Identification and management of familial hypercholesterolaemia: what does it mean to primary care?

von Qureshi, Nadeem, Humphries, Steve E, Seed, Mary, Rowlands, Philip, Minhas, Rubin
Veröffentlicht 2009

Reductions in all-cause, cancer, and coronary mortality in statin-treated patients with heterozygous familial hypercholesterolaemia: a prospective registry study

von Neil, Andrew, Cooper, Jackie, Betteridge, John, Capps, Nigel, McDowell, Ian, Durrington, Paul, Seed, Mary, Humphries, Steve E.
Veröffentlicht 2008

Normal levels of inflammatory markers in treated patients with familial hypercholesterolaemia: a cross-sectional study

von Seed, Mary, Betteridge, D John, Cooper, Jackie, Caslake, Muriel, Durrington, Paul N, Thompson, Gilbert R, Sattar, Naveed, Humphries, Steve E, Neil, H Andrew W
Veröffentlicht 2012

Identification and biochemical analysis of a novel APOB mutation that causes autosomal dominant hypercholesterolemia

von Thomas, Ellen R A, Atanur, Santosh S, Norsworthy, Penny J, Encheva, Vesela, Snijders, Ambrosius P, Game, Laurence, Vandrovcova, Jana, Siddiq, Afshan, Seed, Mary, Soutar, Anne K, Aitman, Timothy J
Veröffentlicht 2013

Linkage and Association Between Distinct Variants of the APOA1/C3/A4/A5 Gene Cluster and Familial Combined Hyperlipidemia

von Eichenbaum-Voline, Sophie, Olivier, Michael, Jones, Emma L., Naoumova, Rossitza P., Jones, Bethan, Gau, Brian, Patel, Hetal N., Seed, Mary, Betteridge, D. John, Galton, David J., Rubin, Edward M., Scott, James, Shoulders, Carol C., Pennacchio, Len A.
Veröffentlicht 2003

Whole exome sequencing of familial hypercholesterolaemia patients negative for LDLR/APOB/PCSK9 mutations

von Futema, Marta, Plagnol, Vincent, Li, KaWah, Whittall, Ros A, Neil, H Andrew W, Seed, Mary, Bertolini, Stefano, Calandra, Sebastiano, Descamps, Olivier S, Graham, Colin A, Hegele, Robert A, Karpe, Fredrik, Durst, Ronen, Leitersdorf, Eran, Lench, Nicholas, Nair, Devaki R, Soran, Handrean, Van Bockxmeer, Frank M, Humphries, Steve E
Veröffentlicht 2014

Association of a sequence variant in DAB2IP with coronary heart disease

von Harrison, Seamus C., Cooper, Jackie A., Li, Kawah, Talmud, Phillipa J., Sofat, Reecha, Stephens, Jeffery W., Hamsten, Anders, Sanders, Julie, Montgomery, Hugh, Neil, Andrew, Humphries, Steve E., Juhan-Vague, Irène, Margaglione, Maurizio, di Minno, Giovanni, Yudkin, John, Tremoli, Elena, Naoumova, Rossi, Thompson, Gil, Seed, Mary, Durrington, Paul, Miller, Paul, Betteridge, John
Veröffentlicht 2012

CDKN2B expression in adipose tissue of familial combined hyperlipidemia patients

von Horswell, Stuart D., Fryer, Lee G. D., Hutchison, Claire E., Zindrou, Dlear, Speedy, Helen E., Town, Margaret-M., Duncan, Emma J., Sivapackianathan, Rasheeta, Patel, Hetal N., Jones, Emma L., Braithwaite, Adam, Salm, Max P. A., Neuwirth, Claire K. Y., Potter, Elizabeth, Anderson, Jonathan R., Taylor, Kenneth M., Seed, Mary, Betteridge, D. John, Crook, Martin A., Wierzbicki, Anthony S., Scott, James, Naoumova, Rossi P., Shoulders, Carol C.
Veröffentlicht 2013