Zobrazeno 1 - 10
of 1 763
pro vyhledávání: '"S R, Carter"'
Publikováno v:
Sarcoma, Vol 2012 (2012)
Leiomyosarcoma of bone is just one of the variants of spindle cell sarcoma of bone characterised by the expression of desmin and other markers indicating a significant element of smooth muscle in the tumour, without osteoid production we have investi
Externí odkaz:
https://doaj.org/article/dfd71e5f31af4ba5be8844c3fc7aafb3
Autor:
A. M. Malhas, V. P. Sumathi, S. L. James, C. Menna, S. R. Carter, R. M. Tillman, L. Jeys, R. J. Grimer
Publikováno v:
Sarcoma, Vol 2012 (2012)
Low-grade central osteosarcoma (LGCO) is a rare variant of osteosarcoma which is difficult to diagnose. If not treated appropriately, the tumour can recur with higher-grade disease. We reviewed our experience of this condition to try and identify fac
Externí odkaz:
https://doaj.org/article/40adf84393ab4880a11e0655898ebb69
Autor:
J. Haniball, V. P. Sumathi, L.-G. Kindblom, A. Abudu, S. R. Carter, R. M. Tillman, L. Jeys, D. Spooner, D. Peake, R. J. Grimer
Publikováno v:
Sarcoma, Vol 2011 (2011)
Background. This study aimed to investigate prognostic factors for patients with myxoid/round-cell liposarcoma (MRCLS), in particular the significance of the round cell component, and to identify metastatic patterns as well as possibly suggest a suit
Externí odkaz:
https://doaj.org/article/c990aecb5e5242b0b993dd91994e1b83
Publikováno v:
Sarcoma, Vol 2010 (2010)
Introduction. The ‘‘two-week wait’’ was established as a potential means of diagnosing malignant tumours earlier. This paper investigated whether these clinics are leading to earlier diagnosis of malignant soft-tissue lumps. Method. We identi
Externí odkaz:
https://doaj.org/article/254de32741074b4c8638cb6b7560268a
Publikováno v:
Sarcoma, Vol 2009 (2009)
Between 1996 and 2006 a total of 278 patients with soft tissue Leiomyosarcoma were treated at our centre. We identified 16 patients (5.8%) where the tumour directly arose from the blood vessels. These tumours were studied to determine their prognosis
Externí odkaz:
https://doaj.org/article/303283a907e8419fa9406a343cb21673
Autor:
C. R. Chandrasekar, R. J. Grimer, S. R. Carter, R. M. Tillman, A. Abudu, A. M. Davies, V. P. Sumathi
Publikováno v:
Sarcoma, Vol 2008 (2008)
Elastofibroma dorsi is an uncommon benign soft tissue pseudotumour usually located at the lower pole of the scapula, deep to serratus anterior, and often attached to the periosteum of the ribs, presenting with long history of swelling and occasionall
Externí odkaz:
https://doaj.org/article/38fb264d3af74a8d9489b2995b3c42c8
Publikováno v:
The Journal of Bone and Joint Surgery-American Volume. 87:842-849
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bdd77d4b81d0c230a80290fc82e7d4f
https://doi.org/10.2106/00004623-200504000-00021
https://doi.org/10.2106/00004623-200504000-00021
Autor:
Kimberley Talbot, Linda M. Vickars, Cedric J. Carter, Shannon Jackson, A. L. Vanden Hoek, Isis S. R. Carter, Ross T. A. MacGillivray, Edward L.G. Pryzdial
Publikováno v:
Journal of Thrombosis and Haemostasis. 10:2613-2615
Vanden Hoek AL, Talbot K, Carter ISR, Vickars L, Carter CJ, Jackson SC, MacGillivray RTA, Pryzdial ELG. Coagulation factor X Arg386 specifically affects activation by the intrinsic pathway: a novel patient mutation. J Thromb Haemost 2012; 10: 2613–
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86cdfa2bd5e3119716aaf3f6ae22571e
https://doi.org/10.1111/jth.12021
https://doi.org/10.1111/jth.12021
Autor:
F. Fiorenza, A. Abudu, R. J. Grimer, S. R. Carter, R. M. Tillman, K. Ayoub, D. C. Mangham, A. M. Davies
Publikováno v:
The Journal of Bone and Joint Surgery. British volume. :93-99
We studied 153 patients with non-metastatic chondrosarcoma of bone to determine the risk factors for survival and local tumour control. The minimum follow-up was for five years; 52 patients had axial and 101 appendicular tumours. Surgical treatment w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c89022169d09234118f42a59642d418b
https://doi.org/10.1302/0301-620x.84b1.0840093
https://doi.org/10.1302/0301-620x.84b1.0840093