Raal FJ - Search Results

1

A double mutant LDL receptor allele in a cypriot family with heterozygous familial hypercholesterolemia.

Kotze MJ, de Villiers JN, Loubser O, Thiart R, Scholtz CL, Raal FJ. Kotze MJ, et al. Among authors: raal fj. Hum Genet. 1997 Jul;100(1):101-3. doi: 10.1007/s004390050473. Hum Genet. 1997. PMID: 9225977

2

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. Rubinsztein DC, et al. Among authors: raal fj. Arterioscler Thromb. 1993 Jul;13(7):1076-81. doi: 10.1161/01.atv.13.7.1076. Arterioscler Thromb. 1993. PMID: 8318509

3

CpG hotspot mutations at the LDL receptor locus are a frequent cause of familial hypercholesterolaemia among South African Indians.

Kotze MJ, Loubser O, Thiart R, de Villiers JN, Langenhoven E, Theart L, Steyn K, Marais AD, Raal FJ. Kotze MJ, et al. Among authors: raal fj. Clin Genet. 1997 Jun;51(6):394-8. doi: 10.1111/j.1399-0004.1997.tb02497.x. Clin Genet. 1997. PMID: 9237502

4

Two novel and two known low-density lipoprotein receptor gene mutations in German patients with familial hypercholesterolemia.

Thiart R, Loubser O, de Villiers JN, Marx MP, Zaire R, Raal FJ, Kotze MJ. Thiart R, et al. Among authors: raal fj. Hum Mutat. 1998;Suppl 1:S232-3. doi: 10.1002/humu.1380110174. Hum Mutat. 1998. PMID: 9452095 No abstract available.

5

Mutation analysis in familial hypercholesterolemia patients of different ancestries: identification of three novel LDLR gene mutations.

Callis M, Jansen S, Thiart R, de Villiers JN, Raal FJ, Kotze MJ. Callis M, et al. Among authors: raal fj. Mol Cell Probes. 1998 Jun;12(3):149-52. doi: 10.1006/mcpr.1998.0164. Mol Cell Probes. 1998. PMID: 9664576

6

Familial hypercholesterolemia: potential diagnostic value of mutation screening in a pediatric population of South Africa.

Kotze MJ, Peeters AV, Loubser O, Theart L, du Plessis L, Hayes VM, de Jong G, de Villiers JN, Lombard CJ, Hansen PS, Raal FJ. Kotze MJ, et al. Among authors: raal fj. Clin Genet. 1998 Jul;54(1):74-8. doi: 10.1111/j.1399-0004.1998.tb03698.x. Clin Genet. 1998. PMID: 9727745

7

Efficacy of vitamin E compared with either simvastatin or atorvastatin in preventing the progression of atherosclerosis in homozygous familial hypercholesterolemia.

Raal FJ, Pilcher GJ, Veller MG, Kotze MJ, Joffe BI. Raal FJ, et al. Am J Cardiol. 1999 Dec 1;84(11):1344-6, A7. doi: 10.1016/s0002-9149(99)00570-6. Am J Cardiol. 1999. PMID: 10614803

8

Lipoprotein(a) in homozygous familial hypercholesterolemia.

Kraft HG, Lingenhel A, Raal FJ, Hohenegger M, Utermann G. Kraft HG, et al. Among authors: raal fj. Arterioscler Thromb Vasc Biol. 2000 Feb;20(2):522-8. doi: 10.1161/01.atv.20.2.522. Arterioscler Thromb Vasc Biol. 2000. PMID: 10669652

9

Inhibition of cholesterol synthesis by atorvastatin in homozygous familial hypercholesterolaemia.

Raal FJ, Pappu AS, Illingworth DR, Pilcher GJ, Marais AD, Firth JC, Kotze MJ, Heinonen TM, Black DM. Raal FJ, et al. Atherosclerosis. 2000 Jun;150(2):421-8. doi: 10.1016/s0021-9150(99)00435-9. Atherosclerosis. 2000. PMID: 10856535 Clinical Trial.

10

Recent origin and spread of a common Lithuanian mutation, G197del LDLR, causing familial hypercholesterolemia: positive selection is not always necessary to account for disease incidence among Ashkenazi Jews.

Durst R, Colombo R, Shpitzen S, Avi LB, Friedlander Y, Wexler R, Raal FJ, Marais DA, Defesche JC, Mandelshtam MY, Kotze MJ, Leitersdorf E, Meiner V. Durst R, et al. Among authors: raal fj. Am J Hum Genet. 2001 May;68(5):1172-88. doi: 10.1086/320123. Epub 2001 Apr 17. Am J Hum Genet. 2001. PMID: 11309683 Free PMC article.

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