Carla Damiano
Naples, 80122, Italy
Last Updated: 09/26/2026
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Found 15 publications
Uncovering mitochondrial defects in photoreceptors opens therapeutic opportunities for Stargardt disease.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 15, 2026
TRPML1 agonists synergize with enzyme replacement therapy in fibroblasts from Pompe disease patients.
Journal: Journal of translational medicine
Published: March 10, 2026
Crosstalk between inflammation and autophagy in CeD organoids.
Journal: Scientific reports
Published: November 13, 2025
GMPPB-CDG Results in Lysosomal Dysfunction and Acid Alpha-Glucosidase Deficiency.
Journal: Journal of inherited metabolic disease
Published: September 12, 2025
MiR-21-5p and miR-223-3p as Treatment Response Biomarkers in Pediatric Eosinophilic Esophagitis.
Journal: International journal of molecular sciences
Published: January 20, 2025
Characterization of a WAS splice-site variant in a patient with Wiskott-Aldrich syndrome.
Journal: Frontiers in immunology
Published: October 25, 2024
MicroRNA dysregulation in ataxia telangiectasia.
Journal: Frontiers in immunology
Published: June 05, 2024
Postbiotic Preparation of Lacticaseibacillus rhamnosus GG against Diarrhea and Oxidative Stress Induced by Spike Protein of SARS-CoV-2 in Human Enterocytes.
Journal: Antioxidants (Basel, Switzerland)
Published: September 10, 2023
How dietary advanced glycation end products could facilitate the occurrence of food allergy.
Journal: The Journal of allergy and clinical immunology
Published: June 27, 2023
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
Last Updated: 09/26/2026