74 related articles for article (PubMed ID: 8888978)
1. Familial defective apolipoprotein B-100: a study of patients from lipid clinics in Scotland and Wales.
Wenham PR; Bloomfield P; Blundell G; Penney MD; Rae PW; Walker SW
Ann Clin Biochem; 1996 Sep; 33 ( Pt 5)():443-50. PubMed ID: 8888978
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Familial ligand-defective apolipoprotein B-100: detection, biochemical features and haplotype analysis of the R3531C mutation in the UK.
Wenham PR; Henderson BG; Penney MD; Ashby JP; Rae PW; Walker SW
Atherosclerosis; 1997 Mar; 129(2):185-92. PubMed ID: 9105560
[TBL] [Abstract][Full Text] [Related]
4. Familial defective apolipoprotein B-100 (R3500Q) in Northern Ireland.
McClean E; Graham CA; Ward AJ; Young IS; Martin S; Nicholls DP
Br J Biomed Sci; 1999; 56(4):258-62. PubMed ID: 10795369
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Familial defective apolipoprotein B-100: haplotype analysis of the arginine(3500)----glutamine mutation.
Rauh G; Schuster H; Fischer J; Keller C; Wolfram G; Zöllner N
Atherosclerosis; 1991 Jun; 88(2-3):219-26. PubMed ID: 1892487
[TBL] [Abstract][Full Text] [Related]
7. Detection of familial defective apolipoprotein B-100 among patients clinically diagnosed with heterozygous familial hypercholesterolemia in maritime Canada.
Morash B; Guernsey DL; Tan MH; Dempsey G; Nassar BA
Clin Biochem; 1994 Aug; 27(4):265-72. PubMed ID: 8001287
[TBL] [Abstract][Full Text] [Related]
8. Familial defective apolipoprotein B-100: a review, including some comparisons with familial hypercholesterolaemia.
Myant NB
Atherosclerosis; 1993 Dec; 104(1-2):1-18. PubMed ID: 8141833
[TBL] [Abstract][Full Text] [Related]
9. Familial defective apolipoprotein B-100 in hypercholesterolemic Chinese Canadians: identification of a unique haplotype of the apolipoprotein B-100 allele.
Abdel-Wareth LO; Pimstone SN; Lagarde JP; Raisonnier A; Benlian P; Pritchard H; Hayden MR; Frohlich JJ
Atherosclerosis; 1997 Dec; 135(2):181-5. PubMed ID: 9430367
[TBL] [Abstract][Full Text] [Related]
10. Familial defective apolipoprotein B-100.
Hansen PS
Dan Med Bull; 1998 Sep; 45(4):370-82. PubMed ID: 9777289
[TBL] [Abstract][Full Text] [Related]
11. Familial defective apolipoprotein B-100 in a group of hypercholesterolaemic patients in Poland. Identification of a new mutation Thr3492Ile in the apolipoprotein B gene.
Bednarska-Makaruk M; Bisko M; Pulawska MF; Hoffman-Zacharska D; Rodo M; Roszczynko M; Solik-Tomassi A; Broda G; Polakowska M; Pytlak A; Wehr H
Eur J Hum Genet; 2001 Nov; 9(11):836-42. PubMed ID: 11781700
[TBL] [Abstract][Full Text] [Related]
12. Identification of a heterozygous compound individual with familial hypercholesterolemia and familial defective apolipoprotein B-100.
Rauh G; Schuster H; Fischer J; Keller C; Wolfram G; Zöllner N
Klin Wochenschr; 1991 May; 69(7):320-4. PubMed ID: 2067318
[TBL] [Abstract][Full Text] [Related]
13. Familial defective apolipoprotein B-100. Comparison with familial hypercholesterolemia in 18 cases detected in Munich.
Schuster H; Rauh G; Kormann B; Hepp T; Humphries S; Keller C; Wolfram G; Zöllner N
Arteriosclerosis; 1990; 10(4):577-81. PubMed ID: 2164382
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Familial defective apolipoprotein B-100 is clinically indistinguishable from familial hypercholesterolemia.
Defesche JC; Pricker KL; Hayden MR; van der Ende BE; Kastelein JJ
Arch Intern Med; 1993 Oct; 153(20):2349-56. PubMed ID: 8215738
[TBL] [Abstract][Full Text] [Related]
16. [Screening for mutations in apolipoprotein B genes in a group of patients with hyperlipoproteinemia].
Grombiríková H; Freiberger T; Kuhrová V; Soska V; Nedomová K
Cas Lek Cesk; 2001 Jan; 140(1):18-21. PubMed ID: 11242979
[TBL] [Abstract][Full Text] [Related]
17. Detecting familial defective apolipoprotein B-100: three molecular scanning methods compared.
Henderson BG; Wenham PR; Ashby JP; Blundell G
Clin Chem; 1997 Sep; 43(9):1630-4. PubMed ID: 9299944
[TBL] [Abstract][Full Text] [Related]
18. [Identification and characterization of the first Spanish familial ligand-defective apolipoprotein B homozygote].
Ejarque I; Civer M; Francisco Ascaso J; Knecht E; Eugenia Armengod M; Carmen R; Tomás Real J; Francisco Chaves J; Javier Martín De Llano J
Med Clin (Barc); 2001 Feb; 116(4):138-41. PubMed ID: 11222161
[TBL] [Abstract][Full Text] [Related]
19. [Familial apolipoprotein B-100 defect, a newly discovered lipid metabolism disorder].
Ceska R
Cas Lek Cesk; 1994 Nov; 133(22):686-9. PubMed ID: 7805094
[TBL] [Abstract][Full Text] [Related]
20. Rapid diagnosis of familial defective apolipoprotein B-100.
Geisel J; Schleifenbaum T; Weisshaar B; Oette K
Eur J Clin Chem Clin Biochem; 1991 Jun; 29(6):395-9. PubMed ID: 1912089
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]