Items where Subject is "32 BIOMEDICAL AND CLINICAL SCIENCES > 3202 Clinical sciences > 320214 Nephrology and urology"

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Number of items at this level: 74.

A

Anton Sagayanathan, Prasanth, Loganathan, Ajanthan, and Pridgeon, Simon (2022) Recurrent renal stone in thoracic ectopic kidney due to diaphragmatic hernia. ANZ Journal of Surgery, 92 (3). pp. 611-613.

Al-Shinnag, Mohammad, Marfan, Helen, Susman, Rachel, Wakeling, Jan, Gustafson, Sonja, Wood, Simon, and Mallett, Andrew John (2021) Birt-Hogg-Dubé Syndrome and Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome: An Effective Multidisciplinary Approach to Hereditary Renal Cancer Predisposing Syndromes. Frontiers in Oncology, 11. 738822.

Aldridge, Melanie, Patel, Chirag, Mallett, Andrew J., and Trnka, Peter (2018) Antenatally diagnosed ADPKD. Kidney International Reports, 3 (5). pp. 1214-1217.

B

Brennan, Sonja, Watson, David L., Rudd, Donna M., and Kandasamy, Yogavijayan (2022) Kidney growth following preterm birth: evaluation with renal parenchyma ultrasonography. Pediatric Research. (In Press)

Brennan, Sonja, Watson, David, Schneider, Michal, Rudd, Donna, and Kandasamy, Yogavijayan (2021) Can measurement of the foetal renal parenchymal thickness with ultrasound be used as an indirect measure of nephron number? Journal of Developmental Origins of Health and Disease, 12 (2). pp. 184-192.

Burke, Joseph Patrick, Aljishi, Manaf, Francis, Leo, Hoy, Wendy, Divi, Dakshinamurthy, Cherian, Roy, Frazier, Jeremy, Gobe, Glenda, Gois, Pedro, Govindarajulu, Sridevi, Huynh, Sonny, Jesudason, Shilpanjali, John, George, Madhan, Krishan, Mallett, Andrew, Manickam, Valli, Mutatiri, Clyson, Ng, Shu-Kay, Thet, Zaw, Trnka, Peter, Venuthurupalli, Sree Krishna, and Ranganathan, Dwarakanathan (2020) Protocol and establishment of a Queensland renal biopsy registry in Australia. BMC Nephrology, 21. 320.

Brennan, Sonja, Kandasamy, Yogavijayan, Rudd, Donna, Schneider, Michal, and Watson, David (2020) Fetal kidney charts of a novel measurement of the renal parenchymal thickness to evaluate fetal kidney growth and potential function. Prenatal Diagnosis, 40. pp. 860-869.

Brailsford, Gabrielle, Cash, Ellie, Burke, Jo, Kirkland, Geoff, Wallis, Mathew, Mallett, Andrew, and Jose, Matthew D. (2020) Genetic kidney disease in Southern Tasmania. Kidney International Reports, 5 (4). pp. 534-537.

Brennan, Sonja, Kandasamy, Yogavijayan, Rudd, Donna M., Schneider, Michal E., Jones, Rhondda E., and Watson, David L. (2020) The effect of diabetes during pregnancy on fetal renal parenchymal growth. Journal of Nephrology, 33. pp. 1079-1089.

Brennan, Sonja (2020) The renal parenchyma – evaluation of a novel ultrasound measurement to assess fetal renal development. PhD thesis, James Cook University.

C

Chan, Samuel, Patel, Chirag, and Mallett, Andrew (2020) Pilot clinical and validation study of the PROPKD score in clinical practice amongst patients with Autosomal Dominant Polycystic Kidney Disease. Nephrology, 25 (2). pp. 274-275.

Connor, Thomas M., Hoer, Simon, Mallett, Andrew, Gale, Daniel P., Gomez-Duran, Aurora, Posse, Viktor, Antrobus, Robin, Moreno, Pablo, Sciacovelli, Marco, Frezza, Christian, Duff, Jennifer, Sheerin, Neil S., Sayer, John A., Ashcroft, Margaret, Wiesener, Michael S., Hudson, Gavin, Gustafsson, Claes M., Chinnery, Patrick F., and Maxwell, Patrick H. (2017) Mutations in mitochondrial DNA causing tubulointerstitial kidney disease. PLoS Genetics, 13. e1006620.

