Spracklen TF - Search Results

1

Genetics of Peripartum Cardiomyopathy: Current Knowledge, Future Directions and Clinical Implications.

Spracklen TF, Chakafana G, Schwartz PJ, Kotta MC, Shaboodien G, Ntusi NAB, Sliwa K. Spracklen TF, et al. Genes (Basel). 2021 Jan 15;12(1):103. doi: 10.3390/genes12010103. Genes (Basel). 2021. PMID: 33467574 Free PMC article. Review.

2

Peripartum cardiomyopathy: from genetics to management.

Sliwa K, Bauersachs J, Arany Z, Spracklen TF, Hilfiker-Kleiner D. Sliwa K, et al. Among authors: spracklen tf. Eur Heart J. 2021 Aug 21;42(32):3094-3102. doi: 10.1093/eurheartj/ehab458. Eur Heart J. 2021. PMID: 34322694 Review.

3

Genetics of inherited cardiomyopathies in Africa.

Shaboodien G, Spracklen TF, Kamuli S, Ndibangwi P, Van Niekerk C, Ntusi NAB. Shaboodien G, et al. Among authors: spracklen tf. Cardiovasc Diagn Ther. 2020 Apr;10(2):262-278. doi: 10.21037/cdt.2019.10.03. Cardiovasc Diagn Ther. 2020. PMID: 32420109 Free PMC article. Review.

4

Heat Shock Proteins: Potential Modulators and Candidate Biomarkers of Peripartum Cardiomyopathy.

Chakafana G, Spracklen TF, Kamuli S, Zininga T, Shonhai A, Ntusi NAB, Sliwa K. Chakafana G, et al. Among authors: spracklen tf. Front Cardiovasc Med. 2021 Jun 16;8:633013. doi: 10.3389/fcvm.2021.633013. eCollection 2021. Front Cardiovasc Med. 2021. PMID: 34222357 Free PMC article. Review.

5

Modern genomic techniques in the identification of genetic causes of cardiomyopathy.

Spracklen TF, Keavney B, Laing N, Ntusi N, Shaboodien G. Spracklen TF, et al. Heart. 2022 Nov 10;108(23):1843-1850. doi: 10.1136/heartjnl-2021-320424. Heart. 2022. PMID: 35140110 Review.

6

Identification of a POLG Variant in a Family With Arrhythmogenic Cardiomyopathy and Left Ventricular Fibrosis.

Spracklen TF, Kasher PR, Kraus S, Botha TL, Page DJ, Kamuli S, Booi Z, Chin A, Laing N, Keavney BD, Ntusi NAB, Shaboodien G. Spracklen TF, et al. Circ Genom Precis Med. 2021 Feb;14(1):e003138. doi: 10.1161/CIRCGEN.120.003138. Epub 2020 Dec 4. Circ Genom Precis Med. 2021. PMID: 33276707 No abstract available.

7

Investigation of Copy Number Variation in South African Patients With Congenital Heart Defects.

Saacks NA, Eales J, Spracklen TF, Aldersley T, Human P, Verryn M, Lawrenson J, Cupido B, Comitis G, De Decker R, Fourie B, Swanson L, Joachim A, Brooks A, Ramesar R, Shaboodien G, Keavney BD, Zühlke LJ. Saacks NA, et al. Among authors: spracklen tf. Circ Genom Precis Med. 2022 Dec;15(6):e003510. doi: 10.1161/CIRCGEN.121.003510. Epub 2022 Oct 7. Circ Genom Precis Med. 2022. PMID: 36205932 Free PMC article.

8

Mutations of FAM111B gene are not associated with Systemic Sclerosis.

Gcelu A, Deshpande G, Shaboodien G, Spracklen TF, Kalla A, Tikly M, Mayosi BM, Hodkinson B. Gcelu A, et al. Among authors: spracklen tf. Sci Rep. 2018 Oct 30;8(1):15988. doi: 10.1038/s41598-018-34341-7. Sci Rep. 2018. PMID: 30375432 Free PMC article.

9

Promoter region variation in NFE2L2 influences susceptibility to ototoxicity in patients exposed to high cumulative doses of cisplatin.

Spracklen TF, Vorster AA, Ramma L, Dalvie S, Ramesar RS. Spracklen TF, et al. Pharmacogenomics J. 2017 Dec;17(6):515-520. doi: 10.1038/tpj.2016.52. Epub 2016 Jul 26. Pharmacogenomics J. 2017. PMID: 27457817

10

IL27 gene expression distinguishes multisystem inflammatory syndrome in children from febrile illness in a South African cohort.

Spracklen TF, Mendelsohn SC, Butters C, Facey-Thomas H, Stander R, Abrahams D, Erasmus M, Baguma R, Day J, Scott C, Zühlke LJ, Kassiotis G, Scriba TJ, Webb K. Spracklen TF, et al. Front Immunol. 2022 Sep 6;13:992022. doi: 10.3389/fimmu.2022.992022. eCollection 2022. Front Immunol. 2022. PMID: 36148243 Free PMC article.

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