Complement factor H and the hemolytic uremic syndrome

por Atkinson, John P., Goodship, Timothy H.J.
Publicado 2007

Plasma therapy in atypical haemolytic uremic syndrome: lessons from a family with a factor H mutation

por Davin, Jean Claude, Strain, Lisa, Goodship, Tim H. J.
Publicado 2008

Complement therapy in atypical haemolytic uraemic syndrome (aHUS)

por Wong, Edwin K.S., Goodship, Tim H.J., Kavanagh, David
Publicado 2013

Use of eculizumab in crescentic IgA nephropathy: proof of principle and conundrum?

por Ring, Troels, Pedersen, Birgitte Bang, Salkus, Giedrius, Goodship, Timothy H.J.
Publicado 2015

Prevalence in the General Population of a CFH Sequence Variant Associated with Atypical Haemolytic Uraemic Syndrome in an Extensive Family from Southwest England

por Hamilton, Alexander J., Lyons, Carl B.A., Goodship, Timothy H.J., Bingham, Coralie
Publicado 2013

Atypical haemolytic uraemic syndrome associated with a CD46 mutation triggered by Shigella flexneri

por Brocklebank, Vicky, Wong, Edwin K.S., Fielding, Rick, Goodship, Timothy H.J., Kavanagh, David
Publicado 2014

Prevention of large-vessel stenoses in atypical hemolytic uremic syndrome associated with complement dysregulation

por Davin, Jean-Claude, Majoie, Charles, Groothoff, Jaap, Gracchi, Valentina, Bouts, Antonia, Goodship, Timothy H. J., Loirat, Chantal
Publicado 2010

Clinical Relapses of Atypical HUS on Eculizumab: Clinical Gap for Monitoring and Individualised Therapy

por Teoh, Chia Wei, Gorman, Kathleen Mary, Lynch, Bryan, Goodship, Timothy H. J., Dolan, Niamh Marie, Waldron, Mary, Riordan, Michael, Awan, Atif
Publicado 2018

Mitochondrial Haplogroup and the Risk of Acute Kidney Injury Following Cardiac Bypass Surgery

por Kanagasundaram, Nigel S., Baudouin, Simon V., Rowling, Sarah, Prabhu, Mahesh, Dark, John H., Goodship, Timothy H. J., Chinnery, Patrick F., Hudson, Gavin
Publicado 2019

Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS

por Ermini, Luca, Goodship, Timothy H.J., Strain, Lisa, Weale, Michael E., Sacks, Steven H., Cordell, Heather J., Fremeaux-Bacchi, Veronique, Sheerin, Neil S.
Publicado 2012

Determining the Population Frequency of the CFHR3/CFHR1 Deletion at 1q32

por Holmes, Lucy V., Strain, Lisa, Staniforth, Scott J., Moore, Iain, Marchbank, Kevin, Kavanagh, David, Goodship, Judith A., Cordell, Heather J., Goodship, Timothy H. J.
Publicado 2013

The role of ADAMTS‐13 activity and complement mutational analysis in differentiating acute thrombotic microangiopathies

por Phillips, E. H., Westwood, J. P., Brocklebank, V., Wong, E. K. S., Tellez, J. O., Marchbank, K. J., McGuckin, S., Gale, D. P., Connolly, J., Goodship, T. H. J., Kavanagh, D., Scully, M. A.
Publicado 2016

Deletion of Complement Factor H–Related Genes CFHR1 and CFHR3 Is Associated with Atypical Hemolytic Uremic Syndrome

por 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
Publicado 2007

Atypical Haemolytic Uraemic Syndrome Associated with a Hybrid Complement Gene

por 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
Publicado 2006

Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux

por 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.
Publicado 2017

Publisher Correction: Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux

por 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.
Publicado 2018

Association of Genetic Variants in Complement Factor H and Factor H-Related Genes with Systemic Lupus Erythematosus Susceptibility

por Zhao, Jian, Wu, Hui, Khosravi, Melanie, Cui, Huijuan, Qian, Xiaoxia, Kelly, Jennifer A., Kaufman, Kenneth M., Langefeld, Carl D., Williams, Adrienne H., Comeau, Mary E., Ziegler, Julie T., Marion, Miranda C., Adler, Adam, Glenn, Stuart B., Alarcón-Riquelme, Marta E., Pons-Estel, Bernardo A., Harley, John B., Bae, Sang-Cheol, Bang, So-Young, Cho, Soo-Kyung, Jacob, Chaim O., Vyse, Timothy J., Niewold, Timothy B., Gaffney, Patrick M., Moser, Kathy L., Kimberly, Robert P., Edberg, Jeffrey C., Brown, Elizabeth E., Alarcon, Graciela S., Petri, Michelle A., Ramsey-Goldman, Rosalind, Vilá, Luis M., Reveille, John D., James, Judith A., Gilkeson, Gary S., Kamen, Diane L., Freedman, Barry I., Anaya, Juan-Manuel, Merrill, Joan T., Criswell, Lindsey A., Scofield, R. Hal, Stevens, Anne M., Guthridge, Joel M., Chang, Deh-Ming, Song, Yeong Wook, Park, Ji Ah, Lee, Eun Young, Boackle, Susan A., Grossman, Jennifer M., Hahn, Bevra H., Goodship, Timothy H. J., Cantor, Rita M., Yu, Chack-Yung, Shen, Nan, Tsao, Betty P.
Publicado 2011