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Francesca Falvo

Showing results (1-10 of 5) with videos related to

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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.
Aging Clinical and Experimental Research|June 8, 2018
Werner syndrome: a rare mutationAlberto Castagna, Pietro Gareri, Francesca Falvo, et al.
European Journal of Medical Genetics|May 14, 2018
Assessment of intrafamilial clinical variability of poikiloderma with neutropenia by a 10-year follow-up of three affected siblingsDaniela Concolino, Simona Sestito, Francesca Falvo, 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.
Oncotarget|January 4, 2018
Genetic variants associated with Fabry disease progression despite enzyme replacement therapyFrancesca Scionti, Maria Teresa Di Martino, Simona Sestito, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
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.
Aging Clinical and Experimental Research|June 8, 2018
Werner syndrome: a rare mutationAlberto Castagna, Pietro Gareri, Francesca Falvo, et al.
European Journal of Medical Genetics|May 14, 2018
Assessment of intrafamilial clinical variability of poikiloderma with neutropenia by a 10-year follow-up of three affected siblingsDaniela Concolino, Simona Sestito, Francesca Falvo, 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.
Oncotarget|January 4, 2018
Genetic variants associated with Fabry disease progression despite enzyme replacement therapyFrancesca Scionti, Maria Teresa Di Martino, Simona Sestito, et al.
Pageof 1