Arq Bras Endocrinol Metab vol.56 número2

reported that the T allele of rs7903146 SNP at the TCF7L2 locus is associated with a 1.57 increase in the risk of T2D in a sample of patients with documented multivessel

In this study, we analyzed the TAC3 and TACR3 genes in a cohort of patients with central pubertal di- sorders, including patients with central precocious pu- berty, normosmic

In the presence of activating mutations in the gene encoding GDH, there is a reduction in the sensitivity of the enzyme to allosteric inhibition by GTP and ATP, followed by

However, spontaneous pubertal development may be arrested in any of its stages, including lack of pro- gression of breast development associated with high levels of gonadotropins,

he main aim of the present study was to assess vitamin D status in new onset diabetes in the younger age group (< 25 years), and in age- and gender-matched controls without

A novel mutation in DAX1 (NR0B1) causing X-linked adrenal hypoplasia congenita: clinical, hormonal and genetic analysis. Jadhav U, Harris RM,

he aim of this study was to assess plasma levels of ho­ mocysteine under fasting and ater methionine overload, besides analyzing hyperhomocysteinemia during fasting, according

To illustrate the importance of AIP expression in the response to SSAs therapy in acromegaly, we de- scribe two patients whose somatotropinomas presented high SSTR2