Corrie E. Erasmus

Mutations in DDHD2, Encoding an Intracellular Phospholipase A1, Cause a Recessive Form of Complex Hereditary Spastic Paraplegia

Janneke Schuurs-Hoeijmakers, Michael T. Geraghty, Erik‐Jan Kamsteeg et al. · The American Journal of Human Genetics · 2012 · 182 citations · Full text

Medicine, Genetics, Molecular Genetics +6

Botulinum toxin assessment, intervention and aftercare for paediatric and adult drooling: international consensus statement

Dinah Reddihough, Corrie E. Erasmus, Hilary Johnson et al. · European Journal of Neurology · 2010 · 123 citations

Health Professions, Speech-language Pathology, Dysphagia +16

Drooling in cerebral palsy: hypersalivation or dysfunctional oral motor control?

Corrie E. Erasmus, Karen van Hulst, Liselotte J. C. Rotteveel et al. · Developmental Medicine & Child Neurology · 2009 · 119 citations · Full text

Health Professions, Speech-language Pathology, Dysphagia +12

De novo mutations in PLXND1 and REV3L cause Möbius syndrome

Laura Tomás‐Roca, Anastasia Tsaalbi‐Shtylik, Jacob G. Jansen et al. · Nature Communications · 2015 · 101 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Oral muscles are progressively affected in Duchenne muscular dystrophy: implications for dysphagia treatment

L. van de Engel-Hoek, Corrie E. Erasmus, Jan C.M. Hendriks et al. · Journal of Neurology · 2012 · 97 citations

Medicine, Rehabilitation Medicine, Dysphagia +9