Zobrazeno 1 - 10
of 83
pro vyhledávání: '"P L, Lukinmaa"'
Publikováno v:
British Journal of Oral and Maxillofacial Surgery. 28:311-316
Benign osteoblastoma is a rare osteoblastic tumour with osteoid and bone deposition. A rapidly growing osteoblastoma involving the area of the mandibular first and second molar of a 20-year-old female is described. Investigation of the collagenous co
Publikováno v:
European journal of paediatric dentistry. 6(2)
This epidemiological study in a group of Italian children was undertaken in order to increase our knowledge of the prevalence of Molar Incisor Hypomineralisation (MIH) in different European countries.A population of school children aged 7.3 - 8.3 yea
Nonfluoride hypomineralizations in the permanent first molars and their impact on the treatment need
Publikováno v:
Caries research. 35(1)
To determine the prevalence of nonfluoride enamel hypomineralization in the permanent first molars, we examined 488 7– to 13–year–old children. We further examined the impact of such defects on the treatment need by evaluating the number of car
Publikováno v:
Journal of oral pathologymedicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology. 29(4)
Solitary fibrous tumour (SFT) is an uncommon mesenchymal neoplasm rarely located in the oral cavity. To characterize further oral SFT, we describe three new cases. Each tumour originated in the buccal mucosa of a middle-aged/elderly patient. Histolog
Autor:
A M, Partanen, S, Alaluusua, P J, Miettinen, I, Thesleff, J, Tuomisto, R, Pohjanvirta, P L, Lukinmaa
Publikováno v:
Laboratory investigation; a journal of technical methods and pathology. 78(12)
We have previously shown that dioxins at prevailing levels in mothers' milk may cause mineralization defects in the developing teeth of their children. Developmental dental defects have also been reported in rhesus macaques and rats experimentally ex
Publikováno v:
Journal of craniofacial genetics and developmental biology. 16(4)
We describe a developmental dentin disorder distinct from dentin defects characterized thus far. The proband was a 9-year-old boy who was the only family member known to be affected in five generations. The dental defect was not associated with any g
Publikováno v:
Journal of craniofacial genetics and developmental biology. 16(3)
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is an autosomal recessive disease composed of failure of various endocrine glands, chronic mucocutaneous candidiasis, and an ectodermal dystrophy complex including hypoplasia of
Publikováno v:
Journal of craniofacial genetics and developmental biology. 15(4)
Cleidocranial dysplasia (CCD) is a heritable generalized bone dysplasia presenting with a variety of dental abnormalities. To delineate morphological features of the dental tissues, we have analyzed histologically the structure of teeth and peridenta
Publikováno v:
Scanning microscopy. 9(1)
Heritable dentin defects form a group of diseases which exclusively affect dentin among the various dental tissues. While one type is associated with the generalized connective tissue disorder, osteogenesis imperfecta, other types occur as single tra
Autor:
J C Waltimo, Leena Peltonen, Anders Paetau, P L Lukinmaa, Elina Ikonen, Aarno Palotie, N E Enomaa
Publikováno v:
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society. 41(7)
Aspartylglucosaminidase (AGA: E.C. 3.5.1.26) is a lysosomal amidase that hydrolyzes the N-acetylglucosamine-asparagine linkage as one of the final steps in the breakdown of glycoproteins. Deficiency of this enzyme results in aspartylglucosaminuria (A