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Results: 1-25/31
Authors:
Gok, F
Duzova, A
Baskin, E
Ozen, S
Besbas, N
Bakkaloglu, A
Citation: F. Gok et al., Comparative study of cefixime alone versus intramuscular ceftizoxime followed by cefixime in the treatment of urinary tract infections in children, J CHEMOTHER, 13(3), 2001, pp. 277-280
Authors:
Yilmaz, E
Ozen, S
Balci, B
Duzova, A
Topaloglu, R
Besbas, N
Saatci, U
Bakkaloglu, A
Ozguc, M
Citation: E. Yilmaz et al., Mutation frequency of Familial Mediterranean Fever and evidence for a highcarrier rate in the Turkish population, EUR J HUM G, 9(7), 2001, pp. 553-555
Authors:
Bakkaloglu, A
Citation: A. Bakkaloglu, Lupus nephropathy in children, NEPH DIAL T, 16, 2001, pp. 126-128
Authors:
Ozen, S
Usta, Y
Sahin-Erdemli, I
Orhan, D
Gumusel, B
Yang, B
Gursoy, Y
Tulunay, O
Dalkara, T
Bakkaloglu, A
El-Nahas, M
Citation: S. Ozen et al., Association of nitric oxide production and apoptosis in a model of experimental nephropathy, NEPH DIAL T, 16(1), 2001, pp. 32-38
Authors:
Duzova, A
Topaloglu, R
Sanal, O
Kilic, S
Mazza, C
Besbas, N
Bakkaloglu, A
Citation: A. Duzova et al., Henoch-Schonlein purpura in Wiskott-Aldrich syndrome, PED NEPHROL, 16(6), 2001, pp. 500-502
Authors:
Yetgin, S
Ozen, S
Yenicesu, I
Cetin, M
Bakkaloglu, A
Citation: S. Yetgin et al., Myelodysplastic features in polyarteritis nodosa, PED HEM ONC, 18(2), 2001, pp. 157-160
Authors:
Topaloglu, R
Akierli, C
Bakkaloglu, A
Aydintug, O
Ozen, S
Besbas, N
Ozcelik, T
Citation: R. Topaloglu et al., Survey of factor V Leiden and prothrombin gene mutations in systemic lupuserythematosus, CLIN RHEUMA, 20(4), 2001, pp. 259-261
Authors:
Besbas, N
Duzova, A
Topaloglu, R
Gok, F
Ozaltin, F
Ozen, S
Bakkaloglu, A
Citation: N. Besbas et al., Pulmonary haemorrhage in a 6-year-old boy with Henoch-Schonlein purpura, CLIN RHEUMA, 20(4), 2001, pp. 293-296
Authors:
Ozen, S
Uckan, D
Baskin, E
Besbas, N
Okur, H
Saatci, U
Bakkaloglu, A
Citation: S. Ozen et al., Increased neutrophil apoptosis during attacks of familial Mediterranean fever, CLIN EXP RH, 19(5), 2001, pp. S68-S71
Authors:
Ozaltin, F
Bakkaloglu, A
Orhon, M
Duzova, A
Irkec, M
Citation: F. Ozaltin et al., Bilateral uveitis in a 7-year-old patient with familial Mediterranean fever. An extremely rare complication, CLIN EXP RH, 19(5), 2001, pp. S80-S81
Authors:
Ozdogan, H
Ruperto, N
Kasapcopur, O
Bakkaloglu, A
Arisoy, N
Ozen, S
Ugurlu, U
Unsal, E
Melikoglu, A
Citation: H. Ozdogan et al., The Turkish version of the Childhood Health Assessment Questionnaire (CHAQ) and the Child Health Questionnaire (CHQ), CLIN EXP RH, 19(4), 2001, pp. S158-S162
Authors:
Emir, S
Kutluk, T
Topaloglu, R
Bakkaloglu, A
Buyukpamukcu, M
Citation: S. Emir et al., Scleroderma in a child after chemotherapy for cancer, CLIN EXP RH, 19(2), 2001, pp. 221-223
Authors:
Duzova, A
Bakkaloglu, A
Yuce, A
Ozen, S
Kocak, N
