Genes and Podocytes – New Insights into Mechanisms of Podocytopathy

por Bierzynska, Agnieszka, Soderquest, Katrina, Koziell, Ania
Publicado 2015

Acute Presentation and Persistent Glomerulonephritis Following Streptococcal Infection in a Patient With Heterozygous Complement Factor H–Related Protein 5 Deficiency

por Vernon, Katherine A., Goicoechea de Jorge, Elena, Hall, Angela E., Fremeaux-Bacchi, Veronique, Aitman, Timothy J., Cook, H. Terence, Hangartner, Robert, Koziell, Ania, Pickering, Matthew C.
Publicado 2012

Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease

por Lennon, Rachel, Stuart, Helen M., Bierzynska, Agnieszka, Randles, Michael J., Kerr, Bronwyn, Hillman, Katherine A., Batra, Gauri, Campbell, Joanna, Storey, Helen, Flinter, Frances A., Koziell, Ania, Welsh, Gavin I., Saleem, Moin A., Webb, Nicholas J. A., Woolf, Adrian S.
Publicado 2015

Shared genetic risk across different presentations of gene test–negative idiopathic nephrotic syndrome

por Downie, Mallory L., Gupta, Sanjana, Chan, Melanie M. Y., Sadeghi-Alavijeh, Omid, Cao, Jingjing, Parekh, Rulan S., Diz, Carmen Bugarin, Bierzynska, Agnieszka, Levine, Adam P., Pepper, Ruth J., Stanescu, Horia, Saleem, Moin A., Kleta, Robert, Bockenhauer, Detlef, Koziell, Ania B., Gale, Daniel P.
Publicado 2022

Short course daily prednisolone therapy during an upper respiratory tract infection in children with relapsing steroid-sensitive nephrotic syndrome (PREDNOS 2): protocol for a rand...

por Webb, Nicholas J A, Frew, Emma, Brettell, Elizabeth A, Milford, David V, Bockenhauer, Detlef, Saleem, Moin A, Christian, Martin, Hall, Angela S, Koziell, Ania, Maxwell, Heather, Hegde, Shivram, Finlay, Eric R, Gilbert, Rodney D, Booth, Jenny, Jones, Caroline, McKeever, Karl, Cook, Wendy, Ives, Natalie J
Publicado 2014

Evaluation of Daily Low-Dose Prednisolone During Upper Respiratory Tract Infection to Prevent Relapse in Children With Relapsing Steroid-Sensitive Nephrotic Syndrome: The PREDNOS 2...

por Christian, Martin T., Webb, Nicholas J. A., Mehta, Samir, Woolley, Rebecca L., Afentou, Nafsika, Frew, Emma, Brettell, Elizabeth A., Khan, Adam R., Milford, David V., Bockenhauer, Detlef, Saleem, Moin A., Hall, Angela S., Koziell, Ania, Maxwell, Heather, Hegde, Shivaram, Prajapati, Hitesh, Gilbert, Rodney D., Jones, Caroline, McKeever, Karl, Cook, Wendy, Ives, Natalie
Publicado 2021

Economic Evaluation of Using Daily Prednisolone versus Placebo at the Time of an Upper Respiratory Tract Infection for the Management of Children with Steroid-Sensitive Nephrotic S...

por Afentou, Nafsika, Frew, Emma, Mehta, Samir, Ives, Natalie J., Woolley, Rebecca L., Brettell, Elizabeth A., Khan, Adam R., Milford, David V., Bockenhauer, Detlef, Saleem, Moin A., Hall, Angela S., Koziell, Ania, Maxwell, Heather, Hegde, Shivaram, Finlay, Eric, Gilbert, Rodney D., Jones, Caroline, McKeever, Karl, Cook, Wendy, Webb, Nicholas J. A., Christian, Martin T.
Publicado 2022

Exploring the relevance of NUP93 variants in steroid-resistant nephrotic syndrome using next generation sequencing and a fly kidney model

por Bierzynska, Agnieszka, Bull, Katherine, Miellet, Sara, Dean, Philip, Neal, Chris, Colby, Elizabeth, McCarthy, Hugh J., Hegde, Shivaram, Sinha, Manish D., Bugarin Diz, Carmen, Stirrups, Kathleen, Megy, Karyn, Mapeta, Rutendo, Penkett, Chris, Marsh, Sarah, Forrester, Natalie, Afzal, Maryam, Stark, Hannah, BioResource, NIHR, Williams, Maggie, Welsh, Gavin I., Koziell, Ania B., Hartley, Paul S., Saleem, Moin A.
Publicado 2022

Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria

por Savige, Judy, Storey, Helen, Watson, Elizabeth, Hertz, Jens Michael, Deltas, Constantinos, Renieri, Alessandra, Mari, Francesca, Hilbert, Pascale, Plevova, Pavlina, Byers, Peter, Cerkauskaite, Agne, Gregory, Martin, Cerkauskiene, Rimante, Ljubanovic, Danica Galesic, Becherucci, Francesca, Errichiello, Carmela, Massella, Laura, Aiello, Valeria, Lennon, Rachel, Hopkinson, Louise, Koziell, Ania, Lungu, Adrian, Rothe, Hansjorg Martin, Hoefele, Julia, Zacchia, Miriam, Martic, Tamara Nikuseva, Gupta, Asheeta, van Eerde, Albertien, Gear, Susie, Landini, Samuela, Palazzo, Viviana, al-Rabadi, Laith, Claes, Kathleen, Corveleyn, Anniek, Van Hoof, Evelien, van Geel, Micheel, Williams, Maggie, Ashton, Emma, Belge, Hendica, Ars, Elisabeth, Bierzynska, Agnieszka, Gangemi, Concetta, Lipska-Ziętkiewicz, Beata S.
Publicado 2021

FAT1 mutations cause a glomerulotubular nephropathy

por Gee, Heon Yung, Sadowski, Carolin E., Aggarwal, Pardeep K., Porath, Jonathan D., Yakulov, Toma A., Schueler, Markus, Lovric, Svjetlana, Ashraf, Shazia, Braun, Daniela A., Halbritter, Jan, Fang, Humphrey, Airik, Rannar, Vega-Warner, Virginia, Cho, Kyeong Jee, Chan, Timothy A., Morris, Luc G. T., ffrench-Constant, Charles, Allen, Nicholas, McNeill, Helen, Büscher, Rainer, Kyrieleis, Henriette, Wallot, Michael, Gaspert, Ariana, Kistler, Thomas, Milford, David V., Saleem, Moin A., Keng, Wee Teik, Alexander, Stephen I., Valentini, Rudolph P., Licht, Christoph, Teh, Jun C., Bogdanovic, Radovan, Koziell, Ania, Bierzynska, Agnieszka, Soliman, Neveen A., Otto, Edgar A., Lifton, Richard P., Holzman, Lawrence B., Sibinga, Nicholas E. S., Walz, Gerd, Tufro, Alda, Hildebrandt, Friedhelm
Publicado 2016