Krause A - Search Results

1

The hereditary adult-onset ataxias in South Africa.

Bryer A, Krause A, Bill P, Davids V, Bryant D, Butler J, Heckmann J, Ramesar R, Greenberg J. Bryer A, et al. Among authors: krause a. J Neurol Sci. 2003 Dec 15;216(1):47-54. doi: 10.1016/s0022-510x(03)00209-0. J Neurol Sci. 2003. PMID: 14607302

2

Genetic testing for Huntington's disease in South Africa.

Krause A, Greenberg J. Krause A, et al. S Afr Med J. 2008 Mar;98(3):193-4. S Afr Med J. 2008. PMID: 18350219 No abstract available.

3

The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population.

Kay C, Collins JA, Wright GEB, Baine F, Miedzybrodzka Z, Aminkeng F, Semaka AJ, McDonald C, Davidson M, Madore SJ, Gordon ES, Gerry NP, Cornejo-Olivas M, Squitieri F, Tishkoff S, Greenberg JL, Krause A, Hayden MR. Kay C, et al. Among authors: krause a. Am J Med Genet B Neuropsychiatr Genet. 2018 Apr;177(3):346-357. doi: 10.1002/ajmg.b.32618. Epub 2018 Feb 20. Am J Med Genet B Neuropsychiatr Genet. 2018. PMID: 29460498

4

A study of Huntington disease-like syndromes in black South African patients reveals a single SCA2 mutation and a unique distribution of normal alleles across five repeat loci.

Baine FK, Peerbhai N, Krause A. Baine FK, et al. Among authors: krause a. J Neurol Sci. 2018 Jul 15;390:200-204. doi: 10.1016/j.jns.2018.04.031. Epub 2018 Apr 21. J Neurol Sci. 2018. PMID: 29801887

5

A Comprehensive Haplotype-Targeting Strategy for Allele-Specific HTT Suppression in Huntington Disease.

Kay C, Collins JA, Caron NS, Agostinho LA, Findlay-Black H, Casal L, Sumathipala D, Dissanayake VHW, Cornejo-Olivas M, Baine F, Krause A, Greenberg JL, Paiva CLA, Squitieri F, Hayden MR. Kay C, et al. Among authors: krause a. Am J Hum Genet. 2019 Dec 5;105(6):1112-1125. doi: 10.1016/j.ajhg.2019.10.011. Epub 2019 Nov 7. Am J Hum Genet. 2019. PMID: 31708117 Free PMC article.

6

Different molecular basis for spinal muscular atrophy in South African black patients.

Stevens G, Yawitch T, Rodda J, Verhaart S, Krause A. Stevens G, et al. Among authors: krause a. Am J Med Genet. 1999 Oct 29;86(5):420-6. Am J Med Genet. 1999. PMID: 10508982

7

The molecular basis of spinal muscular atrophy (SMA) in South African black patients.

Labrum R, Rodda J, Krause A. Labrum R, et al. Among authors: krause a. Neuromuscul Disord. 2007 Oct;17(9-10):684-92. doi: 10.1016/j.nmd.2007.05.005. Epub 2007 Jul 12. Neuromuscul Disord. 2007. PMID: 17627822

8

The utilization and outcome of diagnostic, predictive, and prenatal genetic testing for huntington disease in johannesburg, South Africa.

Sizer EB, Haw T, Wessels TM, Kromberg JG, Krause A. Sizer EB, et al. Among authors: krause a. Genet Test Mol Biomarkers. 2012 Jan;16(1):58-62. doi: 10.1089/gtmb.2011.0007. Epub 2011 Aug 12. Genet Test Mol Biomarkers. 2012. PMID: 21838519

9

Huntington disease in the South African population occurs on diverse and ethnically distinct genetic haplotypes.

Baine FK, Kay C, Ketelaar ME, Collins JA, Semaka A, Doty CN, Krause A, Greenberg LJ, Hayden MR. Baine FK, et al. Among authors: krause a. Eur J Hum Genet. 2013 Oct;21(10):1120-7. doi: 10.1038/ejhg.2013.2. Epub 2013 Mar 6. Eur J Hum Genet. 2013. PMID: 23463025 Free PMC article.

10

Roles of genetic counselors in South Africa.

Kromberg JG, Wessels TM, Krause A. Kromberg JG, et al. Among authors: krause a. J Genet Couns. 2013 Dec;22(6):753-61. doi: 10.1007/s10897-013-9606-2. Epub 2013 May 31. J Genet Couns. 2013. PMID: 23723047

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