Francesca Falvo
Catanzaro, Italy
Last Updated: 09/26/2026
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Found 9 publications
Renal involvement in paediatric Fabry disease.
Journal: Journal of biological regulators and homeostatic agents
Published: October 22, 2019
Alport's syndrome.
Journal: Journal of biological regulators and homeostatic agents
Published: October 22, 2019
Werner syndrome: a rare mutation.
Journal: Aging clinical and experimental research
Published: February 21, 2018
Genetics and Gene Therapy in Hunter Disease.
Journal: Current gene therapy
Published: December 31, 2017
Assessment of intrafamilial clinical variability of poikiloderma with neutropenia by a 10-year follow-up of three affected siblings.
Journal: European journal of medical genetics
Published: December 13, 2017
Genetic variants associated with Fabry disease progression despite enzyme replacement therapy.
Journal: Oncotarget
Published: August 24, 2017
Home infusion program with enzyme replacement therapy for Fabry disease: The experience of a large Italian collaborative group.
Journal: Molecular genetics and metabolism reports
Published: February 22, 2017
Combination therapy in a patient with chronic neuronopathic Gaucher disease: a case report.
Journal: Journal of medical case reports
Published: April 11, 2016
Norrbottnian clinical variant of Gaucher disease in Southern Italy.
Journal: Journal of human genetics
Published: March 23, 2016
Showing 1-9 of 9
Last Updated: 09/26/2026