Lipids, Lipoproteins, Atherosclerosis and Cardiovascular Disease

Por Burnett, John R.
Publicado em 2004

HDL Revisited: New Opportunities for Managing Dyslipoproteinaemia and Cardiovascular Disease

Por Watts, Gerald F, Burnett, John R
Publicado em 2004

Common and Rare Gene Variants Affecting Plasma LDL Cholesterol

Por Burnett, John R, Hooper, Amanda J
Publicado em 2008

Phenylketonuria: An Inborn Error of Phenylalanine Metabolism

Por Williams, Robin A, Mamotte, Cyril DS, Burnett, John R
Publicado em 2008

Genetic determinants of hepatic steatosis in man

Por Hooper, Amanda J., Adams, Leon A., Burnett, John R.
Publicado em 2011

Filiarial chyluria with nephrotic-range proteinuria and associated hypoalbuminaemia and hypogammaglobulinaemia secondary to bilateral lymphorenal fistulae

Por Faraj, Joseph, Mander, Julian, Burnett, John R, Prentice, David
Publicado no BMJ Case Rep (2017)

Lipoprotein lipase deficiency presenting with neonatal perianal abscesses

Por Akesson, Lauren S, Burnett, John R, Mehta, Divyesh K, Martin, Andrew C
Publicado no BMJ Case Rep (2016)

Isolated brachydactyly type E and idiopathic pancreatitis in a patient presenting to a lipid disorders clinic

Por Page, Michael M, Hooper, Amanda J, Glendenning, Paul, Burnett, John R
Publicado no BMJ Case Rep (2017)

Clinical utility gene card for: Abetalipoproteinaemia

Por Burnett, John R, Bell, Damon A, Hooper, Amanda J, Hegele, Robert A
Publicado em 2012

Clinical utility gene card for: Familial Hypobetalipoproteinaemia (APOB)

Por Burnett, John R, Bell, Damon A, Hooper, Amanda J, Hegele, Robert A
Publicado em 2012

Mipomersen and other therapies for the treatment of severe familial hypercholesterolemia

Por Bell, Damon A, Hooper, Amanda J, Watts, Gerald F, Burnett, John R
Publicado em 2012

Clinical utility gene card for: Familial hypobetalipoproteinaemia (APOB) – Update 2014

Por Burnett, John R, Bell, Damon A, Hooper, Amanda J, Hegele, Robert A
Publicado no Eur J Hum Genet (2015)

Clinical utility gene card for: Abetalipoproteinaemia – Update 2014

Por Burnett, John R, Bell, Damon A, Hooper, Amanda J, Hegele, Robert A
Publicado no Eur J Hum Genet (2015)

Clinical utility gene card for: Sitosterolaemia

Por Hooper, Amanda J, Bell, Damon A, Hegele, Robert A, Burnett, John R
Publicado no Eur J Hum Genet (2017)

Protein Kinase C Controls Vesicular Transport and Secretion of Apolipoprotein E from Primary Human Macrophages

Por Karunakaran, Denuja, Kockx, Maaike, Owen, Dylan M., Burnett, John R., Jessup, Wendy, Kritharides, Leonard
Publicado em 2013

Clinical utility gene card for: Tangier disease

Por Hooper, Amanda J, McCormick, Sally P A, Hegele, Robert A, Burnett, John R
Publicado no Eur J Hum Genet (2017)

Lipoprotein Lipase Deficiency in an Infant With Chylomicronemia, Hepatomegaly, and Lipemia Retinalis

Por Vidanapathirana, Dinesha Maduri, Rodrigo, Thushara, Waidyanatha, Samantha, Jasinge, Eresha, Hooper, Amanda J., Burnett, John R.
Publicado no Glob Pediatr Health (2017)

High-density lipoprotein subpopulation profiles in lipoprotein lipase and hepatic lipase deficiency

Por Tani, Mariko, Horvath, Katalin V., Lamarche, Benoit, Couture, Patrick, Burnett, John R., Schaefer, Ernst J., Asztalos, Bela F.
Publicado no Atherosclerosis (2016)

A Model of Care for Familial Hypercholesterolaemia: Key Role for Clinical Biochemistry

Por Watts, Gerald F, Sullivan, David R, van Bockxmeer, Frank M, Poplawski, Nicola, Hamilton-Craig, Ian, Clifton, Peter M, O’Brien, Richard C, George, Peter M, Burnett, John R
Publicado em 2012

Cyclosporin A Decreases Apolipoprotein E Secretion from Human Macrophages via a Protein Phosphatase 2B-dependent and ATP-binding Cassette Transporter A1 (ABCA1)-independent Pathway

Por Kockx, Maaike, Guo, Dongni Lily, Traini, Mathew, Gaus, Katharina, Kay, Jason, Wimmer-Kleikamp, Sabine, Rentero, Carles, Burnett, John R., Le Goff, Wilfried, Van Eck, Miranda, Stow, Jennifer L., Jessup, Wendy, Kritharides, Leonard
Publicado em 2009