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EJNMMI Research|September 6, 2021
Quantitative SPECT/CT parameters of myocardial 99mTechnetium-3,3-diphosphono-1,2-propanodicarboxylic acid (DPD) uptake in suspected cardiac transthyretin amyloidosisSimona Ben-Haim, A Chicheportiche, E Goshen, et al.
BMJ (Clinical Research Ed.)|February 4, 1989
Changing character of cervical cancer in young womenP M Elliott, M H Tattersall, M Coppleson, et al.
Journal of Medical Virology|October 1, 1988
Papillomavirus and cervical cancer: a clinical and laboratory studyW H Zhang, M Coppleson, B R Rose, et al.
International Journal of Cardiology|June 7, 2018
Assessment of a conduction-repolarisation metric to predict Arrhythmogenesis in right ventricular disordersC A Martin, M Orini, N T Srinivasan, et al.
The British Journal of Dermatology|November 2, 2018
Loss-of-function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotypeT Maruthappu, A Posafalvi, S Castelletti, et al.
Heart (British Cardiac Society)|May 10, 2008
Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genesJ P Kaski, P Syrris, M Burch, et al.
Heart (British Cardiac Society)|November 23, 2007
Prevalence of exercise-induced left ventricular outflow tract obstruction in symptomatic patients with non-obstructive hypertrophic cardiomyopathyJ S Shah, M T T Esteban, R Thaman, et al.
International Journal of Cardiology|December 3, 2014
Uncertain diagnosis of Fabry disease: consensus recommendation on diagnosis in adults with left ventricular hypertrophy and genetic variants of unknown significanceB E Smid, L van der Tol, F Cecchi, et al.
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