A selective IgA deficiency in a boy who presented recurrent parotitis von Akar, H H, Patıroglu, T, Duman, L

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Edoxaban for Thromboembolism Prevention in Pediatric Patients With Cardiac Disease von Portman, Michael A., Jacobs, Jeffrey P., Newburger, Jane W., Berger, Felix, Grosso, Michael A., Duggal, Anil, Tao, Ben, Goldenberg, Neil A., Brothers, Matthew, Marino, Bradley, Canter, Charles, Law, Mark, Nguyen, Nguyenvu, Sang, Charlie, Shimano, Kristin, Gupta, Dipankar, Portman, Michael, Williams, Derek, Glass, Lauren, Sperrazza, Charles, Herold, Steven, Garg, Ruchira, Vranicar, Mark, Awad, Sawsan, Asante-Korang, Alfred, Druzgal, Colleen, Ozment, Caroline, Del Toro, Kamill, Roses, Ferran, Jux, Christian, Gravenhorst, Verena, Schweigmann, Ulrich, Bhatt, Mihir, Sabapathy, Christine, Dahdah, Nagib, Bartonicek, Dototea, Tulzer, Gerald, Basargina, Elena, Zvereva, Tatiana, Pertels, Tatiana, Plotnikova, Irina, Pierre-Emmanuel, S.E.G.U.E.L.A., Amedro, Pascal, Yves, Dulac, BONNET, Damien, Saraco, Paola, Rimini, Alessandro, Digtiar, Valerii, Gonchar, Margaryta, Kryuchko, Tetyana, Yablon, Olga, Bedi, Varinder Singh, Patel, Jashvant, Mitra, Monjori, Kusa, Jacek, Domagala, Kowalczyk, KÖRNYEI, László, BERECZKI, Csaba, ABLONCZY, László, Levitas, Vivianne Aviva, Mishali, David, Revel-Vilk, Shoshana, Harlev, Dan, Sasmaz, Hatice Ilgen, Ozbek, Namik Yasar, Unal, Sule, Patıroglu, Türkan, Malbora, Baris, Agin, Hasan, Karakas, Zeynep, Kavakli, Ramazan Kaan, Chalmers, Elizabeth, Bu'Lock, Frances, Daubeney, Piers, Hamza, Hala, Badr, Mohamed, Elalfy, Mohsen, Mansour, Ahmed, Hassab, Hoda, Sabry, Ayman, Daou, Linda, Bitar, Fadi

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PB2024 A RARE CAUSE OF NEUTROPHIL FUNCTION DISORDER: THE MUTATION IN IKBKB GENE von Patıroglu, T., Gungor, H., Cansever, M., Unal, E., Klein, C.

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Four different NCF2 mutations in six families from Turkey and an overview of NCF2 gene mutations von Köker, M. Y., Sanal, Ö., Van Leeuwen, K., De Boer, M., Metin, A., Patıroğlu, T., Özgür, T. T., Tezcan, I., Roos, D.

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PB1860 A TURKISH CHILD PRESENTED WITH NEONATAL THROMBOCYTOPENIA ASSOCIATED WITH GNE MUTATION WITHOUT ASSOCIATED MUSCLE WASTING von Yilmaz, E., Ozcan, A., Verboon, J.M., Karakukcu, M., Sankaran, V.G., Unal, E., Patıroglu, T.

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PB2442 BRONCHOSCOPIC TREATMENT WITH FRESH FROZEN PLASMA AND TISSUE PLASMINOGEN ACTIVATOR FOR A CHILD WITH TYPE 1 PLASMINOGEN DEFICIENCY von Hangul, M., Tuzuner, A. B., Somekh, I., Klein, C., Patıroglu, T., Unal, E., Kose, M.

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PB1974 PYRUVATE KINASE DEFICIENCY IN FOUR CHILDREN WITH TWO UNPUBLISHED MUTATIONS von Unal, E., Gok, V., Roy, N.B.A., Hipkiss, R., Howard, K., Ozcan, A., Yilmaz, E., Karakukcu, M., Henderson, S., Patıroglu, T.

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PB1865 SINUS BRADYCARDIA AS A SIGN OF CENTRAL NERVOUS SYSTEM INVOLVEMENT IN A CHILD WITH GRISCELLI SYNDROME TYPE 2 von Kilic, O., Ay Tuncel, D., Gorkem, B.S., Ozcan, A., Akyol, S., Yuregir, O.O., Pamukcu, O., Unal, E., Karakukcu, M., Patıroglu, T.

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Chronic mucocutaneous candidiasis with agammaglobulinaemia von Patiroglu, T, Tahan, F

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Congenital IL-12R1B receptor deficiency and thrombophilia in a girl homozygous for an IL12RB1 mutation and compound heterozygous for MTFHR mutations: A case report and literature r... von Akar, H.H, Kose, M, Ceylan, O, Patiroglu, T, Bustamante, J, Casanova, J.L, Akyildiz, B.N, Doganay, S

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Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis von Walne, Amanda J, Collopy, Laura, Cardoso, Shirleny, Ellison, Alicia, Plagnol, Vincent, Albayrak, Canan, Albayrak, Davut, Kilic, Sara Sebnem, Patıroglu, Turkan, Akar, Haluk, Godfrey, Keith, Carter, Tina, Marafie, Makia, Vora, Ajay, Sundin, Mikael, Vulliamy, Thomas, Tummala, Hemanth, Dokal, Inderjeet

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Congenital IL-12R1β receptor deficiency and thrombophilia in a girl homozygous for an IL12RB1 mutation and compound heterozygous for MTFHR mutations: A case report and literature r... von Akar, H H, Kose, M, Ceylan, O, Patiroglu, T, Bustamante, J, Casanova, J L, Akyildiz, B N, Doganay, S

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Case Report. Acremonium falciforme fungemia in a patient with acute leukaemia von Nedret Koç, A., Erdem, Fatma, Patıroğlu, T.

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Antibody response to influenza A vaccination in children with nephrotic syndrome von Poyrazoglu, Hakan M., D s nsel, Ruhan, G nd z, Z beyde, Patiroglu, T rkan, K kl, Selmin

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DMP06 Have trisomy 21 babies more proteins in their cells' nuclei than those of controls? von Hamurcu, Z, Demirtas, H, Kumandas, S, Patiroglu, T

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A case of XMEN syndrome presented with severe auto-immune disorders mimicking autoimmune lymphoproliferative disease von Patiroglu, Turkan, Haluk Akar, H, Gilmour, Kimberly, Unal, Ekrem, Akif Ozdemir, M, Bibi, Shahnaz, Burns, Siobhan, Chiang, Samuel C, Schlums, Henrich, Bryceson, Yenan T, Karakukcu, Musa

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Heterotopic Bone Formation in Two Cases of Colon Carcinoma von Alper, M, Akyürek, N, Patiroğlu, T E, Yüksel, O, Belenli, O

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Lymphocytic hypophysitis in a patient with Graves' disease von BAYRAM, F, KELESTIMUR, F, ÖZTÜRK, F, SELCUKLU, A, PATIROGLU, T. E, BEYHAN, Z

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Plasma Soluble Human Leukocyte Antigen G Levels in Asthmatic Children von Tahan, Fulya, Patıroglu, Turkan

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Antifungal susceptibility testing of Candida albicans by flow cytometry von Gökahmetoglu, Selma, Nedret Koç, A, Patiroglu, T

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