Zobrazeno 1 - 2
of 2
pro vyhledávání: '"R. I. Wadman"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-10 (2017)
Abstract Background Hereditary proximal spinal muscular atrophy (SMA) is a severe neuromuscular disease of childhood caused by homozygous loss of function of the survival motor neuron (SMN) 1 gene. The presence of a second, nearly identical SMN gene
Externí odkaz:
https://doaj.org/article/8c70df5be7ba4814b7799e91771fa9d1
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