Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Clare Oni"'
Autor:
Thompson Olaoni, Chandan Saha, Claire N. Harrison, Monika Ciesielska, Yurina Miki, Priya Sriskandarajah, Jennifer O'Sullivan, Chienye Asinobi, Deepti Radia, Donal P. McLornan, Clare Oni, Claire Woodley, Rebecca Todd, Anna Green, Mark Ong, Susan Asirvatham, Clive Grattan, Natalia Curto-Garcia
Publikováno v:
Blood. 138:3625-3625
Background: Systemic mastocytosis (SM) is a disorder of neoplastic mast cells ranging from indolent to aggressive multi-system disease. We previously reported our large single centre experience managing SM. Since 2019 patients have had access to new
Publikováno v:
British journal of haematologyReferences. 188(5)
Mastocytosis is a rare disease with varied presentation, myriad symptomatology and variable prognosis. Most patients present with cutaneous disease and mediator-related symptomatology with a small subset having systemic disease (systemic mastocytosis
Autor:
Deimante Drasutyte, Nicholas C.P. Cross, Natalia Curto-Garcia, Joana M. P. Desterro, Clive Grattan, Mark Ong, Clare Oni, Miki Yurina, Yvonne Francis, Jennifer O'Sullivan, Thompson Olaoni, Donal P. McLornan, Mufaddal Moonim, Anna Green, Claire Woodley, Monika Ciesielska, Deepti Radia
Publikováno v:
Blood. 134:2960-2960
Introduction: Systemic mastocytosis (SM) is a heterogeneous disorder of neoplastic mast cells ranging from an indolent to aggressive multi-system disease. We registered our UK Mastocytosis Centre of Excellence with the European Competence Network of
Autor:
Saaeha Rauz, Adrian Jones, Ben Fisher, Wan-Fai Ng, Costantino Pitzalis, Ian Giles, Peter Lanyon, Simon J. Bowman, John McLaren, David Coady, Clare Oni, Paul Emery, Sheryl Mitchell, John Hunter, N Gendi, Mohammed Akil, Victoria Hindmarsh, Neil McHugh, Robert J. Moots, Nurhan Sutcliffe, Vadivelu Saravanan, Elizabeth Price, Michele Bombardieri, Annie Cooper, David A. Isenberg, Marian Regan, Bhaskar Dasgupta, Katherine James, Steven Young-Min, Francesca Barone, Monica Gupta, Bridget Griffiths, Andrea Richards, Colin T. Pease
Publikováno v:
Oni, C, Mitchell, S, James, K, Ng, W-F, Griffiths, B, Hindmarsh, V, Price, E, Pease, C T, Emery, P, Lanyon, P, Jones, A, Bombardieri, M, Sutcliffe, N, Pitzalis, C, Hunter, J, Gupta, M, McLaren, J, Cooper, A, Regan, M, Giles, I, Isenberg, D, Saravanan, V, Coady, D, Dasgupta, B, McHugh, N, Young-Min, S, Moots, R, Gendi, N, Akil, M, Barone, F, Fisher, B, Rauz, S, Richards, A, Bowman, S J 2016, ' Eligibility for clinical trials in primary Sjögren's syndrome : lessons from the UK Primary Sjögren's Syndrome Registry ', Rheumatology, vol. 55, no. 3, pp. 544-552 . https://doi.org/10.1093/rheumatology/kev373
OBJECTIVE: To identify numbers of participants in the UK Primary Sjögren's Syndrome Registry (UKPSSR) who would fulfil eligibility criteria for previous/current or potential clinical trials in primary SS (pSS) in order to optimize recruitment.METHOD