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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2014 | 2 |
2015 | 1 |
2016 | 1 |
2018 | 1 |
2021 | 2 |
2024 | 0 |
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Page 1
Pyle metaphyseal dysplasia in an African child: Case report and review of the literature.
S Afr Med J. 2016 May 25;106(6 Suppl 1):S110-3. doi: 10.7196/SAMJ.2016.v106i6.11011.
S Afr Med J. 2016.
PMID: 27245543
Review.
Heat-Stable Carbetocin versus Oxytocin to Prevent Hemorrhage after Vaginal Birth.
Widmer M, Piaggio G, Nguyen TMH, Osoti A, Owa OO, Misra S, Coomarasamy A, Abdel-Aleem H, Mallapur AA, Qureshi Z, Lumbiganon P, Patel AB, Carroli G, Fawole B, Goudar SS, Pujar YV, Neilson J, Hofmeyr GJ, Su LL, Ferreira de Carvalho J, Pandey U, Mugerwa K, Shiragur SS, Byamugisha J, Giordano D, Gülmezoglu AM; WHO CHAMPION Trial Group.
Widmer M, et al.
N Engl J Med. 2018 Aug 23;379(8):743-752. doi: 10.1056/NEJMoa1805489. Epub 2018 Jun 27.
N Engl J Med. 2018.
PMID: 29949473
Free article.
Clinical Trial.
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Parental access to hospitalised children during infectious disease pandemics such as COVID-19.
Goga A, Feucht U, Pillay S, Reubenson G, Jeena P, Mahdi S, Mayet NT, Velaphi S, McKerrow N, Mathivha LR, Makubalo N, Green RJ, Gray G.
Goga A, et al. Among authors: makubalo n.
S Afr Med J. 2021 Jan 20;111(2):100-105. doi: 10.7196/SAMJ.2021.v111i2.15388.
S Afr Med J. 2021.
PMID: 33944717
Free article.
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Rationale and design of the African Cardiomyopathy and Myocarditis Registry Program: The IMHOTEP study.
Kraus SM, Shaboodien G, Francis V, Laing N, Cirota J, Chin A, Pandie S, Lawrenson J, Comitis GAM, Fourie B, Zühlke L, Wonkam A, Wainwright H, Damasceno A, Mocumbi AO, Pepeta L, Moeketsi K, Thomas BM, Thomas K, Makotoko M, Brown S, Ntsekhe M, Sliwa K, Badri M, Gumedze F, Cordell HJ, Keavney B, Ferreira V, Mahmod M, Cooper LT, Yacoub M, Neubauer S, Watkins H, Mayosi BM, Ntusi NAB; IMHOTEP Investigators.
Kraus SM, et al.
Int J Cardiol. 2021 Jun 15;333:119-126. doi: 10.1016/j.ijcard.2021.02.026. Epub 2021 Feb 16.
Int J Cardiol. 2021.
PMID: 33607192
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No evidence for clinical utility in investigating the connexin genes GJB2, GJB6 and GJA1 in non-syndromic hearing loss in black Africans.
Wonkam A, Bosch J, Noubiap JJ, Lebeko K, Makubalo N, Dandara C.
Wonkam A, et al. Among authors: makubalo n.
S Afr Med J. 2015 Jan;105(1):23-6. doi: 10.7196/samj.8814.
S Afr Med J. 2015.
PMID: 26046157
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In search of genetic markers for nonsyndromic deafness in Africa: a study in Cameroonians and Black South Africans with the GJB6 and GJA1 candidate genes.
Bosch J, Lebeko K, Nziale JJ, Dandara C, Makubalo N, Wonkam A.
Bosch J, et al. Among authors: makubalo n.
OMICS. 2014 Jul;18(7):481-5. doi: 10.1089/omi.2013.0166. Epub 2014 May 2.
OMICS. 2014.
PMID: 24785695
Free PMC article.
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Sequencing of GJB2 in Cameroonians and Black South Africans and comparison to 1000 Genomes Project Data Support Need to Revise Strategy for Discovery of Nonsyndromic Deafness Genes in Africans.
Bosch J, Noubiap JJ, Dandara C, Makubalo N, Wright G, Entfellner JB, Tiffin N, Wonkam A.
Bosch J, et al. Among authors: makubalo n.
OMICS. 2014 Nov;18(11):705-10. doi: 10.1089/omi.2014.0063. Epub 2014 Aug 27.
OMICS. 2014.
PMID: 25162826
Free PMC article.
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