Nadia Minopoli
Via S. Pansini 5
Naples, Italy
Naples, Italy
Last Updated: 09/26/2026
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Found 8 publications
TRPML1 agonists synergize with enzyme replacement therapy in fibroblasts from Pompe disease patients.
Journal: Journal of translational medicine
Published: March 10, 2026
C-Branched Iminosugars as Selective Pharmacological Chaperones of Lysosomal α-Glucosidase for the Treatment of Pompe Disease.
Journal: Journal of medicinal chemistry
Published: September 15, 2025
GMPPB-CDG Results in Lysosomal Dysfunction and Acid Alpha-Glucosidase Deficiency.
Journal: Journal of inherited metabolic disease
Published: September 12, 2025
Carnitine is a pharmacological allosteric chaperone of the human lysosomal α-glucosidase.
Journal: Journal of enzyme inhibition and medicinal chemistry
Published: September 27, 2021
Correction of oxidative stress enhances enzyme replacement therapy in Pompe disease.
Journal: EMBO molecular medicine
Published: April 15, 2021
Pathogenesis of Mucopolysaccharidoses, an Update.
Journal: International journal of molecular sciences
Published: March 05, 2020
microRNAs as biomarkers in Pompe disease.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: February 06, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026