Search for dissertations about: "remaining teeth"
Showing result 16 - 20 of 26 swedish dissertations containing the words remaining teeth.
-
16. Amelogenesis imperfecta : an epidemiologic, genetic, morphologic and clinical study
Abstract : Amelogenesis imperfecta (AI) is a genetically determined enamel defect characterized by genetic and clinical heterogeneity .The prevalence and incidence of AI were established in the county of Västerbotten, northern Sweden, in 3-19-yr-olds born 1963-79, as were the mode of inheritance and clinical manifestation of AI. READ MORE
-
17. Oral health and self-perceived oral treatment need of adults in Sweden
Abstract : Ett mål med denna avhandling var att undersöka vilka faktorer som har samband med den vuxna patientens syn på sitt tandvårds-behov i Sverige. Ett annat mål var att beskriva hur den vuxna skånska befolkningen såg på sitt behov av tandvård. READ MORE
-
18. On implementation of an endodontic program : change of practice, treatment outcome and cost-effectiveness
Abstract : It is widely accepted that the uptake of research findings by practitionersis unpredictable, yet until they are adopted, advances intechnology and clinical research cannot improve health outcomesin patients. Despite extensive research there is limited knowledgeof the processes by which changes occur and ways of measuringthe effectiveness of change of practice. READ MORE
-
19. Factors shaping demand for prostethic dentistry treatment with special focus on implant dentistry
Abstract : Aim: The main aim of this thesis was to investigate how attitudesinfluence the latent and manifest need, desire, demand, and utilizationfor dental implant treatment, considering the gatekeeping processbetween need and demand, and between demand and utilization ofdental treatment.Material and Methods: A conceptual analysis of the need anddemand concept from the literature was a first step in the study. READ MORE
-
20. Laurence-Moon-Bardet-Biedl syndrome. Clinical,electrophysiological and genetic aspects
Abstract : The study included 44 Scandinavian individuals with the autosomal recessive inherited Laurence-Moon-Bardet-Biedl syndrome. Inclusion criteria were retinal dystrophy plus at least 2 more of the remaining traditional cardinal signs of the syndrome: obesity, polydactyly, hypogenitalism and mental retardation. READ MORE