Results 131 to 140 of about 12,368 (291)
Asthma, a chronic disease whose manifestations go beyond respiratory distress, physical limitation and impaired quality of life [PDF]
Universidade Federal de São Paulo (UNIFESP) Escola Paulista de MedicinaUNIFESP ...
Fernandes, Ana Luisa Godoy
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Editorial: Tooth enamel research: Enamel 10 and beyond
Pamela K. Den Besten+1 more
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Skeletal dysplasia with multiple dislocations are severe disorders characterized by dislocations of large joints and short stature. The majority of them have been linked to pathogenic variants in genes encoding glycosyltransferases, sulfotransferases or ...
J. Dubail+23 more
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Aetiological factors for developmental defects of enamel [PDF]
Developmental defects of enamel remain as a permanent record of a disturbance during amelogenesis. They may present in different forms, some of which may be perceived by an individual as being disfiguring and so requiring treatment to improve the ...
Wong, HM
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Summary of the IADR Cariology Research, Craniofacial Biology, and Mineralized Tissue Groups Symposium, Iguaçu Falls, Brazil, June 2012: Gene-environment Interactions and Epigenetics in Oral Diseases: Enamel Formation and its Clinical Impact on Tooth Defects, Caries, and Erosion. [PDF]
Characteristics of enamel may influence or modulate individual susceptibility to caries and erosion. These characteristics are defined during development, which is under strict genetic control, but can easily be modified in many ways by environmental ...
Gerlach, Raquel F+4 more
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Amelogenesis imperfecta in a family
Introduction: amelogenesis imperfecta consists of a group of hereditary disorders that affect the development of the dental enamel in such a way that the clinical appearance of all or almost all primary and permanent teeth is compromised.
Paula Hurtado-Villa+3 more
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Enamel and dentin mineralization in familial hypophosphatemic rickets: a micro-CT study [PDF]
Objectives: The aim of the present study was to analyse the mineralization pattern of enamel and dentin in patients affected by X-linked hypophosphatemic rickets (XLHR) using micro-CT (µCT), and to associate enamel and dentin mineralization in primary ...
Costa, F. W. G.+4 more
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Amelogenesis imperfecta (AI) is a heterogeneous group of rare inherited diseases presenting with enamel defects. More than 30 genes have been reported to be involved in syndromic or non-syndromic AI and new genes are continuously discovered (Smith et al.,
V. Laugel-Haushalter+13 more
semanticscholar +1 more source
Avopurenta ja sen konservatiivinen hoito [PDF]
Avopurenta on yksi vaikeimmin hoidettavista purentavirheistä johtuen suuresta palautumisriskistä. Sen etiologia on monitekijäinen ja hoitovaihtoehtoja on useita.
Vehviläinen, Mari
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