Simona Rodighiero

Functional Characterization of Wild-Type and a Mutated Form of SLC26A4 Identified in a Patient with Pendred Syndrome

Markus Ritter, Luca Persani, Johannes Fürst, 2006, Cellular Physiology and Biochemistry.

Mechanisms Sensing and Modulating Signals Arising From Cell Swelling

Markus Ritter, Martin Jakab, M. Ritter, 2002, Cellular Physiology and Biochemistry.

Correlative scanning electron and confocal microscopy imaging of labeled cells coated by indium‐tin‐oxide

Andrea Falqui, Enzo Di Fabrizio, Bruno Torre, 2015, Microscopy research and technique.

Fast Fluorometric Method for Measuring Pendrin (SLC26A4) Cl-/I- Transport Activity

Markus Ritter, Paolo Beck-Peccoz, Luca Persani, 2006, Cellular Physiology and Biochemistry.

Molecular and functional studies of 4 candidate loci in Pendred syndrome and nonsyndromic hearing loss

Paolo Beck-Peccoz, Luca Persani, P. Beck‐Peccoz, 2012, Molecular and Cellular Endocrinology.

Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA

Felipe Moreno, Marta Gandía, F. Moreno, 2008, Proceedings of the National Academy of Sciences.

High phenotypic intrafamilial variability in patients with Pendred syndrome and a novel duplication in the SLC26A4 gene: clinical characterization and functional studies of the mutated SLC26A4 protein.

Umberto Ambrosetti, Paolo Beck-Peccoz, P. Beck‐Peccoz, 2007, European journal of endocrinology.

Versatile fabrication of vascularizable scaffolds for large tissue engineering in bioreactor.

Alessandro Tocchio, Paolo Milani, Cristina Lenardi, 2015, Biomaterials.