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Frontiers in Physiology|September 11, 2019
Corrigendum: Normal Calcium-Activated Anion Secretion in a Mouse Selectively Lacking TMEM16A in Intestinal EpitheliumGénesis Vega, Anita Guequén, Malin E V Johansson, et al.
Scientific Reports|October 28, 2016
Goblet Cell Hyperplasia Requires High Bicarbonate Transport To Support Mucin ReleaseGiulia Gorrieri, Paolo Scudieri, Emanuela Caci, et al.
The American Journal of Pathology|November 19, 2018
The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan-Deficient Muscular DystrophyElisabetta Gazzerro, Serena Baratto, Stefania Assereto, et al.
Human Mutation|April 14, 2025
Somatic Double Inactivation of <i>NF1</i> Associated with NF1-Related Pectus Excavatum DeformityCristina Chelleri, Marcello Scala, Patrizia De Marco, et al.
Kidney International Reports|June 19, 2026
IgM Hyposialylation Modulates Podocyte Vulnerability in Patients With Idiopathic Nephrotic SyndromeSonia Spinelli, Sofia Gaudiano, Andrea Garbarino, et al.
The EMBO Journal|March 11, 2020
Light-responsive microRNA miR-211 targets Ezrin to modulate lysosomal biogenesis and retinal cell clearanceFederica Naso, Daniela Intartaglia, Danila Falanga, et al.
Kidney International Reports|June 30, 2026
Steroid-Resistant Idiopathic Nephrotic Syndrome Reveals a Distinct Maladaptive Molecular StateSonia Spinelli, Sofia Gaudiano, Andrea Garbarino, et al.
Frontiers in Pediatrics|May 16, 2022
A Phenotypic-Driven Approach for the Diagnosis of WOREE SyndromeAntonella Riva, Giulia Nobile, Thea Giacomini, et al.
Cancers|April 30, 2021
Genotype-Phenotype Correlations in Neurofibromatosis Type 1: A Single-Center Cohort StudyMarcello Scala, Irene Schiavetti, Francesca Madia, et al.
Frontiers in Molecular Neuroscience|April 23, 2024
Allelic heterogeneity and abnormal vesicle recycling in <i>PLAA</i>-related neurodevelopmental disordersMichele Iacomino, Nadia Houerbi, Sara Fortuna, et al.
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