Zobrazeno 1 - 10
of 19
pro vyhledávání: '"R. G. H. Wallace"'
Publikováno v:
European Journal of Trauma and Emergency Surgery. 41:273-276
The routine use of thromboprophylaxis during cast immobilisation for lower leg trauma is controversial. The concern involves the perceived increased risk of deep vein thrombosis (DVT) and its sequelae following leg immobilisation. However, immobilisa
Publikováno v:
The Journal of Bone and Joint Surgery. British volume. :1362-1366
Controversy surrounds the most appropriate treatment method for patients with a rupture of the tendo Achillis. The aim of this study was to assess the long term rate of re-rupture following management with a non-operative functional protocol. We repo
Publikováno v:
The Journal of Bone and Joint Surgery. British volume. :488-491
We report a 45-year follow-up of a patient with Engelmann’s disease previously described in 1950, showing progression of the disease with unique involvement of the femoral capital epiphyses. The case is compared with others to add some information
Publikováno v:
The Journal of Bone and Joint Surgery. British volume. :769-771
A randomised double-blind study was carried out on 60 patients undergoing elective lumbar discectomy. Patients in the study group (n = 30) received an injection of 10 ml of 0.5% bupivacaine into the wound; the control group (n = 30) received none. Po
Publikováno v:
European Journal of Trauma and Emergency Surgery. 41:277-277
Autor:
Stuart H. Ralston, L. Hovy, W. Van Hul, D. M. Anderson, Michael P. Whyte, R. G. H. Wallace, J. Marken, Heather MacPherson, Anne E. Hughes, C. Bell, Kiyoshi Nakatsuka
Publikováno v:
Hughes, A, Ralston, S H, Marken, J, Bell, C, McPherson, H, Wallace, R G H, Van Hul, W, Whyte, M P, Nakatsuka, K, Hovy, L & Anderson, D M 2000, ' Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis ', Nature Genetics, vol. 24, no. 1, pp. 45-48 .
Nature genetics
Nature genetics
Familial expansile osteolysis (FEO, MIM 174810) is a rare, autosomal dominant bone disorder characterized by focal areas of increased bone remodelling. The osteolytic lesions, which develop usually in the long bones during early adulthood, show incre
Autor:
R. A. .B Mollan, Norman C. Nevin, R. J. Barr, A. M. Shearman, J. L. Weber, P. H. Osterberg, Anne E. Hughes, R. G. H. Wallace
Publikováno v:
Human molecular genetics. 3(2)
Familial expansile osteolysis is a rare bone dysplasia which is transmitted as an autosomal dominant trait in a large kindred in Northern Ireland. The gene which causes the disease shows tight linkage with several polymorphic markers on chromosome 18
Autor:
G. Levin, M R Lumb, F. Assinder, G. Seddon, M. White, A. B Otlet, G. Atkin, M. Whittet, W E Brooke, R. G H Wallace, A. Bird
Publikováno v:
BMJ. 318:1701-1701
Arthur Levin {#article-title-2} Founder of the Wellington Hospital and pioneer of day surgery ( b 1913; q Cambridge/St Bartholomew's 1939), d 29 April 1999. Early in the war he was appointed to the Royal Masonic Hospital, which was an officers' hospi
Publikováno v:
The Journal of Hand Surgery: Journal of the British Society for Surgery of the Hand. 10:269-272
This preliminary report proposes to show that an objective auscultatory method exists as an aid to diagnosis of some hand conditions. The signals so produced are both distinctive and reproducible. The conditions investigated were:- Cavitation finger
Autor:
Rab Mollan, D. A. Adams, P. G. Toner, P. H. Osterberg, J. Sloan, G. R. Dickson, R. G. H. Wallace, N. C. Nevin, R. S. Crone, J. A. Kanis
Publikováno v:
The Journal of bone and joint surgery. British volume. 70(2)
We report 40 cases in one family of an autosomal dominant bone dysplasia, which, though similar in some aspects to Paget's disease, seems unique in some features and in its natural history. The disease shows both general and focal skeletal changes, t