabolic and catabolic hormones to inluence protein turnover and, in turn, their inluence on the structural status of skel- etal muscles, led us to speculate as to wh[r] ... See full document

... Activating mutations in the TSH Receptor (TSHR) gene have been identiied as the molecular basis for congenital non-autoimmune hyperthyroidism. We describe the clinical indings and molecular characterization in a girl who ... See full document

... Objective: To evaluate inlammatory, oxidizing, and reducing responses during the progression of type 1 diabetes mellitus (T1DM) in patients without chronic complications. Subjects and methods: Plasma antioxidant status, ... See full document

... Many cases have been published showing a co-existence of autoimmune thyroid diseases (AITDs) and other autoimmune diseases. About a quarter of patients with achalasia have a con- current thyroid disease, most commonly ... See full document

... A enzima 17b-hidroxiesteroide desidrogenase tipo 3 (17-b-HSD3) catalisa a conversão de an- drostenediona a testosterona nos testículos, e sua deiciência é uma forma rara de distúrbio do desenvolvimento do sexo em ... See full document

... Objective: We made a prospective study evaluating the prevalence of thyroid nodular disease in acromegalic patients. Subjects and methods: Thyroid ultrasound and ultrasound-guided ine needle aspiration biopsy were ... See full document

... A deiciência isolada do hormônio do crescimento (DIGH) pode ser resultado de deleções/mu- tações no gene GH1 ou no gene GHRHR. O objetivo deste estudo foi caracterizar o defeito mo- lecular em uma menina que apresenta ... See full document

... Objective: To study the prevalence of shoulder pain and dysfunction in patients from Southern Brazil with diabetes mellitus (DM) and to evaluate the association of pain and dysfunction with diabetes control and ... See full document

... Objetivo: O objetivo deste estudo foi determinar a incidência e etiologia do hipotireoidismo congênito (HC) em Uberaba, MG. Pacientes e métodos: Mediante revisão dos prontuários de pacientes atendidos no ambulatório de ... See full document

... tive papillary thyroid carcinoma, displaying lymph node metastases at diagnosis and short-term recurrence after surgery, in whom we evaluated the expression pattern of the miRNAs miR[r] ... See full document

... Está bem estabelecido que fatores genéticos têm papel importante no desenvolvimento do diabetes melito tipo 2 (DM2) e obesidade e que indivíduos suscetíveis geneticamente podem desenvolver essas doenças metabólicas após ... See full document

... We report a novel GNRHR mutation in a male with normosmic isolated hypogonadotropic hy- pogonadism (nIHH). The coding region of the GNRHR gene was ampliied and sequenced. Three variants p.[Asn10Lys;Gln11Lys]; [Tyr283His] ... See full document

... Destaco, também, que esse efeito parece ser independente do tempo, mas sim regulado pela disponibilidade de acetil-CoA e citrato durante o metabolismo de lipídeos, favorecendo o ciclo [r] ... See full document