Giancarlo Parenti

6PUBLICATIONS
18CO-AUTHORS
Gene and molecular therapyMedical biochemistry - proteins and peptides (incl. medical proteomics)Metabolic medicineEnzymesInformation systems organisation and management
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Publications (6)

|Jun 12, 2026
TRPML1 agonists synergize with enzyme replacement therapy in fibroblasts from Pompe disease patients.

|Nov 01, 2024
The European reference network for metabolic diseases (MetabERN) clinical pathway recommendations for Pompe disease (acid maltase deficiency, glycogen storage disease type II).

Giancarlo Parenti, Simona Fecarotta, Marianna Alagia

|Mar 31, 2024
Endocrine involvement in hepatic glycogen storage diseases: pathophysiology and implications for care.

Alessandro Rossi, Chiara Simeoli, Rosario Pivonello

|Oct 04, 2021
Correction of oxidative stress enhances enzyme replacement therapy in Pompe disease.

Antonietta Tarallo, Carla Damiano, Sandra Strollo

|Jan 18, 2021
The rapidly evolving view of lysosomal storage diseases.

Giancarlo Parenti, Diego L Medina, Andrea Ballabio

|May 16, 2020
Ensuring continuity of care for children with inherited metabolic diseases at the time of COVID-19: the experience of a metabolic unit in Italy.

Nicola Brunetti-Pierri, Simona Fecarotta, Annamaria Staiano

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Frequent Collaborators

2 joint publications

Diego Luis Medina

1 joint publications

Andrea Ballabio

1 joint publications

Sandra Strollo

1 joint publications

Nadia Minopoli