Chan, Samuel, Mallett, Andrew J., Patel, Chirag, Francis, Ross S., Johnson, David W., Mudge, David W., and Isbel, Nicole M. (2017) Recurrent atypical haemolytic uraemic syndrome post kidney transplant due to aCD46mutation in the setting ofSMARCAL1-mediated inherited kidney disease. Nephrology, 22 (S1). pp. 11-14.

D

Davis, Justin, Tjipto, Alwie, Hegerty, Katharine, and Mallett, Andrew (2019) An audit of electron microscopy in the diagnosis of focal segmental glomerulosclerosis: are current pathological techniques missing important abnormalities in the glomerular basement membrane? F1000Research, 8. 1204.

E

El-damanawi, Ragada, Viecelli, Andrea K., Pascoe, Elaine M., Craig, Jonathan C., Johnson, David W., Mallett, Andrew J., Hawley, Carmel M., and Hiemstra, Thomas F. (2019) Metformin for preventing the progression of chronic kidney disease. Cochrane Database of Systematic Reviews, 9. CD013414.

F

Forbes, Thomas A., Howden, Sara E., Lawlor, Kynan, Phipson, Belinda, Maksimovic, Jovana, Hale, Lorna, Wilson, Sean, Quinlan, Catherine, Ho, Gladys, Holman, Katherine, Bennetts, Bruce, Crawford, Joanna, Trnka, Peter, Oshlack, Alicia, Patel, Chirag, Mallett, Andrew, Simons, Cas, and Little, Melissa H. (2018) Patient-iPSC-derived kidney organoids show functional validation of a ciliopathic renal phenotype and reveal underlying pathogenetic mechanisms. American Journal of Human Genetics, 102 (5). pp. 816-831.

Furyk, Jeremy S., Chu, Kevin, Banks, Colin, Greenslade, Jaimi, Keijzers, Gerben, Thom, Ogilvie, Torpie, Tom, Dux, Carl, and Narula, Rajan (2016) Distal ureteric stones and tamsulosin: a double-blind, placebo-controlled, randomized, multicenter trial. Annals of Emergency Medicine, 67 (1). pp. 86-95.

Francis, Anna, Burke, John, Francis, Leo, McTaggart, Steven, and Mallett, Andrew (2016) Polypoid change of the glomerular basement membrane in a child with steroid resistant nephrotic syndrome and arhgap24 mutation: a case report. The Open Urology & Nephrology Journal, 9. pp. 88-93.

G

Gately, Ryan, Lock, Gregory, Patel, Chirag, Clouston, John, Hawley, Carmel, and Mallett, Andrew (2021) Multiple cerebral aneurysms in an adult with autosomal recessive polycystic kidney disease. Kidney International Reports, 6 (1). pp. 219-223.

Gois, Pedro Henrique Franca, Healy, Helen G., Ranganathan, Dwarakanathan, Mallett, Andrew John, Webster, Angela C., Kanellis, John, Barraclough, Katherine, Wainstein, Marina, Johnson, David W., and Kerr, Peter G. (2021) Nephrology in Australia. In: Moura-Neto, José A., Ronco, Claudio, and Divino-Filho, José Carolino, (eds.) Nephrology Worldwide. Springer, Cham, pp. 701-721.

Gale, Daniel P., Mallett, Andrew, Patel, Chirag, Sneddon, Tam P., Rehm, Heidi L., Sampson, Matthew G., and Bockenhauer, Detlef (2020) Diagnoses of uncertain significance: kidney genetics in the 21st century. Nature Reviews Nephrology, 16. pp. 616-618.

