Paolo Cavarzere

7PUBLICATIONS
12CO-AUTHORS
Infant and child healthCharacterisation of biological macromoleculesDevelopmental genetics (incl. sex determination)Occupational epidemiologyBehavioural genetics
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Publications (7)

|Jun 08, 2026
Improvements in screening test, diagnosis, and outcomes of children with congenital hypothyroidism: lessons learned from 50 years of newborn screening.

|Dec 29, 2025
Rare forms of congenital adrenal hyperplasia: pathogenesis, clinical, treatment and management.

Paolo Cavarzere, Valentina Lupieri, Riccardo Battiston

|Dec 12, 2023
Role of genetic investigation in the diagnosis of short stature in a cohort of Italian children.

P Cavarzere, A Pietrobelli, A Gandini

|Jul 28, 2022
Benefits of rescreening newborns of mothers affected by autoimmune hypothyroidism.

Paolo Cavarzere, Laura Palma, Lara Nicolussi Principe

|Apr 20, 2022
Correction to: A complex pheotype in a girl with a novel heterozygous missense variant (p.Ile56Phe) of the GNAS gene.

Paolo Cavarzere, Andrea Gastaldi, Francesca Marta Elli

|Feb 24, 2022
A complex pheotype in a girl with a novel heterozygous missense variant (p.Ile56Phe) of the GNAS gene.

Paolo Cavarzere, Andrea Gastaldi, Francesca Marta Elli

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Frequent Collaborators

1 joint publications

Franco Antoniazzi

1 joint publications

Elisa Tadiotto

1 joint publications

Giorgio Piacentini

1 joint publications

Mariacarolina Salerno