Krause A - Search Results

1

Junctophilin 3 (JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype.

Krause A, Mitchell C, Essop F, Tager S, Temlett J, Stevanin G, Ross C, Rudnicki D, Margolis R. Krause A, et al. Am J Med Genet B Neuropsychiatr Genet. 2015 Oct;168(7):573-85. doi: 10.1002/ajmg.b.32332. Epub 2015 Jun 16. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 26079385 Free PMC article.

2

Beta-globin haplotype analysis suggests that a major source of Malagasy ancestry is derived from Bantu-speaking Negroids.

Hewitt R, Krause A, Goldman A, Campbell G, Jenkins T. Hewitt R, et al. Among authors: krause a. Am J Hum Genet. 1996 Jun;58(6):1303-8. Am J Hum Genet. 1996. PMID: 8651308 Free PMC article.

3

Founder effect and prevalence of myotonic dystrophy in South Africans: molecular studies.

Goldman A, Krause A, Ramsay M, Jenkins T. Goldman A, et al. Among authors: krause a. Am J Hum Genet. 1996 Aug;59(2):445-52. Am J Hum Genet. 1996. PMID: 8755933 Free PMC article.

4

Feasibility of prenatal diagnosis and carrier detection in South African haemophilia A patients.

Dangerfield BT, Manga P, Field SP, Hartman E, Jenkins T, Krause A. Dangerfield BT, et al. Among authors: krause a. Br J Haematol. 1997 Jun;97(3):558-60. doi: 10.1046/j.1365-2141.1997.892905.x. Br J Haematol. 1997. PMID: 9207400 Free article.

5

Huntington's disease confirmed by genetic testing in five African families.

Silber E, Kromberg J, Temlett JA, Krause A, Saffer D. Silber E, et al. Among authors: krause a. Mov Disord. 1998 Jul;13(4):726-30. doi: 10.1002/mds.870130420. Mov Disord. 1998. PMID: 9686782

6

Utilisation of predictive, prenatal and diagnostic testing for Huntington's disease in Johannesburg.

Kromberg JG, Krause A, Spurdle AB, Temlett JA, Lucas M, Rodseth D, Stevens G, Jenkins T. Kromberg JG, et al. Among authors: krause a. S Afr Med J. 1999 Jul;89(7):774-8. S Afr Med J. 1999. PMID: 10470316

7

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

8

Evidence that a dodecamer duplication in the gene HOPA in Xq13 is not associated with mental retardation.

Friez MJ, Essop FB, Krause A, Castiglia L, Ragusa A, Sossey-Alaoui K, Nelson RL, May MM, Michaelis RC, Srivastava AK, Schwartz CE, Stevenson RE, Goldman A, Villard L, Longshore JW. Friez MJ, et al. Among authors: krause a. Hum Genet. 2000 Jan;106(1):36-9. doi: 10.1007/s004390051006. Hum Genet. 2000. PMID: 10982179

9

Huntington's Disease-like 2 (HDL2) in North America and Japan.

Margolis RL, Holmes SE, Rosenblatt A, Gourley L, O'Hearn E, Ross CA, Seltzer WK, Walker RH, Ashizawa T, Rasmussen A, Hayden M, Almqvist EW, Harris J, Fahn S, MacDonald ME, Mysore J, Shimohata T, Tsuji S, Potter N, Nakaso K, Adachi Y, Nakashima K, Bird T, Krause A, Greenstein P. Margolis RL, et al. Among authors: krause a. Ann Neurol. 2004 Nov;56(5):670-4. doi: 10.1002/ana.20248. Ann Neurol. 2004. PMID: 15468075

10

A common Fanconi anemia mutation in black populations of sub-Saharan Africa.

Morgan NV, Essop F, Demuth I, de Ravel T, Jansen S, Tischkowitz M, Lewis CM, Wainwright L, Poole J, Joenje H, Digweed M, Krause A, Mathew CG. Morgan NV, et al. Among authors: krause a. Blood. 2005 May 1;105(9):3542-4. doi: 10.1182/blood-2004-10-3968. Epub 2005 Jan 18. Blood. 2005. PMID: 15657175 Free article.

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