{ "items": [ "\n\n
We aim to further improve the clinical value of Cardiovascular Magnetic Resonance with application of advanced image analysis techniques.
\n \n\n \n \nWe use multi-parametric cardiac magnetic resonance imaging and multinuclear magnetic resonance spectroscopy to non-invasively investigate the relationship between cardiac metabolism and cardiac function.
\n \n\n \n \nWe have expertise in the study of heart disease using cardiovascular magnetic resonance (CMR), particularly quantitative techniques such as myocardial T1-mapping.
\n \n\n \n \nWe investigate diseases of the heart valves \u2013 how widespread the problem is, what the causes are, who is at risk from future problems and what treatments can improve outcomes for patients.
\n \n\n \n \nOCMR uses sophisticated cardiac MR imaging and spectroscopy methods to phenotype cardiovascular disease \u2013 in small-scale proof-of-principle studies, large-scale multicentre clinical trials and ultra-large scale population imaging programmes. As well as running their own research programmes, OCMR serves as a collaboration partner to any group wanting to strengthen their clinical research with state of the art non-invasive phenotyping tools.
\n \n\n \n \nThe Radcliffe Department of Medicine provides tailored advice and guidance to all researchers and students within RDM who would like support in obtaining funding.
\n \n\n \n \nThe Clinical Genetics Service offers a family-based service providing genetic counselling for children and adults who have or who may be at risk of inheriting a genetic condition, and for conditions where genetic testing can be used for carrier detection or prenatal diagnosis. The Clinical Genetics Service liaises closely with many other departments in the hospital but particularly the Medical Genetics Laboratories and the Prenatal Diagnosis Service.
\n \n\n \n \nThe Clinical Genetics Service offers a family-based service providing genetic counselling for children and adults who have or who may be at risk of inheriting a genetic condition, and for conditions where genetic testing can be used for carrier detection or prenatal diagnosis. The Clinical Genetics Service liaises closely with many other departments in the hospital but particularly the Medical Genetics Laboratories and the Prenatal Diagnosis Service.
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