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Derralynn Hughes
Derralynn Hughes
Verified email at ucl.ac.uk
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Year
Treatment of Fabry’s disease with the pharmacologic chaperone migalastat
DP Germain, DA Hughes, K Nicholls, DG Bichet, R Giugliani, WR Wilcox, ...
New england journal of medicine 375 (6), 545-555, 2016
5852016
Identification and assessment of Anderson-Fabry disease by cardiovascular magnetic resonance noncontrast myocardial T1 mapping
DM Sado, SK White, SK Piechnik, SM Banypersad, T Treibel, G Captur, ...
Circulation: Cardiovascular Imaging 6 (3), 392-398, 2013
5452013
Oral pharmacological chaperone migalastat compared with enzyme replacement therapy in Fabry disease: 18-month results from the randomised phase III ATTRACT study
DA Hughes, K Nicholls, SP Shankar, G Sunder-Plassmann, D Koeller, ...
Journal of medical genetics 54 (4), 288-296, 2017
4282017
Divalent cation-independent macrophage adhesion inhibited by monoclonal antibody to murine scavenger receptor
I Fraser, D Hughes, S Gordon
Nature 364 (6435), 343-346, 1993
4171993
Effects of enzyme replacement therapy on the cardiomyopathy of Anderson–Fabry disease: a randomised, double-blind, placebo-controlled clinical trial of agalsidase alfa
DA Hughes, PM Elliott, J Shah, J Zuckerman, G Coghlan, J Brookes, ...
Heart 94 (2), 153-158, 2008
4012008
Natural history of Fabry disease in females in the Fabry Outcome Survey
PB Deegan, AF Baehner, MAB Romero, DA Hughes, C Kampmann, ...
Journal of medical genetics 43 (4), 347-352, 2006
3752006
Cardiovascular magnetic resonance measurement of myocardial extracellular volume in health and disease
DM Sado, AS Flett, SM Banypersad, SK White, V Maestrini, G Quarta, ...
Heart 98 (19), 1436-1441, 2012
3722012
Recommendations for initiation and cessation of enzyme replacement therapy in patients with Fabry disease: the European Fabry Working Group consensus document
M Biegstraaten, R ArngrÝmsson, F Barbey, L Boks, F Cecchi, PB Deegan, ...
Orphanet journal of rare diseases 10, 1-10, 2015
3512015
Macrophage recruitment during limb development and wound healing in the embryonic and foetal mouse
J Hopkinson-Woolley, D Hughes, S Gordon, P Martin
Journal of cell science 107 (5), 1159-1167, 1994
3511994
Characterization of classical and nonclassical Fabry disease: a multicenter study
M Arends, C Wanner, D Hughes, A Mehta, D Oder, OT Watkinson, ...
Journal of the American Society of Nephrology 28 (5), 1631-1641, 2017
3482017
The macrophage scavenger receptor type A is expressed by activated macrophages and protects the host against lethal endotoxic shock
R Haworth, N Platt, S Keshav, D Hughes, E Darley, H Suzuki, Y Kurihara, ...
The Journal of experimental medicine 186 (9), 1431-1439, 1997
3461997
Estimated impact of the COVID-19 pandemic on cancer services and excess 1-year mortality in people with cancer and multimorbidity: near real-time data on cancer care, cancerá…
AG Lai, L Pasea, A Banerjee, G Hall, S Denaxas, WH Chang, M Katsoulis, ...
BMJ open 10 (11), e043828, 2020
2742020
Prevalence and clinical significance of cardiac arrhythmia in Anderson-Fabry disease
JS Shah, DA Hughes, B Sachdev, M Tome, D Ward, P Lee, AB Mehta, ...
The American journal of cardiology 96 (6), 842-846, 2005
2732005
Identification of macrophages and dendritic cells in the osteopetrotic (op/op) mouse
MD Witmer-Pack, DA Hughes, G Schuler, L Lawson, A McWilliam, K Inaba, ...
Journal of cell science 104 (4), 1021-1029, 1993
2691993
Murine macrophage scavenger receptor: in vivo expression and function as receptor for macrophage adhesion in lymphoid and non‐lymphoid organs
DA Hughes, IP Fraser, S Gordon
European journal of immunology 25 (2), 466-473, 1995
2591995
Gaucher disease
GM Pastores, DA Hughes
2422018
The validation of pharmacogenetics for the identification of Fabry patients to be treated with migalastat
ER Benjamin, MC Della Valle, X Wu, E Katz, F Pruthi, S Bond, B Bronfin, ...
Genetics in Medicine 19 (4), 430-438, 2017
2422017
Multiple myeloma: causes and consequences of delay in diagnosis
CC Kariyawasan, DA Hughes, MM Jayatillake, AB Mehta
QJM: An International Journal of Medicine 100 (10), 635-640, 2007
2392007
Prevalence of Anderson–Fabry disease in patients with hypertrophic cardiomyopathy: the European Anderson–Fabry Disease Survey
P Elliott, R Baker, F Pasquale, G Quarta, H Ebrahim, AB Mehta, ...
Heart 97 (23), 1957-1960, 2011
2282011
Evolution of prodromal clinical markers of Parkinson disease in a GBA mutation–positive cohort
M Beavan, A McNeill, C Proukakis, DA Hughes, A Mehta, AHV Schapira
JAMA neurology 72 (2), 201-208, 2015
2252015
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