Chiara Satta

Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features

Elena Pardi, Simona Borsari, Federica Saponaro et al. · PLoS ONE · 2017 · 45 citations · Full text

Genetics, Parathyroid Disease, Gynecology +17

Functional characterization of a CDKN1B mutation in a Sardinian kindred with multiple endocrine neoplasia type 4

Elena Pardi, Stefano Mariotti, Natalia S. Pellegata et al. · Endocrine Connections · 2014 · 40 citations · Full text

Genetics, Pathology, Cdkn1b Mutation +18

An Italian Survey of Compliance With Major Guidelines for L-Thyroxine of Primary Hypothyroidism

Silvia Vezzani, Elisa Giannetta, Barbara Altieri et al. · Endocrine Practice · 2018 · 19 citations · Full text

Iodine Deficiency Disorders, Parathyroid Hormone, Primary Hypothyroidism +5

High prevalence of diabetes‐specific autoimmunity in first‐degree relatives of Sardinian patients with type 1 diabetes

Michela Incani, C. Serafini, Chiara Satta et al. · Diabetes/Metabolism Research and Reviews · 2016 · 13 citations