Pre-diagnosing and managing patients with GM1 gangliosidosis and related disorders by the evaluation of GM1 ganglioside content
Rodolfo Tonin(Meyer Children's Hospital), Amelia Morrone(Meyer Children's Hospital), Anna Ardissone(Fondazione IRCCS Istituto Neurologico Carlo Besta), Arianna Casini(Nuovo Ospedale San Giovanni di Dio), Elena Procopio(Meyer Children's Hospital), Maria Margherita Mancardi(Istituto Giannina Gaslini), Alessandro Salviati(University of Verona), Antonio Marangi(University of Verona), Rita Fischetto(Ospedale Pediatrico Giovanni XXIII), Maja Di Rocco(Istituto Giannina Gaslini), Pietro Strisciuglio(Federico II University Hospital), Francesco S. Pavone(National Research Council), Anna Caciotti(Meyer Children's Hospital), Federica Deodato(Bambino Gesù Children's Hospital), Martino Calamai(National Research Council), Giusi Mangone(Meyer Children's Hospital), Rossella Parini(MRC Epidemiology Unit), Agata Fiumara, Silvia Ricci(Meyer Children's Hospital), Renzo Guerrini(Meyer Children's Hospital)
Cited by 15
Related Papers
The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission1
|Epilepsia|2010|1.7k
A developmental and genetic classification for malformations of cortical development: update 2012
|Brain|2012|1.1k
A developmental and genetic classification for malformations of cortical development
|Neurology|2005|720
Classification system for malformations of cortical development
|Neurology|2001|537
Somatic Mutations in Cerebral Cortical Malformations
|New England Journal of Medicine|2014|394