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	1.	aHUS caused by complement dysregulation: new therapies on the horizon. [electronic resource] by Waters, Aoife M Licht, Christoph Producer: 20110325 In: Pediatric nephrology (Berlin, Germany) vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Paediatrics: Long-term effects of Wilms tumour therapy on renal function. [electronic resource] by Waters, Aoife M Pritchard-Jones, Kathy Producer: 20151022 In: Nature reviews. Urology vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Ciliopathies: an expanding disease spectrum. [electronic resource] by Waters, Aoife M Beales, Philip L Producer: 20110916 In: Pediatric nephrology (Berlin, Germany) vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Malformations in the Murine Kidney Caused by Loss of CENP-F Function. [electronic resource] by Haley, Chanell O Waters, Aoife M Bader, D M Producer: 20200403 In: Anatomical record (Hoboken, N.J. : 2007) vol. 302 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Tubulointerstitial nephritis as an extraintestinal manifestation of Crohn's disease. [electronic resource] by Waters, Aoife M Zachos, Mary Herzenberg, Andrew M Harvey, Elizabeth Rosenblum, Norman D Producer: 20090505 In: Nature clinical practice. Nephrology vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Severe atypical HUS caused by CFH S1191L--case presentation and review of treatment options. [electronic resource] by De, Sudarsana Waters, Aoife M Segal, Audrey O Trautmann, Agnes Harvey, Elizabeth A Licht, Christoph Producer: 20110628 In: Pediatric nephrology (Berlin, Germany) vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Ectopic notch activation in developing podocytes causes glomerulosclerosis. [electronic resource] by Waters, Aoife M Wu, Megan Y J Onay, Tuncer Scutaru, Jacob Liu, Ju Lobe, Corrinne G Quaggin, Susan E Piscione, Tino D Producer: 20080729 In: Journal of the American Society of Nephrology : JASN vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Growth in PHEX-associated X-linked hypophosphatemic rickets: the importance of early treatment. [electronic resource] by Quinlan, Catherine Guegan, Katie Offiah, Amaka Neill, Richard O' Hiorns, Melanie P Ellard, Sian Bockenhauer, Detlef Hoff, William Van't Waters, Aoife M Producer: 20120618 In: Pediatric nephrology (Berlin, Germany) vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Notch promotes dynamin-dependent endocytosis of nephrin. [electronic resource] by Waters, Aoife M Wu, Megan Yi Jun Huang, Yi-Wei Liu, Guang Ying Holmyard, Doug Onay, Tuncer Jones, Nina Egan, Sean E Robinson, Lisa A Piscione, Tino D Producer: 20120309 In: Journal of the American Society of Nephrology : JASN vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Activation of podocyte Notch mediates early Wt1 glomerulopathy. [electronic resource] by Asfahani, Rowan I Tahoun, Mona M Miller-Hodges, Eve V Bellerby, Jack Virasami, Alex K Sampson, Robert D Moulding, Dale Sebire, Neil J Hohenstein, Peter Scambler, Peter J Waters, Aoife M Producer: 20190102 In: Kidney international vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Mutations in LAMB2 Are Associated With Albuminuria and Optic Nerve Hypoplasia With Hypopituitarism. [electronic resource] by Tahoun, Mona Chandler, Jennifer C Ashton, Emma Haston, Scott Hannan, Athia Kim, Ji Soo D'Arco, Felipe Bockenhauer, D Anderson, G Lin, Meei-Hua Marzouk, Salah Saied, Marwa H Miner, Jeffrey H Dattani, Mehul T Waters, Aoife M Producer: 20201105 In: The Journal of clinical endocrinology and metabolism vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Hemolytic uremic syndrome associated with invasive pneumococcal disease: the United kingdom experience. [electronic resource] by Waters, Aoife M Kerecuk, Larissa Luk, David Haq, Mushfequr R Fitzpatrick, Margaret M Gilbert, Rodney D Inward, Carol Jones, Caroline Pichon, Bruno Reid, Christopher Slack, Mary P E Van't Hoff, William Dillon, Michael J Taylor, C M Tullus, Kjell Producer: 20070822 In: The Journal of pediatrics vol. 151 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis. [electronic resource] by Zivony-Elboum, Yifat Westbroek, Wendy Kfir, Nehama Savitzki, David Shoval, Yishay Bloom, Assnat Rod, Raya Khayat, Morad Gross, Bella Samri, Walid Cohen, Hector Sonkin, Vadim Freidman, Tatiana Geiger, Dan Fattal-Valevski, Aviva Anikster, Yair Waters, Aoife M Kleta, Robert Falik-Zaccai, Tzipora C Producer: 20130107 In: Journal of medical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes. [electronic resource] by Waters, Aoife M Asfahani, Rowan Carroll, Paula Bicknell, Louise Lescai, Francesco Bright, Alison Chanudet, Estelle Brooks, Anthony Christou-Savina, Sonja Osman, Guled Walsh, Patrick Bacchelli, Chiara Chapgier, Ariane Vernay, Bertrand Bader, David M Deshpande, Charu O' Sullivan, Mary Ocaka, Louise Stanescu, Horia Stewart, Helen S Hildebrandt, Friedhelm Otto, Edgar Johnson, Colin A Szymanska, Katarzyna Katsanis, Nicholas Davis, Erica Kleta, Robert Hubank, Mike Doxsey, Stephen Jackson, Andrew Stupka, Elia Winey, Mark Beales, Philip L Producer: 20160301 In: Journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)