141 related articles for article (PubMed ID: 8305410)
1. Characteristics of 46 heterozygous carriers and 57 unaffected relatives in five Danish families with familial defective apolipoprotein B-100.
Hansen PS; Meinertz H; Jensen HK; Fruergaard P; Launbjerg J; Klausen IC; Lemming L; Gerdes U; Gregersen N; Faergeman O
Arterioscler Thromb; 1994 Feb; 14(2):207-13. PubMed ID: 8305410
[TBL] [Abstract][Full Text] [Related]
2. Phenotypic heterogeneity associated with defective apolipoprotein B-100 and occurrence of the familial hypercholesterolemia phenotype in the absence of an LDL-receptor defect within a Canadian kindred.
Davignon J; Dufour R; Roy M; Bétard C; Ma Y; Ouellette S; Boulet L; Lussier-Cacan S
Eur J Epidemiol; 1992 May; 8 Suppl 1():10-7. PubMed ID: 1505645
[TBL] [Abstract][Full Text] [Related]
3. Differences in the phenotype between children with familial defective apolipoprotein B-100 and familial hypercholesterolemia.
Pimstone SN; Defesche JC; Clee SM; Bakker HD; Hayden MR; Kastelein JJ
Arterioscler Thromb Vasc Biol; 1997 May; 17(5):826-33. PubMed ID: 9157944
[TBL] [Abstract][Full Text] [Related]
4. Familial defective apolipoprotein B-100.
Hansen PS
Dan Med Bull; 1998 Sep; 45(4):370-82. PubMed ID: 9777289
[TBL] [Abstract][Full Text] [Related]
5. Clinical signs of familial hypercholesterolemia in patients with familial defective apolipoprotein B-100 and normal low density lipoprotein receptor function.
Myant NB; Gallagher JJ; Knight BL; McCarthy SN; Frostegård J; Nilsson J; Hamsten A; Talmud P; Humphries SE
Arterioscler Thromb; 1991; 11(3):691-703. PubMed ID: 1674216
[TBL] [Abstract][Full Text] [Related]
6. The effect of the apolipoprotein E polymorphism on lipid levels in patients with familial defective apolipoprotein B-100.
Manke C; Schuster H; Keller C; Wolfram G
Clin Investig; 1993 Apr; 71(4):277-80. PubMed ID: 8471813
[TBL] [Abstract][Full Text] [Related]
7. Decreased binding of apolipoprotein (a) to familial defective apolipoprotein B-100 (Arg3500-->Gln). A study of the assembly of recombinant apolipoprotein (a) with mutant low density lipoproteins.
Durovic S; März W; Frank S; Scharnagl H; Baumstark MW; Zechner R; Kostner GM
J Biol Chem; 1994 Dec; 269(48):30320-5. PubMed ID: 7982944
[TBL] [Abstract][Full Text] [Related]
8. Sib-pair analysis detects elevated Lp(a) levels and large variation of Lp(a) concentration in subjects with familial defective ApoB.
van der Hoek YY; Lingenhel A; Kraft HG; Defesche JC; Kastelein JJ; Utermann G
J Clin Invest; 1997 May; 99(9):2269-73. PubMed ID: 9151801
[TBL] [Abstract][Full Text] [Related]
9. Differences in the phenotypic characteristics of subjects with familial defective apolipoprotein B-100 and familial hypercholesterolemia.
Miserez AR; Keller U
Arterioscler Thromb Vasc Biol; 1995 Oct; 15(10):1719-29. PubMed ID: 7583549
[TBL] [Abstract][Full Text] [Related]
10. Phenotypic variation in patients heterozygous for familial defective apolipoprotein B (FDB) in three European countries.
