Ontology highlight
ABSTRACT:
SUBMITTER: Kirschner J
PROVIDER: S-EPMC7347351 | biostudies-literature | 2020 Sep
REPOSITORIES: biostudies-literature
Kirschner Janbernd J Butoianu Nina N Goemans Nathalie N Haberlova Jana J Kostera-Pruszczyk Anna A Mercuri Eugenio E van der Pol W Ludo WL Quijano-Roy Susana S Sejersen Thomas T Tizzano Eduardo F EF Ziegler Andreas A Servais Laurent L Muntoni Francesco F
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 20200709
Spinal muscular atrophy (SMA) used to be one of the most common genetic causes of infant mortality. New disease modifying treatments have changed the disease trajectories and most impressive results are seen if treatment is initiated in the presymptomatic phase of the disease. Very recently, the European Medicine Agency approved Onasemnogene abeparvovec (Zolgensma®) for the treatment of patients with SMA with up to three copies of the SMN2 gene or the clinical presentation of SMA type 1. While t ...[more]