Webinar Nusinersen in pre-symptomatic SMA
30 November, 2020
This event has been organized and sponsored by Biogen.
- Provide an overview of the NURTURE study and discuss new results from the study
- Understand the benefit of both prompt diagnosis and early and longer-term treatment with nusinersen
Meet the speaker
Kathryn J Swoboda, MD
Massachusetts General Hospital, Boston, MA, USA
Kathryn J Swoboda is a neurologist and geneticist with particular expertise in motor disorders with childhood onset. Her primary research efforts include genotype/phenotype studies targeting the underlying molecular disease pathogenesis, biomarker development and treatment of inherited motor disorders. She has directed or collaborated in numerous clinical trials and studies in children and adults with spinal muscular atrophy (SMA), alternating hemiplegia of childhood (AHC), inherited disorders of neurotransmitter biosynthesis and metabolism (Segawa disease, dihydropteridine reductase [DHPR] and 6-pyruvoyl-tetrahydropterin synthase [PTPS] deficiency), and other disorders, including childhood-onset ataxias and neurodegenerative disorders. She is actively engaged in pilot initiatives to support newborn screening for neurodegenerative disorders with onset in infancy or childhood, including SMA, Pompe and other rare neurological disorders.