Determining the population frequency of the CFHR3/CFHR1 deletion at 1q32 von Holmes, Lucy V, Strain, Lisa, Staniforth, Scott J, Moore, Iain, Marchbank, Kevin, Kavanagh, David, Goodship, Judith A, Cordell, Heather J, Goodship, Timothy H J

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Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome von Zipfel, Peter F, Edey, Matthew, Heinen, Stefan, Józsi, Mihály, Richter, Heiko, Misselwitz, Joachim, Hoppe, Bernd, Routledge, Danny, Strain, Lisa, Hughes, Anne E, Goodship, Judith A, Licht, Christoph, Goodship, Timothy H J, Skerka, Christine

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Atypical haemolytic uraemic syndrome associated with a hybrid complement gene von Venables, Julian P, Strain, Lisa, Routledge, Danny, Bourn, David, Powell, Helen M, Warwicker, Paul, Diaz-Torres, Martha L, Sampson, Anne, Mead, Paul, Webb, Michelle, Pirson, Yves, Jackson, Michael S, Hughes, Anne, Wood, Katrina M, Goodship, Judith A, Goodship, Timothy H J

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A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome von Francis, Nigel J., McNicholas, Bairbre, Awan, Atif, Waldron, Mary, Reddan, Donal, Sadlier, Denise, Kavanagh, David, Strain, Lisa, Marchbank, Kevin J., Harris, Claire L., Goodship, Timothy H.J.

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Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome von Fang, Celia J., Fremeaux-Bacchi, Veronique, Liszewski, M. Kathryn, Pianetti, Gaia, Noris, Marina, Goodship, Timothy H.J., Atkinson, John P.

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Combined Complement Gene Mutations in Atypical Hemolytic Uremic Syndrome Influence Clinical Phenotype von BRESIN, Elena, RURALI, Erica, VALOTI, Elisabetta, REMUZZI, Giuseppe, NORIS, Marina, CAPRIOLI, Jessica, SANCHEZ-CORRAL, Pilar, FREMEAUX-BACCHI, Veronique, DE CORDOBA, Santiago Rodriguez, PINTO, Sheila, GOODSHIP, Timothy H. J, ALBERTI, Marta, RIBES, David

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Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy von Osborne, Amy J, Breno, Matteo, Borsa, Nicolo Ghiringhelli, Bu, Fengxiao, Frémeaux-Bacchi, Véronique, Gale, Daniel P, van den Heuvel, Lambertus P, Kavanagh, David, Noris, Marina, Pinto, Sheila, Rallapalli, Pavithra M, Remuzzi, Giuseppe, Rodríguez de Cordoba, Santiago, Ruiz, Angela, Smith, Richard J H, Vieira-Martins, Paula, Volokhina, Elena, Wilson, Valerie, Goodship, Timothy H J, Perkins, Stephen J

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Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome von Moore, Iain, Strain, Lisa, Pappworth, Isabel, Kavanagh, David, Barlow, Paul N., Herbert, Andrew P., Schmidt, Christoph Q., Staniforth, Scott J., Holmes, Lucy V., Ward, Roy, Morgan, Lynn, Goodship, Timothy H.J., Marchbank, Kevin J.

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Atypical hemolytic uremic syndrome von Kavanagh, David, Goodship, Timothy HJ

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Case report: Benefits and challenges of long-term eculizumab in atypical hemolytic uremic syndrome von Cullinan, Noelle, Gorman, Kathleen Mary, Riordan, Michael, Waldron, Mary, Goodship, Timothy H J, Awan, Atif

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Mutations in Human Complement Regulator, Membrane Cofactor Protein (CD46), Predispose to Development of Familial Hemolytic Uremic Syndrome von Richards, Anna, Kemp, Elizabeth J., Liszewski, M. Kathryn, Goodship, Judith A., Lampe, Anne K., Decorte, Ronny, Müslümanoǧglu, M. Hamza, Kavukcu, Salih, Filler, Guido, Pirson, Yves, Wen, Leana S., Atkinson, John P., Timothy H. J. Goodship

