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Feeding and Swallowing Problems in Infants with Spinal Muscular Atrophy Type 1: an Observational Study

A.M.B. van der Heul; I. Cuppen; R.I. Wadman; F. Asselman; M.A.G.C. Schoenmakers; D.R. van der Woude; E. Gerrits (Lector); W.L. van der Pol; L. van den Engel-Hoek

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. Dysphagia is a common complication but has not been studied in detail. Objective: To study feeding and swallowing problems …

2020GezondheidArtikel

Employment status of patients with neuromuscular diseases in relation to personal factors, fatigue and health status : A secondary analysis

Marie-Antoinett van Minis; Joke Kalkman; Reinier Akkermans; Josephine Engels; Peter Huijbregts; Gijs Bleijenberg; Rob Oostendorp; B.G.M. van Engelen

To determine the number of employed people in a group of patients with neuromuscular diseases and in 3 separate subgroups (facioscapulo-humeral dystrophy, hereditary motor and sensory neuropathy, and myotonic dystrophy) to investigate any differences in employment status between the patient groups, and …

2010AlgemeenArtikel

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Feeding and Swallowing Problems in Infants with Spinal Muscular Atrophy Type 1: an Observational Study

Employment status of patients with neuromuscular diseases in relation to personal factors, fatigue and health status : A secondary analysis

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