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Visar resultat 1 - 5 av 10 avhandlingar som matchar ovanstående sökkriterier.
1. Sensorimotor Brain Plasticity in Stroke Patients with Dysphagia : A Methodological Study on Investigation and Treatment
Sammanfattning : AimsThe aims of the thesis were to validate investigation instruments for stroke patients with dysphagia, and to improve oropharyngeal dysphagia therapies.Methods/ResultsA Lip Force Meter, LF 100, affirmed excellent intra- and inter-reliability, sensitivity and specificity. LÄS MER
2. Gait strategy in myelomeningocele : movements, mechanics and methods
Sammanfattning : The overall aim of this thesis was to describe the movement patterns employed in self-ambulatory children with a range of muscle paresis due to nervous tissue damage resulting from myelomeningocele, a common congenital malformation of the spinal column resulting in sensory and motor paresis. Using 3D movement analysis, the upper and lower body kinematics, movement of the center of mass, and joint moments, powers, and work done during gait in 32 children with lumbo-sacral myelomeningocele were analyzed and divided into 5 groups based on the severity of paresis. LÄS MER
3. Associations between body functions, activities and health-related quality of life from onset until 18 months after stroke
Sammanfattning : Introduction and aims: In planning rehabilitation services for patients with stroke, it is important to know the frequency of the impairments and activity limitations presented by the patients and also how each body function and activity is associated with other body functions and activities, as well as the patients health-related quality of life (HRQL) at different time-points after stroke. The overall aims of the thesis were to describe body functions, activities and HRQL in patients with stroke and to analyse the associations between those variables, in the first week and at three and 18 months after stroke onset. LÄS MER
4. Ambulation in persons with myelomeningocele
Sammanfattning : The aim was to study ambulatory function in persons with myelomeningocele. Different systems used to classify the extent of motor paresis were compared. The classification according to five commonly used systems showed a lack of congruence in classes L3 level and downward. LÄS MER
5. Biomarkers for diagnosis and prognosis in amyotrophic lateral sclerosis
Sammanfattning : Background: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder characterized by loss of upper and lower motor neurons, leading to paresis, muscle atrophy, and respiratory failure. ALS can be difficult to diagnose and prognosticate early. LÄS MER