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Vito Guarnieri

6PUBLICATIONS

39CO-AUTHORS

Medical biotechnology diagnostics (incl. biosensors)Structural properties of condensed matterInfant and child healthHaematological tumoursCancer therapy (excl. chemotherapy and radiation therapy)

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Publications (6)

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|Nov 12, 2025

The clinical challenge of MEN1 phenocopies: insights from a multicentric national retrospective study.

Rosaria M Ruggeri, Elio Benevento, Iderina Hasballa

|Feb 06, 2025

Hypophosphatemic rickets in an Italian multicentric cohort of 24 subjects: a clinical and molecular characterisation.

R Chimenz, C Columbu, F Pugliese

|Jun 09, 2024

Correction to: The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinion.

G I Baroncelli, G Carlucci, E Freri

|Sep 26, 2023

The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinion.

G I Baroncelli, G Carlucci, E Freri

|May 16, 2020

Rare Somatic MEN1 Gene Pathogenic Variant in a Patient Affected by Atypical Parathyroid Adenoma.

Luigia Cinque, Flavia Pugliese, Celeste Clemente

|Aug 05, 2017

Large intragenic deletion of CDC73 (exons 4-10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family.

Vito Guarnieri, Raewyn M Seaberg, Catherine Kelly

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Frequent Collaborators

2 joint publications

G I Baroncelli

2 joint publications

E Freri

2 joint publications

M R Giuca

2 joint publications

B Toschi

2 joint publications

S Mora

2 joint publications

Flavia Pugliese

1 joint publications

R Chimenz

1 joint publications

A Arena

1 joint publications

L Bonifazi Meffe

1 joint publications

L di Filippo

Frequent Collaborators

2 joint publications

G I Baroncelli

2 joint publications

E Freri

2 joint publications

M R Giuca

2 joint publications

B Toschi

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