On Migration, Exile, and Cosmopolitanism: A Brief Survey of South African Art Song von de Villiers, Nico

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Effect of rapamycin on hepatic osteodystrophy in rats with portasystemic shunting von van der Merwe, Schalk W, Conradie, Maria M, Bond, Robert, Olivier, Brenda J, Fritz, Elongo, Nieuwoudt, Martin, Delport, Rhena, Slavik, Tomas, Engelbrecht, Gert, Kahn, Del, Shephard, Enid G, Kotze, Maritha J, de Villiers, Nico P, Hough, Stephen

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A novel LYST mutation causing Chédiak Higashi syndrome in a South African child von Dame, Joycelyn Assimeng, Phillips, Lee-Ann, de Villiers, Nico, Pillay, Komala, Hlela, Carol, Eley, Brian

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Analysis of viral and genetic factors in South African patients with multiple sclerosis von de Villiers, J Nico P, Treurnicht, Florette K, Warnich, Louise, Carr, Jonathan, van Rensburg, Susan J, Kotze, Maritha J

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Spectrum of Mutations in the HFE Gene Implicated in Haemochromatosis and Porphyria von de Villiers, J. Nico P., Hillermann, Renate, Loubser, Lynzie, Kotze, Maritha J.

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Abacavir: it’s use and hypersensitivity von Rabie, Helena, Henning, Kristin Lorenc, Schoeman, Pierre, de Villiers, Nico, Pretrorius, G.H.J "Oubaas", Cotton, Mark F

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Sounding Out A Poet In Disguise: Richard Hageman's Five Robert Nathan Songs von de Villiers, Nico

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Overrepresentation of the founder PPOX gene mutation R59W in a South African patient with severe clinical manifestation of porphyria von De Villiers, J. Nico P., Kotze, Maritha J., Van Heerden, Carel J., Sadie, Annalene, Gardner, Helena F. J., Liebenberg, Juanita, Van Zyl, René, Du Plessis, Lana, Kimberg, Matti, Frank, Jorge, Warnich, Louise

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Singing the Songs of Rabindranath Tagore: Richard Hageman's Settings from The Gardener von De Villiers, Nico

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Lack of clinical manifestation of hereditary haemochromatosis in South African patients with multiple sclerosis von Kotze, Maritha J, de Villiers, J Nico P, Warnich, Louise, Schmidt, Stephen, Carr, Jonathan, Mansvelt, Erna, Fourie, Elba, van Rensburg, Susan J

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Challenging beliefs : only a genetic diagnosis of primary immunodeficiency disorders will suffice for some patients, even in a resource-poor setting von van Rooyen, Cathy, van Niekerk, André, Walters, Sarah, de Villiers, Nico, Green, Robin J., van den Berg, Sylvia, van Bruwaene, L.

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Predominance of a 6 bp deletion in exon 2 of the LDL receptor gene in Africans with familial hypercholesterolaemia von Thiart, Rochelle, Scholtz, Charlotte L, Vergotine, Joseph, Hoogendijk, Christiaan F, de Villiers, J Nico P, Nissen, Henrik, Brusgaard, Klaus, Gaffney, Dairena, Hoffs, Michael S, Vermaak, W J Hayward, Kotze, Maritha J

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Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry von Loubser, Odell, Marais, A David, Kotze2, Maritha J, Godenir, Nicole, Thiart2, Rochelle, Scholtz2, Charlotte L, De Villiers2, J Nico P, Hillermann2, Renate, Firth, Jean C, Weich, Hellmuth Fh, Maritz, Frans, Jones2, Sheena, Van Der Westhuyzen, Deneys R

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5- and 6-Glycosylation of transferrin in patients with Alzheimer's disease von VAN RENSBURG, Susan J, BERMAN, Peter, POTOCNIK, Felix, MACGREGOR, Pam, HON, Dinie, DE VILLIERS, Nico

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Abacavir: its use and hypersensitivity : clinical von De Villiers, Nico, Pretorius, G.H.J (Oubaas), Schoeman, Pierre, Henning, Kristin Lorenc, Rabie, Helena, Cotton, Mark F.

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Analysis of the NRAMP1 Gene Implicated in Iron Transport: Association with Multiple Sclerosis and Age Effects von Kotze, Maritha J., de Villiers, J.Nico P., Rooney, Roberta N., Grobbelaar, Johanna J., Mansvelt, Erna P.G., Bouwens, Christianne S.H., Carr, Jonathan, Stander, Ilse, du Plessis, Lana

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Identification of Three Mutations and Associated Haplotypes in the Protoporphyrinogen Oxidase Gene in South African Families with Variegate Porphyria von Warnich, Louise, Kotze, Maritha J., Groenewald, Ilse M., Groenewald, Johannes Z., van Brakel, Maléne G., van Heerden, Carel J., de Villiers, J. Nico P., van de Ven, Wim J. M., Schoenmakers, Eric F.P.M., Taketani, Shigeru, Retief, Andries E.

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CpG hotspot mutations at the LDL receptor locus are a frequent cause of familial hypercholesterolaemia among South African Indians von KOTZE, M. J, LOUBSER, O, THIART, R, DE VILLIERS, J. N. P, LANGENHOVEN, E, THEART, L, STEYN, K, MARAIS, A. D, RAAL, F. J

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High prevalence of the CYS282TYR HFE mutation facilitates an improved diagnostic service for hereditary haemochromatosis in South Africa von DE VILLIERS, J. N. P, HILLERMAN, R, DE JONG, G, LANGENHOVEN, E, ROSSOUW, H, MARX, M. P, KOTZE, M. J

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Familial hypercholesterolemia: potential diagnostic value of mutation screening in a pediatric population of South Africa von Kotze, Maritha J., Peeters, Armand V., Loubser, Odell, Theart, Leonora, du Plessis, Lana, Hayes, Vanessa M., de Jong, Greetje, de Villiers, J. Nico P., Lombard, Carl J., Hansen, Peter S., Raal, Frederick J.

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