OBJECTIVE: This study explores the use of quantitative data on strength and fatigability of orofacial muscles in patients with facioscapulohumeral muscular dystrophy (FSHD) and assesses the frequency of swallowing and communication difficulties and their relationship to orofacial muscle involvement. METHODS: We included 43 patients with FSHD and 35 healthy controls and used the Iowa Oral Performance Instrument (IOPI) to obtain quantitative measurements of strength and endurance of lip compression, cheek (buccodental) compression, and tongue elevation. For the assessment of swallowing and communication difficulties, we used the dysphagia-specific quality of life (SWAL-QOL) and Communicative Participation Item Bank questionnaires. RESULTS: Ch...
Purpose This study describes swallow-related quality of life (SWAL-QOL) in patients with myotonic dy...
Background: Spinal and bulbar muscular atrophy (SBMA) is an X-lined motor neuron disease characteriz...
Purpose This study describes swallow-related quality of life (SWAL-QOL) in patients with myotonic dy...
This study compared orofacial muscle strength between normal and dysarthric speakers and across type...
Dysphagia is reported in advanced stages of Duchenne muscular dystrophy (DMD). The population of DMD...
Dysphagia is reported in advanced stages of Duchenne muscular dystrophy (DMD). The population of DMD...
Contains fulltext : 50260.pdf (publisher's version ) (Closed access)Dysphagia is n...
Dysphagia is not considered a symptom of facioscapulohumeral muscular dystrophy (FSHD). In this stud...
OBJECTIVE: To evaluate facial weakness in patients with FSHD to better define clinical signs, and pi...
Facioscapulohumeral muscular dystrophy (FSHD) is not a recognized neuromuscular cause of dysphagia. ...
Contains fulltext : 232742.pdf (Publisher’s version ) (Open Access)OBJECTIVE: To e...
Introduction Herein we present an exploratory study of orofacial function in children with congenita...
Purpose This study describes swallow-related quality of life (SWAL-QOL) in patients with myotonic dy...
Contains fulltext : 167750.pdf (publisher's version ) (Closed access)Dysphagia in ...
Purpose This study describes swallow-related quality of life (SWAL-QOL) in patients with myotonic dy...
Purpose This study describes swallow-related quality of life (SWAL-QOL) in patients with myotonic dy...
Background: Spinal and bulbar muscular atrophy (SBMA) is an X-lined motor neuron disease characteriz...
Purpose This study describes swallow-related quality of life (SWAL-QOL) in patients with myotonic dy...
This study compared orofacial muscle strength between normal and dysarthric speakers and across type...
Dysphagia is reported in advanced stages of Duchenne muscular dystrophy (DMD). The population of DMD...
Dysphagia is reported in advanced stages of Duchenne muscular dystrophy (DMD). The population of DMD...
Contains fulltext : 50260.pdf (publisher's version ) (Closed access)Dysphagia is n...
Dysphagia is not considered a symptom of facioscapulohumeral muscular dystrophy (FSHD). In this stud...
OBJECTIVE: To evaluate facial weakness in patients with FSHD to better define clinical signs, and pi...
Facioscapulohumeral muscular dystrophy (FSHD) is not a recognized neuromuscular cause of dysphagia. ...
Contains fulltext : 232742.pdf (Publisher’s version ) (Open Access)OBJECTIVE: To e...
Introduction Herein we present an exploratory study of orofacial function in children with congenita...
Purpose This study describes swallow-related quality of life (SWAL-QOL) in patients with myotonic dy...
Contains fulltext : 167750.pdf (publisher's version ) (Closed access)Dysphagia in ...
Purpose This study describes swallow-related quality of life (SWAL-QOL) in patients with myotonic dy...
Purpose This study describes swallow-related quality of life (SWAL-QOL) in patients with myotonic dy...
Background: Spinal and bulbar muscular atrophy (SBMA) is an X-lined motor neuron disease characteriz...
Purpose This study describes swallow-related quality of life (SWAL-QOL) in patients with myotonic dy...