Zobrazeno 1 - 10
of 26
pro vyhledávání: '"D E Porter"'
Publikováno v:
Sarcoma, Vol 2009 (2009)
We studied 123 patients with malignant peripheral nerve sheath tumours (MPNSTs) between 1979 and 2002. However, 90 occurred sporadically whereas 33 were associated with neurofibromatosis type 1 (NF1). Survival was calculated using Kaplan-Meier surviv
Externí odkaz:
https://doaj.org/article/66c6d0b6ba41431bb208e35069f2bd26
Autor:
N D Clement, D E Porter
Publikováno v:
Journal of Bone and Joint Surgery. 95:1586-1592
Background: There is a high rate of forearm deformity in patients with hereditary multiple exostoses, with many patients developing radial head dislocation associated with ulnar shortening. Methods: One hundred and six patients with hereditary multip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::446bf09d014995ec532cae5b43cf00de
https://doi.org/10.2106/jbjs.l.00736
https://doi.org/10.2106/jbjs.l.00736
Publikováno v:
The Journal of Bone and Joint Surgery. British volume. :988-995
We defined the characteristics of dysplasia and coxa valga in hereditary multiple exostoses (HME) by radiological analysis of 24 hips in 12 patients. The degree and effect of the ‘osteochondroma load’ around the hip were quantified. We investigat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fece5ced3b29e88cd258937410908092
https://doi.org/10.1302/0301-620x.83b7.0830988
https://doi.org/10.1302/0301-620x.83b7.0830988
Publikováno v:
Journal of Pediatric Orthopedics. 20:246-250
Hereditary multiple exostoses (HME) is traditionally described as a skeletal dysplasia. However, the discovery that the EXT family of tumour suppressor genes are responsible for HME suggests that it is more appropriate to classify HME as a familial n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5b2239bbbddd5f759a01fcdf337eec5
https://doi.org/10.1097/00004694-200003000-00022
https://doi.org/10.1097/00004694-200003000-00022
Publikováno v:
Journal of Pediatric Orthopaedics. 20:246-250
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::086a9039fa4f132a981d4852a71bbcc9
https://doi.org/10.1097/01241398-200003000-00022
https://doi.org/10.1097/01241398-200003000-00022
Autor:
D. E. Porter, A. H. R. W. Simpson
Publikováno v:
The Journal of Pathology. 188:119-125
Many theories of osteochondroma pathogenesis have been advanced. Genetic research into the inherited multiple form, hereditary multiple exostoses, has revealed a new family of tumour suppressor genes denoted EXT. Patterns of EXT gene mutation in here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::502ca3a8b135d776e22cf9688c7a34a1
https://doi.org/10.1002/(sici)1096-9896(199906)188:2<119::aid-path321>3.0.co
https://doi.org/10.1002/(sici)1096-9896(199906)188:2<119::aid-path321>3.0.co
Autor:
D. E. Porter, G. Spowart, J. Mackay, Alastair M. Thompson, C. M. Steel, M. Mitchell, C. M. Gosden, H. Morrison
Publikováno v:
The Breast. 3:209-214
Cultured stimulated peripheral blood lymphocytes from members of 18 breast and breast/ovarian cancer pedigrees each containing between 2 and 9 cases of breast cancer in a single line of descent were subjected to metaphase analysis for chromosomal rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6dd260abb6a62592a3f9fc551cbc6cb8
https://doi.org/10.1016/0960-9776(94)90047-7
https://doi.org/10.1016/0960-9776(94)90047-7
Publikováno v:
Scottish medical journal. 57(1)
To our knowledge there are no reports of a primary multifocal spindle cell sarcoma affecting both long bones of the lower limb in an elderly patient. An 83-year-old man presented with a progressively painful right ankle, without a history of trauma.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ce2cc8e5c664ca51cda9949e4ae53aa
https://pubmed.ncbi.nlm.nih.gov/22194402
https://pubmed.ncbi.nlm.nih.gov/22194402
Publikováno v:
International Journal of Cancer. 53:188-198
Fifteen pedigrees with a total of 75 cases of breast cancer, 10 of ovarian cancer and 53 of other cancers have been collected. Polymorphic markers on chromosome 17q have been screened to locate a putative breast-cancer gene using DNA from relevant in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39f74ac79dc7a6419b9efb634f547458
https://doi.org/10.1002/ijc.2910530203
https://doi.org/10.1002/ijc.2910530203
Autor:
D. E. Porter, C. M. Steel
Publikováno v:
Disease Markers, Vol 11, Iss 1, Pp 11-21 (1993)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f317467f1a43b306318d3519ffa68a7
https://doi.org/10.1155/1993/721892
https://doi.org/10.1155/1993/721892