Sitosterolemia, Hypercholesterolemia, and Coronary Artery Disease-Reference-Cited by-同舟云学术

Sitosterolemia, Hypercholesterolemia, and Coronary Artery Disease

Published:2018-09-01 Issue:9 Volume:25 Page:783-789
ISSN:1340-3478
Container-title:Journal of Atherosclerosis and Thrombosis
language:en
Short-container-title:JAT

Author:

Tada Hayato¹,Nohara Atsushi¹,Inazu Akihiro²,Sakuma Nagahiko³,Mabuchi Hiroshi¹,Kawashiri Masa-aki¹

Affiliation:

1. Department of Cardiovascular and Internal Medicine, Kanazawa University Graduate School of Medical Science

2. Department of Laboratory Science, Molecular Biochemistry and Molecular Biology, Graduate School of Medical Science, Kanazawa University

3. Department of Cardio-Renal Medicine and Hypertension, Nagoya City University Graduate School of Medical Sciences

Publisher

Japan Atherosclerosis Society

Subject

Biochemistry (medical),Cardiology and Cardiovascular Medicine,Internal Medicine

Link

https://www.jstage.jst.go.jp/article/jat/25/9/25_RV17024/_pdf

Reference30 articles.

1. 1) Goldstein JL, Hobbs HH, Brown MS. Familial hypercholesterolemia. In The Metabolic and Molecular Bases of Inherited Diseases. 8th edition. Scriver CR, Beaudet AL, Sly WS, Valle D, editors. McGraw- Hill, New York. 2001; 2863-2913

2. 2) Soutar AK, Naoumova RP. Mechanisms of Disease: genetic causes of familial hypercholesterolemia. Nat Pract Cardiovasc Med. 2007; 4: 214-225

3. 3) Escolà-Gil JC, Quesada H, Julve J, Martín-Campos JM, Cedó L, Blanco-Vaca F. Sitosterolemia: diagnosis, investigation, and management. Curr Atheroscler Rep. 2014; 16: 424

4. 4) Tada H, Kawashiri MA, Takata M, Matsunami K, Imamura A, Matsuyama M, Sawada H, Nunoi H, Konno T, Hayashi K, Nohara A, Inazu A, Kobayashi J, Mabuchi H, Yamagishi M. Infantile Cases of Sitosterolaemia with Novel Mutations in the ABCG5 Gene: Extreme Hypercholesterolaemia is Exacerbated by Breastfeeding. JIMD Rep. 2015; 21: 115-122

5. 5) Tada H, Kawashiri MA, Okada H, Endo S, Toyoshima Y, Konno T, Nohara A, Inazu A, Takao A, Mabuchi H, Yamagishi M, Hayashi K. A Rare Coincidence of Sitosterolemia and Familial Mediterranean Fever Identified by Whole Exome Sequencing. J Atheroscler Thromb. 2016; 23: 884-890

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