Genetic analyses in familial isolated hyperparathyroidism: implication for clinical assessment and surgical management
Filomena Cetani(University of Pisa), Claudio Marcocci(University of Pisa), Aldo Pinchera(Unknown), Elena Ambrogini(Central Arkansas Veterans Healthcare System), Luisella Cianferotti(University of Florence), Elena Pardi(University of Pisa), Edda Vignali(University of Pisa), Simona Borsari(University of Pisa), Paolo Viacava(Ospedale di Livorno), M Lemmi, Piero Berti(Ospedale di Bolzano), Stefano Mariotti(University of Cagliari)
Cited by 61
Related Papers
PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis
|Nature Genetics|1998|502
Surgery or Surveillance for Mild Asymptomatic Primary Hyperparathyroidism: A Prospective, Randomized Clinical Trial
|The Journal of Clinical Endocrinology & Metabolism|2007|406
Genetic Analyses of the<i>HRPT2</i>Gene in Primary Hyperparathyroidism: Germline and Somatic Mutations in Familial and Sporadic Parathyroid Tumors
|The Journal of Clinical Endocrinology & Metabolism|2004|256
Calcium Intake in Bone Health: A Focus on Calcium-Rich Mineral Waters
|Nutrients|2018|240
A Novel Mutation of the Autoimmune Regulator Gene in an Italian Kindred with Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy, Acting in a Dominant Fashion and Strongly Cosegregating with Hypothyroid Autoimmune Thyroiditis
|The Journal of Clinical Endocrinology & Metabolism|2001|207