[PDF] Top 20 Arq Bras Endocrinol Metab vol.56 número7

... Objectives: Vitamin D deiciency is common at all ages, and low levels of vitamin D have been as- sociated with high incidence of type 1 diabetes. Similar results are not consistent for type 2 diabetes. The aim of the ... 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

... 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

... 7. Ejaz S, Vissilopoulou-Sellin R, Busaidy NL, Hu MI, Waguespack SG, Jimenez C, et al. Cushing syndrome secondary to ectopic ad- renocorticotropic hormone secretion: the University of Texas MD Andersen Cancer Center ... 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

... Objetivo: Determinar os níveis plasmáticos de homocisteína de jejum e após sobrecarga de me- tionina e correlacionar a homocisteinemia com o polimorismo C677T e A1298C da metilenote- tra-hidrofolato redutase (MTHFR) em ... See full document

... O diabetes do tipo MODY (maturity-onset diabetes of the young) caracteriza-se por herança autos- sômica dominante, início precoce da hiperglicemia e defeitos na secreção de insulina. Os subtipos de MODY apresentam ... 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

... A 56-year-old female patient was initially evaluated in February, 1994, referred from the Neurosurgery De- partment, where she had a transsphenoidal surgery. She had a typical history of acromegaly, with a ... 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

... 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

... The enzyme 17b-hydroxysteroid dehydrogenase type 3 (17-b-HSD3) catalyzes the conversion of androstenedione to testosterone in the testes, and its deiciency is a rare disorder of sex devel- opment in 46,XY individuals. It ... 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

... Objective: The rate of reduction of nocturnal blood pressure (NBP) is lesser than normal in patients with type 2 diabetes mellitus (type 2 DM). Hyperhomocysteinemia (HHC) disrupts vascular structure and function, no ... See full document

... Relatamos uma nova mutação no gene GNRHR em um homem com hipogonadismo hipogo- nadotróico isolado normósmico (HHIn). A região codiicadora do gene GNRHR foi ampliicada e sequenciada. Três variantes p.[Asn10Lys;Gln11Lys]; ... See full document

... Objetivo: Realizamos um estudo prospectivo avaliando a prevalência de patologia nodular tireói dea em 34 pacientes acromegálicos. Sujeitos e métodos: Avaliamos os pacientes com ecograia tireóidea e punção biópsia com ... 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

... Objective: The objective of this study was to determine the incidence and etiology of congenital hypothyroidism (CH) in Uberaba, MG. Subjects and methods: From 2001 to 2010, by reviewing patient iles from a public ... See full document