Sökning: "myotonic dystrophy type 1"
Visar resultat 1 - 5 av 11 avhandlingar innehållade orden myotonic dystrophy type 1.
1. Myotonic dystrophy type 1. Cognition, personality and emotion
Sammanfattning : kommer senare.... LÄS MER
2. Personality and facial emotion recognition ability in myotonic dystrophy type 1
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3. Orofacial dysfunctions in children and adolescents with myotonic dystrophy type 1 - evaluation and intervention
Sammanfattning : Myotonic dystrophy type 1 (DM1) is a slowly progressive neuromuscular disease. The overall aim of this thesis was primarily to describe the characteristics, prevalence, and development of orofacial functions in a group of children and adolescents with DM1 and secondly to investigate the effect of lip strengthening exercises. LÄS MER
4. On oral health in children and adults with myotonic dystrophy
Sammanfattning : Background: Myotonic Dystrophy type 1 (DM1) is a hereditary neuromuscular multisystem disease with varying clinical expressions and severity. The prevalence worldwide is 5-20/100 000. It is characterized by progressive muscular waste and myotonia. Facial weakness is one of the earliest and most constant features. LÄS MER
5. Force, falls and fear of falls in myotonic dystrophy type 1. Cross-sectional and longitudinal studies
Sammanfattning : ABSTRACT Background: Myotonic dystrophy type 1 (DM1) is a neuromuscular multisystemic disorder with slowly progressive muscle weakness. The overall purpose of this thesis was, in adult patients with DM1, to investigate factors of importance for functional balance skills and falls, and to investigate the natural course of muscle force and functional balance impairments, with reliable measurement methods. LÄS MER