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R I Wadman

Showing results (1-10 of 8) with videos related to

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Orphanet Journal of Rare Diseases|April 13, 2017
Cardiac pathology in spinal muscular atrophy: a systematic reviewC A Wijngaarde, A C Blank, M Stam, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 16, 2022
Inflammatory markers in cerebrospinal fluid of paediatric spinal muscular atrophy patients receiving nusinersen treatmentF E V Scheijmans, I Cuppen, M M Zwartkruis, et al.
Neuromuscular Disorders : NMD|April 8, 2019
Participation and mental well-being of mothers of home-living patients with spinal muscular atrophyC H Cremers, M J Fischer, E T Kruitwagen-van Reenen, et al.
European Journal of Neurology|December 2, 2017
Muscle strength and motor function throughout life in a cross-sectional cohort of 180 patients with spinal muscular atrophy types 1c-4R I Wadman, C A Wijngaarde, M Stam, et al.
Dysphagia|August 15, 2021
Mastication in Patients with Spinal Muscular Atrophy Types 2 and 3 is Characterized by Abnormal Efficiency, Reduced Endurance, and FatigueA M B van der Heul, R P A van Eijk, R I Wadman, et al.
Journal of Neuromuscular Diseases|April 26, 2020
Feeding and Swallowing Problems in Infants with Spinal Muscular Atrophy Type 1: an Observational StudyA M B van der Heul, I Cuppen, R I Wadman, et al.
Journal of Neuromuscular Diseases|September 3, 2019
Bulbar Problems Self-Reported by Children and Adults with Spinal Muscular AtrophyA M B van der Heul, C A Wijngaarde, R I Wadman, et al.
Genome Medicine|March 22, 2025
Long-read sequencing identifies copy-specific markers of SMN gene conversion in spinal muscular atrophyM M Zwartkruis, M G Elferink, D Gommers, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Orphanet Journal of Rare Diseases|April 13, 2017
Cardiac pathology in spinal muscular atrophy: a systematic reviewC A Wijngaarde, A C Blank, M Stam, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 16, 2022
Inflammatory markers in cerebrospinal fluid of paediatric spinal muscular atrophy patients receiving nusinersen treatmentF E V Scheijmans, I Cuppen, M M Zwartkruis, et al.
Neuromuscular Disorders : NMD|April 8, 2019
Participation and mental well-being of mothers of home-living patients with spinal muscular atrophyC H Cremers, M J Fischer, E T Kruitwagen-van Reenen, et al.
European Journal of Neurology|December 2, 2017
Muscle strength and motor function throughout life in a cross-sectional cohort of 180 patients with spinal muscular atrophy types 1c-4R I Wadman, C A Wijngaarde, M Stam, et al.
Dysphagia|August 15, 2021
Mastication in Patients with Spinal Muscular Atrophy Types 2 and 3 is Characterized by Abnormal Efficiency, Reduced Endurance, and FatigueA M B van der Heul, R P A van Eijk, R I Wadman, et al.
Journal of Neuromuscular Diseases|April 26, 2020
Feeding and Swallowing Problems in Infants with Spinal Muscular Atrophy Type 1: an Observational StudyA M B van der Heul, I Cuppen, R I Wadman, et al.
Journal of Neuromuscular Diseases|September 3, 2019
Bulbar Problems Self-Reported by Children and Adults with Spinal Muscular AtrophyA M B van der Heul, C A Wijngaarde, R I Wadman, et al.
Genome Medicine|March 22, 2025
Long-read sequencing identifies copy-specific markers of SMN gene conversion in spinal muscular atrophyM M Zwartkruis, M G Elferink, D Gommers, et al.
Pageof 1