Giancarlo Parenti

7PUBLICATIONS
48CO-AUTHORS
Cell and nuclear divisionGene and molecular therapyMedical biochemistry - proteins and peptides (incl. medical proteomics)Metabolic medicineEnzymes
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Publications (7)

|Oct 02, 2026
S-Nitrosylation of glycogen phosphorylase regulates nuclear glycogenolysis and is impaired in metabolic liver disorders.

|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

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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