Control of proteinuria with increased doses of agalsidase alfa in a patient with Fabry disease with atypical genotype–phenotype expression Christos Paliouras, Georgios Aperis, Foteini Lamprianou, Giorgos Ntetskas, Konstantinos Roufas, Polichronis Alivanis

Fabry disease as a trigger of immune-mediated glomerular disease: Clinical hypotheses and literature review Javier Martínez de Victoria Carazo, Haylen Marin, Francisco Javier De la Hera Fernández, Carlos Mañero Rodríguez, César Ramírez Tortosa, José Luís Callejas Rubio

Podocyturia in pediatric patients with Fabry disease Miguel Liern, Anabella Collazo, Maylin Valencia, Alejandro Fainboin, Lorena Isse, Cristian Costales-Collaguazo, Federico Ochoa, Graciela Vallejo, Elsa Zotta