Greenwood, Alice M., Gunnarsson, Ronny, Neuen, Brendon L., Oliver, Kimberley, Green, Stella J., and Baer, Richard A. (2017) Clinical presentation, treatment and outcome of focal segmental glomerulosclerosis in Far North Queensland Australian adults. Nephrology, 22 (7). pp. 520-530.

Gilhotra, Rajit A., Rodrigues, Beverly T., Vangaveti, Venkat N., Kan, George, Porter, David, Sangla, Kunwarjit S., and Malabu, Usman H. (2016) Non-traumatic lower limb amputation in patients with end-stage renal failure on dialysis: an Australian perspective. Renal Failure, 38. pp. 1-8.

H

Huppertz, Nina, Beetham, Kassia S., Howden, Erin J., Leicht, Anthony S., Isbel, Nicole M., and Coombes, Jeff S. (2020) A 12-month lifestyle intervention does not improve cardiac autonomic function in patients with chronic kidney disease. Autonomic Neuroscience: Basic and Clinical, 224. 102642.

Hudson, Rebecca, Patel, Chirag, Hawley, Carmel M., O’Shea, Stacey, Snelling, Paul, Ho, Gladys, Holman, Katherine, Bennetts, Bruce, Crawford, Joanna, Francis, Leo, Simons, Cas, and Mallett, Andrew (2020) Adult-Diagnosed Nonsyndromic Nephronophthisis in Australian Families Caused by Biallelic NPHP4 Variants. American Journal of Kidney Diseases, 76 (2). pp. 282-287.

Hill, Kathleen, Sharp, Rebecca, Childs, Jessie, Esterman, Adrian, Leu, Richard Le, Juneja, Rajiv, and Jesudason, Shilpa (2020) Cannulation practices at haemodialysis initiation via an arteriovenous fistula or arteriovenous graft. The Journal of Vascular Acces, 21 (5). pp. 573-581.

Huynh, Vinh T., Audrézet, Marie-Pierre, Sayer, John A., Ong, Albert C., Lefevre, Siriane, Le Brun, Valoris, Després, Aurore, Senum, Sarah R., Chebib, Fouad T., Barroso-Gil, Miguel, Patel, Chirag, Mallett, Andrew, Goel, Himanshu, Mallawaarachchi, Amali C., Van Eerde, Albertien M., Ponlot, Eléonore, Kribs, Marc, Le Meur, Yannick, Harris, Peter C., and Cornec-Le Gall, Emilie (2020) Clinical spectrum, prognosis and estimated prevalence of DNAJB11-kidney disease. Kidney International, 98 (2). pp. 476-487.

Hoy, Wendy E., White, Andrew V., Tipiloura, Bernard, Singh, Gurmeet, Sharma, Suresh, Bloomfield, Hilary, Swanson, Cheryl E., Dowling, Alison, and McCredie, David A. (2016) The influence of birthweight, past poststreptococcal glomerulonephritis and current body mass index on levels of albuminuria in young adults: the multideterminant model of renal disease in a remote Australian Aboriginal population with high rates of renal disease and renal failure. Nephrology Dialysis Transplantation, 31 (6). pp. 971-977.

J

Jeyaruban, A., Hoy, W., Cameron, A., Healy, H., Wang, Z., Zhang, J., and Mallett, A. (2022) Determining the association between the type of intervention for ischaemic heart disease and mortality and morbidity in patients with chronic kidney disease. Internal Medicine Journal. (In Press)

Jayasinghe, Kushani, Quinlan, Catherine, Mallett, Andrew, Kerr, Peter G., McClaren, Belinda, Nisselle, Amy, Mallawaarachchi, Amali, Polkinghorne, Kevan R., Patel, Chirag, Best, Stephanie, and Stark, Zornitza (2021) Attitudes and practices of Australian nephrologists toward implementation of clinical genomics. Kidney International Reports, 6 (2). pp. 272-283.

