Area of research
Cardiology and Cardiovascular Medicine · Endocrinology, Diabetes and Metabolism
Research interest
Research focused on Steatosis and Allele, with related work in Microsomal triglyceride transfer protein, Lipoprotein lipase, Chylomicron. Notable publications include 'Homozygous MTTP and APOB mutations may lead to hepatic steatosis and fibrosis despite metabolic differences in congenital hypocholesterolemia', 'An APOA5 3′ UTR Variant Associated with Plasma Triglycerides Triggers APOA5 Downregulation by Creating a Functional miR-485-5p Binding Site', and 'Molecular and functional analysis of two new MTTP gene mutations in an atypical case of abetalipoproteinemia'.
Efficacy of two vitamin E formulations in patients with abetalipoproteinemia and chylomicron retention disease
Homozygous MTTP and APOB mutations may lead to hepatic steatosis and fibrosis despite metabolic differences in congenital hypocholesterolemia
An APOA5 3′ UTR Variant Associated with Plasma Triglycerides Triggers APOA5 Downregulation by Creating a Functional miR-485-5p Binding Site
Post-Heparin LPL Activity Measurement Using VLDL As a Substrate: A New Robust Method for Routine Assessment of Plasma Triglyceride Lipolysis Defects
Molecular and functional analysis of two new MTTP gene mutations in an atypical case of abetalipoproteinemia