Sökning: "remaining teeth"
Visar resultat 16 - 20 av 26 avhandlingar innehållade orden remaining teeth.
16. Amelogenesis imperfecta : an epidemiologic, genetic, morphologic and clinical study
Sammanfattning : 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. LÄS MER
17. On implementation of an endodontic program : change of practice, treatment outcome and cost-effectiveness
Sammanfattning : 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. LÄS MER
18. Oral health and self-perceived oral treatment need of adults in Sweden
Sammanfattning : 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. LÄS MER
19. Factors shaping demand for prostethic dentistry treatment with special focus on implant dentistry
Sammanfattning : 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. LÄS MER
20. Laurence-Moon-Bardet-Biedl syndrome. Clinical,electrophysiological and genetic aspects
Sammanfattning : 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. LÄS MER