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Metabolites|May 26, 2023
Severe Hypertriglyceridaemia and Chylomicronaemia Syndrome-Causes, Clinical Presentation, and Therapeutic OptionsBilal Bashir, Jan H Ho, Paul Downie, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|September 5, 2024
Ethnic Diversity and Distinctive Features of Familial Versus Multifactorial Chylomicronemia Syndrome: Insights From the UK FCS National RegistryBilal Bashir, Paul Downie, Natalie Forrester, et al.Atherosclerosis|March 6, 2024
Validation of the familial chylomicronaemia syndrome (FCS) score in an ethnically diverse cohort from UK FCS registry: Implications for diagnosis and differentiation from multifactorial chylomicronaemia syndrome (MCS)Bilal Bashir, See Kwok, Anthony S Wierzbicki, et al.Nutrients|October 17, 2019
Nutritional and Metabolic Characteristics of UK Adult Phenylketonuria Patients with Varying Dietary AdherenceBenjamin Green, Robert Browne, Sarah Firman, et al.Genetics in Medicine Open|September 8, 2025
Rare variant genetic landscape of familial chylomicronemia syndrome (FCS) in the United KingdomBilal Bashir, Natalie Forrester, Paul Downie, et al.International Journal of Neonatal Screening|September 23, 2024
Consistency in the Assessment of Dried Blood Spot Specimen Size and Quality in U.K. Newborn Screening LaboratoriesStuart J Moat, James R Bonham, Christine Cavanagh, et al.Pageof 4