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Results: 1-10 |
Results: 10

Authors: Kapelushnik, J Shalev, H Schulman, H Moser, A Tamary, H
Citation: J. Kapelushnik et al., Upper airway obstruction-related sleep apnea in a child with thalassemia intermedia, J PED H ONC, 23(8), 2001, pp. 525-526

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

Authors: Shalev, H Mishori-Dery, A Kapelushnik, J Moser, A Sheffield, VC McClain, A Carmi, R
Citation: H. Shalev et al., Prenatal diagnosis of malignant osteopetrosis in Bedouin families by linkage analysis, PRENAT DIAG, 21(3), 2001, pp. 183-186

Authors: Landau, D Shalev, H Levy-Finer, G Polonsky, A Segev, Y Katchko, L
Citation: D. Landau et al., Familial hemolytic uremic syndrome associated with complement factor H deficiency, J PEDIAT, 138(3), 2001, pp. 412-417

Authors: Zdebska, E Golaszewska, E Fabijanska-Mitek, J Schachter, H Shalev, H Tamary, H Sandstrom, H Wahlin, A Koscielak, J
Citation: E. Zdebska et al., Glycoconjugate abnormalities in patients with congenital dyserythropoieticanaemia type I, II and III, BR J HAEM, 114(4), 2001, pp. 907-913

Authors: Landau, D Shalev, H Shulman, H Barki, Y Maor, E Zmora, E
Citation: D. Landau et al., Oligohydramnion, renal failure and no pulmonary hypoplasia in glomerulocystic kidney disease, PED NEPHROL, 14(4), 2000, pp. 319-321

Authors: Landau, D Tovbin, D Shalev, H
Citation: D. Landau et al., Pediatric urolithiasis in southern Israel: the role of uricosuria, PED NEPHROL, 14(12), 2000, pp. 1105-1110

Authors: Shalev, H Moser, A Kapelushnik, J Karplus, M Zucker, N Yaniv, I Tamary, H
Citation: H. Shalev et al., Congenital dyserythropoietic anemia type I presenting as persistent pulmonary hypertension of the newborn, J PEDIAT, 136(4), 2000, pp. 553-555

Authors: Tamary, H Shalev, H Pinsk, V Zoldan, M Zaizov, R
Citation: H. Tamary et al., No response to recombinant human erythropoietin therapy in patients with congenital dyserythropoietic anemia type I, PED HEM ONC, 16(2), 1999, pp. 165-168

Authors: Ying, LH Katz, Y Schlesinger, M Carmi, R Shalev, H Haider, N Beck, G Sheffield, VC Landau, D
Citation: Lh. Ying et al., Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome, AM J HU GEN, 65(6), 1999, pp. 1538-1546
Risultati: 1-10 |