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Familial Hypercholesterolemia and Lipoprotein Apheresis.
Makino H, Koezuka R, Tamanaha T, Ogura M, Matsuki K, Hosoda K, Harada-Shiba M. Makino H, et al. J Atheroscler Thromb. 2019 Aug 1;26(8):679-687. doi: 10.5551/jat.RV17033. Epub 2019 Jun 22. J Atheroscler Thromb. 2019. PMID: 31231083 Free PMC article. Review.
[LDL-apheresis].
Makino H, Harada-Shiba M. Makino H, et al. Nihon Rinsho. 2007 Jul 28;65 Suppl 7:504-8. Nihon Rinsho. 2007. PMID: 17824079 Review. Japanese. No abstract available.
A novel Thr56Met mutation of the autosomal recessive hypercholesterolemia gene associated with hypercholesterolemia.
Harada K, Miyamoto Y, Morisaki H, Ohta N, Yamanaka I, Kokubo Y, Makino H, Harada-Shiba M, Okayama A, Tomoike H, Okamura T, Saito Y, Yoshimasa Y, Morisaki T. Harada K, et al. Among authors: makino h. J Atheroscler Thromb. 2010 Feb 26;17(2):131-40. doi: 10.5551/jat.2873. Epub 2010 Feb 3. J Atheroscler Thromb. 2010. PMID: 20124734 Free article.
Removal of plasma mature and furin-cleaved proprotein convertase subtilisin/kexin 9 by low-density lipoprotein-apheresis in familial hypercholesterolemia: development and application of a new assay for PCSK9.
Hori M, Ishihara M, Yuasa Y, Makino H, Yanagi K, Tamanaha T, Kishimoto I, Kujiraoka T, Hattori H, Harada-Shiba M. Hori M, et al. Among authors: makino h. J Clin Endocrinol Metab. 2015 Jan;100(1):E41-9. doi: 10.1210/jc.2014-3066. J Clin Endocrinol Metab. 2015. PMID: 25313916
1,950 results