Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Peter J. M. Crawford"'
Publikováno v:
Orthodontic Update. 5:38-47
These two articles aim to outline the importance of combined paediatric dentistry-orthodontic planning in the management of complex cases of the developing dentition. They will use case studies to highlight those patients who would most benefit from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::326af3d296069d9b5c236a03fe869672
https://doi.org/10.12968/ortu.2012.5.2.38
https://doi.org/10.12968/ortu.2012.5.2.38
Publikováno v:
International Journal of Paediatric Dentistry. 22:427-434
International Journal of Paediatric Dentistry 2012; 22: 427–434 Aims. To ascertain whether deproteinization pretreatment of molar-incisor hypomineralization (MIH) enamel affects resin sealant infiltration. Design. Thirty one extracted MIH teeth wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4139d24937b90340674f517ab8e73976
https://doi.org/10.1111/j.1365-263x.2011.01212.x
https://doi.org/10.1111/j.1365-263x.2011.01212.x
Publikováno v:
International Journal of Paediatric Dentistry. 20:293-304
International Journal of Paediatric Dentistry 2010; 20: 293–304 Background. Existing indices to quantify tooth discolouration are mostly aetiology-specific. An index of tooth appearance (IOTA), derived from all types of tooth discolouration and sur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5162859bfb4ee00a18b40421b45b807
https://doi.org/10.1111/j.1365-263x.2010.01053.x
https://doi.org/10.1111/j.1365-263x.2010.01053.x
Publikováno v:
Clinical Genetics. 38:44-50
Various authors have allocated a diagnosis of tricho-dento-osseous syndrome to cases originally reported as amelogenesis imperfecta (hypomaturation-hypoplasia type) with taurodontism. The resulting confusion has prompted this critical review of the l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2007c19844a57938dbc429418642d265
https://doi.org/10.1111/j.1399-0004.1990.tb03546.x
https://doi.org/10.1111/j.1399-0004.1990.tb03546.x
Publikováno v:
Clinical Genetics. 63:333-339
Dental genetic disorders can cause severe social and psychological effects in affected individuals. The cost of treatment can be considerable, not only in financial terms but also in time spent during treatment. In theory it is, or will soon be, poss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8766b24e697578884beabf9ba393789b
https://doi.org/10.1034/j.1399-0004.2003.00045.x
https://doi.org/10.1034/j.1399-0004.2003.00045.x
Publikováno v:
Oral Diseases. 9:19-23
Amelogenesis imperfecta (AI) is a collective term for a number of conditions with abnormal enamel formation. Many cases are inherited, either as an X-linked, autosomal dominant or autosomal recessive trait. Several classifications have evolved since
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a3c7e4c7ce0e16f137116d2cf2ca1cf
https://doi.org/10.1034/j.1601-0825.2003.00843.x
https://doi.org/10.1034/j.1601-0825.2003.00843.x
Autor:
Thomas C. Hart, S. P. Hong, Carolyn W. Gibson, John Tim Wright, P.S. Hart, Peter J. M. Crawford, Michael J. Aldred, Kim Seow
Publikováno v:
Connective Tissue Research. 44:72-78
X-linked amelogenesis imperfectas (AI) resulting from mutations in the amelogenin gene (AMELX) are phenotypically and genetically diverse. Amelogenin is the predominant matrix protein in developing enamel and is essential for normal enamel formation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f9f4a1d0d4a0d11ee61fc9b05ca6f48
https://doi.org/10.1080/03008200390152124
https://doi.org/10.1080/03008200390152124
Autor:
Peter J. M. Crawford, Thomas C. Hart, Nicholas J. Wright, P.S. Hart, John Tim Wright, Michael J. Aldred
Publikováno v:
Archives of Oral Biology. 47:261-265
Amelogenin, the predominant matrix protein in developing dental enamel, is considered essential for normal enamel formation, but its exact functions are undefined. Mutations in the AMELX gene that encodes for amelogenin protein cause X-linked ameloge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a28d8945bd7b280393ab4a535a2bde91
https://doi.org/10.1016/s0003-9969(02)00003-1
https://doi.org/10.1016/s0003-9969(02)00003-1
Autor:
M. J. Aldred, John Tim Wright, S. J. Walker, Jennifer A. Price, Peter J. M. Crawford, Thomas C. Hart
Publikováno v:
Clinical Genetics. 56:35-40
Amelogenesis imperfecta of the hypomaturation-hypoplasia type with taurodontism (AIHHT) is inherited as a highly penetrant autosomal dominant trait. These dental findings are similar to those of another autosomal dominant condition, the tricho-dento-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1a866b4a48e54a614e24e70a112b337
https://doi.org/10.1034/j.1399-0004.1999.550105.x
https://doi.org/10.1034/j.1399-0004.1999.550105.x
Autor:
S. J. Merrett, Peter J. M. Crawford
Publikováno v:
International Journal of Paediatric Dentistry. 13:127-129
This paper describes the case of a day old baby who was admitted to hospital because of the presence of a large intraoral swelling that was preventing her from breast feeding. Clinical examination showed a firm, pedunculated, lobulated nodule protrud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2860d69346eff7d2e8c573593f8a2a52
https://doi.org/10.1046/j.1365-263x.2003.00435.x
https://doi.org/10.1046/j.1365-263x.2003.00435.x