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Results: 1-10 |
Results: 10

Authors: Leclerc, D Wu, Q Ellis, JR Goodyer, P Rozen, R
Citation: D. Leclerc et al., Is the SLC7A10 gene on chromosome 19 a candidate locus for cystinuria?, MOL GEN MET, 73(4), 2001, pp. 333-339

Authors: Langlois, V Geary, D Murray, L Champoux, S Hebert, D Goodyer, P
Citation: V. Langlois et al., Polyuria and proteinuria in cystinosis have no impact on renal transplantation - A report of the North American Pediatric Renal Transplant Cooperative Study (vol 15, pg 7, 2000), PED NEPHROL, 16(2), 2001, pp. 201-201

Authors: Goodyer, P Boutros, M Rozen, R
Citation: P. Goodyer et al., The molecular basis of cystinuria: An update, EXP NEPHROL, 8(3), 2000, pp. 123-127

Authors: Porteous, S Torban, E Cho, NP Cunliffe, H Chua, L McNoe, L Ward, T Souza, C Gus, P Giugliani, R Sato, T Yun, K Favor, J Sicotte, M Goodyer, P Eccles, M
Citation: S. Porteous et al., Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2(1Neu) +/- mutant mice, HUM MOL GEN, 9(1), 2000, pp. 1-11

Authors: Goodyer, P Langlois, V Geary, D Murray, L Champoux, S Hebert, D
Citation: P. Goodyer et al., Polyuria and proteinuria in cystinosis have no impact on renal transplantation - A report of the North American Pediatric Renal Transplant Cooperative Study, PED NEPHROL, 15(1-2), 2000, pp. 7-10

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: McGowan-Jordan, J Stoddard, K Podolsky, L Orrbine, E McLaine, P Town, M Goodyer, P MacKenzie, A Heick, H
Citation: J. Mcgowan-jordan et al., Molecular analysis of cystinosis: Probable Irish origin of the most commonFrench Canadian mutation, EUR J HUM G, 7(6), 1999, pp. 671-678

Authors: Blydt-Hansen, TD Tenenhouse, HS Goodyer, P
Citation: Td. Blydt-hansen et al., PHEX expression in parathyroid gland and parathyroid hormone dysregulationin X-linked hypophosphatemia, PED NEPHROL, 13(7), 1999, pp. 607-611

Authors: Rodd, C Goodyer, P
Citation: C. Rodd et P. Goodyer, Hypercalcemia of the newborn: etiology, evaluation, and management, PED NEPHROL, 13(6), 1999, pp. 542-547

Authors: Kim, J Prawitt, D Bardeesy, N Torban, E Vicaner, C Goodyer, P Zabel, B Pelletier, J
Citation: J. Kim et al., The Wilms' tumor suppressor gene (wt1) product regulates Dax-1 gene expression during gonadal differentiation, MOL CELL B, 19(3), 1999, pp. 2289-2299
Risultati: 1-10 |