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Results: 1-8 |
Results: 8
Arterial changes in paediatric haemodialysis patients undergoing renal transplantation
Authors: Nayir, A Bilge, I Kilicaslan, I Ander, H Emre, S Sirin, A
Citation: A. Nayir et al., Arterial changes in paediatric haemodialysis patients undergoing renal transplantation, NEPH DIAL T, 16(10), 2001, pp. 2041-2047
Lupus nephritis in children: Prognostic significance of clinicopathological findings
Authors: Emre, S Bilge, I Sirin, A Kilicaslan, I Nayir, A Oktem, F Uysal, V
Citation: S. Emre et al., Lupus nephritis in children: Prognostic significance of clinicopathological findings, NEPHRON, 87(2), 2001, pp. 118-126
Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing
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
Hemostatic problems and thromboembolic complications in nephrotic children
Authors: Citak, A Emre, S Sirin, A Bilge, I Nayir, A
Citation: A. Citak et al., Hemostatic problems and thromboembolic complications in nephrotic children, PED NEPHROL, 14(2), 2000, pp. 138-142
Frequency of renal malformations in Turner syndrome: analysis of 82 Turkish children
Authors: Bilge, I Kayserili, H Emre, S Nayir, A Sirin, A Tukel, T Bas, F Kilic, G Basaran, S Gunoz, H Apak, M
Citation: I. Bilge et al., Frequency of renal malformations in Turner syndrome: analysis of 82 Turkish children, PED NEPHROL, 14(12), 2000, pp. 1111-1114
Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubularacidosis with sensorineural deafness
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
Endovascular treatment of arteriovenous fistulas complicating percutaneousrenal biopsy in three paediatric cases
Authors: Bilge, I Rozanes, I Acunas, B Minareci, O Nayir, A Oktem, F Tonguc, E Kozok, Y Emre, S Ander, H Sirin, A Poyanli, A
Citation: I. Bilge et al., Endovascular treatment of arteriovenous fistulas complicating percutaneousrenal biopsy in three paediatric cases, NEPH DIAL T, 14(11), 1999, pp. 2726-2730
Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34
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
Risultati: 1-8 |