Roberta Giordano

Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia.

Tom Vulliamy, Michele D’Urso, G. Battistuzzi et al. · Proceedings of the National Academy of Sciences · 1988 · 255 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Long-Term Follow-Up in Adrenal Incidentalomas: An Italian Multicenter Study

Valentina Morelli, Giuseppe Reimondo, Roberta Giordano et al. · The Journal of Clinical Endocrinology & Metabolism · 2014 · 223 citations · Full text

Medicine, Endocrinology, Internal Medicine +17

Metabolic and cardiovascular outcomes in patients with Cushing’s syndrome of different aetiologies during active disease and 1 year after remission

Roberta Giordano, Andreea Picu, Elisa Marinazzo et al. · Clinical Endocrinology · 2011 · 123 citations

Medicine, Clinical Sciences, Endocrinology +17

Long-term morphological, hormonal, and clinical follow-up in a single unit on 118 patients with adrenal incidentalomas

Roberta Giordano, Elisa Marinazzo, Rita Berardelli et al. · European Journal of Endocrinology · 2010 · 99 citations

Medicine, Endocrinology, Surgery +17

Improvement of anthropometric and metabolic parameters, and quality of life following treatment with dual-release hydrocortisone in patients with Addison’s disease

Roberta Giordano, Federica Guaraldi, Elisa Marinazzo et al. · Endocrine · 2015 · 96 citations

Medicine, Endocrinology, Internal Medicine +3