[PDF] Top 20 Arq Bras Endocrinol Metab vol.52 número2

... It is clear that beta-cells of the mouse can regenerate with recovery from acute destruction and severe hyper- glycemia (47). Islet beta-cells appear to arise primarily from replication of existing beta-cells in the ... See full document

... Direct evidence of ER stress markers expression in beta-cells from diabetic patients is still limited. Immu- nostaining of islets from T2D patients (autopsy mate- rial) showed an increased expression of Chop, BiP and p58 ... See full document

... the feasibility of glucose control by the combined implantation of a pump for peritoneal insulin delivery and a central intravenous glucose sensor, connect- ed physically by a subcutaneous lead and functionally by PID ... See full document

... O risco de doença arterial coronariana (DAC) nos pacientes com diabetes me- lito tipo 1 (DM1) é conhecido desde o final dos anos 1970, sendo atualmente a principal causa de mortalidade na população adulta com diabetes ... See full document

... Type 1 diabetes mellitus is the result of the autoimmune response against pancreatic β-cell(s). At the time of clinical diagnosis near 70% of β-cell mass is been destroyed as a consequence of the auto-destruction that ... 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

... 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

... 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

... 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

... 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

... Diabetes insípido neuro-hipofi sário com herança autossômica dominante (adFNDI) é uma doença autossômica dominante rara, caracterizada por poliúria e polidipsia devido à defi ciência de arginina-vasopressina (AVP). Mais ... 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

... 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

... 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

... 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

... 38. Chen X, Song F, Dai Y, Bao X, Jin Y. A novel mutation of the growth hormone receptor gene (GHR) in a Chinese girl with Laron syndrome. J Pediatr Endocrinol Metab. 2003;16:1183-9. 39. Amselem S, ... 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

... 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