Teeth fragments from members of a family clinically and genetically diagnosed as having amelogenesis imperfecta were studied by scanning electron microscopy and X-ray microprobe analysis to establish the morphological patterns and the quantitative concentration of calcium in the enamel of anterior (canine, incisor) and posterior (premolar and molar) teeth. The prism patterns in the enamel of teeth from both regions were parallel or irregularly decussate, with occasional filamentous prisms accompanied by small, irregularly rounded formations. Prismless enamel showed the R- and P-type patterns. Calcium levels in enamel of amelogenesis imperfecta and control teeth differed significantly between anterior and posterior teeth, indicating t...
Amelogenesis imperfecta (AI) is a group of inherited disorders primarily affecting dental enamel. Va...
The present investigation studied dental development in 23 subjects with amelogenesis imperfecta (AI...
Amelogenesis imperfecta is a rare, genetically determined disorder charaterized by the presence of a...
Teeth fragments from members of a family clinically and genetically diagnosed as having amelogenesis...
Teeth fragments from members of a famil? clinically and genetically diagnosed as having amelogenesis...
Objectives: The purpose of this study was to use quantitative x-ray microprobe analysis with scannin...
Objectives: The purpose of this study was to use quantitative x-ray microprobe analysis with scannin...
To explore the mineral features of dentin and cementum in hypoplastic Amelogenesis imperfecta AI tee...
Successful bonding of resins to teeth affected by amelogenesis imperfecta (AI) may be highly depende...
The purpose of this study was to clarify the structural and ultrastructural alterations of the ename...
Amelogenesis imperfecta (AI) is the name given to a clinically and genetically heterogeneous group o...
The teeth of the Homo erectus child (Garba IV) recovered from Melka Kunture Ethiopia and dated to 1....
Objectives: The aim of this investigation was to describe the dental and craniofacial. characteristi...
Abstract Amelogenesis imperfecta (AI) represents a group of developmental conditions, genomic in ori...
Twelve teeth from three patients with enamel and dentin dysplasia were investigated by polarized lig...
Amelogenesis imperfecta (AI) is a group of inherited disorders primarily affecting dental enamel. Va...
The present investigation studied dental development in 23 subjects with amelogenesis imperfecta (AI...
Amelogenesis imperfecta is a rare, genetically determined disorder charaterized by the presence of a...
Teeth fragments from members of a family clinically and genetically diagnosed as having amelogenesis...
Teeth fragments from members of a famil? clinically and genetically diagnosed as having amelogenesis...
Objectives: The purpose of this study was to use quantitative x-ray microprobe analysis with scannin...
Objectives: The purpose of this study was to use quantitative x-ray microprobe analysis with scannin...
To explore the mineral features of dentin and cementum in hypoplastic Amelogenesis imperfecta AI tee...
Successful bonding of resins to teeth affected by amelogenesis imperfecta (AI) may be highly depende...
The purpose of this study was to clarify the structural and ultrastructural alterations of the ename...
Amelogenesis imperfecta (AI) is the name given to a clinically and genetically heterogeneous group o...
The teeth of the Homo erectus child (Garba IV) recovered from Melka Kunture Ethiopia and dated to 1....
Objectives: The aim of this investigation was to describe the dental and craniofacial. characteristi...
Abstract Amelogenesis imperfecta (AI) represents a group of developmental conditions, genomic in ori...
Twelve teeth from three patients with enamel and dentin dysplasia were investigated by polarized lig...
Amelogenesis imperfecta (AI) is a group of inherited disorders primarily affecting dental enamel. Va...
The present investigation studied dental development in 23 subjects with amelogenesis imperfecta (AI...
Amelogenesis imperfecta is a rare, genetically determined disorder charaterized by the presence of a...