Grete H. Andersen
Copenhagen, 2100, Denmark
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 13 publications
High-intensity training in patients with spinal and bulbar muscular atrophy.
Journal: Journal of neurology
Published: March 06, 2019
High-intensity interval training in facioscapulohumeral muscular dystrophy type 1: a randomized clinical trial.
Journal: Journal of neurology
Published: February 21, 2017
The antimyotonic effect of lamotrigine in non-dystrophic myotonias: a double-blind randomized study.
The antimyotonic effect of lamotrigine in non-dystrophic myotonias: a double-blind randomized study.
Journal: Brain : a journal of neurology
Published: February 08, 2017
Aerobic training in myotonia congenita: Effect on myotonia and fitness.
Journal: Muscle & nerve
Published: September 27, 2016
MRI as outcome measure in facioscapulohumeral muscular dystrophy: 1-year follow-up of 45 patients.
Journal: Journal of neurology
Published: August 17, 2016
Mitochondrial DNA mutation load in a family with the m.8344A>G point mutation and lipomas: a case study.
Journal: Clinical case reports
Published: April 09, 2016
Protein-carbohydrate supplements improve muscle protein balance in muscular dystrophy patients after endurance exercise: a placebo-controlled crossover study.
Journal: American journal of physiology. Regulatory, integrative and comparative physiology
Published: November 21, 2014
Aerobic training and postexercise protein in facioscapulohumeral muscular dystrophy: RCT study.
Journal: Neurology
Published: November 18, 2014
Bezafibrate in skeletal muscle fatty acid oxidation disorders: a randomized clinical trial.
Journal: Neurology
Published: January 24, 2014
Muscle phenotype in patients with myotonic dystrophy type 1.
Journal: Muscle & nerve
Published: July 23, 2012
Last Updated: 09/26/2026