PedAM
Pediatric Disease Annotations & Medicines
| Disease | vascular disease |
| Phenotype | C0020445|familial hypercholesterolemia |
| Sentences | 7 |
| PubMedID- 22819221 | Lrp1 gene polymorphisms are associated with premature risk of cardiovascular disease in patients with familial hypercholesterolemia. |
| PubMedID- 25525746 | We investigated whether anxa5 genetic variations and plasma anxa5 levels were associated with carotid atherosclerosis and contributed to cardiovascular disease (cvd) risk in patients with familial hypercholesterolemia (fh). |
| PubMedID- 23882283 | familial hypercholesterolemia (fh) is associated with premature atherosclerotic cardiovascular diseases, and is inherited as an autosomal dominant trait. |
| PubMedID- 23757599 | Previous studies have reported that cimt is increased in children at high risk for cardiovascular disease because of familial hypercholesterolemia, type 1 diabetes, having parents with premature myocardial infarction, or elevated levels of ultrasensitive c-reactive protein compared with other children (jarvisalo et al. |
| PubMedID- 22119890 | The logarithm of the triglyceride/hdl-cholesterol ratio is related to the history of cardiovascular disease in patients with familial hypercholesterolemia. |
| PubMedID- 25029472 | Association of peripheral arterial and cardiovascular diseases in familial hypercholesterolemia. |
| PubMedID- 20169164 | Background: the risk of premature cardiovascular disease in patients with familial hypercholesterolemia (fh) can be profoundly reduced by cholesterol-lowering therapy, and current guidelines for fh advocate ambitious low-density lipoprotein cholesterol (ldl-c) goals. |
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