163,582 research outputs found

    Is cholesteryl ester transfer protein inhibition an effective strategy to reduce cardiovascular risk? CETP inhibition as a strategy to reduce cardiovascular risk: The pro case

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    Originally published August 3, 2015. Includes Response to Barter et al. by G. Kees Hovingh, Kausik K. Ray, S. Matthijs Boekholdt on pg. 432Philip J. Barter, Stephen J. Nicholls, John J. P. Kastelein, Kerry-Anne Ry

    UvA-DARE (Digital Academic Repository) HUMU 780 A Single Ser259Arg Mutation in the Gene for Lipoprotein Lipase Causes Chylomicronemia in Moroccans of Berber Ancestry

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    A single Ser 259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestry Foubert, L.; Bruin, T.; de Gennes, J.L.; Ehrenborg, E.; Furioli, J.; Kastelein, J.J.P.; Benlian, P.; Hayden, M.R. Published in: Human Mutation Link to publication Citation for published version (APA): Foubert, L., Bruin, T., de Gennes, J. L., Ehrenborg, E., Furioli, J., Kastelein, J. J. P., ... Hayden, M. R. (1997). A single Ser 259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestry. Human Mutation, 10, 179-185. General rights It is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), other than for strictly personal, individual use, unless the work is under an open content license (like Creative Commons). Disclaimer/Complaints regulations If you believe that digital publication of certain material infringes any of your rights or (privacy) interests, please let the Library know, stating your reasons. In case of a legitimate complaint, the Library will make the material inaccessible and/or remove it from the website. Please Ask the Library: https://uba.uva.nl/en/contact, or a letter to: Library of the University of Amsterdam, Secretariat, Singel 425, 1012 WP Amsterdam, The Netherlands. You will be contacted as soon as possible

    [Report to Chief J. E. Curry, by an unknown author #1]

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    Report to Chief J. E. Curry, by an unknown author. The report contains a list of officers who gave depositions to the United States Attorney

    [Report to Chief J. E. Curry, by an unknown author #2]

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    Report to Chief J. E. Curry, by an unknown author. The report contains a list of officers who gave depositions to the United States Attorney

    Murder on the mountain: author talk with Peter J. Wosh

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    Author talk by Peter J. Wosh on May 5th, 2022, on his book, "Murder on the Mountain: crime, passion, and punishment in gilded age New Jersey.

    Homozygous autosomal dominant hypercholesterolaemia: prevalence, diagnosis, and current and future treatment perspectives

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    Homozygous autosomal dominant hypercholesterolemia (hoADH) is a rare genetic disorder caused by mutations in LDL receptor, apolipoprotein B, and/or proprotein convertase subtilisin-kexin type 9. Both the genetic mutations and the clinical phenotype vary largely among individual patients, but patients with hoADH are typically characterized by extremely elevated LDL-cholesterol (LDL-C) levels, and a very high-risk for premature cardiovascular disease. Current lipid-lowering therapies include bile acid sequestrants, statins, and ezetimibe. To further decrease LDL-C levels in hoADH, lipoprotein apheresis is recommended, but this therapy is not available in all countries

    Mr. Melvin J. Collier, RWWL AUC, June 2011

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    This video is a conversation with Mr. Melvin J. Collier. Mr. Collier talks about his book, "From Mississippi to Africa: A Journey of Discovery". Daniel Le, AUC Woodruff Library, is the interviewer

    Effect of evolocumab on coronary plaque composition

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    Abstract not availableStephen J. Nicholls, Rishi Puri, Todd Anderson, Christie M. Ballantyne, Leslie Cho, John J.P. Kastelein, Wolfgang Koenig, Ransi Somaratne, Helina Kassahun, Jingyuan Yang, Scott M. Wasserman, Satoshi Honda, Daisuke Shishikura, Daniel J. Scherer, Marilyn Borgman, Danielle M. Brennan, Kathy Wolski, Steven E. Nisse
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