A novel mutation in the NR0B1 (DAX1) gene in a large family with two boys affected by congenital adrenal hypoplasia Posted on by Read More
Rare case of Cushing’s disease due to double ACTH-producing adenomas, one located in the pituitary gland and one into the stalk Posted on by Read More
Biological activity of the e domain of the IGF-1Ec as addressed by synthetic peptides Posted on by Read More
Adipsic diabetes insipidus and venous thromboembolism (VTE): recommendations for addressing its hypercoagulability Posted on by Read More
Non-alcoholic fatty liver disease in women with polycystic ovary syndrome: assessment of non-invasive indices predicting hepatic steatosis and fibrosis Posted on by Read More
Insights into the coexistence of two mutations in the same LHCGR gene locus causing severe Leydig cell hypoplasia Posted on by Read More