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Results: 1-9 |
Results: 9
Familial inheritance of crossed fused renal ectopia
Authors: Rinat, C Farkas, A Frishberg, Y
Citation: C. Rinat et al., Familial inheritance of crossed fused renal ectopia, PED NEPHROL, 16(3), 2001, pp. 269-270
Severe reversible renal failure doe to naproxen-associated acute interstitial nephritis
Authors: Becker-Cohen, R Frishberg, Y
Citation: R. Becker-cohen et Y. Frishberg, Severe reversible renal failure doe to naproxen-associated acute interstitial nephritis, EUR J PED, 160(5), 2001, pp. 293-295
Erythropoietin deficiency causes anemia in nephrotic children with normal kidney function
Authors: Feinstein, S Becker-Cohen, R Algur, N Raveh, D Shalev, H Shvil, Y Frishberg, Y
Citation: S. Feinstein et al., Erythropoietin deficiency causes anemia in nephrotic children with normal kidney function, AM J KIDNEY, 37(4), 2001, pp. 736-742
Kelley-Seegmiller syndrome due to a unique variant of hypoxanthine-guaninephosphoribosyltransferase: reduced affinity for 5-phosphoribosyl-1-pyrophosphate manifested only at low, physiological substrate concentrations
Authors: Zoref-Shani, E Feinstein, S Frishberg, Y Bromberg, Y Sperling, O
Citation: E. Zoref-shani et al., Kelley-Seegmiller syndrome due to a unique variant of hypoxanthine-guaninephosphoribosyltransferase: reduced affinity for 5-phosphoribosyl-1-pyrophosphate manifested only at low, physiological substrate concentrations, BBA-MOL BAS, 1500(2), 2000, pp. 197-203
The use of Luria's method for the neurobehavioral assessment of encephalopathy in an adolescent: Application in a rehabilitation setting
Authors: Guedalia, J Finkelstein, Y Drukker, A Frishberg, Y
Citation: J. Guedalia et al., The use of Luria's method for the neurobehavioral assessment of encephalopathy in an adolescent: Application in a rehabilitation setting, ARCH CLIN N, 15(2), 2000, pp. 177-184
Genetic polymorphism in paraoxonase is a risk factor for childhood focal segmental glomerulosclerosis
Authors: Frishberg, Y Toledano, H Becker-Cohen, R Feigin, E Halle, D
Citation: Y. Frishberg et al., Genetic polymorphism in paraoxonase is a risk factor for childhood focal segmental glomerulosclerosis, AM J KIDNEY, 36(6), 2000, pp. 1253-1261
Hypothyroidism in primary hyperoxaluria type 1
Authors: Frishberg, Y Feinstein, S Rinat, C Drukker, A
Citation: Y. Frishberg et al., Hypothyroidism in primary hyperoxaluria type 1, J PEDIAT, 136(2), 2000, pp. 255-257
Primary hyperoxaluria type I: A model for multiple mutations in a monogenic disease within a distinct ethnic group
Authors: Rinat, C Wanders, RJA Drukker, A Halle, D Frishberg, Y
Citation: C. Rinat et al., Primary hyperoxaluria type I: A model for multiple mutations in a monogenic disease within a distinct ethnic group, J AM S NEPH, 10(11), 1999, pp. 2352-2358
Refined mapping of the CSNU3 gene to a 1.8-Mb region on chromosome 19q13.1using historical recombinants in libyan Jewish cystinuria patients
Authors: Pras, E Pras, E Kreiss, Y Frishberg, Y Prosen, L Aksentijevich, I Kastner, DL
Citation: E. Pras et al., Refined mapping of the CSNU3 gene to a 1.8-Mb region on chromosome 19q13.1using historical recombinants in libyan Jewish cystinuria patients, GENOMICS, 60(2), 1999, pp. 248-250
Risultati: 1-9 |