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Items: 1 to 20 of 358

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Hyperlipidemia in coronary heart disease. I. Lipid levels in 500 survivors of myocardial infarction.

Goldstein JL, Hazzard WR, Schrott HG, Bierman EL, Motulsky AG.

J Clin Invest. 1973 Jul;52(7):1533-43.

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Genetic analysis of total cholesterol and triglycerides in a pedigree of St. Thomas rabbits.

Beaty TH, Kwiterovich PO, Laville A, Lewis B.

J Lipid Res. 1989 Mar;30(3):387-94.

7.

Bivariate analyses of cholesterol and triglyceride levels in families in which probands have type IIb lipoprotein phenotype.

Namboodiri KK, Elston RC, Glueck CJ, Fallat R, Buncher CR, Tsang R.

Am J Hum Genet. 1975 Jul;27(4):454-71.

8.

Study of the genetic transmission of hypercholesterolemia and hypertriglyceridemia in a 195 member kindred.

Elston RC, Namboodiri KK, Glueck CJ, Fallat R, Tsang R, Leuba V.

Ann Hum Genet. 1975 Jul;39(1):67-87.

PMID:
1180488
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Myocardial infarction in the familial forms of hypertriglyceridemia.

Brunzell JD, Schrott HG, Motulsky AG, Bierman EL.

Metabolism. 1976 Mar;25(3):313-20.

PMID:
1250165
11.

Prevalence and expression of familial combined hyperlipidemia in childhood.

Cortner JA, Coates PM, Gallagher PR.

J Pediatr. 1990 Apr;116(4):514-9.

PMID:
2319396
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Population-based frequency of dyslipidemia syndromes in coronary-prone families in Utah.

Williams RR, Hopkins PN, Hunt SC, Wu LL, Hasstedt SJ, Lalouel JM, Ash KO, Stults BM, Kuida H.

Arch Intern Med. 1990 Mar;150(3):582-8.

PMID:
2310276
14.

Plasma lipoproteins in familial combined hyperlipidemia and monogenic familial hypertriglyceridemia.

Brunzell JD, Albers JJ, Chait A, Grundy SM, Groszek E, McDonald GB.

J Lipid Res. 1983 Feb;24(2):147-55.

16.

The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.

Jensen HK.

Dan Med Bull. 2002 Nov;49(4):318-45. Review.

PMID:
12553167
17.

Diagnosis of familial combined hyperlipidemia based on lipid phenotype expression in 32 families: results of a 5-year follow-up study.

Veerkamp MJ, de Graaf J, Bredie SJ, Hendriks JC, Demacker PN, Stalenhoef AF.

Arterioscler Thromb Vasc Biol. 2002 Feb 1;22(2):274-82.

18.

No evidence of linkage between familial combined hyperlipidemia and genes encoding lipolytic enzymes in Finnish families.

Pajukanta P, Porkka KV, Antikainen M, Taskinen MR, Perola M, Murtomäki-Repo S, Ehnholm S, Nuotio I, Suurinkeroinen L, Lahdenkari AT, Syvänen AC, Viikari JS, Ehnholm C, Peltonen L.

Arterioscler Thromb Vasc Biol. 1997 May;17(5):841-50.

19.

Apolipoprotein B is associated with metabolic syndrome in Chinese families with familial combined hyperlipidemia, familial hypertriglyceridemia and familial hypercholesterolemia.

Pei WD, Sun YH, Lu B, Liu Q, Zhang CY, Zhang J, Jia YH, Lu ZL, Hui RT, Liu LS, Yang YJ.

Int J Cardiol. 2007 Mar 20;116(2):194-200. Epub 2006 Jul 10.

PMID:
16828905
20.

[Familial combined hyperlipidemia: detection and characterisation of the hyperlipidemic profile among children and adolescents].

Ribalta J, La Ville AE, Heras M, Plana N, Masana L.

Med Clin (Barc). 1997 Jun 28;109(5):161-4. Spanish.

PMID:
9289537
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