Zobrazeno 1 - 10
of 72
pro vyhledávání: '"S.E. Handfield‐Jones"'
Autor:
I. Zaki, K.E. McKenna, R. E. A. Williams, S. M. Wilkinson, D. Bilsland, Lesley E. Rhodes, S.E. Handfield-Jones
Publikováno v:
ResearcherID
Following publication of treatment guidelines for patients with psoriasis, a six-centre audit was undertaken to assess current therapeutic practice for two second-line treatments, PUVA and methotrexate. The audit consisted of random sampling of casen
Autor:
J.C. Sterling, S. Gibbs, S.S. Haque Hussain, M.F. Mohd Mustapa, S.E. Handfield‐Jones, J.R. Hughes, M. Griffiths, A.J. McDonagh, S. Punjabi, D.A. Buckley, I. Nasr, V.J. Swale, C.E. Duarte Williamson, P.M. McHenry, N.J. Levell, T. Leslie, E. Mallon, K. Towers, R. Davis, C. Saunders, A.G. Brian, L.S. Exton
Publikováno v:
The British journal of dermatology. 171(4)
British Association of Dermatologists’ guidelines for the management of cutaneous warts 2014 J.C. Sterling, S. Gibbs, S.S. Haque Hussain, M.F. Mohd Mustapa and S.E. Handfield-Jones Addenbrooke’s Hospital, Cambridge University Hospitals NHS Founda
Publikováno v:
British Journal of Dermatology. 144:890-893
We present a family with Buschke-Ollendorff syndrome presenting as elastic tissue naevi without evidence of osteopoikilosis. We discuss the variable expression of this syndrome in other families previously reported in the literature, the association
Autor:
S.E. Handfield-Jones
Publikováno v:
British Journal of Dermatology. 138:273-276
Immediate hypersensitivity to latex protein is a serious and potentially life-threatening problem. This study found that eight of 867 (0.9%) medical and nursing staff in a district general hospital were allergic to latex with resultant hand eczema an
Autor:
S.L. Woodrow, S.E. Handfield-Jones
Publikováno v:
Clinical and Experimental Dermatology. 22:283-286
We report the case of a 39-year-old woman with a persistent congenital vascular lesion, which unusually is continuing to enlarge. Histologically, the lesion is a thin-walled haemangioma with numerous mast cells. Currently, the precise mechanism of ve
Publikováno v:
Clinical and experimental dermatology. 38(8)
Summary Waldenström macroglobulinaemia (WM) is a chronic lymphoproliferative disorder characterized by the presence of a monoclonal IgM paraprotein. Specific cutaneous features of WM include neoplastic cell infiltrates, IgM storage papules and IgM b
Autor:
N.P. Smith, S.E. Handfield-Jones
Publikováno v:
British Journal of Dermatology. 134:607-616
Malignant melanoma (MM) is rare in childhood. We report 24 cases of MM in children 16 years old or less, whose histopathological specimens were referred to our department from 1981 to 1993. In only three cases was the diagnosis of MM made clinically.
Autor:
J.L. Rees, M. Malone, P. Goodwin, S.E. Handfield-Jones, R. Coleman, John I. Harper, D. J. Atherton
Publikováno v:
Clinical and Experimental Dermatology. 19:173-176
Summary Three cases of waxy keratoses of childhood occurring in two families are described. The disorder seen in these three cases appears to be clinically and histopathologicaly distinct from previously distinct from previously described familial di
Publikováno v:
British Journal of Dermatology.
Publikováno v:
British Journal of Dermatology. 129:619-624
Summary Two patients with widespread, chronic, relapsing panniculitis resulting in disfiguring lipoatrophy are reported. Histology in both cases showed a mixed septal and lobular panniculitis, with lipophagia. The clinical appearance and histology su