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American Journal of Medical Genetics. Part A
|
June 5, 2025
Severe Nerve Enlargement in SOS2-Related Noonan Syndrome
Erika Leenders, Fieke Draaisma, Corrie E Erasmus, et al.
Journal of Neuromuscular Diseases
|
March 17, 2020
Dysphagia and Dysarthria in Children with Neuromuscular Diseases, a Prevalence Study
Mieke Kooi-van Es, Corrie E Erasmus, Bert J M de Swart, et al.
Neuromuscular Disorders : NMD
|
March 5, 2026
Framing childhood-onset facioscapulohumeral dystrophy: from first symptoms to future trials
Jildou N Dijkstra, Corrie E Erasmus, Pierre Laurian, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 1, 2024
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, et al.
BMC Pediatrics
|
October 9, 2025
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, et al.
Neurology
|
February 19, 2024
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, et al.
Neurology
|
October 4, 2022
Neuromuscular Features in XL-MTM Carriers: A Cross-sectional Study in an Unselected Cohort
Daniëlle K Franken, Karlijn Bouman, Stacha F I Reumers, et al.
European Journal of Human Genetics : EJHG
|
May 11, 2021
Solving unsolved rare neurological diseases-a Solve-RD viewpoint
Rebecca Schüle, Dagmar Timmann, Corrie E Erasmus, et al.
European Journal of Human Genetics : EJHG
|
August 25, 2021
Correction: Solving unsolved rare neurological diseases-a Solve-RD viewpoint
Rebecca Schüle, Dagmar Timmann, Corrie E Erasmus, et al.
Neurology
|
October 22, 2021
Natural History of Facioscapulohumeral Dystrophy in Children: A 2-Year Follow-up
Jildou N Dijkstra, Rianne J M Goselink, Nens van Alfen, et al.
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Search research articles
Search
Showing results (51-60 of 91) with videos related to
Sort By:
Page
of 10
American Journal of Medical Genetics. Part A
|
June 5, 2025
Severe Nerve Enlargement in SOS2-Related Noonan Syndrome
Erika Leenders, Fieke Draaisma, Corrie E Erasmus, et al.
Journal of Neuromuscular Diseases
|
March 17, 2020
Dysphagia and Dysarthria in Children with Neuromuscular Diseases, a Prevalence Study
Mieke Kooi-van Es, Corrie E Erasmus, Bert J M de Swart, et al.
Neuromuscular Disorders : NMD
|
March 5, 2026
Framing childhood-onset facioscapulohumeral dystrophy: from first symptoms to future trials
Jildou N Dijkstra, Corrie E Erasmus, Pierre Laurian, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 1, 2024
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, et al.
BMC Pediatrics
|
October 9, 2025
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, et al.
Neurology
|
February 19, 2024
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, et al.
Neurology
|
October 4, 2022
Neuromuscular Features in XL-MTM Carriers: A Cross-sectional Study in an Unselected Cohort
Daniëlle K Franken, Karlijn Bouman, Stacha F I Reumers, et al.
European Journal of Human Genetics : EJHG
|
May 11, 2021
Solving unsolved rare neurological diseases-a Solve-RD viewpoint
Rebecca Schüle, Dagmar Timmann, Corrie E Erasmus, et al.
European Journal of Human Genetics : EJHG
|
August 25, 2021
Correction: Solving unsolved rare neurological diseases-a Solve-RD viewpoint
Rebecca Schüle, Dagmar Timmann, Corrie E Erasmus, et al.
Neurology
|
October 22, 2021
Natural History of Facioscapulohumeral Dystrophy in Children: A 2-Year Follow-up
Jildou N Dijkstra, Rianne J M Goselink, Nens van Alfen, et al.
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of 10