Search Results - "Asselman, F"

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  1. 1

    Mastication in Patients with Spinal Muscular Atrophy Types 2 and 3 is Characterized by Abnormal Efficiency, Reduced Endurance, and Fatigue by van der Heul, A. M. B., van Eijk, R. P. A., Wadman, R. I., Asselman, F., Cuppen, I., Nievelstein, R. A. J., Gerrits, E., van der Pol, W. L., van den Engel-Hoek, L.

    Published in Dysphagia (01-08-2022)
    “…Mastication problems can have a negative impact on the intake of food and quality of life. This cross-sectional study characterizes mastication problems using…”
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    Journal Article
  2. 2

    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.

    Published in European journal of paediatric neurology (01-01-2023)
    “…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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    Journal Article
  3. 3

    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

    Published in Journal of neuromuscular diseases (01-01-2020)
    “…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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    Journal Article
  4. 4

    Swallowing Problems in Spinal Muscular Atrophy Types 2 and 3: A Clinical, Videofluoroscopic and Ultrasound Study by van der Heul, A M B, Nievelstein, R A J, van Eijk, R P A, Asselman, F, Erasmus, C E, Cuppen, I, Bittermann, A J N, Gerrits, E, van der Pol, W L, van den Engel-Hoek, L

    Published in Journal of neuromuscular diseases (01-01-2023)
    “…Spinal muscular atrophy (SMA) is a hereditary motor neuron disorder, characterized by the degeneration of motor neurons and progressive muscle weakness. There…”
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    Journal Article
  5. 5

    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

    Published in Journal of neuromuscular diseases (01-01-2019)
    “…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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    Journal Article
  6. 6

    Cost-effectiveness of trauma CT in the trauma room versus the radiology department: the REACT trial by Saltzherr, T. P., Goslings, J. C., Bakker, F. C., Beenen, L. F. M., Olff, M., Meijssen, K., Asselman, F. F., Reitsma, J. B., Dijkgraaf, M. G. W.

    Published in European radiology (2013)
    “…Objective To determine the cost-effectiveness of trauma room CT compared with CT performed at the radiology department. Methods In this randomised controlled…”
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  7. 7

    Cost-effectiveness of early versus selectively invasive strategy in patients with acute coronary syndromes without ST-segment elevation by Dijksman, L.M, Hirsch, A, Windhausen, F, Asselman, F.F, Tijssen, J.G.P, Dijkgraaf, M.G.W, de Winter, R.J

    Published in International journal of cardiology (09-01-2009)
    “…Abstract Aims The ICTUS trial compared an early invasive versus a selectively invasive strategy in high risk patients with a non-ST-segment elevation acute…”
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  8. 8

    Ontwerp, implementatie en toepassing van kostprijzen in het AMC by Asselman, F. F.

    Published in MAB ('s-Gravenhage. Online) (01-03-2007)
    “…Door een toenemende druk op de financiële middelen en de invoering van marktwerking in de zorg kreeg het AMC behoefte aan gedetailleerde kosteninformatie. Het…”
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  9. 9

    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.

    Published in Clinical neurophysiology (01-03-2022)
    “…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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    Journal Article