High Prevalence of Cerebral Small Vessel Disease on 7T Magnetic Resonance Imaging in Familial Hypercholesterolemia
Author:
Affiliation:
1. Division of Diabetes, Metabolism and Endocrinology, Department of Internal Medicine, Iwate Medical University
2. Division of Ultra-high Field MRI, Institute for Biomedical Sciences, Iwate Medical University
Publisher
Japan Atherosclerosis Society
Subject
Biochemistry (medical),Cardiology and Cardiovascular Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/jat/26/12/26_48553/_pdf
Reference39 articles.
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2. 2) Harada-Shiba M, Arai H, Ishigaki Y, Ishibashi S, Okamura T, Ogura M, Dobashi K, Nohara A, Bujo H, Miyauchi K, Yamashita S and Yokote K: Guidelines for Diagnosis and Treatment of Familial Hypercholesterolemia 2017. J Atheroscler Thromb, 2018; 25: 751-770
3. 3) Mabuchi H, Nohara A, Noguchi T, Kobayashi J, Kawashiri MA, Inoue T, Mori M, Tada H, Nakanishi C, Yagi K, Yamagishi M, Ueda K, Takegoshi T, Miyamoto S, Inazu A and Koizumi J: Genotypic and phenotypic features in homozygous familial hypercholesterolemia caused by proprotein convertase subtilisin/kexin type 9 (PCSK9) gain-of-function mutation. Atherosclerosis, 2014; 236: 54-61
4. 4) Stone NJ, Levy RI, Fredrickson DS and Verter J: Coronary artery disease in 116 kindred with familial type II hyperlipoproteinemia. Circulation, 1974; 49: 476-488
5. 5) Versmissen J, Oosterveer DM, Yazdanpanah M, Defesche JC, Basart DC, Liem AH, Heeringa J, Witteman JC, Lansberg PJ, Kastelein JJ and Sijbrands EJ: Efficacy of statins in familial hypercholesterolaemia: a long term cohort study. BMJ, 2008; 337: a2423
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