de Villiers JN - Search Results

1

Pediatric meningitis in the Western Cape Province of South Africa.

Donald PR, Cotton MF, Hendricks MK, Schaaf HS, de Villiers JN, Willemse TE. Donald PR, et al. Among authors: de villiers jn. J Trop Pediatr. 1996 Oct;42(5):256-61. doi: 10.1093/tropej/42.5.256. J Trop Pediatr. 1996. PMID: 8936954

2

Isoniazid elimination kinetics in children with protein-energy malnutrition treated for tuberculous meningitis with a four-component antimicrobial regimen.

Seifart HI, Donald PR, de Villiers JN, Parkin DP, Jaarsveld PP. Seifart HI, et al. Among authors: de villiers jn. Ann Trop Paediatr. 1995 Sep;15(3):249-54. doi: 10.1080/02724936.1995.11747780. Ann Trop Paediatr. 1995. PMID: 8534045

3

Intensive short course chemotherapy in the management of tuberculous meningitis.

Donald PR, Schoeman JF, Van Zyl LE, De Villiers JN, Pretorius M, Springer P. Donald PR, et al. Among authors: de villiers jn. Int J Tuberc Lung Dis. 1998 Sep;2(9):704-11. Int J Tuberc Lung Dis. 1998. PMID: 9755923

4

BCG vaccination status of children with tuberculous meningitis and the use of unsupervised isoniazid prophylaxis.

Donald PR, van Zyl LE, de Villiers J. Donald PR, et al. S Afr Med J. 1995 Mar;85(3):167-70. S Afr Med J. 1995. PMID: 7777968

5

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: de villiers jn, de jong g. Clin Genet. 1998 Jul;54(1):74-8. doi: 10.1111/j.1399-0004.1998.tb03698.x. Clin Genet. 1998. PMID: 9727745

6

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: de villiers jn. Clin Genet. 1997 Jun;51(6):394-8. doi: 10.1111/j.1399-0004.1997.tb02497.x. Clin Genet. 1997. PMID: 9237502

7

Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry.

Loubser O, Marais AD, Kotze MJ, Godenir N, Thiart R, Scholtz CL, de Villiers JN, Hillermann R, Firth JC, Weich HF, Maritz F, Jones S, van der Westhuyzen DR. Loubser O, et al. Among authors: de villiers jn. Clin Genet. 1999 May;55(5):340-5. doi: 10.1034/j.1399-0004.1999.550507.x. Clin Genet. 1999. PMID: 10422804

8

Mutation -59c-->t in repeat 2 of the LDL receptor promoter: reduction in transcriptional activity and possible allelic interaction in a South African family with familial hypercholesterolaemia.

Scholtz CL, Peeters AV, Hoogendijk CF, Thiart R, de Villiers JN, Hillermann R, Liu J, Marais AD, Kotze MJ. Scholtz CL, et al. Among authors: de villiers jn. Hum Mol Genet. 1999 Oct;8(11):2025-30. doi: 10.1093/hmg/8.11.2025. Hum Mol Genet. 1999. PMID: 10484771

9

Predominance of a 6 bp deletion in exon 2 of the LDL receptor gene in Africans with familial hypercholesterolaemia.

Thiart R, Scholtz CL, Vergotine J, Hoogendijk CF, de Villiers JN, Nissen H, Brusgaard K, Gaffney D, Hoffs MS, Vermaak WJ, Kotze MJ. Thiart R, et al. Among authors: de villiers jn. J Med Genet. 2000 Jul;37(7):514-9. doi: 10.1136/jmg.37.7.514. J Med Genet. 2000. PMID: 10882754 Free PMC article.

10

Significance of linkage disequilibrium between mutation C282Y and a MseI polymorphism in population screening and DNA diagnosis of hemochromatosis.

de Villiers JN, Kotze MJ. de Villiers JN, et al. Blood Cells Mol Dis. 1999 Jun-Aug;25(3-4):250-2; discussion 253-4. doi: 10.1006/bcmd.1999.0250. Blood Cells Mol Dis. 1999. PMID: 10575550

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