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Children with MEN1 gene mutations may present first (and at a young age) with Cushing disease.
Pituitary abnormalities in patients with Fanconi anaemia.
A gender-dependent analysis of Cushing's disease in childhood: pre- and postoperative follow-up.
Correlation of TSH with the risk of paediatric thyroid carcinoma.
Identification of novel genetic variants in phosphodiesterase 8B (PDE8B), a cAMP-specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort of patients with adrenal tumours.
Identification, characterization and rescue of a novel vasopressin-2 receptor mutation causing nephrogenic diabetes insipidus.