Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Anthony F. Winder"'
Autor:
Anthony F. Winder, John A Papadakis, Dimitri P. Mikhailidis, Emanuel S Ganotakis, Indera Anita Jagroop
Publikováno v:
International Journal of Cardiology. 69:237-244
We evaluated the use of combination therapy (ciprofibrate 100 mg or bezafibrate 400 mg plus fluvastatin 40 mg) in 23 patients (n=13 in the ciprofibrate group) with established cardiovascular disease. Both treatments achieved a significant (P less tha
Publikováno v:
Clinical Chemistry. 41:1599-1604
Molecular epidemiological research has identified the association of a common apolipoprotein E (apo E) isoform (E4 as opposed to E3), with risk both of coronary artery disease and of Alzheimer dementia. In addition, the role of apo E genotype (usuall
Publikováno v:
Clinica Chimica Acta. 227:17-22
Direct DNA sequence determination of PCR amplified exons of the tyrosinase gene of three British patients suffering from tyrosinase negative oculocutaneous albinism has revealed three new missense point mutations: (1) an adenine to guanine transition
Autor:
Anthony F Winder
Publikováno v:
Journal of the Royal Society of Medicine. 91:189-191
Publikováno v:
Circulation. 101
To the Editor: The comprehensive review by Furberg1 of natural statins and stroke raises a number of issues. Stroke was a secondary end point in these studies in patients with cardiovascular disease (CVD). Primary end-point trials in stroke are await
Autor:
Anthony F. Winder, Lars H. Breimer, Barrie Jay, Anthony T. Moore, Panos Panayiotidis, Marcelle Jay
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 243(1)
Molecular analysis of the human tyrosinage gene in two patients suffering from a temperature-sensitive form of albinism has identified a thymine triplet deletion at codon 439 which is accompanied by a duplication of the immediately preceding cytosine
Autor:
France Mailly, Yesim Tugrul, Paul W. A. Reymer, Taco Bruin, Mary Seed, Björn F. Groenemeyer, Anette Asplund-Carlson, David Vallance, Anthony F. Winder, George J. Miller, John J. P. Kastelein, Anders Hamsten, Gunilla Olivecrona, Steve E. Humphries, Philippa J. Talmud
Publikováno v:
Arteriosclerosis, thrombosis, and vascular biology. 15(4)
Abstract Subjects with combined hyperlipidemia (CHL) were screened for mutations in the lipoprotein lipase (LPL) gene by single-strand conformational polymorphism, and a previously reported G→A DNA sequence change in exon 2, causing substitution of
Publikováno v:
Biochemical Society Transactions. 20:41S-41S
Autor:
Anthony F Winder
Publikováno v:
Proceedings of the Royal Society of Medicine. 69:270-272
Publikováno v:
Biochemical Society Transactions. 15:912-913