Jayasinghe, Kushani, Stark, Zornitza, Kerr, Peter G., Gaff, Clara, Martyn, Melissa, Whitlam, John, Creighton, Belinda, Donaldson, Elizabeth, Hunter, Matthew, Jarmolowicz, Anna, Johnstone, Lilian, Krzesinski, Emma, Lunke, Sebastian, Lynch, Elly, Nicholls, Kathleen, Patel, Chirag, Prawer, Yael, Ryan, Jessica, See, Emily J., Talbot, Andrew, Trainer, Alison, Tytherleigh, Rigan, Valente, Giulia, Wallis, Mathew, Wardrop, Louise, West, Kirsty H., White, Susan M., Wilkins, Ella, Mallett, Andrew, and Quinlan, Catherine (2021) Clinical impact of genomic testing in patients with suspected monogenic kidney disease. Genetics in Medicine, 23 (1). pp. 183-191.

Jayasinghe, Kushani, Wu, You, Stark, Zornitza, Kerr, Peter G., Mallett, Andrew J., Gaff, Clara, Martyn, Melissa, Goranitis, Ilias, and Quinlan, Catherine (2021) Cost-effectiveness of targeted exome analysis as a diagnostic test in glomerular diseases. Kidney International Reports, 6 (11). pp. 2850-2861.

Jacups, Susan P., Carter, Angus W., and Murray, Andrew (2020) Acute kidney injury in Indigenous intensive care patients. Australian Critical Care, 33 (5). pp. 452-457.

Jones, Scott A., Hegerty, Katharine, Scuderi, Carla, Eglington, Jessica, Green, Ben, and Mallett, Andrew (2020) Clinical and healthcare utilization outcomes of parathyroidectomy in CKD and dialysis patients. Kidney International Reports, 5 (7). pp. 1086-1089.

Jeyaruban, Andrew, Hoy, Wendy, Cameron, Anne, Healy, Helen, Wang, Zaimin, Zhang, Jianzhen, and Mallett, Andrew (2020) Impact of cardiovascular events on mortality and progression of renal dysfunction in a Queensland CKD cohort. Nephrology, 25 (11). pp. 839-844.

Jahan, Sadia, Sarathchandran, Subashini, Akhter, Shamina, Goldblatt, Jack, Stark, Samantha, Crawford, Douglas, Mallett, Andrew, and Thomas, Mark (2020) Prevalence of Fabry disease in dialysis patients: Western Australia Fabry disease screening study - the FoRWARD study. Orphanet Journal of Rare Diseases, 15. 10.

Jones, Lynelle K., Lam, Rachel, McKee, Karen K., Aleksandrova, Maya, Dowling, John, Alexander, Stephen I., Mallawaarachchi, Amali, Cottle, Denny L., Short, Kieran M., Pais, Lynn, Miner, Jeffery H., Mallett, Andrew, Simons, Cas, McCarthy, Hugh, Yurchenco, Peter D., and Smyth, Ian M. (2020) A mutation affecting laminin alpha 5 polymerisation gives rise to a syndromic developmental disorder. Development, 147 (21). dev189183.

Jayasinghe, Kushani, White, Susan M., Kerr, Peter G., MacGregor, Duncan, Stark, Zornitza, Wilkins, Ella, Simons, Cas, Mallett, Andrew, and Quinlan, Catherine (2019) Isolated proteinuria due to CUBN homozygous mutation – challenging the investigative paradigm. BMC Nephrology, 20. 330.

K

Kumuthini, Judit, van Woerden, Christiaan, Mallett, Andrew, Zass, Lyndon, Chaouch, Melek, Thompson, Michael, Johnston, Katherine, Mbiyavanga, Mamana, Baichoo, Shakuntala, Mungloo-Dilmohamud, Zahra, Patel, Chirag, and Mulder, Nicola (2019) Proposed minimum information guideline for kidney disease—research and clinical data reporting: a cross-sectional study. BMJ Open, 9 (11). e029539.

