Zobrazeno 1 - 10
of 26
pro vyhledávání: '"N. M. Isbel"'
Autor:
Kevan R. Polkinghorne, N. M. Isbel, John Kanellis, Emily J See, Peter G. Kerr, Vanessa C Heron
Publikováno v:
Transplantation Proceedings. 53:839-847
Background End-stage kidney disease secondary to hyperoxaluria presents a major challenge for transplant physicians given concern regarding disease recurrence. Few contemporary studies have reported long-term outcomes following transplantation in thi
Autor:
Keren Papier, Kiarash Khosrotehrani, Scott B. Campbell, N. M. Isbel, Adèle C. Green, Louisa G. Gordon, A. Griffin
Publikováno v:
British Journal of Dermatology. 180
Autor:
Keren Papier, Astrid J. Rodriguez-Acevedo, Kiarash Khosrotehrani, Scott B. Campbell, Adèle C. Green, Louisa G. Gordon, A. Griffin, N. M. Isbel
Publikováno v:
Journal of the European Academy of Dermatology and Venereology : JEADV. 33(7)
Background A long‐term complication among organ transplant recipients (OTRs) is skin malignancies which are associated with level and duration of immunosuppressive treatment, sun exposure and age. Dermatological surveillance is recommended for OTRs
Autor:
Louisa G. Gordon, A. Griffin, Scott B. Campbell, Keren Papier, N. M. Isbel, Adèle C. Green, Kiarash Khosrotehrani
Publikováno v:
British Journal of Dermatology. 179(5)
Autor:
Adèle C. Green, Louisa G. Gordon, Scott B. Campbell, Keren Papier, Kiarash Khosrotehrani, N. M. Isbel, A. Griffin
Publikováno v:
Papier, K, Gordon, L G, Khosrotehrani, K, Isbel, N, Campbell, S, Griffin, A & Green, A C 2018, ' Management of organ transplant recipients attending a high-throughput skin cancer surgery and surveillance clinic in Queensland ', The British journal of dermatology . https://doi.org/10.1111/bjd.17001
Background The incidence of skin cancer in organ transplant recipients (OTRs) is very high, due mainly to long‐term immunosuppressive therapy. The problem is particularly severe for OTRs living in Queensland, Australia, and results in significant m
Autor:
Kyoko Miura, Elsemieke I. Plasmeijer, Steven C. Campbell, N. M. Isbel, Mandy Way, Louise Marquart, Zainab Jiyad, Hans Peter Soyer, Peter O'Rourke, Jamie Fawcett, Adèle C. Green, Lisa Ferguson, David C. Whiteman, Marcia Davis
Publikováno v:
Acta Dermato-Venereologica, Vol 99, Iss 10, Pp 929-930 (2019)
Acta Dermato-Venereologica, 99(10), 929-930. Medical Journals/Acta D-V
Plasmeijer, E I, Jiyad, Z, Way, M, Marquart, L, Miura, K, Campbell, S, Isbel, N, Fawcett, J, Ferguson, L E, Davis, M, Whiteman, D C, Soyer, H P, O'Rourke, P & Green, A C 2019, ' Extreme Incidence of Skin Cancer in Kidney and Liver Transplant Recipients Living with High Sun Exposure ', Acta Dermato-Venereologica . https://doi.org/10.2340/00015555-3234
Acta Dermato-Venereologica, 99(10), 929-930. Medical Journals/Acta D-V
Plasmeijer, E I, Jiyad, Z, Way, M, Marquart, L, Miura, K, Campbell, S, Isbel, N, Fawcett, J, Ferguson, L E, Davis, M, Whiteman, D C, Soyer, H P, O'Rourke, P & Green, A C 2019, ' Extreme Incidence of Skin Cancer in Kidney and Liver Transplant Recipients Living with High Sun Exposure ', Acta Dermato-Venereologica . https://doi.org/10.2340/00015555-3234
is missing (Short communication)
Autor:
Kirsty Armstrong, Linda Orazio, Ingrid J. Hickman, N. M. Isbel, David W. Johnson, Merrilyn Banks
Publikováno v:
Nutrition & Dietetics. 64:200-206
Aim: Obesity following renal transplantation is common and may be associated with cardiovascular disease. We sought to investigate the prevalence of central obesity in renal transplant recipients (RTR) and its association with cardiovascular risk fac
Autor:
N. M. Isbel
Publikováno v:
Nephrology. 7:S58-S61
Autor:
Troy D. Kay, Gavin Cull, Paula Marlton, Devinder Gill, Carmel M. Hawley, David W. Johnson, Ralph Cobcroft, N. M. Isbel, Scott B. Campbell, Glen A Kennedy
Publikováno v:
Pathology. 34:263-266
Aim: The pseudo-Pelger-Huet (PH) anomaly has been associated with a variety of primary haematological disorders, infections and drugs. Recently, the development of dysgranulopoiesis characterised by a pseudo-PH anomaly has been reported in two patien
Autor:
Michael Uder, Kai-Uwe Eckardt, Kerstin Amann, George Mangos, Daniela Soreth-Rieke, Corinne Antignac, Bodo B. Beck, Ingo Hermann, Tobias B. Huber, Maike Buettner, Arif B. Ekici, Michael S. Wiesener, Stella McGinn, Steffen Uebe, Martin Hornberger, Thomas Hackenbeck, Antje Wiesener, Andrea Pannes, Sina Grupp, André Reis, N. M. Isbel, Vincent Morinière, Rolf Janka
Publikováno v:
Kidney international. 86(3)
For decades, ill-defined autosomal dominant renal diseases have been reported, which originate from tubular cells and lead to tubular atrophy and interstitial fibrosis. These diseases are clinically indistinguishable, but caused by mutations in at le