A P Fitzpatrick

Guidelines for the Prevention of Stroke in Patients With Stroke and Transient Ischemic Attack

Re-theorising mobility and the formation of culture and language among the Corded Ware Culture in Europe

A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation

Mapping a Gene for Familial Hypertrophic Cardiomyopathy to Chromosome 14q1

Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes

Cardiac Myxomas

Defining the Anthropocene

Restrictive Cardiomyopathy

Familial cardiomyopathy underlies syndrome of right bundle branch block, ST segment elevation and sudden death

Chronic Kidney Disease Diagnosis and Management

Sudden Death and Cardiovascular Collapse in Children With Restrictive Cardiomyopathy

Assignment of patients into the classification of cardiomyopathies.

Guidelines for the Primary Prevention of Stroke

Brugada Syndrome: Report of the Second Consensus Conference

2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death

Contemporary Definitions and Classification of the Cardiomyopathies

Population history in third-millennium-BC Europe: assessing the contribution of genetics

The Palaeoanthropocene – The beginnings of anthropogenic environmental change

Risk-Based Triage for Nephrology Referrals Using the Kidney Failure Risk Equation

Familial neurofibromatosis and hypertrophic cardiomyopathy.

Initial experience with a rapid access blackouts triage clinic

Familial restrictive cardiomyopathy with atrioventricular block and skeletal myopathy.

BRONZE AGE CHILDHOOD MIGRATION OF INDIVIDUALS NEAR STONEHENGE, REVEALED BY STRONTIUM AND OXYGEN ISOTOPE TOOTH ENAMEL ANALYSIS*

Cardiac tumours simulating collagen vascular disease.