L

Lopez-Garcia, Sergio Camilo, Emma, Francesco, Walsh, Stephen B., Fila, Marc, Hooman, Nakysa, Zaniew, Marcin, Bertholet-Thomas, Aurélia, Colussi, Giacomo, Burgmaier, Kathrin, Levtchenko, Elena, Sharma, Jyoti, Singhal, Jyoti, Soliman, Neveen A., Ariceta, Gema, Basu, Biswanath, Murer, Luisa, Tasic, Velibor, Tsygin, Alexey, Decramer, Stéphane, Gil-Peña, Helena, Koster-Kamphuis, Linda, La Scola, Claudio, Gellermann, Jutta, Konrad, Martin, Lilien, Marc, Francisco, Telma, Tramma, Despoina, Trnka, Peter, Yüksel, Selçuk, Caruso, Maria Rosa, Chromek, Milan, Ekinci, Zelal, Gambaro, Giovanni, Kari, Jameela A., König, Jens, Taroni, Francesca, Thumfart, Julia, Trepiccione, Francesco, Winding, Louise, Wühl, Elke, Ağbaş, Ayşe, Belkevich, Anna, Vargas-Poussou, Rosa, Blanchard, Anne, Conti, Giovanni, Boyer, Olivia, Dursun, Ismail, Pınarbaşı, Ayşe Seda, Melek, Engin, Miglinas, Marius, Novo, Robert, Mallett, Andrew, Milosevic, Danko, Szczepanska, Maria, Wente, Sarah, Cheong, Hae Il, Sinha, Rajiv, Gucev, Zoran, Dufek, Stephanie, Iancu, Daniela, European dRTA Consortium, , Kleta, Robert, Schaefer, Franz, and Bockenhauer, Detlef (2019) Treatment and long-term outcome in primary distal renal tubular acidosis. Nephrology Dialysis Transplantation, 34 (6). pp. 981-991.

M

Mallett, Andrew, Kearey, Phoebe Jane, Cameron, Anne, Healy, Helen G., Denaro, Charles, Thomas, Mark, Lee, Vincent W., Stark, Samantha Louise, Fuller, Maria, Wang, Zaimin, and Hoy, Wendy E. (2022) The prevalence of Fabry disease in a statewide chronic kidney disease cohort – Outcomes of the aCQuiRE (Ckd.Qld fabRy Epidemiology) study. BMC Nephrology, 23 (1). 169.

Mallett, Andrew J., Knoers, Nine, Sayer, John, and Stark, Zornitza (2021) Clinical versus research genomics in kidney disease. Nature Reviews Nephrology, 17 (9). pp. 570-571.

McConnachie, Dominique J., Stow, Jennifer, and Mallett, Andrew (2021) Ciliopathies and the kidney: a review. American Journal of Kidney Diseases, 77 (3). pp. 410-419.

Mallawaarachchi, Amali C., Lundie, Ben, Hort, Yvonne, Schonrock, Nicole, Senum, Sarah R., Gayevskiy, Velimir, Minoche, Andre E., Hollway, Georgina, Ohnesorg, Thomas, Hinchcliffe, Marcus, Patel, Chirag, Tchan, Michel, Mallett, Andrew, Dinger, Marcel E., Rangan, Gopala, Cowley, Mark J., Harris, Peter C., Burnett, Leslie, Shine, John, and Furlong, Timothy J. (2021) Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencing. European Journal of Human Genetics, 29. pp. 760-770.

Mallett, Andrew (2021) Monogenic nephrolithiasis-collision of phenotypes, genotypes, and phenocopies. Kidney International Reports, 6 (11). pp. 2737-2739.

Mallett, Andrew J., Perrone, Ronald D., Rangan, Gopala, Hawley, Carmel, El-Damanawi, Ragada, Hiemstra, Thomas F., Townsend Arellano, Carolina, Lee, Jennifer, and Torres, Vicente E. (2021) Per-treatment post-hoc analysis of clinical trial outcomes with Tolvaptan in autosomal dominant polycystic kidney disease. Kidney International Reports, 6. pp. 1032-1040.

Mallett, Andrew, Kearey, Phoebe, Cameron, Anne, Healy, Helen, Denaro, Charles, Thomas, Mark, Lee, Vincent W., Stark, Samantha, Fuller, Maria, and Hoy, Wendy E. (2020) The Ckd. Qld fabRy Epidemiology (aCQuiRE) study protocol: identifying the prevalence of Fabry disease amongst patients with kidney disease in Queensland, Australia. BMC Nephrology, 21. 58.

