A. Biason

Quality of care to institutionalized patients with diabetes in Italy: a national survey

A. Salzano, A. Coracina, L. Fontana, 2020, European Geriatric Medicine.

Deletion within the CYP17 gene together with insertion of foreign DNA is the cause of combined complete 17 alpha-hydroxylase/17,20-lyase deficiency in an Italian patient.

M. Waterman, C. Scaroni, E. Simpson, 1991, Molecular endocrinology.

17-α-hydroxylase deficiency in three siblings: short- and long-term studies

C. Scaroni, F. Mantero, G. Opocher, 1991 .

Low-dose ketoconazole treatment in hirsute women

M. Boscaro, C. Scaroni, N. Sonino, 1990, Journal of endocrinological investigation.

17-alpha-hydroxylase deficiency in three siblings: short- and long-term studies.

C. Scaroni, F. Mantero, G. Opocher, 1991, Journal of endocrinological investigation.

New aspects of mineralocorticoid hypertension.

D. Armanini, M. Boscaro, N. Sonino, 1990, Hormone research.