The effect of iron deficiency anemia on the function of the immune system von Ekiz, Ceyda, Agaoglu, Leyla, Karakas, Zeynep, Gurel, Nuray, Yalcin, Işik

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Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency von Quartier, Pierre, Bustamante, Jacinta, Sanal, Ozden, Plebani, Alessandro, Debré, Marianne, Deville, Anne, Litzman, Jiri, Levy, Jacov, Fermand, Jean-Paul, Lane, Peter, Horneff, Gerd, Aksu, Guzide, Yalçin, Isik, Davies, Graham, Tezcan, Ilhan, Ersoy, Furgen, Catalan, Nadia, Imai, Kohsuhe, Fischer, Alain, Durandy, Anne

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Role of Mycoplasma pneumoniae and Chlamydia pneumoniae in Children with Community-Acquired Pneumonia in Istanbul, Turkey von Somer, Ayper, Salman, Nuran, Yalçın, Işık, Ağaçfidan, Ali

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Multiuser detection with neural network and PIC in CDMA systems for AWGN and Rayleigh fading asynchronous channels von Işık, Yalçın, Taşpınar, Necmi

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Neuro-Behçet disease presenting as secondary pseudotumor syndrome: Case report von Can, Emrah, Kara, Bülent, Somer, Ayper, Keser, Melike, Salman, Nuran, Yalçın, Işık

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Neuro-Behçet syndrome presentıng as acute meningeal syndrome von Kara, Bülent, Somer, Ayper, Pişkin, Sanem, Aydınlı, Nur, Salman, Nuran, Yalçın, Işık

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Multiuser detection with neural network MAI detector in CDMA systems for AWGN and rayleigh fading asynchronous channels von Taspinar, Necmi, Isik, Yalcin

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Sonographic assessment of ceftriaxone-associated biliary pseudolithiasis in children von Palanduz, Ayşe, Yalçın, Işık, Tonguç, Erdem, Güler, Nermin, Öneş, Ülker, Salman, Nuran, Somer, Ayper

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Serotype distribution and antibiotic susceptibility of invasive Streptococcus pneumoniae disease isolates from children in Turkey, 2001-2004 von YALCIN, Isik, GURLER, Nezahat, ALHAN, Emre, YAMAN, Akgün, TURGUT, Mehmet, CELIK, Ümit, AKCAKAYA, Necla, CAMCIOGLU, Yildiz, DIREN, Sukufe, YILDIRIM, Bülent

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Myofibroblastic tumors involving bilateral adrenal glands and skin in a patient with common variable immunodeficiency von Yalçın, Işık, Somer, Ayper, Akçay, Ahmet, Büyükbabani, Nesimi, Salman, Nuran, Güler, Nermin

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Investigation of mycotoxin residues in poultry feeds by LC MS/MS method von Nihayet Fadime, IŞIK, YALÇIN

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Presentation of Interleukin-12/-23 Receptor beta 1 Deficiency with Various Clinical Symptoms of Salmonella Infections von Sanal, Ozden, Turul, Tuba, Boer, Tijtske, Vosse, Esther Van De, Yalcin, Isik, Tezcan, Ilhan, Sun, Cagman, Memis, L, Ottenhoff, Tom HM, Ersoy, Fugen

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The Multi-User Detection in Code Division Multiple Access with Adaptive Neuro-Fuzzy Inference System von ISIK, Yalcin, TASPINAR, Necmi

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Presentation of Interleukin-12/-23 Receptor β1 Deficiency with Various Clinical Symptoms of Salmonella Infections von Sanal, Ozden, Turul, Tuba, De Boer, Tijtske, Vosse, Esther Van De, Yalcin, Işik, Tezcan, Ilhan, Sun, Cağman, Memis, L., Ottenhoff, Tom H. M., Ersoy, Fugen

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Spread of nontuberculous mycobacteria from 1993 to 2006 in Koreans von Ryoo, Sung Weon, Shin, Sonya, Shim, Myung-shup, Park, Yoon-Sung, Lew, Woo Jin, Park, Sue-Nie, Park, Young Kil, Kang, Seongman

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Relationship of Fibronectin to C-Reactive Protein, Ceruloplasmin, Alpha-1 Antitrypsin, and Transferrin in Septicemic Children von GÜLER, Nermin, ÖNES, Ülker, SALMAYENLI, Nihal, YALÇIN, Isik, SIVAS, Ahmet, SALMAN, Nuran

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Nasal carriage of methicillin-resistant Staphylococcus aureus in the children of hospital staff von Palanduz, Ayse, Guler, Nermin, Yalcn, Isk

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Presentation of Interleukin-12/-23 Receptor [beta]1 Deficiency with Various Clinical Symptoms of Salmonella Infections von Sanal, Ozden, Turul, Tuba, De Boer, Tijtske, Van De Vosse, Esther, Yalcin, Isik, Tezcan, Ilhan, Sun, Cagman, Memis, L, Ottenhoff, Tom H M, Ersoy, Fugen

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Presentation of interleukin-12/-23 receptor beta1 deficiency with various clinical symptoms of Salmonella infections von Sanal, Ozden, Turul, Tuba, De Boer, Tijtske, Van de Vosse, Esther, Yalcin, Işik, Tezcan, Ilhan, Sun, Cağman, Memis, L, Ottenhoff, Tom H M, Ersoy, Fugen

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Corrigendum to “Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency” [Clin... von Quartier, Pierre, Bustamante, Jacinta, Sanal, Ozden, Plebani, Alessandro, Debré, Marianne, Deville, Anne, Litzman, Jiri, Levy, Jacov, Fermand, Jean-Paul, Lane, Peter, Horneff, Gerd, Aksu, Guzide, Yalçin, Isik, Davies, Graham, Tezcan, Ilhan, Ersoy, Furgen, Catalan, Nadia, Imai, Kohsuhe, Fischer, Alain, Durandy, Anne

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