Publications by authors named "Corrie Erasmus"

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Long-Term Outcomes of Surgical Drooling Treatment in Individuals with Neurodevelopmental Disabilities: A Retrospective Cohort Study.
Daan W A van den Nieuwenhof, Esther J P C van Bergen, Corrie E Erasmus, Corinne P A Delsing, Karen van Hulst

J Pediatr· January 2026

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The ins and outs of glycopyrronium treatment for paediatric drooling: exploring the treatment journey using real-world data.
Lynn B Orriëns, Karen van Hulst, Joyce M Geelen, Frank J A van den Hoogen, Anne T M Dittrich, Corrie E Erasmus

Eur J Paediatr Neurol· November 2025

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Validity, Reliability and Application of the Paediatric Posterior Drooling Scale.
Denise C R M Koeken, Karen van Hulst, Marloes L J Lagarde, Robert F Pangalila, Corrie E Erasmus

Child Care Health Dev· November 2025

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Severe Nerve Enlargement in SOS2-Related Noonan Syndrome.
Erika Leenders, Fieke Draaisma, Corrie E Erasmus, Catelijne Coppens, Lotte E R Kleimeier

Am J Med Genet A· October 2025

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Understanding posterior drooling in children and young people with neurodevelopmental disabilities: a parental perspective.
Lynn B Orriëns, Jan J W van der Burg, Petra Maille-Wisse, Angret de Boer, Frank J A van den Hoogen, Corrie E Erasmus

BMC Pediatr· October 2025

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279th ENMC international workshop: Classification, clinical care, outcome measures and biomarkers in childhood onset facioscapulohumeral dystrophy: towards standardizing clinical care and ensuring clinical trial readiness. Hoofddorp, The Netherlands, 1-3 November 2024.
Jildou N Dijkstra, Bettina C Henzi, Katherine D Mathews, Corrie E Erasmus, Renatta Knox

Neuromuscul Disord· October 2025

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Significance of incidental copy number variants in the Duchenne muscular dystrophy gene.
Ieke B Ginjaar, Marjolein Kriek, Mariëtte J V Hoffer, Renske Oegema, Ellen van Binsbergen, Corrie E Erasmus

Neuromuscul Disord· September 2025

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Clinical Outcome and Risk Factors for Progression of Prenatally Diagnosed Fetal Ventriculomegaly: A Retrospective Multicenter Study.
Anouk Moens, Zoe Albersnagel, Marieke B Veenhof, Phebe N Adama van Scheltema, Esther Sikkel, Corrie E Erasmus

Prenat Diagn· August 2025

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Negative effects on oral motor function after submandibular and parotid botulinum neurotoxin A injections for drooling in children with developmental disabilities.
Reva M van Eck, Lynn B Orriëns, Corinne P A Delsing, Frank J A van den Hoogen, Corrie E Erasmus

Dev Med Child Neurol· May 2025

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Quantitative ultrasound of submental and masticatory muscles in children with cerebral palsy.
Marloes L J Lagarde, Karen van Hulst, Corrie E Erasmus, Lenie van den Engel-Hoek, Alexander C H Geurts

J Pediatr Rehabil Med· February 2025

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Longitudinal Insights Into Childhood Onset Facioscapulohumeral Dystrophy: A 5-Year Natural History Study.
Jildou N Dijkstra, Helena T M Boon, Anne Koekkoek, Rianne J M Goselink, Maaike M Pelsma, Corrie E Erasmus

Neurology· January 2025

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Nerve enlargement in patients with Noonan syndrome: A retrospective cohort study.
Fieke Draaisma, Erika K S M Leenders, Corrie E Erasmus, Hilde M H Braakman, Melanie C J Burgers

Am J Med Genet A· November 2024

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Social and emotional impact of anterior drooling in school-age children and young people with neurodevelopmental disabilities.
Lynn B Orriëns, Lieke G J M van Aarle, Corrie E Erasmus, Karen van Hulst, Jan J W van der Burg

