Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Aoife Waters"'
Autor:
Natalie Ives, Rebecca Woolley, Moin A Saleem, Catherine A Moakes, Aoife Waters, Rodney D Gilbert, Hugh Jarrett, Elizabeth Brettell, Steve Nash, Louise K Farmer, Khadija Ourradi, Sally A Johnson
Publikováno v:
Efficacy and Mechanism Evaluation, Vol 11, Iss 11 (2024)
Background Shiga-toxin-producing Escherichia coli haemolytic uraemic syndrome affects ~100 United Kingdom children each year. Around half need dialysis, a quarter develop serious complications with long-term consequences and ~3% die. No effective int
Externí odkaz:
https://doaj.org/article/d211a98eb57e4132bc1c294a564bffab
Autor:
Richard M. Lynn, Sarah J. O’Brien, C. Mark Taylor, Goutam K. Adak, Henrik Chart, Tom Cheasty, John E. Coia, Iain A. Gillespie, Mary E. Locking, William J. Reilly, Henry R. Smith, Aoife Waters, Geraldine A. Willshaw
Publikováno v:
Emerging Infectious Diseases, Vol 11, Iss 4, Pp 590-596 (2005)
We conducted prospective surveillance of childhood hemolytic uremic syndrome (HUS) from 1997 to 2001 to describe disease incidence and clinical, epidemiologic and microbiologic characteristics. We compared our findings, where possible, with those of
Externí odkaz:
https://doaj.org/article/07eb6032ea8645ee86c12c4df7904d11
Autor:
Francesco Lescai, Silvia Bonfiglio, Chiara Bacchelli, Estelle Chanudet, Aoife Waters, Sanjay M Sisodiya, Dalia Kasperavičiūtė, Julie Williams, Denise Harold, John Hardy, Robert Kleta, Sebahattin Cirak, Richard Williams, John C Achermann, John Anderson, David Kelsell, Tom Vulliamy, Henry Houlden, Nicholas Wood, Una Sheerin, Gian Paolo Tonini, Donna Mackay, Khalid Hussain, Jane Sowden, Veronica Kinsler, Justyna Osinska, Tony Brooks, Mike Hubank, Philip Beales, Elia Stupka
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e51292 (2012)
Recent advances in genomics technologies have spurred unprecedented efforts in genome and exome re-sequencing aiming to unravel the genetic component of rare and complex disorders. While in rare disorders this allowed the identification of novel caus
Externí odkaz:
https://doaj.org/article/a5b135f4e56341478420eb0c8b20e8d2
Autor:
Georgia Malakasioti, Daniela Iancu, Anastasiia Milovanova, Alexey Tsygin, Tomoko Horinouchi, China Nagano, Kandai Nozu, Koichi Kamei, Shuichiro Fujinaga, Kazumoto Iijima, Rajiv Sinha, Biswanath Basu, William Morello, Giovanni Montini, Aoife Waters, Olivia Boyer, Zeynep Yürük Yıldırım, Sibel Yel, İsmail Dursun, Hugh J. McCarthy, Marina Vivarelli, Larisa Prikhodina, Martine T.P. Besouw, Eugene Yu-hin Chan, Wenyan Huang, Markus J. Kemper, Sebastian Loos, Chanel Prestidge, William Wong, Galia Zlatanova, Rasmus Ehren, Lutz T. Weber, Hassib Chehade, Nakysa Hooman, Marcin Tkaczyk, Małgorzata Stańczyk, Michael Miligkos, Kjell Tullus
Publikováno v:
Kidney International, 103(5), 962-972. ELSEVIER SCIENCE INC
While 44-83% of children with steroid-resistant nephrotic syndrome (SRNS) without a proven genetic cause respond to treatment with a calcineurin inhibitor (CNI), current guidelines recommend against the use of immunosuppression in monogenic SRNS. Thi
Autor:
Zainab Arslan, Hazel Webb, Emma Ashton, Becky Foxler, Kjell Tullus, Aoife Waters, Detlef Bockenhauer
Publikováno v:
Pediatric Nephrology. 38:1051-1056
Primary steroid resistant nephrotic syndrome (SRNS) is thought to have either genetic or immune-mediated aetiology. Knowing which children to screen for genetic causes can be difficult. Several studies have described the prevalence of genetic causes
Autor:
Chang Woo Lee, Ashleigh Ivy, Brittany Brownlee, Mohammed Bahgat, Aoife Waters, Lakhbinder Pabla, Claire Mclarnon, Gerard Siou, Steven Powell
Background: There is an increasing importance to increasing the day-case rate for children undergoing adenotonsillectomy. The primary aim of this study was to evaluate the immediate post-operative complication (IPOC) rate of children undergoing adeno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c446d174856d0ae97a152ee83e7aa712
https://doi.org/10.22541/au.167463375.50299313/v1
https://doi.org/10.22541/au.167463375.50299313/v1
Autor:
Aoife Waters, Mathieu Lemaire
Publikováno v:
Pediatric Kidney Disease ISBN: 9783031116643
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8dfe9e6cc6b2b5f64b495e67cd03d94b
https://doi.org/10.1007/978-3-031-11665-0_4
https://doi.org/10.1007/978-3-031-11665-0_4
Autor:
Aoife Waters
Publikováno v:
Pediatric Kidney Disease ISBN: 9783031116643
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6358b90e6a5dfd173b4060fb4da95f87
https://doi.org/10.1007/978-3-031-11665-0_6
https://doi.org/10.1007/978-3-031-11665-0_6
Autor:
Jelena, Stojanovic, Anna, Adamusiak, Aoife, Waters, Neil J, Sebire, Nicos, Kessaris, Nizam, Mamode, Stephen D, Marks
Publikováno v:
Pediatric nephrology (Berlin, Germany). 36(10)
A 3-year-old girl with clinical features of atypical HUS (complement Factor I mutation inherited from an asymptomatic mother and Factor H autoantibodies) was treated with plasma exchange, progressed to kidney failure (KF) aged 4 years, and received a
Publikováno v:
Pediatric nephrology (Berlin, Germany). 37(7)
Long-term steroid treatment in children is known to cause obesity and negatively affect growth. The objective of this study was to determine the prevalence of obesity and overweight and analyze linear growth in children with nephrotic syndrome.The st