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Current Pharmaceutical Design|March 2, 2013
Anderson-Fabry disease in childrenSimona Sestito, Ferdinando Ceravolo, Daniela Concolino
Alzheimer'S & Dementia (New York, N. Y.)|March 27, 2020
Perspective: Is therapeutic plasma exchange a viable option for treating Alzheimer's disease?Bruno P Imbimbo, Stefania Ippati, 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.
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.
Molecular Genetics and Metabolism|August 27, 2013
Efficacy of miglustat in Niemann-Pick C disease: a single centre experienceVirginia Maria Ginocchio, Adele D'Amico, Enrico Bertini, 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.
Journal of Inherited Metabolic Disease|February 28, 2023
Long-term safety and efficacy of velmanase alfa treatment in children under 6 years of age with alpha-mannosidosis: A phase 2, open label, multicenter studyNathalie Guffon, Vassiliki Konstantopoulou, Julia B Hennermann, et al.
Orphanet Journal of Rare Diseases|September 30, 2020
The SPARKLE registry: protocol for an international prospective cohort study in patients with alpha-mannosidosisJulia B Hennermann, Nathalie Guffon, Federica Cattaneo, et al.
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