Medicine and Dentistry
Familial Hypercholesterolemia
100%
Patient
69%
Low Density Lipoprotein Cholesterol
45%
Lipid
42%
Diseases
39%
Therapeutic Procedure
35%
Gene
30%
Plasma
26%
Apolipoprotein B
25%
Diagnosis
24%
Lipoprotein Lipase
24%
Lipoprotein
23%
Genetic Screening
22%
Familial Hypobetalipoproteinemia
20%
Child
19%
Coronary Artery Disease
17%
Family
17%
Lipoprotein Lipase Deficiency
16%
Screening
16%
Hypercholesterolemia
15%
Gene Mutation
15%
Inpatient
15%
Proprotein Convertase 9
14%
Cholesterol
14%
Ischemic Heart Disease
12%
LDL Receptor
12%
Triacylglycerol
12%
Exon
12%
Arteriosclerotic Heart Disease
11%
Prematurity
11%
Association
11%
Hypertriglyceridemia
10%
Predictor
10%
Pancreatitis
9%
Lipoprotein Apheresis
9%
Heterozygote
9%
Metabolism
9%
Hyperlipidemia
9%
Risk Assessment
9%
Experience
9%
Abetalipoproteinemia
8%
Xanthoma
8%
Age
8%
Adult
7%
Statin
7%
Hypertension
6%
Index Case
6%
Serum
6%
Diabetes
6%
High Density Lipoprotein Cholesterol
6%
Biochemistry, Genetics and Molecular Biology
Familial Hypercholesterolemia
68%
Mutation
62%
Cholesterol
45%
Nested Gene
45%
Hypobetalipoproteinemia
36%
Lipid Disorders
35%
Gene Mutation
34%
Apolipoprotein B
33%
Lipoprotein
33%
Low-Density Lipoprotein
29%
Lipoprotein Lipase
25%
Genetic Screening
24%
Genetics
21%
Lipid
17%
Missense Mutation
14%
Microsomal Triglyceride Transfer Protein
14%
Hypertriglyceridemia
13%
Lipoprotein Metabolism
13%
Abetalipoproteinemia
13%
Hypercholesterolemia
12%
Lipoprotein Lipase Deficiency
11%
Secretion (Process)
10%
LDL Receptor
9%
Proband
9%
Blood Level
9%
ABC Transporter
9%
Patient Registry
9%
Association
8%
Protein
8%
Metabolic Pathway
8%
Genetic Carrier
8%
Development
7%
Low Density Lipoprotein Cholesterol Level
7%
Cholesterol Blood Level
7%
Regulatory Mechanism
6%
Electric Potential
6%
Kinetics
6%
Dyslipidemia
6%
Sequencing
6%
Very Low-Density Lipoprotein
5%
Genetic Risk
5%
Data Base
5%
Kexin
5%
Proprotein Convertase
5%
Subtilisin
5%
Nonsense Mutation
5%
Autosomal Recessive Inheritance
5%
Alipogene Tiparvovec
5%
Lipase
5%
Fat
5%