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Results: 1-9 |
Results: 9
Intensive care and immediate follow-up of children after renal transplantation
Authors: Seikaly, MG Sanjad, SA
Citation: Mg. Seikaly et Sa. Sanjad, Intensive care and immediate follow-up of children after renal transplantation, TRANSPLAN P, 33(5), 2001, pp. 2821-2824
Renal tubular dysfunction following kidney transplantation: A prospective study in 31 children
Authors: Sanjad, SA Ibrahim, A Al Shorafa, S Al Abbad, A Khauli, RB Shaibani, KA Al Sabban, E
Citation: Sa. Sanjad et al., Renal tubular dysfunction following kidney transplantation: A prospective study in 31 children, TRANSPLAN P, 33(5), 2001, pp. 2830-2831
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
Bartter syndrome in a neonate: early treatment with indomethacin
Authors: Mourani, CC Sanjad, SA Akatcherian, CY
Citation: Cc. Mourani et al., Bartter syndrome in a neonate: early treatment with indomethacin, PED NEPHROL, 14(2), 2000, pp. 143-145
Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome 1q42-43
Authors: Kelly, TE Blanton, S Saif, R Sanjad, SA Sakati, NA
Citation: Te. Kelly et al., Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome 1q42-43, J MED GENET, 37(1), 2000, pp. 63-64
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
A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renalglycogenosis with Fanconi syndrome and low phosphorylase kinase activity
Authors: Burwinkel, B Sanjad, SA Al-Sabban, E Al-Abbad, A Kilimann, MW
Citation: B. Burwinkel et al., A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renalglycogenosis with Fanconi syndrome and low phosphorylase kinase activity, HUM GENET, 105(3), 1999, pp. 240-243
Primary hyperoxaluria type I: An underestimated cause of nephrocalcinosis and chronic renal failure in Saudi Arabian children
Authors: Sanjad, SA Al-Abbad, A Al-Sabban, E
Citation: Sa. Sanjad et al., Primary hyperoxaluria type I: An underestimated cause of nephrocalcinosis and chronic renal failure in Saudi Arabian children, ANN SAUDI M, 19(1), 1999, pp. 4-7
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: 1-9 |