Mallett, Andrew J., Quinlan, Catherine, Patel, Chirag, Fowles, Lindsay, Crawford, Joanna, Gattas, Michael, Baer, Richard, Bennetts, Bruce, Ho, Gladys, Holman, Katherine, and Simons, Cas (2019) Precision medicine diagnostics for rare kidney disease: Twitter as a tool in clinical genomic translation. Kidney Medicine, 1 (5). pp. 315-318.

Mallett, Andrew J., McCarthy, Hugh J., Ho, Gladys, Holman, Katherine, Farnsworth, Elizabeth, Patel, Chirag, Fletcher, Jeffery T., Mallawaarachchi, Amali, Quinlan, Catherine, Bennetts, Bruce, and Alexander, Stephen I. (2017) Massively parallel sequencing and targeted exomes in familial kidney disease can diagnose underlying genetic disorders. Kidney International, 92. pp. 1493-1506.

Mahmood, Usman, Isbel, Nicole, Mollee, Peter, Mallett, Andrew, Govindarajulu, Sridevi, and Francis, Ross (2017) Monoclonal gammopathy of renal significance triggering atypical haemolytic uraemic syndrome. Nephrology, 22 (Suppl. 1). pp. 15-17.

Maple-Brown, Louise J., Hughes, Jaquelyne T., Ritte, Rebecca, Barzi, Federica, Hoy, Wendy E., Lawton, Paul D., Jones, Graham R.D., Death, Elizabeth, Simmonds, Alison, Sinha, Ashim K., Cherian, Sajiv, Thomas, Mark A.B., McDermott, Robyn, Brown, Alex D.H., O'dea, Kerin, Jerums, George, Cass, Alan, and MacIsaac, Richard J. (2016) Progression of kidney disease in Indigenous Australians: the eGFR follow-up study. Clinical Journal of the American Society of Nephrology, 11 (6). pp. 993-1004.

Mallett, Andrew, Fowles, Lindsay F., McGaughran, Julie, Healy, Helen, and Patel, Chirag (2016) A multidisciplinary renal genetics clinic improves patient diagnosis. Medical Journal of Australia, 204 (2). pp. 58-59.

Mallett, Andrew, Tang, Wen, Hart, Gareth, McDonald, Stephen P., Hawley, Carmel M., Badve, Sunil V., Boudville, Neil, Brown, Fiona G., Campbell, Scott B., Clayton, Philip A., and Johnson, David W. (2015) End-Stage Kidney Disease Due to Fibrillary Glomerulonephritis and Immunotactoid Glomerulopathy - Outcomes in 66 Consecutive ANZDATA Registry Cases. American Journal of Nephrology, 42. pp. 177-184.

N

Ng, Monica S.Y., Charu, Vivek, Johnson, David W., O’Shaughnessy, Michelle M., and Mallett, Andrew (2022) National and international kidney failure registries: characteristics, commonalities, and contrasts. Kidney International, 101 (1). pp. 23-35.

Ng, Monica S., Malacova, Eva, Hurst, Cameron, Johnson, David W., and Mallett, Andrew (2021) Clinical Outcomes of People With Fabry Disease — ANZDATA Registry Study. Kidney International Reports, 6 (9). pp. 2481-2485.

