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2. 4 years' cascade genetic testing for familial hypercholesterolaemia in England – Increased referrals and ascertainment. (December 2016)

4. Contribution of NOTCH1 genetic variants to bicuspid aortic valve and other congenital lesions. Issue 14 (14th March 2022)

5. Diagnosis, natural history, and management in vascular Ehlers–Danlos syndrome. Issue 1 (March 2017)

6. Effect of remote ischaemic conditioning on clinical outcomes in patients with acute myocardial infarction (CONDI-2/ERIC-PPCI): a single-blind randomised controlled trial. Issue 10207 (19th October 2019)

7. Globotriaosylsphingosine (Lyso‐Gb3) as a biomarker for cardiac variant (N215S) Fabry disease. Issue 2 (2nd January 2018)

8. Irbesartan in Marfan syndrome (AIMS): a double-blind, placebo-controlled randomised trial. Issue 10216 (21st December 2019)

9. Study of indications for cardiac device implantation and utilisation in Fabry cardiomyopathy. Issue 23 (24th August 2019)

10. The 2017 international classification of the Ehlers–Danlos syndromes. Issue 1 (March 2017)