Rare Neuromuscular Disorders (RND) research group at Oslo University Hospital aims to contribute to a better understanding of rare neuromuscular disorders through enhancing diagnostic methods, development of better treatments and multidisciplinary standards of care. The RND research group is a part of the movement disorders group. The research group is closely linked with the unit for inborn and hereditary neuromuscular disorders (EMAN) at Oslo University Hospital.
Novel mutations in the HADHB gene causing a mild phenotype of mitochondrial trifunctional protein (MTP) deficiency
JIMD Rep, 63 (3), 193-198
The Physical Activity and Fitness in Childhood Cancer Survivors (PACCS) Study: Protocol for an International Mixed Methods Study
JMIR Res Protoc, 11 (3), e35838
Functional Ability and Physical Activity in Hereditary Neuromuscular Diseases
J Neuromuscul Dis, 9 (3), 437-446