Nisselle, Amy, Janinski, Monika, Martyn, Melissa, McClaren, Belinda, Kaunein, Nadia, Maguire, Jane, Riggs, Erin Rooney, Barlow-Stewart, Kristine, Belcher, Andrea, Bernat, John A., Best, Stephanie, Bishop, Michelle, Carroll, June C., Cornel, Martina, Dissanayake, Vajira H.W., Dodds, Agnes, Dunlop, Kate, Garg, Gunjan, Gear, Russell, Graves, Debra, Knight, Ken, Korf, Bruce, Kumar, Dhavendra, Laurino, Mercy, Ma, Alan, Mallett, Andrew, McCarthy, Maria, McEwen, Alison, Mulder, Nicola, Patel, Chirag, Quinlan, Catherine, Reed, Kate, Sinnerbrink, Ingrid, Slavotinek, Anne, Suppiah, Vijayaprakash, Terrill, Bronwyn, Tobias, Edward S., Tonkin, Emma, Trumble, Steve, Wessels, Tina-Marie, Metcalfe, Sylvia, Jordan, Helen, and Gaff, Clara (2021) Ensuring best practice in genomics education and evaluation: reporting item standards for education and its evaluation in genomics (RISE2 Genomics). Genetics in Medicine, 23 (7). pp. 1356-1365.

Ng, Monica S.Y., Ullah, Shahid, Wilson, Gregory, McDonald, Stephen, Sypek, Matthew, and Mallett, Andrew J. (2020) ABO blood group relationships to kidney transplant recipient and graft outcomes. PLoS ONE, 15 (7). e0236396.

Nesbitt, Alexander L., Kapoor, Jada, Piesse, Charlotte, Evans, Garrath, Antoniou, Stefan, Smith, Philip, and Pridgeon, Simon W. (2019) Prediction of pathological stage at radical prostatectomy: do commonly used prostate cancer nomograms apply to men from Far North Queensland? Australian and New Zealand Journal of Surgery, 89 (1-2). pp. 111-114.

Ng, Monica S.Y., McClymont, Kelly, McCallum, Naomi, Dua, Rahul, Holman, Katherine, Bennetts, Bruce, Ho, Gladys, Patel, Chirag, and Mallett, Andrew (2018) CFHR5 nephropathy in a Greek-Cypriot Australian family: ancestry-informed precision medicine. Kidney International Reports, 3 (5). pp. 1222-1228.

Ng, Monica Suet Ying, Francis, Leo, Pillai, Elango, and Mallett, Andrew John (2018) Paraneoplastic immunoglobulin A nephropathy and associated focal segmental glomerulosclerosis in asymptomatic low volume B-cell lymphoma – a case report. BMC Nephrology, 19 (1). 224.

Neuen, Brendon L., Leather, Nicole, Greenwood, Alice M., Gunnarsson, Ronny, Cho, Yeoungjee, and Mantha, Murty L. (2016) Neutrophil–lymphocyte ratio predicts cardiovascular and all-cause mortality in hemodialysis patients. Renal Failure, 38 (1). pp. 70-76.

R

Ritte, Rebecca E., Lawton, Paul, Hughes, Jaquelyne T., Barzi, Federica, Brown, Alex, Mills, Phillip, Hoy, Wendy, O'dea, Kerin, Cass, Alan, and Maple-Brown, Louise (2020) Chronic kidney disease and socio-economic status: a cross sectional study. Ethnicity and Health, 25 (1). pp. 93-109.

S

Scuderi, Carla E., Parker, Suzanne L., Jacks, Margaret, John, George, McWhinney, Brett, Ungerer, Jacobus, Mallett, Andrew, Roberts, Jason A., Healy, Helen, and Staatz, Christine E. (2020) Kidney transplant recipient's perceptions of blood testing through microsampling and venepuncture. Bioanalysis, 12 (13). pp. 873-881.

Sutherland, Megan R., Vojisavljevic, Danica, and Black, Mary Jane (2020) A practical guide to the stereological assessment of glomerular number, size, and cellular composition. The Anatomical Record, 303 (10). pp. 2679-2692.

Sutherland, Megan R., Chatfield, Mark D., Davison, Belinda, Vojisavljevic, Danica, Alison, Kent L., Hoy, Wendy E., Singh, Gurmeet R., and Black, Mary Jane (2019) Renal dysfunction is already evident within the first month of life in Australian Indigenous infants born preterm. Kidney International, 96 (5). pp. 1205-1216.

T

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, Bennetts, Bruce, Alexander, Stephen I., and McCarthy, Hugh J. (2021) Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families. npj Genomic Medicine, 6. 20.

