The human Ec peptide: the active core of a progression growth factor with species-specific mode of action Posted on by Read More
A rare missense variant in RET exon 8 in a Portuguese family with atypical multiple endocrine neoplasia type 2A Posted on by Read More
A novel truncating AIP mutation, p.W279*, in a familial isolated pituitary adenoma (FIPA) kindred Posted on by Read More
A novel MC4R deletion coexisting with FTO and MC1R gene variants, causes severe early onset obesity Posted on by Read More
Thyrotoxic hypokalemic periodic paralysis in a Turkish patient presenting with a U wave on ECG Posted on by Read More