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We have 6 University of Liverpool, Institute of Life Course and Medical Sciences PhD Projects, Programmes & Scholarships PhD Projects, Programmes & Scholarships
University of Liverpool, Institute of Life Course and Medical Sciences PhD Projects, Programmes & Scholarships PhD Projects, Programmes & Scholarships
We have 6 University of Liverpool, Institute of Life Course and Medical Sciences PhD Projects, Programmes & Scholarships PhD Projects, Programmes & Scholarships
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Examination of the effectiveness and cost-effectiveness of the introduction of a novel patient-centered community metabolic liver clinic
Background. Non-alcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease in the UK due to the obesity and type 2 diabetes (T2D) epidemics. Read more
THROMB-AI: Computational risk stratification of thrombus formation and lysis in post-stroke patients
Cardiovascular disease is the leading cause of mortality and morbidity in developed countries. Often, the main pathological process responsible is the development of an arterial thrombus (or blood clot). Read more
Exploration of the multi-causality and multi-morbidity in patients with lifestyle related liver disease using the UK Biobank
Background. Non-alcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease in the UK due to the obesity and type 2 diabetes epidemics. Read more
ITCH-CF: Investigating The Cardiovascular Health of people living with Cystic Fibrosis in the CFTR modulator era
As life-expectancy improves for people living with cystic fibrosis (pwCF), new challenges in optimally managing an older, co-morbid population are likely to arise. Read more
Assessment of the stiffness of the aortic wall by Pulse Wave Velocity to predict risk of thoracic aortic aneurysm among hypertensive patients: The T-watch study
Thoracic Aortic Aneurysm (TAA) is a silent but lethal, disease, with 95% of TAAs being asymptomatic before an acute event, such as dissection or rupture, occurs. Read more
Investigating the role of calmodulin in human muscular hypotonia and immunodeficiency
Recently, human gene mutations in the calcium channels Orai1 and STIM1 have been identified in patients with immunodeficiency and muscular hypotonia syndromes. Read more
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