A clinical approach to tubulopathies in children and young adults

por Kermond, Rachael, Mallett, Andrew, McCarthy, Hugh
Publicado 2022

Genomics in the renal clinic - translating nephrogenetics for clinical practice

por Mallett, Andrew, Corney, Christopher, McCarthy, Hugh, Alexander, Stephen I., Healy, Helen
Publicado 2015

Adrenocorticotrophic Hormone−Induced Remission of Pediatric Post-transplantation Recurrent Focal Segmental Glomerulosclerosis

por Raaijmakers, Anke, Craig, Elizabeth, Kim, Siah, Kennedy, Sean E., McCarthy, Hugh J.
Publicado 2019

Participant Choice towards Receiving Potential Additional Findings in an Australian Nephrology Research Genomics Study

por O’Shea, Rosie, Wood, Alasdair, Patel, Chirag, McCarthy, Hugh J., Mallawaarachchi, Amali, Quinlan, Catherine, Simons, Cas, Stark, Zornitza, Mallett, Andrew J.
Publicado 2022

Immunologic response to SARS-CoV-2 mRNA vaccination in pediatric kidney transplant recipients

por Kermond, Rachael F., Ozimek-Kulik, Justyna E., Kim, Siah, Alexander, Stephen I., Hahn, Deirdre, Kesson, Alison, Wood, Nicholas, McCarthy, Hugh J., Durkan, Anne M.
Publicado 2022

Membranous nephropathy: Clearer pathology and mechanisms identify potential strategies for treatment

por Chung, Edmund Y. M., Wang, Yuan M., Keung, Karen, Hu, Min, McCarthy, Hugh, Wong, Germaine, Kairaitis, Lukas, Bose, Bhadran, Harris, David C. H., Alexander, Stephen I.
Publicado 2022

Molecular Analysis of Goodpasture’s Disease Following Hematopoietic Stem Cell Transplant in a Pediatric Patient, Recalls the Conformeropathy of Wild-Type Anti-GBM Disease

por Gray, Paul E., McCarthy, Hugh, Siggs, Owen M., Saleem, Moin A., O' Brien, Tracy, Frith, Katie, Ziegler, John B., Kitching, A. Richard, Fogo, Agnes B., Hudson, Billy G., Pedchenko, Vadim
Publicado 2019

Predictive Models for Recurrent Membranous Nephropathy After Kidney Transplantation

por Chung, Edmund Y. M., Blazek, Katrina, Teixeira-Pinto, Armando, Sharma, Ankit, Kim, Siah, Lin, Yingxin, Keung, Karen, Bose, Bhadran, Kairaitis, Lukas, McCarthy, Hugh, Ronco, Pierre, Alexander, Stephen I., Wong, Germaine
Publicado 2022

Understanding the ongoing learning needs of Australian paediatricians: Evaluation of a pilot paediatric video teaching programme

por Le Marne, Fleur A, Briggs, Nancy, Frith, Katie, Kariyawasam, Didu, McCarthy, Hugh J, Nunn, Kenneth, Rao, Arjun, Sachdev, Rani, Sarkozy, Vanessa, Teng, Arthur, Trethewie, Susan, Williams, Gary D, Bye, Ann ME
Publicado 2022

Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol

por Jayasinghe, Kushani, Stark, Zornitza, Patel, Chirag, Mallawaarachchi, Amali, McCarthy, Hugh, Faull, Randall, Chakera, Aron, Sundaram, Madhivanan, Jose, Matthew, Kerr, Peter, Wu, You, Wardrop, Louise, Goranitis, Ilias, Best, Stephanie, Martyn, Melissa, Quinlan, Catherine, Mallett, Andrew J
Publicado 2019

Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families

por Tanudisastro, Hope A., Holman, Katherine, Ho, Gladys, Farnsworth, Elizabeth, Fisk, Katrina, Gayagay, Thet, Hackett, Emma, Jenkins, Gemma, Krishnaraj, Rahul, Lai, Tiffany, Wong, Karen, Patel, Chirag, Mallawaarachchi, Amali, Mallett, Andrew J., Bennetts, Bruce, Alexander, Stephen I., McCarthy, Hugh J.
Publicado 2021

