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Mitochondrion|March 23, 2007
Molecular genetic and clinical aspects of mitochondrial disorders in childhoodAli-Reza Moslemi, Niklas DarinEuropean Journal of Human Genetics : EJHG|October 3, 2013
B3GALNT2 is a gene associated with congenital muscular dystrophy with brain malformationsCarola Hedberg, Anders Oldfors, Niklas DarinNeurology|March 15, 2013
Increased childhood incidence of narcolepsy in western Sweden after H1N1 influenza vaccinationAttila Szakács, Niklas Darin, Tove HallböökNeuromuscular Disorders : NMD|June 19, 2017
Muscle pathology in Vici syndrome-A case study with a novel mutation in EPG5 and a summary of the literatureCarola Hedberg-Oldfors, Niklas Darin, Anders OldforsNeuromuscular Disorders : NMD|March 29, 2005
Early onset myopathy with a novel mutation in the Selenoprotein N gene (SEPN1)Homa Tajsharghi, Niklas Darin, Mar Tulinius, et al.Pediatric Neurology|June 18, 2026
Progressive Orexin Deficiency and Age-Dependent Glial and Axonal Biomarkers in juvenile neuronal ceroid lipofuscinosis type 3 (CLN3) DiseasePontus Wasling, Jonathan Blomqvist, Mia Olsson-Engman, et al.Health and Quality of Life Outcomes|July 6, 2017
The development of a health-related quality-of-life instrument for young people with narcolepsy: NARQoL-21John E Chaplin, Attila Szakács, Tove Hallböök, et al.The Journal of Pediatrics|January 30, 2002
Multiple congenital contractures: birth prevalence, etiology, and outcomeNiklas Darin, Eva Kimber, Anna-Karin Kroksmark, et al.Sleep|October 18, 2014
Psychiatric comorbidity and cognitive profile in children with narcolepsy with or without association to the H1N1 influenza vaccinationAttila Szakács, Tove Hallböök, Pontus Tideman, et al.Acta Paediatrica (Oslo, Norway : 1992)|October 3, 2014
Epidemiology of lysosomal storage diseases in SwedenMalin Hult, Niklas Darin, Ulrika von Döbeln, et al.Pageof 10