Bardien S - Search Results

1

Factors influencing the development of early- or late-onset Parkinson's disease in a cohort of South African patients.

van der Merwe C, Haylett W, Harvey J, Lombard D, Bardien S, Carr J. van der Merwe C, et al. Among authors: bardien s. S Afr Med J. 2012 Oct 1;102(11 Pt 1):848-51. doi: 10.7196/samj.5879. S Afr Med J. 2012. PMID: 23116741

2

A South African mixed ancestry family with Huntington disease-like 2: clinical and genetic features.

Bardien S, Abrahams F, Soodyall H, van der Merwe L, Greenberg J, Brink T, Carr J. Bardien S, et al. Mov Disord. 2007 Oct 31;22(14):2083-9. doi: 10.1002/mds.21672. Mov Disord. 2007. PMID: 17708569

3

Huntington's disease--like 2 in South Africa.

Greenberg J, Bardien S, Carr J. Greenberg J, et al. Among authors: bardien s. S Afr Med J. 2008 Mar;98(3):166. S Afr Med J. 2008. PMID: 18350210 No abstract available.

4

Molecular analysis of the parkin gene in South African patients diagnosed with Parkinson's disease.

Bardien S, Keyser R, Yako Y, Lombard D, Carr J. Bardien S, et al. Parkinsonism Relat Disord. 2009 Feb;15(2):116-21. doi: 10.1016/j.parkreldis.2008.04.005. Epub 2008 Jun 2. Parkinsonism Relat Disord. 2009. PMID: 18514563

5

A South African family with the mitochondrial A1555G mutation on haplogroup L0d.

Human H, Lombard D, de Jong G, Bardien S. Human H, et al. Among authors: bardien s. Biochem Biophys Res Commun. 2009 May 1;382(2):390-4. doi: 10.1016/j.bbrc.2009.03.032. Epub 2009 Mar 12. Biochem Biophys Res Commun. 2009. PMID: 19285484

6

Novel non-sense GCH1 mutation in a South African family diagnosed with dopa-responsive dystonia.

Bardien S, Keyser R, Lombard D, du Plessis M, Human H, Carr J. Bardien S, et al. Eur J Neurol. 2010 Mar;17(3):510-2. doi: 10.1111/j.1468-1331.2009.02725.x. Epub 2009 Jun 29. Eur J Neurol. 2010. PMID: 19566901

7

Identification of a novel functional deletion variant in the 5'-UTR of the DJ-1 gene.

Keyser RJ, van der Merwe L, Venter M, Kinnear C, Warnich L, Carr J, Bardien S. Keyser RJ, et al. Among authors: bardien s. BMC Med Genet. 2009 Oct 13;10:105. doi: 10.1186/1471-2350-10-105. BMC Med Genet. 2009. PMID: 19825160 Free PMC article.

8

Analysis of exon dosage using MLPA in South African Parkinson's disease patients.

Keyser RJ, Lombard D, Veikondis R, Carr J, Bardien S. Keyser RJ, et al. Among authors: bardien s. Neurogenetics. 2010 Jul;11(3):305-12. doi: 10.1007/s10048-009-0229-6. Epub 2009 Dec 15. Neurogenetics. 2010. PMID: 20013014

9

Investigation of mitochondrial sequence variants associated with aminoglycoside-induced ototoxicity in South African TB patients on aminoglycosides.

Human H, Hagen CM, de Jong G, Harris T, Lombard D, Christiansen M, Bardien S. Human H, et al. Among authors: bardien s. Biochem Biophys Res Commun. 2010 Mar 19;393(4):751-6. doi: 10.1016/j.bbrc.2010.02.075. Epub 2010 Feb 18. Biochem Biophys Res Commun. 2010. PMID: 20171168

10

LRRK2 G2019S mutation: frequency and haplotype data in South African Parkinson's disease patients.

Bardien S, Marsberg A, Keyser R, Lombard D, Lesage S, Brice A, Carr J. Bardien S, et al. J Neural Transm (Vienna). 2010 Jul;117(7):847-53. doi: 10.1007/s00702-010-0423-6. Epub 2010 Jun 11. J Neural Transm (Vienna). 2010. PMID: 20544233

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