NAV-KIDS(2) trial: protocol for a multi-centre, staggered randomised controlled trial of a patient navigator intervention in children with chronic kidney disease

por van Zwieten, Anita, Caldwell, Patrina, Howard, Kirsten, Tong, Allison, Craig, Jonathan C., Alexander, Stephen, Howell, Martin, Armando, Teixeira-Pinto, Hawley, Carmel, Jesudason, Shilpa, Walker, Amanda, Mackie, Fiona, Kennedy, Sean, McTaggart, Steve, McCarthy, Hugh, Carter, Simon, Kim, Siah, Crafter, Sam, Woodleigh, Reginald, Guha, Chandana, Wong, Germaine
Publicado 2019

A protocol for the identification and validation of novel genetic causes of kidney disease

por Mallett, Andrew, Patel, Chirag, Maier, Barbara, McGaughran, Julie, Gabbett, Michael, Takasato, Minoru, Cameron, Anne, Trnka, Peter, I. Alexander, Stephen, Rangan, Gopala, Tchan, Michel C., Caruana, Georgina, John, George, Quinlan, Cathy, McCarthy, Hugh J., Hyland, Valentine, E. Hoy, Wendy, Wolvetang, Ernst, Taft, Ryan, Simons, Cas, Healy, Helen, Little, Melissa
Publicado 2015

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

NAVKIDS(2) trial: a multi-centre, waitlisted randomised controlled trial of a patient navigator intervention in children with chronic kidney disease — statistical analysis plan and...

por van Zwieten, Anita, Ryan, Elizabeth G., Caldwell, Patrina, Howard, Kirsten, Tong, Allison, Craig, Jonathan C., Alexander, Stephen I., Howell, Martin, Teixeira-Pinto, Armando, Hawley, Carmel M., Jesudason, Shilpanjali, Walker, Amanda, Mackie, Fiona, Kennedy, Sean E., McTaggart, Steven, McCarthy, Hugh J., Carter, Simon A., Kim, Siah, Woodleigh, Reginald, Francis, Anna, Mallard, Alistair R., Bernier-Jean, Amélie, Johnson, David W., Hahn, Deirdre, Reidlinger, Donna, Pascoe, Elaine, Varghese, Julie, Kiriwandeniya, Charani, Vergara, Liza, Larkins, Nicholas, Macauley, Luke, Irving, Michelle, Khalid, Rabia, Guha, Chandana, Wong, Germaine
Publicado 2022

Baseline characteristics of participants in the NAVKIDS(2) trial: a patient navigator program in children with chronic kidney disease

por Guha, Chandana, Khalid, Rabia, van Zwieten, Anita, Francis, Anna, Hawley, Carmel M., Jauré, Allison, Teixeira-Pinto, Armando, Mallard, Alistair R., Bernier-Jean, Amelie, Johnson, David W., Hahn, Deirdre, Reidlinger, Donna, Pascoe, Elaine M., Ryan, Elizabeth G., Mackie, Fiona, McCarthy, Hugh J., Craig, Jonathan C., Varghese, Julie, Kiriwandeniya, Charani, Howard, Kirsten, Larkins, Nicholas G., Macauley, Luke, Walker, Amanda, Howell, Martin, Irving, Michelle, Caldwell, Patrina H. Y., Woodleigh, Reginald, Jesudason, Shilpanjali, Carter, Simon A., Kennedy, Sean E., Alexander, Stephen I., McTaggart, Steven, Wong, Germaine
Publicado 2022

Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant

por Hoorntje, Edgar T., Burns, Charlotte, Marsili, Luisa, Corden, Ben, Parikh, Victoria N., te Meerman, Gerard J., Gray, Belinda, Adiyaman, Ahmet, Bagnall, Richard D., Barge-Schaapveld, Daniela Q.C.M., van den Berg, Maarten P., Bootsma, Marianne, Bosman, Laurens P., Correnti, Gemma, Duflou, Johan, Eppinga, Ruben N., Fatkin, Diane, Fietz, Michael, Haan, Eric, Jongbloed, Jan D.H., Hauer, Arnaud D., Lam, Lien, van Lint, Freyja H.M., Lota, Amrit, Marcelis, Carlo, McCarthy, Hugh J., van Mil, Anneke M., Oldenburg, Rogier A., Pachter, Nicholas, Planken, R. Nils, Reuter, Chloe, Semsarian, Christopher, van der Smagt, Jasper J., Thompson, Tina, Vohra, Jitendra, Volders, Paul G.A., van Waning, Jaap I., Whiffin, Nicola, van den Wijngaard, Arthur, Amin, Ahmad S., Wilde, Arthur A.M., van Woerden, Gijs, Yeates, Laura, Zentner, Dominica, Ashley, Euan A., Wheeler, Matthew T., Ware, James S., van Tintelen, J. Peter, Ingles, Jodie
Publicado 2022