Complement factor 5 (C5) p.A252T mutation is prevalent in, but not restricted to, sub‐Saharan Africa: implications for the susceptibility to meningococcal disease von Franco‐Jarava, C., Comas, D., Orren, A., Hernández‐González, M., Colobran, R.

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Complete deficiency of the sixth complement component (C6Q0), susceptibility to Neisseria meningitidis infections and analysis of the frequencies of C6Q0 gene defects in South Afri... von Orren, A., Owen, E. P., Henderson, H. E., van der Merwe, L., Leisegang, F., Stassen, C., Potter, P. C.

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Methotrexate, Doxorubicin, and Cisplatin (MAP) Plus Maintenance Pegylated Interferon Alfa-2b Versus MAP Alone in Patients With Resectable High-Grade Osteosarcoma and Good Histologi... von Bielack, Stefan S, Smeland, Sigbjørn, Whelan, Jeremy S, Marina, Neyssa, Jovic, Gordana, Hook, Jane M, Krailo, Mark D, Gebhardt, Mark, Pápai, Zsuzsanna, Meyer, James, Nadel, Helen, Randall, R Lor, Deffenbaugh, Claudia, Nagarajan, Rajaram, Brennan, Bernadette, Letson, G Douglas, Teot, Lisa A, Goorin, Allen, Baumhoer, Daniel, Kager, Leo, Werner, Mathias, Lau, Ching C, Sundby Hall, Kirsten, Gelderblom, Hans, Meyers, Paul, Gorlick, Richard, Windhager, Reinhard, Helmke, Knut, Eriksson, Mikael, Hoogerbrugge, Peter M, Schomberg, Paula, Tunn, Per-Ulf, Kühne, Thomas, Jürgens, Heribert, van den Berg, Henk, Böhling, Tom, Picton, Susan, Renard, Marleen, Reichardt, Peter, Gerss, Joachim, Butterfass-Bahloul, Trude, Morris, Carol, Hogendoorn, Pancras C W, Seddon, Beatrice, Calaminus, Gabriele, Michelagnoli, Maria, Dhooge, Catharina, Sydes, Matthew R, Bernstein, Mark

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Complement component C5 and C6 mutation screening indicated in meningococcal disease in South Africa von Owen, E P, Leisegang, F, Whitelaw, A, Simpson, J, Baker, S, Würzner, R, Potter, P, Orren, A

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Characterization of a large genomic deletion in four Irish families with C7 deficiency von Thomas, A.D., Orren, A., Connaughton, J., Feighery, C., Morgan, B.P., Roberts, A.G.

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Complement component 5 deficiency (C5D) in South Africa von Orren, A., Owen, T., Potter, P.C., Leisegang, F., Morgan, B.P., Wurzner, R.

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SOUTH AFRICAN PATIENTS WITH GENETIC DEFICIENCIES OF COMPLEMENT COMPONENTS C5 AND C6 SUFFER A MARKED INCREASE IN SUSCEPTIBILITY TO MENINGOCOCCAL DISEASE von Orren, A, Thomas, A, Leisegang, F, Wurzner, R, Owen, E P, Potter, P C

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Molecular mechanisms of complement component C6 deficiency; a hypervariable exon 6 region responsible for three of six reported defects von Orren, A

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Vaccination against meningococcus in complement‐deficient individuals von Morgan, B P, Orren, A

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How do mammals distinguish between pathogens and non-self? von Orren, Ann

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Complement‐mediated lipopolysaccharide release and outer membrane damage in Escherichia coli J5: requirement for C9 von O'Hara, A. M., Moran, A. P., Würzner, R., Orren, A.

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The molecular basis of C6 deficiency in the western Cape, South Africa von HOBART, M. J, FERNIE, B. A, FIJEN, K. A. P. M. J, ORREN, A

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Meningococcal septicaemia in a C6-deficient patient and effects of plasma transfusion on lipopolysaccharide release von Lehner, P.J., Cohen, J., Davies, K.A., Walport, M.I., Cape, A.P., Wurzner, R., Orren, A., Morgan, B.P.

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South African patients with genetic deficiencies of complement components C5 and C6 suffer a marked increase in susceptibility to meningococcal disease : invited review von Orren, A., Owen, E.P., Wurzner, R., Thomas, A., Leisegang, F., Potter, P.C., Leisegang, F., Orren, A.

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Characterization of strains of Neisseria meningitidis recovered from complement-sufficient and complement-deficient patients in the Western Cape Province, South Africa von Orren, A, Caugant, D A, Fijen, C A, Dankert, J, van Schalkwyk, E J, Poolman, J T, Coetzee, G J

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C7 deficiency in an Irish family: a deletion defect which is predominant in the Irish von O'HARA, A. M, FERNIE, B. A, MORAN, A. P, WILLIAMS, Y. E, CONNAUGHTON, J. J, ORREN, A, HOBART, M. J

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Complement component C5 and C6 mutation screening indicated in meningococcal disease in South Africa : research von Leisegang, F, Orren, A, Baker, S, Whitelaw, A, Potter, P, Simpson, J, Orren, A, Owen, E.P, Owen, E.P, Leisegang, F, Orren, A, Whitelaw, A, Wurzner, R, Simpson, J

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Complement component C7 deficiency in four Irish families: The characterisation of a large genomic deletion within the C7 gene von Thomas, A.D., Roberts, A.G., Chuzhanova, N., Cooper, D.N., Feighery, C., Connaughton, J., Morgan, B.P., Orren, A.

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Complement component C5 and C6 mutation screening indicated in meningococcal disease in South Africa: University of Cape Town (UCT) Faculty of Health Sciences Centenary 1912-2012 von OWEN, E. P, LEISEGANG, F, WHITELAW, A, SIMPSON, J, BAKER, S, WÜRZNER, R, POTTER, P, ORREN, A

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How partial C7 deficiency with chronic and recurrent bacterial infections can mimic total C7 deficiency: temporary restoration of host C7 levels following plasma transfusion von WÜRZNER, R., PLATONOV, A. E., BELOBORODOV, V. B., PEREVERZEV, A. I., VERSHININA, I. V., FERNIE, B. A., HOBART, M. J., LACHMANN, P. J., ORREN, A.

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