Results 211 to 220 of about 6,798 (252)
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Ameloblastic Carcinoma in a Horse
Journal of Comparative Pathology, 2003The clinical, gross morphological, histological and immunohistochemical characteristics of an ameloblastic carcinoma in a 30-year-old Quarter Horse mare are reported. This tumour was fast growing, locally invasive and destructive. Histologically, it showed an infiltrative pattern of large islands, broad sheets and, at the periphery, small cords of ...
H E V, De Cock +2 more
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Hypoxia increases the expression of enamel genes and cytokines in an ameloblast-derived cell line
European Journal of Oral Sciences, 2015The aim of this study was to investigate the effect of hypoxic conditions on the expression of enamel genes and on the secretion of alkaline phosphatase (ALP), lactate dehydrogenase (LDH), cytokines, and interleukins by an ameloblast-derived cell line ...
Rivan Sidaly +5 more
semanticscholar +1 more source
International Journal of Oral Surgery, 1979
An ameloblastic fibro-odontoma in a 14-year-old girl is reported. The case has clinical interest because of the location and the size of the tumor which was surgically enucleated. The different views about clinical, radiographical and histopathological characteristics and the classification of this benign tumor are discussed.
C H, Bernhoft, G, Bang, O, Gilhuus-Moe
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An ameloblastic fibro-odontoma in a 14-year-old girl is reported. The case has clinical interest because of the location and the size of the tumor which was surgically enucleated. The different views about clinical, radiographical and histopathological characteristics and the classification of this benign tumor are discussed.
C H, Bernhoft, G, Bang, O, Gilhuus-Moe
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Ameloblastic odontoma in a dog
Journal of the American Veterinary Medical Association, 1984An ameloblastic odontoma in the right maxilla of a 10-week-old, female Springer Spaniel was treated by extensive curettage. Twelve months after surgery there was no recurrence of the neoplasm.
J B, Nold +3 more
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Papilliferous ameloblastic fibroma
Oral Surgery, Oral Medicine, Oral Pathology, 1972Abstract An interesting and unusual histologic variant of ameloblastic fibroma is reported in a 15-year-old Negro girl. The case represents the first published report of papilliferous ameloblastic fibroma. The available follow-up suggests that the biologic behavior of this variant is identical to that of the ameloblastic fibroma.
T F, Christ +2 more
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Ameloblastic carcinoma of the maxilla
Oral Oncology, 2003The maxilla is an unusual site for an ameloblastoma, and certainly for an ameloblastic carcinoma. Ameloblastomas are considered as benign, yet locally aggressive neoplasms in the vast majority of cases. However, very rarely, these tumors demonstrate a clinical course of malignancy. Recently, a classification system was published differentiating between
Karan, Dhir +2 more
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Ameloblastic sarcoma of the mandible
Journal of Oral and Maxillofacial Surgery, 1985Malignant ameloblastic odontogenic tumors have traditionally been classified as either ameloblastic fibrosarcomas, dentinosarcomas or odontosarcomas. This separation is based on the presence of either dentine or dentine and enamel in some lesions. To date, 28 cases of ameloblastic fibrosarcoma, one case of ameloblastic dentinosarcoma, and seven cases ...
M, Altini +3 more
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Ameloblastic fibroma in an infant
Journal of Oral and Maxillofacial Surgery, 1985A case of ameloblastic fibroma associated with a hypoplastic lesion in an unerupted deciduous central incisor is presented. Whether this case provides new evidence concerning the time and source of origin of the ameloblastic fibroma is open to debate, but the possible implications may be worthy of further study.
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Ameloblastic fibroma of the mandible
British Journal of Oral and Maxillofacial Surgery, 1986A case of an ameloblastic fibroma in the mandible is presented. The ameloblastic fibroma is a benign neoplasm belonging to the group of mixed odontogenic tumours. Enucleation is the treatment of choice. Recurrence of the tumour is very rare, but follow up is necessary. Fewer than 75 cases are described in the literature. An additional case is presented
Blankestijn, J. +2 more
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Journal of Oral and Maxillofacial Surgery, 1987
J P, Cassidy, D J, Crocker, W H, Grau
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J P, Cassidy, D J, Crocker, W H, Grau
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