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Corrie E Erasmus

Showing results (71-80 of 91) with videos related to

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Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|June 9, 2020
A closer look at the paralyzed face; a narrative review of the neurobiological basis for functional and aesthetic appreciation between patients with a left and a right peripheral facial palsyThomas E Tieman, Scott R Chaiet, Robin Luijmes, et al.
Journal of Neuromuscular Diseases|March 22, 2024
Treatment Approaches for Altered Facial Expression: A Systematic Review in Facioscapulohumeral Muscular Dystrophy and Other Neurological DiseasesNathaniël B Rasing, Willianne A van de Geest-Buit, On Ying A Chan, et al.
Prenatal Diagnosis|May 19, 2025
Clinical Outcome and Risk Factors for Progression of Prenatally Diagnosed Fetal Ventriculomegaly: A Retrospective Multicenter StudyAnouk Moens, Zoe Albersnagel, Marieke B Veenhof, et al.
Clinical Genetics|August 31, 2021
Clinical, genetic, and histological features of centronuclear myopathy in the NetherlandsStacha F I Reumers, Corrie E Erasmus, Karlijn Bouman, et al.
BMC Neurology|August 18, 2016
Facioscapulohumeral dystrophy in children: design of a prospective, observational study on natural history, predictors and clinical impact (iFocus FSHD)Rianne J M Goselink, Tim H A Schreuder, Karlien Mul, et al.
American Journal of Medical Genetics. Part A|July 3, 2024
Nerve enlargement in patients with Noonan syndrome: A retrospective cohort studyFieke Draaisma, Erika K S M Leenders, Corrie E Erasmus, et al.
Neuromuscular Disorders : NMD|September 29, 2025
Significance of incidental copy number variants in the Duchenne muscular dystrophy geneIeke B Ginjaar, Marjolein Kriek, Mariëtte J V Hoffer, et al.
Journal of Neuromuscular Diseases|October 9, 2023
SELENON-Related Myopathy Across the Life Span, a Cross-Sectional Study for Preparing Trial ReadinessKarlijn Bouman, Jan T Groothuis, Jonne Doorduin, et al.
Neurology. Genetics|July 21, 2023
<i>LAMA2</i>-Related Muscular Dystrophy Across the Life Span: A Cross-sectional StudyKarlijn Bouman, Jan T Groothuis, Jonne Doorduin, et al.
Annals of Neurology|September 5, 2018
Facioscapulohumeral Dystrophy in Childhood: A Nationwide Natural History StudyRianne J M Goselink, Tim H A Schreuder, Nens van Alfen, et al.
Pageof 10

Showing results (71-80 of 91) with videos related to

Sort By:
Pageof 10
Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS|June 9, 2020
A closer look at the paralyzed face; a narrative review of the neurobiological basis for functional and aesthetic appreciation between patients with a left and a right peripheral facial palsyThomas E Tieman, Scott R Chaiet, Robin Luijmes, et al.
Journal of Neuromuscular Diseases|March 22, 2024
Treatment Approaches for Altered Facial Expression: A Systematic Review in Facioscapulohumeral Muscular Dystrophy and Other Neurological DiseasesNathaniël B Rasing, Willianne A van de Geest-Buit, On Ying A Chan, et al.
Prenatal Diagnosis|May 19, 2025
Clinical Outcome and Risk Factors for Progression of Prenatally Diagnosed Fetal Ventriculomegaly: A Retrospective Multicenter StudyAnouk Moens, Zoe Albersnagel, Marieke B Veenhof, et al.
Clinical Genetics|August 31, 2021
Clinical, genetic, and histological features of centronuclear myopathy in the NetherlandsStacha F I Reumers, Corrie E Erasmus, Karlijn Bouman, et al.
BMC Neurology|August 18, 2016
Facioscapulohumeral dystrophy in children: design of a prospective, observational study on natural history, predictors and clinical impact (iFocus FSHD)Rianne J M Goselink, Tim H A Schreuder, Karlien Mul, et al.
American Journal of Medical Genetics. Part A|July 3, 2024
Nerve enlargement in patients with Noonan syndrome: A retrospective cohort studyFieke Draaisma, Erika K S M Leenders, Corrie E Erasmus, et al.
Neuromuscular Disorders : NMD|September 29, 2025
Significance of incidental copy number variants in the Duchenne muscular dystrophy geneIeke B Ginjaar, Marjolein Kriek, Mariëtte J V Hoffer, et al.
Journal of Neuromuscular Diseases|October 9, 2023
SELENON-Related Myopathy Across the Life Span, a Cross-Sectional Study for Preparing Trial ReadinessKarlijn Bouman, Jan T Groothuis, Jonne Doorduin, et al.
Neurology. Genetics|July 21, 2023
<i>LAMA2</i>-Related Muscular Dystrophy Across the Life Span: A Cross-sectional StudyKarlijn Bouman, Jan T Groothuis, Jonne Doorduin, et al.
Annals of Neurology|September 5, 2018
Facioscapulohumeral Dystrophy in Childhood: A Nationwide Natural History StudyRianne J M Goselink, Tim H A Schreuder, Nens van Alfen, et al.
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