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Joint EASPS-AAPS conference in Tanzania 2023: a beginning of the pragmatic efforts to promote physiology education, research, and practice in East Africa.
Alagbonsi AI, Essop F, Njelekela M, Leminie AA, Ojiambo R, Malindisa EK, Alkizim FO, Ninsiima HI, Kediso TE, Mashili FL, Chillo O, Ebrahim AA, Dionis I, Ruhighira JJ, Obonyo NG. Alagbonsi AI, et al. Among authors: essop f. Adv Physiol Educ. 2024 Sep 1;48(3):573-577. doi: 10.1152/advan.00091.2024. Epub 2024 Jun 6. Adv Physiol Educ. 2024. PMID: 38841750 Free article.
STAC3 disorder: a common cause of congenital hypotonia in Southern African patients.
Essop F, Dillon B, Mhlongo F, Bhengu L, Naicker T, Lambie L, Smit L, Fieggen K, Lochan A, Dawson J, Mpangase P, Hauptfleisch M, Scher G, Tabane O, Immelman M, Urban M, Krause A. Essop F, et al. Eur J Hum Genet. 2025 Jan;33(1):14-23. doi: 10.1038/s41431-024-01644-5. Epub 2024 Jun 1. Eur J Hum Genet. 2025. PMID: 38824262 Free PMC article.
The First Case of Huntington's Disease like 2 in Mali, West Africa.
Bocoum A, Ouologuem M, Cissé L, Essop F, Dit Papa Coulibaly S, Botha N, Cissé CAK, Dit Baneye Maiga A, Krause A, Landouré G; H3Africa consortium. Bocoum A, et al. Among authors: essop f. Tremor Other Hyperkinet Mov (N Y). 2024 Apr 2;14:15. doi: 10.5334/tohm.859. eCollection 2024. Tremor Other Hyperkinet Mov (N Y). 2024. PMID: 38617831 Free PMC article.
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: essop f. 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.
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. Among authors: essop f. 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.
17 results