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Results: 1-5 |
Results: 5

Authors: Ellis, SR Hulton, SA McKiernan, PJ de Goyet, JD Kelly, DA
Citation: Sr. Ellis et al., Combined liver-kidney transplantation for primary hyperoxaluria type 1 in young children, NEPH DIAL T, 16(2), 2001, pp. 348-354

Authors: Hulton, SA
Citation: Sa. Hulton, Evaluation of urinary tract calculi in children, ARCH DIS CH, 84(4), 2001, pp. 320-323

Authors: Smith, AN Skaug, J Choate, KA Nayir, A Bakkaloglu, A Ozen, S Hulton, SA Sanjad, SA Al-Sabban, EA Lifton, RP Scherer, SW Karet, FE
Citation: An. Smith et al., Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing, NAT GENET, 26(1), 2000, pp. 71-75

Authors: Karet, FE Finberg, KE Nelson, RD Nayir, A Mocan, H Sanjad, SA Rodriguez-Soriano, J Santos, F Cremers, CWRJ Di Pietro, A Hoffbrand, BI Winiarski, J Bakkaloglu, A Ozen, S Dusunsel, R Goodyer, P Hulton, SA Wu, DK Skvorak, AB Morton, CC Cunningham, MJ Jha, V Lifton, RP
Citation: Fe. Karet et al., Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubularacidosis with sensorineural deafness, NAT GENET, 21(1), 1999, pp. 84-90

Authors: Karet, FE Finberg, KE Nayir, A Bakkaloglu, A Ozen, S Hulton, SA Sanjad, SA Al-Sabban, EA Medina, JF Lifton, RP
Citation: Fe. Karet et al., Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34, AM J HU GEN, 65(6), 1999, pp. 1656-1665
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