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Ophthalmic Genetics|October 27, 2021
Ectopic vortex veins and varices in Donnai Barrow syndromeAisling Higham, Göran Darius Hildebrand, Katharine A J Graham-Evans, et al.
European Journal of Pediatrics|May 5, 2019
Tolvaptan use in children and adolescents with autosomal dominant polycystic kidney disease: rationale and design of a two-part, randomized, double-blind, placebo-controlled trialFranz Schaefer, Djalila Mekahli, Francesco Emma, et al.
Nephrology (Carlton, Vic.)|April 11, 2024
Characterization of patients with aHUS and associated triggers or clinical conditions: A Global aHUS Registry analysisChristoph Licht, Imad Al-Dakkak, Katerina Anokhina, et al.
BMC Nephrology|August 5, 2025
Demographics and baseline disease characteristics of UK patients within the global aHUS registryRodney D Gilbert, Imad Al-Dakkak, Clare Boothe, et al.
Pediatric Nephrology (Berlin, Germany)|November 4, 2015
Positive trends in paediatric renal biopsy service provision in the UK: a national survey and re-audit of paediatric renal biopsy practiceAsheeta Gupta, Joanna Campion-Smith, Wesley Hayes, et al.
The Journal of Pediatrics|July 24, 2007
Hemolytic uremic syndrome associated with invasive pneumococcal disease: the United kingdom experienceAoife M Waters, Larissa Kerecuk, David Luk, et al.
Kidney International|November 28, 2008
Mutations in phospholipase C epsilon 1 are not sufficient to cause diffuse mesangial sclerosisRodney D Gilbert, Claire L S Turner, Jane Gibson, et al.
Trials|April 29, 2014
Short course daily prednisolone therapy during an upper respiratory tract infection in children with relapsing steroid-sensitive nephrotic syndrome (PREDNOS 2): protocol for a randomised controlled trialNicholas J A Webb, Emma Frew, Elizabeth A Brettell, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 26, 2013
Simultaneous sequencing of 24 genes associated with steroid-resistant nephrotic syndromeHugh J McCarthy, Agnieszka Bierzynska, Matt Wherlock, et al.
American Journal of Human Genetics|April 9, 2013
Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylationBobby G Ng, Kati J Buckingham, Kimiyo Raymond, et al.
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