Eur J Pediatr· October 2024

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A cross-sectional study in 18 patients with typical and mild forms of nemaline myopathy in the Netherlands.
Esmee S B van Kleef, Sanne A J H van de Camp, Jan T Groothuis, Corrie E Erasmus, Michael A Gaytant

Neuromuscul Disord· October 2024

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Interdisciplinary assessment and treatment of paediatric drooling: two decades of experience by the Nijmegen saliva control team reflected in a stepwise algorithm.
Lynn B Orriëns, Sandra A F de Groot, Jan J W van der Burg, Frank J A van den Hoogen, Karen van Hulst, Corrie E Erasmus

Eur J Pediatr· September 2024

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Cardiac Involvement in LAMA2-Related Muscular Dystrophy and SELENON-Related Congenital Myopathy: A Case Series.
Karlijn Bouman, Frederik M A van den Heuvel, Reinder Evertz, Ewout Boesaard, Jan T Groothuis, Corrie E Erasmus

J Neuromuscul Dis· September 2024

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Predicting non-response to intraglandular botulinum neurotoxin A injections for drooling in children with neurodevelopmental disabilities.
Lynn B Orriëns, Karen van Hulst, Michèl A A P Willemsen, Frank J A van den Hoogen, Corrie E Erasmus

Dev Med Child Neurol· July 2024

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The when, why, and how of using glycopyrronium to diminish drooling in children with neurodevelopmental disabilities: Implications for clinical practice.
Lynn B Orriëns, Jan J W van der Burg, Frank J A van den Hoogen, Michèl A A P Willemsen, Karen van Hulst, Corrie E Erasmus

Eur J Paediatr Neurol· July 2024

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Treatment Approaches for Altered Facial Expression: A Systematic Review in Facioscapulohumeral Muscular Dystrophy and Other Neurological Diseases.
Nathaniël B Rasing, Willianne A van de Geest-Buit, On Ying A Chan, Karlien Mul, Anke Lanser, Corrie E Erasmus

J Neuromuscul Dis· May 2024

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Quality of life and support needs in children, adolescents, and young adults with facioscapulohumeral dystrophy, a mixed-method study.
Jildou N Dijkstra, Nathaniël B Rasing, Helena T M Boon, Sandra Altena-Rensen, Edith H C Cup, Corrie E Erasmus

Eur J Paediatr Neurol· May 2024

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Brody Disease, an Early-Onset Myopathy With Delayed Relaxation and Abnormal Gait: A Case Series of 9 Children.
Jamie I Verhoeven, Jasper Kramer, Juergen Seeger, Joery P Molenaar, Hilde Braakman, Corrie E Erasmus

Neurology· March 2024

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Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy.
Ana Töpf, Dan Cox, Irina T Zaharieva, Valeria Di Leo, Jaakko Sarparanta, Corrie E Erasmus

Nat Genet· March 2024

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Comparing the evidence for botulinum neurotoxin injections in paediatric anterior drooling: a scoping review.
Lynn B Orriëns, Karen van Hulst, Jan J W van der Burg, Frank J A van den Hoogen, Michèl A A P Willemsen, Corrie E Erasmus

Eur J Pediatr· January 2024

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Respiratory function in LAMA2-related muscular dystrophy and SELENON-related congenital myopathy, a 1.5-year natural history study.
Karlijn Bouman, Jeroen L M van Doorn, Jan T Groothuis, Peter J Wijkstra, Baziel G M van Engelen, Corrie E Erasmus

Eur J Paediatr Neurol· January 2024

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Bone quality in LAMA2-related muscular dystrophy and SELENON-related congenital myopathy, a one-year prospective natural history study.
Karlijn Bouman, Anne T M Dittrich, Jan T Groothuis, Baziel G M van Engelen, Heidi Zweers-van Essen, Corrie E Erasmus

Neuromuscul Disord· January 2024

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