Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Hanna A Scheuer"'
Publikováno v:
Journal of Cranio-Maxillofacial Surgery. 48:98-104
Purpose The purpose of the study was the investigation of supernumerary teeth (ST) in the permanent dentition of patients with neurofibromatosis type 1 (NF1). Material and methods The panoramic radiographs of 200 NF1 patients were analysed for ST. Th
Publikováno v:
Anticancer research. 42(5)
Neurofibromatosis type 1 (NF1) is an autosomal dominant tumor predisposition syndrome that is also characterized by skeletal abnormalities. In the cranial region, skeletal dysplasia is observed that is associated with a characteristic peripheral nerv
A Posterior-Anterior Cephalometric Study of Skull Symmetry in Patients With Neurofibromatosis Type 1
Publikováno v:
Anticancer research. 41(10)
BACKGROUND/AIM Neurofibromatosis type 1 (NF1) is a tumor predisposition syndrome. Bone findings make a significant contribution to the clinical diagnosis of NF1. It has been suggested that there are characteristic skeletal features of the NF1 patient
Publikováno v:
In Vivo
Background Radiological cephalometry is an important diagnostic tool for analyzing the shape and proportions of the skull. Standardized teleradiography of the skull in posterior-anterior (PA) projection provides orientation data on the symmetry and v
Autor:
Hannah T Scheuer, Hanna A Scheuer, Reinhard E Friedrich, Jozef Zustin, Andreas M. Luebke, Christian Hagel
Publikováno v:
Anticancer research. 41(4)
Background/aim Numerical aberrations of permanent dentition and dystopic tooth eruption are part of the phenotype of the tumor predisposition syndrome neurofibromatosis type 1 (NF1). In these cases, surplus tooth germs usually develop in the alveolar
Autor:
Hanna A Scheuer, Reinhard E Friedrich
Publikováno v:
Anticancer Research. 38:4083-4091
Neurofibromatosis type (NF1) is an autosomal dominant inherited tumor-suppressor gene syndrome of significant phenotypic variability with probable complete penetrance of the disease. Skeletal malformations of the skull belong to the phenotype of NF1.
Publikováno v:
GMS Interdisciplinary Plastic and Reconstructive Surgery DGPW, Vol 6, p Doc05 (2017)
GMS Interdisciplinary Plastic and Reconstructive Surgery DGPW
GMS Interdisciplinary Plastic and Reconstructive Surgery DGPW
The aim of this study was to measure line segments and areas of sella turcica on lateral cephalograms with respect to the clinical diagnosis of facial phenotype of patients with neurofibromatosis type 1 (NF1). Special attention was given to correlate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ebc4b5689c974841e85aa78b5816c5b
Autor:
Georg Christ, Christine Eulenburg, Hanna A Scheuer, Jan-Marten Lehmann, Reinhard E Friedrich, Hannah T Scheuer, Jonathan Rother
Publikováno v:
Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery. 45(6)
Purpose Neurofibromatosis type 1 (NF1) is an autosomal dominant transmitted tumour suppressor syndrome and also a bone disease. Osseous dysplasia affecting the craniofacial region is characteristic of NF1. The aim of this study was to analyse the lat
Publikováno v:
Anticancer research. 36(6)
Odontogenic myxoma (OM) is a rare tumour arising in the jaws. The tumour is purported to be odontogenic in origin due to the frequent localisation of the tumour inside the jaws in close relation to teeth. The aim of this report was to detail the cour
Publikováno v:
Journal of Oral Pathology & Medicine. 39:115-120
J Oral Pathol Med (2010) 39: 115–120 Background: Podoplanin expression was described in mouse tooth germ and apical bud cells. The aim of this study was to analyse the podoplanin expression of human tooth germ tissues, adult teeth and odontogenic l