Showing results (1-10 of 19) with videos related to
Sort By:
Pageof 2
Molecular Genetics and Metabolism|November 25, 2017
Epilepsy in mucopolysaccharidosis disordersMaurizio Scarpa, Charles Marques Lourenço, Hernán AmartinoArchives of Dermatology|December 22, 2004
Fabry disease: a study of 6 hemizygous men and 5 heterozygous women with emphasis on dermatologic manifestationsMargarita Larralde, Paula Boggio, Hernán Amartino, et al.Molecular Genetics and Metabolism Reports|May 17, 2017
Effectiveness of enzyme replacement therapy in Fabry disease: Long term experience in ArgentinaGustavo Cabrera, Juan Politei, Norberto Antongiovani, et al.Archivos Argentinos De Pediatria|October 17, 2012
[Alrternating hemiplegia of childhood: a case report and literature review]Martín Traut, Brian M Cavagnari, José H Méndez, et al.Epilepsia|April 19, 2012
Sulthiame add-on therapy in children with focal epilepsies associated with encephalopathy related to electrical status epilepticus during slow sleep (ESES)Natalio Fejerman, Roberto Caraballo, Ricardo Cersósimo, et al.Archivos Argentinos De Pediatria|January 18, 2021
[Idursulfase desensitization in a child with Hunter syndrome (mucopolysaccharidosis II)]Lucrecia L Bustamante, Luciano Garavaglia, Esteban I Garramone, et al.Molecular Genetics and Metabolism|November 21, 2017
Surgical management of neurological manifestations of mucopolysaccharidosis disordersTord D Alden, Hernán Amartino, Amauri Dalla Corte, et al.Molecular Genetics and Metabolism|November 25, 2017
Practical management of behavioral problems in mucopolysaccharidoses disordersMaria L Escolar, Simon A Jones, Elsa G Shapiro, et al.Medicina|June 24, 2017
Switch from agalsidase beta to agalsidase alfa in the enzyme replacement therapy of patients with Fabry disease in Latin AmericaDiego Ripeau, Hernán Amartino, Martín Cedrolla, et al.Medicina|August 15, 2023
[Argentinean Consensus on the Diagnosis and Treatment of Niemann- Pick Disease Type C]Hernán Amartino, Carolina Azcona, Cristian Calandra, et al.Pageof 2