Hansen PS; Defesche JC; Kastelein JJ; Gerdes LU; Fraza L; Gerdes C; Tato F; Jensen HK; Jensen LG; Klausen IC; Faergeman O; Schuster H
Arterioscler Thromb Vasc Biol; 1997 Apr; 17(4):741-7. PubMed ID: 9108789
[TBL] [Abstract][Full Text] [Related]
11. Lipoprotein(a) in subjects with familial defective apolipoprotein B100.
Perombelon YF; Gallagher JJ; Myant NB; Soutar AK; Knight BL
Atherosclerosis; 1992 Feb; 92(2-3):203-12. PubMed ID: 1385954
[TBL] [Abstract][Full Text] [Related]
12. Homozygous familial defective apolipoprotein B-100. Enhanced removal of apolipoprotein E-containing VLDLs and decreased production of LDLs.
Schaefer JR; Scharnagl H; Baumstark MW; Schweer H; Zech LA; Seyberth H; Winkler K; Steinmetz A; März W
Arterioscler Thromb Vasc Biol; 1997 Feb; 17(2):348-53. PubMed ID: 9081691
[TBL] [Abstract][Full Text] [Related]
13. Statin therapy in a kindred with both apolipoprotein B and low density lipoprotein receptor gene defects.
Raal FJ; Pilcher G; Rubinsztein DC; Lingenhel A; Utermann G
Atherosclerosis; 1997 Feb; 129(1):97-102. PubMed ID: 9069523
[TBL] [Abstract][Full Text] [Related]
14. Familial hypercholesterolemia and familial defective apolipoprotein B-100: comparison of the phenotypic expression In 116 cases.
Brugger D; Schuster H; Zöllner N
Eur J Med Res; 1996 May; 1(8):383-6. PubMed ID: 9360938
[TBL] [Abstract][Full Text] [Related]
15. Characterization of six patients who are double heterozygotes for familial hypercholesterolemia and familial defective apo B-100.
Rubinsztein DC; Raal FJ; Seftel HC; Pilcher G; Coetzee GA; van der Westhuyzen DR
Arterioscler Thromb; 1993 Jul; 13(7):1076-81. PubMed ID: 8318509
[TBL] [Abstract][Full Text] [Related]
16. Familial defective apolipoprotein B-100: a lesson from homozygous and heterozygous patients.
Ceska R; Vrablík M; Horínek A
Physiol Res; 2000; 49 Suppl 1():S125-30. PubMed ID: 10984082
[TBL] [Abstract][Full Text] [Related]
17. A novel LCAT mutation (Phe382-->Val) in a kindred with familial LCAT deficiency and defective apolipoprotein B-100.
Nanjee MN; Stocks J; Cooke CJ; Molhuizen HO; Marcovina S; Crook D; Kastelein JP; Miller NE
Atherosclerosis; 2003 Sep; 170(1):105-13. PubMed ID: 12957688
[TBL] [Abstract][Full Text] [Related]
18. Denaturing gradient-gel electrophoresis screening of familial defective apolipoprotein B-100 in a mixed Asian cohort: two cases of arginine3500-->tryptophan mutation associated with a unique haplotype.
Choong ML; Koay ES; Khoo KL; Khaw MC; Sethi SK
Clin Chem; 1997 Jun; 43(6 Pt 1):916-23. PubMed ID: 9191540
[TBL] [Abstract][Full Text] [Related]
19. [Clinical and biochemical characteristics of familial ligand-defective apo B-100 in a South European population].
Ejarque I; Real JT; Chaves FJ; Blesa S; González V; Milian E; Ascaso JF; Priego MA; Carmena R
Med Clin (Barc); 2004 Oct; 123(12):456-9. PubMed ID: 15498441
[TBL] [Abstract][Full Text] [Related]
20. Serum low density lipoprotein cholesterol level and cholesterol absorption efficiency are influenced by apolipoprotein B and E polymorphism and by the FH-Helsinki mutation of the low density lipoprotein receptor gene in familial hypercholesterolemia.
Gylling H; Aalto-Setälä K; Kontula K; Miettinen TA
Arterioscler Thromb; 1991; 11(5):1368-75. PubMed ID: 1911722
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]