Delphi consensus on recommendations for the treatment of spinal muscular atrophy in Spain (RET-AME consensus)

Introduction: Spinal muscular atrophy (SMA) is a neurodegenerative disease caused by a biallelic mutation of the SMN1 gene, located on the long arm of chromosome 5, and predominantly affects the motor neurons of the anterior horn of the spinal cord, causing progressive muscle weakness and atrophy. T...

Full description

Bibliographic Details
Main Authors: I. Pitarch Castellano, M. Cabrera-Serrano, R. Calvo Medina, M.G. Cattinari, S. Espinosa García, J.A. Fernández-Ramos, O. García Campos, D. Gómez-Andrés, M.A. Grimalt Calatayud, A.J. Gutiérrez Martínez, E. Ibáñez Albert, S. Kapetanovic García, M. Madruga-Garrido, M. Martínez-Moreno, J. Medina Cantillo, A.I. Melián Suárez, A. Moreno Escribano, F. Munell, A. Nascimento Osorio, S.I. Pascual-Pascual, M. Povedano, I.M. Santana Casiano, J.F. Vázquez-Costa
Format: Article
Language:English
Published: Elsevier España 2022-04-01
Series:Neurología (English Edition)
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2173580822000128