Ulrike Heinl-Dunkhase
Aabenraa, Denmark
Last Updated: 09/26/2026
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Found 8 publications
Ryanodine receptor 1 related myasthenia like myopathy responsive to pyridostigmine.
Journal: European journal of medical genetics
Published: March 08, 2022
Impaired glucose-1,6-biphosphate production due to bi-allelic PGM2L1 mutations is associated with a neurodevelopmental disorder.
Journal: American journal of human genetics
Published: January 28, 2021
Gait analysis for individually tailored interdisciplinary interventions in children with cerebral palsy: a randomized controlled trial.
Journal: Developmental medicine and child neurology
Published: December 15, 2018
Is MED13L-related intellectual disability a recognizable syndrome?
Journal: European journal of medical genetics
Published: February 24, 2018
Epidemiology of cerebral palsy in Southern Denmark.
Journal: Danish medical journal
Published: January 06, 2015
The use of instrumented gait analysis for individually tailored interdisciplinary interventions in children with cerebral palsy: a randomised controlled trial protocol.
Journal: BMC pediatrics
Published: June 11, 2014
Post-varicella angiopathy: a series of 4 patients with focus on virologic and neuroimaging findings.
Post-varicella angiopathy: a series of 4 patients with focus on virologic and neuroimaging findings.
Journal: Pediatric neurology
Published: September 24, 2013
Showing 1-8 of 8
Last Updated: 09/26/2026