Giuseppina Del Prete

A novel NKX2.1 mutation in a family with hypothyroidism and benign hereditary chorea.

P. Macchia, G. De Michele, A. Filla, 2008, Thyroid : official journal of the American Thyroid Association.

A new case of familial nonautoimmune hyperthyroidism caused by the M463V mutation in the TSH receptor with anticipation of the disease across generations: a possible role of iodine supplementation.

P. Macchia, G. Fenzi, M. Salerno, 2007, Thyroid : official journal of the American Thyroid Association.

Combined Imaging With 18F-FDG-PET/CT and 111In-Labeled Octreotide SPECT for Evaluation of Thymic Epithelial Tumors

M. Salvatore, L. Pace, S. de Placido, 2013, Clinical nuclear medicine.

Incremental prognostic value of stress myocardial perfusion imaging in asymptomatic diabetic patients.

M. Petretta, W. Acampa, A. Cuocolo, 2013, Atherosclerosis.