S. Wallace

发表

Priority setting at the clinical level: the case of nusinersen and the Norwegian national expert group

M. Magelssen, R. Førde, M. Rasmussen, 2021, BMC medical ethics.

A de novo Mutation in the SCN4A Gene Causing Sodium Channel Myotonia

E. Kerty, K. Ørstavik, T. Torbergsen, 2015, Journal of neuromuscular diseases.

Novel PIGT Variant in Two Brothers: Expansion of the Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 Phenotype

D. Misceo, A. Stray-Pedersen, P. Strømme, 2016, Genes.

Cognitive function, behaviour and quality of life in children with myotonic dystrophy type 1 in South - Eastern Norway.

K. Ørstavik, P. Aden, M. Rasmussen, 2023, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.