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Current Pharmaceutical Design|March 2, 2013
Anderson-Fabry disease in childrenSimona Sestito, Ferdinando Ceravolo, Daniela Concolino
Journal of Medical Case Reports|January 21, 2017
Combination therapy in a patient with chronic neuronopathic Gaucher disease: a case reportFerdinando Ceravolo, Michele Grisolia, Simona Sestito, et al.
Italian Journal of Pediatrics|September 10, 2013
Home treatment in paediatric patients with Hunter syndrome: the first Italian experienceFerdinando Ceravolo, Italia Mascaro, Simona Sestito, et al.
Journal of Human Genetics|December 23, 2016
Norrbottnian clinical variant of Gaucher disease in Southern ItalySimona Sestito, Mirella Filocamo, Ferdinando Ceravolo, et al.
European Journal of Pediatrics|August 31, 2013
Myoglobinuria as first clinical sign of a primary alpha-sarcoglycanopathyFerdinando Ceravolo, Sonia Messina, Carmelo Rodolico, et al.
Gastroenterology Research and Practice|February 17, 2016
Gastrointestinal Symptoms of Patients with Fabry DiseaseLicia Pensabene, Simona Sestito, Angela Nicoletti, et al.
European Journal of Pediatrics|June 12, 2009
Long-term treatment with recombinant insulin-like growth factor 1 (IGF-1) in a child with IGF-1 gene mutationDaniela Concolino, Gianluca Muzzi, Simona Sestito, et al.
Pediatrics and Neonatology|August 11, 2020
Evolution of congenital hypothyroidism in a cohort of preterm born childrenMaria Scavone, Laura Giancotti, Elisa Anastasio, et al.
Nutrients|February 10, 2024
Nutraceuticals and Pain Disorders of the Gut-Brain Interaction in Infants and Children: A Narrative Review and Practical InsightsSilvia Salvatore, Mariagrazia Carlino, Simona Sestito, et al.
Molecular Genetics and Metabolism|September 29, 2023
c.376A>G, (p.Ser126Gly) Alpha-Galactosidase A mutation induces ER stress, unfolded protein response and reduced enzyme trafficking to lysosome: Possible relevance in the pathogenesis of late-onset forms of Fabry DiseaseConcetta Riillo, Giuseppe Bonapace, Maria Teresa Moricca, et al.
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