Krause A - Search Results

1

Mutation analysis and clinical profile of South African patients with Neurofibromatosis type 1 (NF1) phenotype.

Mudau MM, Dillon B, Smal C, Feben C, Honey E, Carstens N, Krause A. Mudau MM, et al. Among authors: krause a. Front Genet. 2024 Mar 26;15:1331278. doi: 10.3389/fgene.2024.1331278. eCollection 2024. Front Genet. 2024. PMID: 38596211 Free PMC article.

2

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

3

Phenotypic consequences in black South African Fanconi anemia patients homozygous for a founder mutation.

Feben C, Kromberg J, Wainwright R, Stones D, Sutton C, Poole J, Haw T, Krause A. Feben C, et al. Among authors: krause a. Genet Med. 2014 May;16(5):400-6. doi: 10.1038/gim.2013.159. Epub 2013 Oct 17. Genet Med. 2014. PMID: 24136620 Free article.

4

Hematological consequences of a FANCG founder mutation in Black South African patients with Fanconi anemia.

Feben C, Kromberg J, Wainwright R, Stones D, Poole J, Haw T, Krause A. Feben C, et al. Among authors: krause a. Blood Cells Mol Dis. 2015 Mar;54(3):270-4. doi: 10.1016/j.bcmd.2014.11.011. Epub 2014 Nov 27. Blood Cells Mol Dis. 2015. PMID: 25477267

5

Mudau MM, Essop F, Krause A. Mudau MM, et al. Among authors: krause a. S Afr Med J. 2016 Dec 21;107(1):80-82. doi: 10.7196/SAMJ.2016.v107.i1.10907. S Afr Med J. 2016. PMID: 28112097

6

Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia.

Feben C, Spencer C, Lochan A, Laing N, Fieggen K, Honey E, Wainstein T, Krause A. Feben C, et al. Among authors: krause a. Fam Cancer. 2017 Jul;16(3):441-446. doi: 10.1007/s10689-017-9968-y. Fam Cancer. 2017. PMID: 28185119

7

Fanconi anaemia in South Africa: Past, present and future.

Feben C, Wainstein T, Kromberg J, Essop F, Krause A. Feben C, et al. Among authors: krause a. S Afr Med J. 2018 Apr 25;108(5):393-398. doi: 10.7196/SAMJ.2018.v108i5.13004. S Afr Med J. 2018. PMID: 29843852 Review.

8

Spinal Muscular Atrophy in the Black South African Population: A Matter of Rearrangement?

Vorster E, Essop FB, Rodda JL, Krause A. Vorster E, et al. Among authors: krause a. Front Genet. 2020 Feb 13;11:54. doi: 10.3389/fgene.2020.00054. eCollection 2020. Front Genet. 2020. PMID: 32117462 Free PMC article.

9

Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation.

Dillon B, Feben C, Segal D, du Plessis J, Reynders D, Wainwright R, Poole J, Krause A. Dillon B, et al. Among authors: krause a. Mol Genet Genomic Med. 2020 Aug;8(8):e1351. doi: 10.1002/mgg3.1351. Epub 2020 Jun 11. Mol Genet Genomic Med. 2020. PMID: 32529760 Free PMC article.

10

Ending a diagnostic odyssey-The first case of Takenouchi-Kosaki syndrome in an African patient.

Flynn K, Feben C, Lamola L, Carstens N, Krause A, Lombard Z; for DDD‐Africa as members of the H3Africa Consortium. Flynn K, et al. Among authors: krause a. Clin Case Rep. 2021 Mar 2;9(4):2144-2148. doi: 10.1002/ccr3.3966. eCollection 2021 Apr. Clin Case Rep. 2021. PMID: 33936654 Free PMC article.

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