Zobrazeno 1 - 6
of 6
pro vyhledávání: '"A M B, van der Heul"'
Autor:
W.L. van der Pol, R.P.A. van Eijk, L. van den Engel-Hoek, Inge Cuppen, Renske I. Wadman, Fay-Lynn Asselman, Rutger A.J. Nievelstein, E Gerrits, A M B van der Heul
Publikováno v:
Dysphagia, 37, 715-723
Dysphagia, 37, 4, pp. 715-723
Dysphagia, 37, 4, pp. 715-723
Mastication problems can have a negative impact on the intake of food and quality of life. This cross-sectional study characterizes mastication problems using clinical and instrumental assessments in patients with spinal muscular atrophy (SMA) types
Autor:
A M B, van der Heul, R P A, van Eijk, R I, Wadman, F, Asselman, I, Cuppen, R A J, Nievelstein, E, Gerrits, W L, van der Pol, L, van den Engel-Hoek
Publikováno v:
Dysphagia. 37(4)
Mastication problems can have a negative impact on the intake of food and quality of life. This cross-sectional study characterizes mastication problems using clinical and instrumental assessments in patients with spinal muscular atrophy (SMA) types
Autor:
Renske I. Wadman, Fay-Lynn Asselman, E Gerrits, W.L. van der Pol, D R van de Woude, Marja A.G.C. Schoenmakers, A M B van der Heul, Inge Cuppen, L. van den Engel-Hoek
Publikováno v:
Journal of Neuromuscular Diseases, 7, 323-330
Journal of Neuromuscular Diseases, 7(3), 323-330
Journal of Neuromuscular Diseases, 7, 3, pp. 323-330
Journal of Neuromuscular Diseases, 7(3), 323-330
Journal of Neuromuscular Diseases, 7, 3, pp. 323-330
Contains fulltext : 220780.pdf (Publisher’s version ) (Closed access) BACKGROUND: 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 weakness.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78d8125a21e4fbbc95ea01f386172847
https://doi.org/10.3233/JND-190465
https://doi.org/10.3233/JND-190465
Autor:
W.L. van der Pol, L.H. van den Berg, M.T. van den Aardweg, L. van den Engel-Hoek, Fay-Lynn Asselman, Inge Cuppen, Camiel A. Wijngaarde, Bart Bartels, E Gerrits, A M B van der Heul, Renske I. Wadman
Publikováno v:
Journal of Neuromuscular Diseases, 6, 361-368
Journal of Neuromuscular Diseases, 6, 3, pp. 361-368
Journal of Neuromuscular Diseases, 6, 3, pp. 361-368
Item does not contain fulltext BACKGROUND: Spinal muscular atrophy (SMA) is hereditary motor neuron disorder, characterised by the degeneration of motor neurons and progressive muscle weakness. It is caused by the homozygous loss of function of the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1464c15dcb72655672d4efb9e27967e
https://doi.org/10.3233/JND-190379
https://doi.org/10.3233/JND-190379
Autor:
I A C, de Vries, C C, Breugem, A M B, van der Heul, M J C, Eijkemans, M, Kon, A B, Mink van der Molen
Publikováno v:
Clinical oral investigations. 18(5)
The purpose of this study in children with cleft palate only (CPO) is to (1) explore the prevalence of feeding problems on a retrospective basis, (2) investigate rates of nasogastric (NG) feeding, (3) examine the prevalence of associated disorders an
Autor:
A. M. B. van der Heul, A. B. Mink van der Molen, Corstiaan C. Breugem, I. A. C. de Vries, M. J. C. Eijkemans, Moshe Kon
Publikováno v:
Clinical Oral Investigations.
The purpose of this study in children with cleft palate only (CPO) is to (1) explore the prevalence of feeding problems on a retrospective basis, (2) investigate rates of nasogastric (NG) feeding, (3) examine the prevalence of associated disorders an