Ulla Werlauff

Congenital Titinopathy: Comprehensive characterization and pathogenic insights

Emily C. Oates, Kristi Jones, Sandra Donkervoort et al. · Annals of Neurology · 2018 · 164 citations · Full text

Medicine, Molecular Genetics, Pathology +13

Loss-of-function mutations in<i>SCN4A</i>cause severe foetal hypokinesia or ‘classical’ congenital myopathy

Irina Zaharieva, Michael G. Thor, Emily C. Oates et al. · Brain · 2015 · 126 citations · Full text

Medicine, Genetics, Molecular Genetics +17

A randomized comparative study of two methods for controlling Tendo Achilles contracture in Duchenne muscular dystrophy

Sylvia A. Hyde, Ida Fløytrup, Sara Glent et al. · Neuromuscular Disorders · 2000 · 83 citations

Medicine, Orthopaedic Surgery, Orthopedic Surgery +16

Phenotypes, genotypes, and prevalence of congenital myopathies older than 5 years in Denmark

Nanna Witting, Ulla Werlauff, John Vissing · Neurology Genetics · 2017 · 52 citations · Full text

Life Sciences, Genetics, Pathology +17

Fatigue in patients with spinal muscular atrophy type II and congenital myopathies: evaluation of the fatigue severity scale

Ulla Werlauff, Ann-Lisbeth Højberg, R. Firla-Holme et al. · Quality of Life Research · 2013 · 44 citations

Medicine, Internal Medicine, Neurology +14