Aim. The aim of this study was to assess the correlation between osteogenesis imperfecta (OI) and dentinogenesis imperfecta (DI) from both a clinical and histological point of view, particularly clarifying the structural and ultrastructural dentine changes. Design. Sixteen children (6-12 years aged) with diagnosis of OI were examined for dental alterations referable to DI. For each patient, the OI type (I,III, or IV) was recorded. Extracted or normally exfoliated primary teeth were subjected to a histological examination (to both optical microscopy and confocal laser-scanning microscopy). Results A total of ten patients had abnormal discolourations referable to DI: four patients were affected by OI type I, three patients by OI type III, a...
Osteogenesis imperfecta (OI) is a heterogeneous group of disorders of connective tissue, caused main...
Dentinogenesis imperfecta (DI) is the result of a dominant genetic defect and affects both the decid...
Osteogenesis imperfecta is a very rare heterogeneous genetic disorder associated with the developmen...
Abstract AIM: The aim of this study was to assess the correlation between osteogenesis imperfecta (...
The purpose of this study was to clarify the structural and ultrastructural alterations of the ename...
Based on three cases(two autopsies and one biopsy) we have conducted a pathological study On dentin...
Background. Osteogenesis imperfecta (OI), also known as ""brittle bone disease,"" can be difficult t...
Background: Dentinogenesis imperfecta type I (DGI-I) is a hereditary alteration of dentin associated...
Dental development is part of the craniofacial organogenesis, starting from the pluripotent cephalic...
Abstract BACKGROUND: Dentinogenesis imperfecta (DI) is an inherited dentine defect which affects bo...
The aims of this thesis were to investigate (1) dental aberrations in a large sample of unrelated pa...
Dental hard tissue is subject to variety of disorders. Dentinogenesis Imperfecta is one such disorde...
Dentinogenesis imperfecta is an example of an inheritable dentinal defect originating during the his...
AbstractDentinogenesis imperfecta (DI) associated with osteogenesis imperfecta (OI) is a genetic dis...
Osteogenesis imperfecta (OI) is a heterogeneous group of disorders of connective tissue, caused main...
Osteogenesis imperfecta (OI) is a heterogeneous group of disorders of connective tissue, caused main...
Dentinogenesis imperfecta (DI) is the result of a dominant genetic defect and affects both the decid...
Osteogenesis imperfecta is a very rare heterogeneous genetic disorder associated with the developmen...
Abstract AIM: The aim of this study was to assess the correlation between osteogenesis imperfecta (...
The purpose of this study was to clarify the structural and ultrastructural alterations of the ename...
Based on three cases(two autopsies and one biopsy) we have conducted a pathological study On dentin...
Background. Osteogenesis imperfecta (OI), also known as ""brittle bone disease,"" can be difficult t...
Background: Dentinogenesis imperfecta type I (DGI-I) is a hereditary alteration of dentin associated...
Dental development is part of the craniofacial organogenesis, starting from the pluripotent cephalic...
Abstract BACKGROUND: Dentinogenesis imperfecta (DI) is an inherited dentine defect which affects bo...
The aims of this thesis were to investigate (1) dental aberrations in a large sample of unrelated pa...
Dental hard tissue is subject to variety of disorders. Dentinogenesis Imperfecta is one such disorde...
Dentinogenesis imperfecta is an example of an inheritable dentinal defect originating during the his...
AbstractDentinogenesis imperfecta (DI) associated with osteogenesis imperfecta (OI) is a genetic dis...
Osteogenesis imperfecta (OI) is a heterogeneous group of disorders of connective tissue, caused main...
Osteogenesis imperfecta (OI) is a heterogeneous group of disorders of connective tissue, caused main...
Dentinogenesis imperfecta (DI) is the result of a dominant genetic defect and affects both the decid...
Osteogenesis imperfecta is a very rare heterogeneous genetic disorder associated with the developmen...