Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development von Vivante, Asaf, Kleppa, Marc-Jens, Schulz, Julian, Kohl, Stefan, Sharma, Amita, Chen, Jing, Shril, Shirlee, Hwang, Daw-Yang, Weiss, Anna-Carina, Kaminski, Michael M., Shukrun, Rachel, Kemper, Markus J., Lehnhardt, Anja, Beetz, Rolf, Sanna-Cherchi, Simone, Verbitsky, Miguel, Gharavi, Ali G., Stuart, Helen M., Feather, Sally A., Goodship, Judith A., Goodship, Timothy H.J., Woolf, Adrian S., Westra, Sjirk J., Doody, Daniel P., Bauer, Stuart B., Lee, Richard S., Adam, Rosalyn M., Lu, Weining, Reutter, Heiko M., Kehinde, Elijah O., Mancini, Erika J., Lifton, Richard P., Tasic, Velibor, Lienkamp, Soeren S., Jüppner, Harald, Kispert, Andreas, Hildebrandt, Friedhelm

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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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Genotype/Phenotype Correlations in Complement Factor H Deficiency Arising From Uniparental Isodisomy von Wilson, Valerie, PhD, Darlay, Rebecca, PhD, Wong, William, MD, Wood, Katrina M., MD, McFarlane, Jeannette, MD, Schejbel, Lone, MD, Schmidt, Ida M., MD, Harris, Claire L., PhD, Tellez, James, BSc, Hunze, Eva-Maria, PhD, Marchbank, Kevin, PhD, Goodship, Judith A., MD, Goodship, Timothy H.J., MD

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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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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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Thrombotic Microangiopathy in Inverted Formin 2 - Mediated Renal Disease von Challis, Rachel C, Ring, Troels, Xu, Yaobo, Wong, Edwin K S, Flossmann, Oliver, Roberts, Ian S D, Ahmed, Saeed, Wetherall, Michael, Salkus, Giedrius, Brocklebank, Vicky, Fester, Julian, Strain, Lisa, Wilson, Valerie, Wood, Katrina M, Marchbank, Kevin J, Santibanez-Koref, Mauro, Goodship, Timothy H J, Kavanagh, David

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Mutations in complement factor i predispose to development of atypical hemolytic uremic syndrome von KAVANAGH, David, KEMP, Elizabeth J, MAYLAND, Elizabeth, WINNEY, Robin J, DUFFIELD, Jeremy S, WARWICK, Graham, RICHARDS, Anna, WARD, Roy, GOODSHIP, Judith A, GOODSHIP, Timothy H. J

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The influence of nutritional status on complications after operations for lung cancer von Jagoe, R.Thomas, Goodship, Timothy H.J, Gibson, G.John

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A De Novo Deletion in the Regulators of Complement Activation Cluster Producing a Hybrid Complement Factor H/Complement Factor H-Related 3 Gene in Atypical Hemolytic Uremic Syndrom... von Challis, Rachel C, Araujo, Geisilaine S R, Wong, Edwin K S, Anderson, Holly E, Awan, Atif, Dorman, Anthony M, Waldron, Mary, Wilson, Valerie, Brocklebank, Vicky, Strain, Lisa, Morgan, B Paul, Harris, Claire L, Marchbank, Kevin J, Goodship, Timothy H J, Kavanagh, David

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Outcome of Renal Transplantation in Patients with Non–Shiga Toxin–Associated Hemolytic Uremic Syndrome: Prognostic Significance of Genetic Background von Bresin, Elena, Daina, Erica, Noris, Marina, Castelletti, Federica, Stefanov, Rumen, Hill, Prudence, Goodship, Timothy H J, Remuzzi, Giuseppe

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Complement factor H and the hemolytic uremic syndrome von Atkinson, John P, Goodship, Timothy H J

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Patient stratification and therapy in atypical haemolytic uraemic syndrome (aHUS) von Wong, Edwin, Challis, Rachel, Sheerin, Neil, Johnson, Sally, Kavanagh, David, Goodship, Timothy H.J

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The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structura... von Saunders, Rebecca E., Abarrategui-Garrido, Cynthia, Frémeaux-Bacchi, Véronique, Goicoechea de Jorge, Elena, Goodship, Timothy H.J., López Trascasa, Margarita, Noris, Marina, Ponce Castro, Isabel Maria, Remuzzi, Giuseppe, Rodríguez de Córdoba, Santiago, Sánchez-Corral, Pilar, Skerka, Christine, Zipfel, Peter F., Perkins, Stephen J.

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Chromosomal rearrangement—A rare cause of complement factor I associated atypical haemolytic uraemic syndrome von Gleeson, Patrick J, Wilson, Valerie, Cox, Thomas E, Sharma, Seema D, Smith-Jackson, Kate, Strain, Lisa, Lappin, David, McHale, Teresa, Kavanagh, David, Goodship, Timothy H.J

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Factor H autoantibodies in membranoproliferative glomerulonephritis von Goodship, Timothy H.J., Pappworth, Isabel Y., Toth, Tibor, Denton, Mark, Houlberg, Kris, McCormick, Frances, Warland, David, Moore, Iain, Hunze, Eva-Maria, Staniforth, Scott J., Hayes, Christine, Cavalcante, Danielle Paixão, Kavanagh, David, Strain, Lisa, Herbert, Andrew P., Schmidt, Christoph Q., Barlow, Paul N., Harris, Claire L., Marchbank, Kevin J.

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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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Factor H Mutations in Hemolytic Uremic Syndrome Cluster in Exons 18–20, a Domain Important for Host Cell Recognition von Richards, Anna, Buddles, Mark R., Donne, Rosemary L., Kaplan, Bernard S., Kirk, Edwin, Venning, Michael C., Tielemans, Christian L., Goodship, Judith A., Goodship, Timothy H.J.

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Use of the complement inhibitor Coversin to treat HSCT-associated TMA von Goodship, Timothy H.J., Pinto, Fernando, Weston-Davies, Wynn H., Silva, Juliana, Nishimura, Jun-ichi, Nunn, Miles A., Mackie, Ian, Machin, Samuel J., Palm, Liina, Pryce, Jeremy W., Chiesa, Robert, Amrolia, Persis, Veys, Paul

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The genetics and pathogenesis of haemolytic uraemic syndrome and thrombotic thrombocytopenic purpura von Richards, Anna, Goodship, Judith A, Goodship, Timothy H.J

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Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndrome von Richards, Anna, Kathryn Liszewski, M., Kavanagh, David, Fang, Celia J., Moulton, Elizabeth, Fremeaux-Bacchi, Veronique, Remuzzi, Giuseppe, Noris, Marina, Goodship, Timothy H.J., Atkinson, John P.

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