同: familial combined hyperlipidemia

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1. LDLコレステロール代謝の遺伝性疾患 inherited disorders of ldl cholesterol metabolism
2. 高トリグリセリド血症患者に対するアプローチ approach to the patient with hypertriglyceridemia

English Journal

Identification of the differentially expressed genes associated with familial combined hyperlipidemia using bioinformatics analysis.

Luo X1, Yu C1, Fu C1, Shi W1, Wang X1, Zeng C1, Wang H1.
Molecular medicine reports.Mol Med Rep.2015 Jan 27. doi: 10.3892/mmr.2015.3263. [Epub ahead of print]
The aim of the present study was to screen the differentially expressed genes (DEGs) associated with familial combined hyperlipidemia (FCHL) and examine the changing patterns. The transcription profile of GSE18965 was obtained from the NCBI Gene Expression Omnibus database, including 12 FCHL samples
PMID 25625967

Determinants of VLDL composition and apo B-containing particles in familial combined hyperlipidemia.

Cruz-Bautista I1, Mehta R1, Cabiedes J2, García-Ulloa C1, Guillen-Pineda LE1, Almeda-Valdés P1, Cuevas-Ramos D1, Aguilar-Salinas CA3.
Clinica chimica acta; international journal of clinical chemistry.Clin Chim Acta.2015 Jan 1;438:160-5. doi: 10.1016/j.cca.2014.08.018. Epub 2014 Aug 27.
BACKGROUND: In familial combined hyperlipidemia (FCHL) the severity of the dyslipidemia is determined by an overproduction of VLDL (very low density lipoprotein) particles and by its abnormal lipid composition. However, few are known regarding the metabolic factors that determine these abnormalities
PMID 25172037

Common genetic variants contribute to primary hypertriglyceridemia without differences between familial combined hyperlipidemia and isolated hypertriglyceridemia.

De Castro-Orós I1, Cenarro A2, Tejedor MT2, Baila-Rueda L2, Mateo-Gallego R2, Lamiquiz-Moneo I2, Pocoví M2, Civeira F2.
Circulation. Cardiovascular genetics.Circ Cardiovasc Genet.2014 Dec;7(6):814-21. doi: 10.1161/CIRCGENETICS.114.000522. Epub 2014 Aug 30.
BACKGROUND: The majority of hypertriglyceridemias are diagnosed as familial combined hyperlipidemia (FCHL) and primary isolated hypertriglyceridemias. The contribution of common genetic variants in primary hypertriglyceridemias and the genetic difference between FCHL and isolated hypertriglyceridemi
PMID 25176936

Japanese Journal

原発性高脂血症 (特集内分泌・代謝領域の「難病」とその克服に向けた取り組みの現状と展望)

山﨑久隆,大須賀淳一,石橋俊
内分泌・糖尿病・代謝内科 37(5), 487-494, 2013-11
NAID 40019890949

アポ蛋白Bと small, dense LDL-C

伊藤康樹
臨床病理 60(4), 336-342, 2012-04-25
NAID 10030762899

Management of Type IIb Dyslipidemia

Arai Hidenori,Ishibashi Shun,Bujo Hideaki,Hayashi Toshio,Yokoyama Shinji,Oikawa Shinichi,Kobayashi Junji,Shirai Kohji,Ota Takao,Yamashita Shizuya,Gotoda Takanari,Harada-Shiba Mariko,Sone Hirohito,Eto Masaaki,Suzuki Hiroaki,Yamada Nobuhiro
Journal of Atherosclerosis and Thrombosis 19(2), 105-114, 2012
… It is also associated with type 2 diabetes mellitus, metabolic syndrome, and chronic kidney disease (CKD), and most patients with familial combined hyperlipidemia (FCHL) show this phenotype; …
NAID 130004444573

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