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The First Case of Riboflavin Transporter Deficiency in sub-Saharan Africa.
Chaya S, Zampoli M, Gray D, Booth J, Riordan G, Ndondo A, Fieggen K, Rusch J, van der Watt G, Pillay K, van der Westhuizen F, Menezes M, Wilmshurst J. Chaya S, et al. Among authors: fieggen k. Semin Pediatr Neurol. 2018 Jul;26:10-14. doi: 10.1016/j.spen.2017.03.002. Epub 2017 Apr 4. Semin Pediatr Neurol. 2018. PMID: 29961494
Personalized care of paediatric drug-resistant epilepsy in Africa: A single-centre pilot study utilizing mobile health and genetic testing.
Olivier IS, Fieggen K, Komarzynski S, Davies EH, Muchada I, McIntosh C, Esterhuizen A, Burman RJ, Wilmshurst JM; And the University of Cape Town (UCT) Human Genetics Precision Medicine Epilepsy Group. Olivier IS, et al. Among authors: fieggen k. Dev Med Child Neurol. 2025 Aug 20. doi: 10.1111/dmcn.16478. Online ahead of print. Dev Med Child Neurol. 2025. PMID: 40836609
The burden of sickle cell disease in Cape Town.
Wonkam A, Ponde C, Nicholson N, Fieggen K, Ramessar R, Davidson A. Wonkam A, et al. Among authors: fieggen k. S Afr Med J. 2012 Jun 28;102(9):752-4. doi: 10.7196/samj.5886. S Afr Med J. 2012. PMID: 22958698
Implications of direct-to-consumer whole-exome sequencing in South Africa.
Lombard Z, Baine F, Krause A, Lochan A, Macualay S, Spencer C, Aldous C, De Vries J, Fieggen K, Henderson B, Hoal E, Kinnear C, Kinsley N, September A, Urban M, Soodyall H, Pepper M, Ramsay M. Lombard Z, et al. Among authors: fieggen k. S Afr Med J. 2016 Jan 12;106(2):139-40. doi: 10.7196/SAMJ.2016.v106i2.10534. S Afr Med J. 2016. PMID: 26821891
48 results