Search Results - "Wadman, R.I"

G.P.98 Dysfunction of the neuromuscular junction in patients with spinal muscular atrophy type 2 and 3 by Van der Pol, W.L, Wadman, R.I, Van den Berg, L.H, Vrancken, A.F.J

“…Abstract Degeneration of the alpha motor neurons in the spinal cord is the pathological hallmark of SMA. Recent pathological studies in mouse models of SMA…”
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P3.14 Drug treatment in spinal muscular atrophy types 1, 2 and 3: An update of the systematic Cochrane review by Wadman, R.I, van der Pol, W.L, Vrancken, A.F.J

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P3.6 Segmental distribution of muscle weakness in Dutch patients with SMA type 2, 3 and 4 by Wadman, R.I, van den Berg, L.H, van der Pol, W.L

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OC09: Patient reported experience with multimodal peripheral electrophysiological studies in children and adults with Spinal Muscular Atrophy (SMA) by Ros, L.A.A., Sleutjes, B.T.H.M., Goedee, H.S., Asselman, F., Pol, L., Der, Van, Wadman, R.I.

“…Purpose: Several electrophysiological tests have been proposed to aid in characterization of motor unit integrity and function in patients with Spinal Muscular…”
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Inflammatory markers in cerebrospinal fluid of paediatric spinal muscular atrophy patients receiving nusinersen treatment by Scheijmans, F.E.V., Cuppen, I., Zwartkruis, M.M., Signoria, I., van Ekris, C., Asselman, F., Wadman, R.I., Knol, E.F., van der Pol, W.L., Groen, E.J.N.

“…Spinal muscular atrophy (SMA) is a progressive motor neuron disease with onset during infancy or early childhood. Recent therapeutic advances targeting the…”
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Participation and mental well-being of mothers of home-living patients with spinal muscular atrophy by Cremers, C.H., Fischer, M.J., Kruitwagen-van Reenen, E.T., Wadman, R.I., Vervoordeldonk, J.J., Verhoef, M., Visser-Meily, J.M., van der Pol, W.L., Schröder, C.D.

“…•A substantial part of mothers of patients with SMA perceive a high caregiver burden.•Emotional well-being is comparable between mothers of children and adults…”
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Feeding and Swallowing Problems in Infants with Spinal Muscular Atrophy Type 1: an Observational Study by van der Heul, A M B, Cuppen, I, Wadman, R I, Asselman, F, Schoenmakers, M A G C, van de Woude, D R, Gerrits, E, van der Pol, W L, van den Engel-Hoek, L

“…Infantile hereditary proximal spinal muscular atrophy (SMA) type 1 is characterized by onset in the first 6 months of life and severe and progressive muscle…”
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Bulbar Problems Self-Reported by Children and Adults with Spinal Muscular Atrophy by van der Heul, A M B, Wijngaarde, C A, Wadman, R I, Asselman, F, van den Aardweg, M T A, Bartels, B, Cuppen, I, Gerrits, E, van den Berg, L H, van der Pol, W L, van den Engel-Hoek, L

“…Spinal muscular atrophy (SMA) is hereditary motor neuron disorder, characterised by the degeneration of motor neurons and progressive muscle weakness. It is…”
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