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A Novel Non-Synonymous Polymorphism (p.Arg240His) in C4b-Binding Protein Is Associated with Atypical Hemolytic Uremic Syndrome and Leads to Impaired Alternative Pathway Cofactor Ac... von Blom, Anna M, Bergstrom, Frida, Edey, Matthew, Diaz-Torres, Martha, Kavanagh, David, Lampe, Anne, Goodship, Judith A, Strain, Lisa, Moghal, Nadeem, McHugh, Mary, Inward, Carol, Tomson, Charles, Fremeaux-Bacchi, Veronique, Villoutreix, Bruno O, Goodship, Timothy H. J

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Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome von Frémeaux-Bacchi, Veronique, Miller, Elizabeth C., Liszewski, M. Kathryn, Strain, Lisa, Blouin, Jacques, Brown, Alison L., Moghal, Nadeem, Kaplan, Bernard S., Weiss, Robert A., Lhotta, Karl, Kapur, Gaurav, Mattoo, Tej, Nivet, Hubert, Wong, William, Gie, Sophie, de Ligny, Bruno Hurault, Fischbach, Michel, Gupta, Ritu, Hauhart, Richard, Meunier, Vincent, Loirat, Chantal, Dragon-Durey, Marie-Agnès, Fridman, Wolf H., Janssen, Bert J.C., Goodship, Timothy H.J., Atkinson, John P.

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Atypical hemolytic uremic syndrome, genetic basis, and clinical manifestations von Kavanagh, David, Goodship, Timothy H J

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Factors determining penetrance in familial atypical haemolytic uraemic syndrome von Sansbury, Francis H, Cordell, Heather J, Bingham, Coralie, Bromilow, Gilly, Nicholls, Anthony, Powell, Roy, Shields, Bev, Smyth, Lucy, Warwicker, Paul, Strain, Lisa, Wilson, Valerie, Goodship, Judith A, Goodship, Timothy H J, Turnpenny, Peter D

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Mitochondrial Haplogroup and the Risk of Acute Kidney Injury Following Cardiac Bypass Surgery von Kanagasundaram, Nigel S., Baudouin, Simon V., Rowling, Sarah, Prabhu, Mahesh, Dark, John H., Goodship, Timothy H. J., Chinnery, Patrick F., Hudson, Gavin

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Atypical haemolytic uraemic syndrome von KAVANAGH, David, GOODSHIP, Timothy H. J, RICHARDS, Anna

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Whole-Genome Linkage and Association Scan in Primary, Nonsyndromic Vesicoureteric Reflux von CORDELL, Heather J, DARLAY, Rebecca, KENDA, Rajko B, GOODSHIP, Judith A, CHAROEN, Pimphen, STEWART, Aisling, GULLETT, Ambrose M, LAMBERT, Heather J, MALCOLM, Sue, FEATHER, Sally A, GOODSHIP, Timothy H. J, WOOLF, Adrian S

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Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux von Darlow, John M., Darlay, Rebecca, Dobson, Mark G., Stewart, Aisling, Charoen, Pimphen, Southgate, Jennifer, Baker, Simon C., Xu, Yaobo, Hunziker, Manuela, Lambert, Heather J., Green, Andrew J., Santibanez-Koref, Mauro, Sayer, John A., Goodship, Timothy H. J., Puri, Prem, Woolf, Adrian S., Kenda, Rajko B., Barton, David E., Cordell, Heather J.

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Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndrome von Kavanagh, David, Richards, Anna, Noris, Marina, Hauhart, Richard, Liszewski, M. Kathryn, Karpman, Diana, Goodship, Judith A., Fremeaux-Bacchi, Veronique, Remuzzi, Giuseppe, Goodship, Timothy H.J., Atkinson, John P.

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