Showing 1 - 6 results of 6 for search 'Elena Pardi', query time: 0.02s Refine Results
  1. 1
    Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features.

    Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features. by Elena Pardi, Simona Borsari, Federica Saponaro, Fausto Bogazzi, Claudio Urbani, Stefano Mariotti, Francesca Pigliaru, Chiara Satta, Fabiana Pani, Gabriele Materazzi, Paolo Miccoli, Lorena Grantaliano, Claudio Marcocci, Filomena Cetani

    Published 2017-01-01
    Get full text
    Article
  2. 2
    Cutaneous lesions and other non-endocrine manifestations of Multiple Endocrine Neoplasia type 1 syndrome

    Cutaneous lesions and other non-endocrine manifestations of Multiple Endocrine Neoplasia type 1 syndrome by Laura Pierotti, Elena Pardi, Elisa Dinoi, Paolo Piaggi, Simona Borsari, Simone Della Valentina, Chiara Sardella, Angela Michelucci, Maria Adelaide Caligo, Fausto Bogazzi, Claudio Marcocci, Claudio Marcocci, Filomena Cetani

    Published 2023-07-01
    Get full text
    Article
  3. 3
    Case report: Early-onset osteoporosis in a patient carrying a novel heterozygous variant of the WNT1 gene

    Case report: Early-onset osteoporosis in a patient carrying a novel heterozygous variant of the WNT1 gene by Maria Cristina Campopiano, Antonella Fogli, Angela Michelucci, Laura Mazoni, Antonella Longo, Simona Borsari, Elena Pardi, Elena Benelli, Chiara Sardella, Laura Pierotti, Elisa Dinoi, Claudio Marcocci, Claudio Marcocci, Filomena Cetani

    Published 2022-08-01
    Get full text
    Article
  4. 4
    Vitamin D measurement and effect on outcome in a cohort of patients with heart failure

    Vitamin D measurement and effect on outcome in a cohort of patients with heart failure by Federica Saponaro, Alessandro Saba, Sabina Frascarelli, Concetta Prontera, Aldo Clerico, Marco Scalese, Maria Rita Sessa, Filomena Cetani, Simona Borsari, Elena Pardi, Antonella Marvelli, Claudio Marcocci, Claudio Passino, Riccardo Zucchi

    Published 2018-10-01
    Get full text
    Article
  5. 5
    A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype.

    A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype. by Gianluca Occhi, Daniela Regazzo, Giampaolo Trivellin, Francesca Boaretto, Denis Ciato, Sara Bobisse, Sergio Ferasin, Filomena Cetani, Elena Pardi, Márta Korbonits, Natalia S Pellegata, Viktoryia Sidarovich, Alessandro Quattrone, Giuseppe Opocher, Franco Mantero, Carla Scaroni

    Published 2013-03-01
    Get full text
    Article
  6. 6
    The Long Non-Coding BC200 Is a Novel Circulating Biomarker of Parathyroid Carcinoma

    The Long Non-Coding BC200 Is a Novel Circulating Biomarker of Parathyroid Carcinoma by Annamaria Morotti, Annamaria Morotti, Filomena Cetani, Giulia Passoni, Simona Borsari, Elena Pardi, Vito Guarnieri, Chiara Verdelli, Giulia Stefania Tavanti, Giulia Stefania Tavanti, Luca Valenti, Luca Valenti, Cristiana Bianco, Stefano Ferrero, Stefano Ferrero, Sabrina Corbetta, Sabrina Corbetta, Valentina Vaira, Valentina Vaira

    Published 2022-05-01
    Get full text
    Article

Search Tools: