Renal tubular function in children with tyrosinaemia type I treated with nitisinone von Santra, S., Preece, M. A., Hulton, S.-A., McKiernan, P. J.

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Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment von COCHAT, Pierre, HULTON, Sally-Anne, JAMIESON, Neville V, KEMPER, Markus J, MANDRILE, Giorgia, MARANGELLA, Martino, PICCA, Stefano, RUMSBY, Gill, SALIDO, Eduardo, STRAUB, Michael, WOERDEN, Christiaan S. Van, ACQUAVIVA, Cecile, DANPURE, Christopher J, DAUDON, Michel, DE MARCHI, Mario, FARGUE, Sonia, GROOTHOFF, Jaap, HARAMBAT, Jerome, HOPPE, Bernd

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Mutations in the gene encoding B1 subunit of H + -ATPase cause renal tubular acidosis with sensorineural deafness von Lifton, Richard P, Karet, Fiona E, Finberg, Karin E, Nelson, Raoul D, Nayir, Ahmet, Mocan, Hilal, Sanjad, Sami A, Rodriguez-Soriano, Juan, Santos, Fernando, Cremers, Cor W.R.J, Pietro, Antonio Di, Hoffbrand, Barry I, Winiarski, Jacek, Bakkaloglu, Aysin, Ozen, Seza, Dusunsel, Ruhan, Goodyer, Paul, Hulton, Sally A, Wu, Doris K, Skvorak, Anne B, Morton, Cynthia C, Cunningham, Michael J, Jha, Vivekanand

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Mutations in the Chloride-Bicarbonate Exchanger Gene AE1 Cause Autosomal Dominant but not Autosomal Recessive Distal Renal Tubular Acidosis von Karet, F. E., Gainza, F. J., Gyory, A. Z., Unwin, R. J., Wrong, O., Tanner, M. J. A., Nayir, A., Alpay, H., Santos, F., Hulton, S. A., Bakkaloglu, A., Ozen, S., Cunningham, M. J., Di Pietro, A., Walker, W. G., Lifton, R. P.

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Evaluation of urinary tract calculi in children von Hulton, S-A

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Antenatal diagnosis of fetal renal calculus von Rhodes, C., Churchill, D., Hulton, S.‐A.

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Localization of a Gene for Autosomal Recessive Distal Renal Tubular Acidosis with Normal Hearing ( rdRTA2 ) to 7q33-34 von Karet, Fiona E., Finberg, Karin E., Nayir, Ahmet, Bakkaloglu, Aysin, Ozen, Seza, Hulton, Sally A., Sanjad, Sami A., Al-Sabban, Essam A., Medina, Juan F., Lifton, Richard P.

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Mutations in ATP6N1B , encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing von Karet, Fiona E, Smith, Annabel N, Skaug, Jennifer, Choate, Keith A, Nayir, Ahmet, Bakkaloglu, Aysin, Ozen, Seza, Hulton, Sally A, Sanjad, Sami A, Al-Sabban, Essam A, Lifton, Richard P, Scherer, Stephen W

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Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss von Stover, E H, Borthwick, K J, Bavalia, C, Eady, N, Fritz, D M, Rungroj, N, Giersch, A B S, Morton, C C, Axon, P R, Akil, I, Al-Sabban, E A, Baguley, D M, Bianca, S, Bakkaloglu, A, Bircan, Z, Chauveau, D, Clermont, M-J, Guala, A, Hulton, S A, Kroes, H, Li Volti, G, Mir, S, Mocan, H, Nayir, A, Ozen, S, Rodriguez Soriano, J, Sanjad, S A, Tasic, V, Taylor, C M, Topaloglu, R, Smith, A N, Karet, F E

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Hypertension: a cause of growth impairment von DESHPANDE, P. V, GILBERT, R. D, WILLIAMS, J, HULTON, S. A, MILFORD, D. V

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Plasma oxalate and eGFR are correlated in primary hyperoxaluria patients with maintained kidney function—data from three placebo-controlled studies von Milliner, Dawn S., Cochat, Pierre, Hulton, Sally-Anne, Harambat, Jerome, Banos, Ana, Dehmel, Bastian, Lindner, Elisabeth

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Characteristics and Outcomes of Children with Primary Oxalosis Requiring Renal Replacement Therapy von Harambat, Jérôme, van Stralen, Karlijn J, Espinosa, Laura, Groothoff, Jaap W, Hulton, Sally-Anne, Cerkauskiene, Rimante, Schaefer, Franz, Verrina, Enrico, Jager, Kitty J, Cochat, Pierre

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Cyclosporin-related nephrotoxicity in children with nephrotic syndrome von Ganesan, V, Milford, D V, Taylor, C M, Hulton, S A, Parvaresh, S, Ramani, P

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Combined liver–kidney transplantation for primary hyperoxaluria type 1 in young children von Ellis, Sally R., Hulton, Sally‐Anne, McKiernan, Patrick J., de Ville de Goyet, Jean, Kelly, Deirdre A.

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Efficacy and safety of Oxalobacter formigenes to reduce urinary oxalate in primary hyperoxaluria von Hoppe, Bernd, Groothoff, Jaap W., Hulton, Sally-Anne, Cochat, Pierre, Niaudet, Patrick, Kemper, Markus J., Deschênes, George, Unwin, Robert, Milliner, Dawn

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Lymphocyte subpopulations, interleukin-2 and interleukin-2 receptor expression in childhood nephrotic syndrome von HULTON, S.-A, SHAH, S, BYRNE, M. R, MORGAN, G, BARRATT, T. M, DILLON, M. J

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The prevalence and treatment of end-stage renal disease in an Asian child population von MOGHAL, N. E, MILFORD, D. V, HULTON, S. A, TAYLOR, C. M

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A case of neonatal Bartter's syndrome von Wong, W, Hulton, S A, Taylor, C M, Raafat, F, Lote, C J, Lindop, G

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Vincristine and focal segmental sclerosis : do we need a multicentre trial? von GOONASEKERA, C. D. A, KOZIELL, A. B, HULTON, S. A, DILLON, M. J

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Urinary l-lactate excretion is increased in renal Fanconi syndrome von Thirumurugan, Arumugavelu, Thewles, Andrew, Gilbert, Rodney D., Hulton, Sally-Anne, Milford, David V., Lote, Christopher J., Taylor, C. Mark

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