Federica Cavalcoli (F Cavalcoli)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 6

Top Topics

Neuroendocrine Tumors

Cross Sectional

Top Venues

Diagnostics (Basel, Switzerland)

Techniques in coloproctology

Orphanet journal of rare diseases

This page only lists publications with an associated author ORCID identifier.

Publications

Marianna Franchina, Federica Cavalcoli, Olga Falco, Marta La Milia, Alessandra Elvevi, Sara Massironi
Biochemical Markers for Neuroendocrine Tumors: Traditional Circulating Markers and Recent Development-A Comprehensive Review. Diagnostics (Basel, Switzerland) 14 (12) (2024)
Marianna Franchina, Federica Cavalcoli, Olga Falco, Marta La Milia, Alessandra Elvevi, Sara Massironi
Biochemical Markers for Neuroendocrine Tumors: Traditional Circulating Markers and Recent Development-A Comprehensive Review. Diagnostics (Basel, Switzerland) 14 (12) (2024)
Federica Cavalcoli, Emanuele Rausa, Davide Ferrari, Roberto Rosa, Marco Maccauro, Sara Pusceddu, Giovanna Sabella, Paolo Cantù, Vitellaro Marco, Jorgelina Coppa, Vincenzo Mazzaferro
Pathological Characteristics, Management, and Prognosis of Rectal Neuroendocrine Tumors: A Retrospective Study from a Tertiary Hospital. Diagnostics (Basel, Switzerland) 14 (17) (2024)
Federica Cavalcoli, A Magarotto, M E Kelly, P Cantù, A Mancini, E Rausa, E Masci
Outcomes of endoscopic full thickness resection in the colon rectum at an Italian tertiary center. Techniques in coloproctology (2023)
Sara Massironi, Federica Cavalcoli, Alessandra Elvevi, Maurizio Quatrini, Pietro Invernizzi
Somatostatin analogs in patients with Zollinger Ellison syndrome (ZES): an observational study. Endocrine (2021)
Federica Cavalcoli, Alberto Gandini, Irene Aglaia Matelloni, Francesca Catalano, Saverio Alicante, Guido Manfredi, Gianfranco Brambilla, Fernanda Menozzi, Federica Perolini, Egon Costi, Roberto Bertè, Elisabetta Buscarini
Dietary iron intake and anemia: food frequency questionnaire in patients with hereditary hemorrhagic telangiectasia. Orphanet journal of rare diseases 15 (1) (2020)