Vito Guarnieri (V Guarnieri)

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 4

Top Topics

Replacement Therapy

Pulmonary Embolism

Clinical Practice

Top Venues

Journal of endocrinological investigation

BMC medical genetics

International journal of endocrinology

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

Publications

Giampiero I Baroncelli, G Carlucci, Elena Freri, M R Giuca, Vito Guarnieri, G Navarra, Benedetta Toschi, Stefano Mora
Correction to: The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinion. Journal of endocrinological investigation (2024)
Giampiero I Baroncelli, G Carlucci, Elena Freri, M R Giuca, Vito Guarnieri, G Navarra, Benedetta Toschi, Stefano Mora
The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinion. Journal of endocrinological investigation (2023)
Luigia Cinque, Flavia Pugliese, Celeste Clemente, Stefano Castellana, Maria Pia Leone, Danilo de Martino, Teresa Balsamo, Claudia Battista, Tommaso Biagini, Paolo Graziano, Marco Castori, Alfredo Scillitani, Vito Guarnieri
Rare Somatic MEN1 Gene Pathogenic Variant in a Patient Affected by Atypical Parathyroid Adenoma. International journal of endocrinology 2020 (2020)
Vito Guarnieri, Raewyn M Seaberg, Catherine Kelly, M Jean Davidson, Simon Raphael, Andrew Y Shuen, Filomena Baorda, Orazio Palumbo, Alfredo Scillitani, Geoffrey N Hendy, David E C Cole
Large intragenic deletion of CDC73 (exons 4-10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family. BMC medical genetics 18 (1) (2017)