van der Merwe L - Search Results

1

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. Among authors: van der merwe l. Mov Disord. 2007 Oct 31;22(14):2083-9. doi: 10.1002/mds.21672. Mov Disord. 2007. PMID: 17708569

2

Patient-control association study of the Leucine-Rich repeat kinase 2 (LRRK2) gene in South African Parkinson's disease patients.

Bardien S, Blanckenberg J, van der Merwe L, Farrer MJ, Ross OA. Bardien S, et al. Among authors: van der merwe l. Mov Disord. 2013 Dec;28(14):2039-40. doi: 10.1002/mds.25637. Epub 2013 Sep 6. Mov Disord. 2013. PMID: 24014121 Free PMC article. No abstract available.

3

Mitochondrial impairment observed in fibroblasts from South African Parkinson's disease patients with parkin mutations.

van der Merwe C, Loos B, Swart C, Kinnear C, Henning F, van der Merwe L, Pillay K, Muller N, Zaharie D, Engelbrecht L, Carr J, Bardien S. van der Merwe C, et al. Among authors: van der merwe l. Biochem Biophys Res Commun. 2014 May 2;447(2):334-40. doi: 10.1016/j.bbrc.2014.03.151. Epub 2014 Apr 8. Biochem Biophys Res Commun. 2014. PMID: 24721425 Free article.

4

The frequency of the H402 allele of CFH and its involvement with age-related maculopathy in an aged Black African Xhosa population.

Ziskind A, Bardien S, van der Merwe L, Webster AR. Ziskind A, et al. Among authors: van der merwe l. Ophthalmic Genet. 2008 Sep;29(3):117-9. doi: 10.1080/13816810802216472. Ophthalmic Genet. 2008. PMID: 18766990

5

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: van der merwe l. BMC Med Genet. 2009 Oct 13;10:105. doi: 10.1186/1471-2350-10-105. BMC Med Genet. 2009. PMID: 19825160 Free PMC article.

6

A study of meningiomas in South Africa: investigating a correlation between clinical presentation, histopathology and genetic markers.

Vivier J, Bardien S, Van der Merwe L, Brusnicky J, Zaharie D, Keyser R, Hewlett R, de Jong G, Hartzenberg B. Vivier J, et al. Among authors: van der merwe l. Br J Neurosurg. 2009 Feb;23(1):63-70. doi: 10.1080/02688690802593064. Br J Neurosurg. 2009. PMID: 19234911

7

Altered Mitochondrial Respiration and Other Features of Mitochondrial Function in Parkin-Mutant Fibroblasts from Parkinson's Disease Patients.

Haylett W, Swart C, van der Westhuizen F, van Dyk H, van der Merwe L, van der Merwe C, Loos B, Carr J, Kinnear C, Bardien S. Haylett W, et al. Among authors: van der westhuizen f, van der merwe l, van der merwe c, van dyk h. Parkinsons Dis. 2016;2016:1819209. doi: 10.1155/2016/1819209. Epub 2016 Mar 8. Parkinsons Dis. 2016. PMID: 27034887 Free PMC article.

8

A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness.

Bardien S, Human H, Harris T, Hefke G, Veikondis R, Schaaf HS, van der Merwe L, Greinwald JH, Fagan J, de Jong G. Bardien S, et al. Among authors: van der merwe l. BMC Med Genet. 2009 Jan 13;10:2. doi: 10.1186/1471-2350-10-2. BMC Med Genet. 2009. PMID: 19144107 Free PMC article.

9

The role of ancestry in TB susceptibility of an admixed South African population.

Daya M, van der Merwe L, van Helden PD, Möller M, Hoal EG. Daya M, et al. Among authors: van der merwe l, van helden pd. Tuberculosis (Edinb). 2014 Jul;94(4):413-20. doi: 10.1016/j.tube.2014.03.012. Epub 2014 Apr 13. Tuberculosis (Edinb). 2014. PMID: 24832562

10

5-HTTLPR polymorphism: analysis in South African autistic individuals.

Arieff Z, Kaur M, Gameeldien H, van der Merwe L, Bajic VB. Arieff Z, et al. Among authors: van der merwe l. Hum Biol. 2010 Jun;82(3):291-300. doi: 10.3378/027.082.0303. Hum Biol. 2010. PMID: 20649385

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