Tran, Ngan K., Lea, Rodney A., Holland, Samuel, Nguyen, Quan, Raghubar, Arti M., Sutherland, Heidi G., Benton, Miles C., Haupt, Larisa M., Blackburn, Nicholas B., Curran, Joanne E., Blangero, John, Mallett, Andrew, and Griffiths, Lyn R. (2021) Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney disease. Scientific Reports, 11. 19425.

Tan, Wei Shen, Teo, Chin Hai, Chan, Delcos, Heinrich, Malgorzata, Feber, Andrew, Sarpong, Rachael, Allan, Jennifer, Williams, Norman, Brew-Graves, Chris, Ng, Chirk Jenn, Kelly, John D., and DETECT II Trail Collaborators, (2019) Mixed-methods approach to exploring patients’ perspectives on the acceptability of a urinary biomarker test in replacing cystoscopy for bladder cancer surveillance. BJU International, 124 (3). pp. 408-417.

Tong, A., Tunnicliffe, David J., Lopez-Vargas, Pamela, Mallett, Andrew, Patel, Chirag, Savige, Judy, Campbell, Katrina, Patel, Manish, Tchan, Michel C., Alexander, Stephen I., Lee, Vincent, Craig, Jonathan C., Fassett, Robert, and Rangan, Gopala K. (2016) Identifying and integrating consumer perspectives in clinical practice guidelines on autosomal-dominant polycystic kidney disease. Nephrology, 21 (2). pp. 122-32.

V

Viering, Daan, Schlingmann, Karl-Peter, Hureaux, Marguerite, Nijhenhuis, Tom, Mallett, Andrew, Chan, Melanie MY, van Beek, André, van Eerde, Albertien M, Coulibaly, Jean-Marie, Vallet, Marion, Decramer, Stéphane, Pelletier, Solenne, Klaus, Günter, Komhoff, Martin, Beetz, Rolf, Patel, Chirag, Shenoy, Mohan, Steenbergen, Eric J., Anderson, Glenn, Bongers, Ernie M.H.F., Bermann, Carsten, Penneman, Daan, Rodenburg, Richard J., Kleta, Robert, Houillier, Pascal, Konrad, Martin, Vargas-Poussou, Rosa, Knoers, Nine, Bockenhauer, Detlef, de Baaij, Jeroen, and Genomics England Research Consortium, (2022) Gitelman-like syndrome caused by pathogenic variants in mtDNA. Journal of the American Society of Nephrology, 33 (2). pp. 305-325.

W

Wilson, Gregory J., Wood, Simon, Patel, Chirag, Oliver, Kimberley, John, George, Ranganathan, Dwarakanathan, Mallett, Andrew, and Isbel, Nicole (2020) DNAJB11-Related Atypical ADPKD in a Kidney Transplant Donor. Kidney International Reports, 5 (8). pp. 1363-1366.

Wu, You, Al-Janabi, Hareth, Mallett, Andrew, Quinlan, Catherine, Scheffer, Ingrid E., Howell, Katherine B., Christodoulou, John, Leventer, Richard J., Lockhart, Paul J., Stark, Zornitza, Boughtwood, Tiffany, and Goranitis, Ilias (2020) Parental health spillover effects of paediatric rare genetic conditions. Quality of Life Research, 29. pp. 2445-2454.

Wu, Yeda, Byrne, Enda M., Zheng, Zhili, Kemper, Kathryn E., Yengo, Loic, Mallett, Andrew J., Yang, Jian, Visscher, Peter M., and Wray, Naomi R. (2019) Genome-wide association study of medication-use and associated disease in the UK Biobank. Nature Communications, 10. 1891.

Wilson, Gregory J., Kark, Adrian L., Francis, Leo P., Hoy, Wendy, Healy, Helen G., and Mallett, Andrew (2017) The increasing rates of acute interstitial nephritis in Australia: a single centre case series. BMC Nephrology, 18. 329.

This list was generated on Mon Feb 6 23:01:41 2023 AEST.