Citation: A. Duzova et al., Successful treatment of polyarteritis nodosa with interferon alpha in a nine-month old girl, EUR J PED, 160(8), 2001, pp. 519-520
Authors:
Topaloglu, R
Sungur, A
Baskin, E
Besbas, N
Saatci, U
Bakkaloglu, A
Citation: R. Topaloglu et al., Vascular endothelial growth factor in Henoch-Schonlein purpura, J RHEUMATOL, 28(10), 2001, pp. 2269-2273
Authors:
Ozen, S
Ben-Chetrit, E
Bakkaloglu, A
Gur, H
Tinaztepe, K
Calguneri, M
Turgan, C
Turkmen, A
Akpolat, I
Danaci, M
Besbas, N
Akpolat, T
Citation: S. Ozen et al., Polyarteritis nodosa in patients with Familial Mediterranean fever (FMF): A concomitant disease or a feature of FMF?, SEM ARTH RH, 30(4), 2001, pp. 281-287
Authors:
Bakkaloglu, A
Citation: A. Bakkaloglu, Effect of different rolling schedules on the mechanical properties and microstructure of X60 type HSLA steel, Z METALLKUN, 92(4), 2001, pp. 355-360
Authors:
Vencovsky, J
Jarosova, K
Ruzickova, S
Nemcova, D
Niederlova, J
Ozen, S
Alikasifoglu, M
Bakkaloglu, A
Ollier, WER
Mageed, RA
Citation: J. Vencovsky et al., Higher frequency of allele 2 of the interleukin-1 receptor antagonist genein patients with juvenile idiopathic arthritis, ARTH RHEUM, 44(10), 2001, pp. 2387-2391
Authors:
Bakkaloglu, A
Ozen, S
Baskin, E
Besbas, N
Gur-Guven, A
Kasapcopur, O
Tinaztepe, K
Citation: A. Bakkaloglu et al., The significance of antineutrophil cytoplasmic antibody in microscopic polyangitis and classic polyarteritis nodosa, ARCH DIS CH, 85(5), 2001, pp. 427-430
Authors:
Rossetti, S
Strmecki, L
Gamble, V
Burton, S
Sneddon, V
Peral, B
Roy, S
Bakkaloglu, A
Komel, R
Winearls, CG
Harris, PC
Citation: S. Rossetti et al., Mutation analysis of the entire PKD1 gene: Genetic and diagnostic implications, AM J HU GEN, 68(1), 2001, pp. 46-63
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
Authors:
Besbas, N
Ozen, S
Saatci, U
Topaloglu, R
Tinaztepe, K
Bakkaloglu, A
Citation: N. Besbas et al., Renal involvement in polyarteritis nodosa: evaluation of 26 Turkish children, PED NEPHROL, 14(4), 2000, pp. 325-327
Authors:
Topaloglu, R
Bakkaloglu, A
Slingsby, JH
Aydintug, O
Besbas, N
Saatci, U
Walport, MJ
Citation: R. Topaloglu et al., Survey of Turkish systemic lupus erythematosus patients for a particular mutation of C1Q deficiency, CLIN EXP RH, 18(1), 2000, pp. 75-77
Authors:
Ozen, S
Tinaztepe, K
Gucer, S
Bakkaloglu, A
Citation: S. Ozen et al., Nephrotic syndrome and arthritis in a 12-year-old girl, AM J KIDNEY, 36(1), 2000, pp. 220-224
Authors:
Yetgin, S
Ozen, S
Saatci, U
Bakkaloglu, A
Topaloglu, R
Yenicesu, I
Olcay, L
Okur, H
Karaagaoglu, E
Tuncer, M
Besbas, N
Citation: S. Yetgin et al., Evaluation of tumour necrosis factor alpha, interferon gamma and granulocyte-macrophage colony stimulating factor levels in juvenile chronic arthritis, RHEUMATOLOG, 38(5), 1999, pp. 468-471
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