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European Journal of Neurology|August 27, 2014
Endocrine function over time in patients with myotonic dystrophy type 1J R Dahlqvist, M C Ørngreen, N Witting, et al.
Neurology. Genetics|October 22, 2016
Muscle involvement in limb-girdle muscular dystrophy with GMPPB deficiency (LGMD2T)S T Oestergaard, T Stojkovic, J R Dahlqvist, et al.
Acta Neurologica Scandinavica|April 11, 2018
Phenotype and genotype of muscle ryanodine receptor rhabdomyolysis-myalgia syndromeN Witting, P Laforêt, N C Voermans, et al.
European Journal of Neurology|July 23, 2020
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imagingG Giacomucci, M Monforte, J Diaz-Manera, et al.
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