Course of IL-2-inducible T-cell kinase deficiency in a family: lymphomatoid granulomatosis, lymphoma and allogeneic bone marrow transplantation in one sibling; and death in the oth... von Çağdaş, D, Erman, B, Hanoğlu, D, Tavil, B, Kuşkonmaz, B, Aydın, B, Akyüz, C, Uçkan, D, Sanal, Ö, Tezcan, İ

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Successful outcome with second hematopoietic stem cell transplantation in a patient with IL-10R deficiency von Kuşkonmaz, B, Ayvaz, D, Aydemir, Y, Erman, B, Tavil, B, Özen, H, Tezcan, İ, Çetinkaya, D U

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Six different CYBA mutations including three novel mutations in ten families from Turkey, resulting in autosomal recessive chronic granulomatous disease von Köker, M. Y., Van Leeuwen, K., De Boer, M., Çelmeli, F., Metin, A., Özgür, T. T., Tezcan, İ., Sanal, Ö., Roos, D.

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Mutations of chronic granulomatous disease in Turkish families von Köker, M. Y., Sanal, Ö., De Boer, M., Tezcan, İ., Metin, A., Ersoy, F., Roos, D.

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Bone marrow transplantation with Favorable outcome in three patients with LPS-responsive beige-like anchor (LRBA) deficiency von Okur, F.V., Kuskonmaz, B., Cagdas, D., Tezcan, I., Uckan-Cetinkaya, D.

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Investigation of Genetic Defects in Severe Combined Immunodeficiency Patients from Turkey by Targeted Sequencing von Erman, B., Bilic, I., Hirschmugl, T., Salzer, E., Boztug, H., Sanal, Ö., Çağdaş Ayvaz, D., Tezcan, I., Boztug, K.

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Clinical and genetic features of the patients with X‐Linked agammaglobulinemia from Turkey: Single‐centre experience von Esenboga, S., Cagdas, D., Ozgur, T. T., Gur Cetinkaya, P., Turkdemir, L. M., Sanal, O., VanDerBurg, M., Tezcan, I.

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A case report of RAS-associated autoimmune lymphoproliferative disorder von Coskun, C., Gumruk, F., Cemaloglu, M., Orhan, M., Tezcan, I., Unal, S.

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A Novel Homozygous Mutation With Different Clinical Presentations in 2 IRAK-4-Deficient Siblings: First Case With Recurrent Salmonellosis and Non-Hodgkin Lymphoma von Gokturk, B, Casanova, J L, Picard, C, Cagdas Ayvaz, D, Erman, B, Tezcan, I, Ozdemir, H, Ozel, A, Reisli, I

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Cernunnos deficiency: a case report von Turul, T, Tezcan, I, Sanal, O

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Life-threatening neurological complications after bone marrow transplantation in children von UCKAN, D, CETIN, M, YIGITKANLI, I, TEZCAN, I, TUNCER, M, KARASIMAV, D, OGUZ, K. K, TOPCU, M

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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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Naturally acquired hepatitis A antibodies after haematopoetic stem cell transplantation von YALÇIN, S. S., KONDOLOT, M., GÖKER, H., KUŞKONMAZ, B., KARACAN, Y., ÇETİN, M., AKSU, S., TEZCAN, İ., UÇKAN, D.

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Economic Burden of Primary Immunodeficiency (PIDD) In Turkey von Malhan, S, Ikinciogullari, A, Dogu, F, Kilic, S, Kutukculer, N, Reisli, İ, Tezcan, İ, Guner, NS, Cekic, S, Karaca, N, Oksuz, E

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PSY58 - Economic Burden of Primary Immunodeficiency (PIDD) In Turkey von Malhan, S, Ikinciogullari, A, Dogu, F, Kilic, S, Kutukculer, N, Reisli, İ, Tezcan, İ, Guner, NS, Cekic, S, Karaca, N, Oksuz, E

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Skewing of X-chromosome inactivation in three generations of carriers with X-linked chronic granulomatous disease within one family von Köker, M. Y., Sanal, Ö., De Boer, M., Tezcan, I., Metin, A., Tan, Ç., Ersoy, F., Roos, D.

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IAP038 Guillain-Barre syndrome in an immunocompromised patient with Wiscott-Aldrich syndrome von Ölmez, A, Turul, T, Tezcan, I, Turanli, G

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Congenital erythropoietic porphyria successfully treated by allogeneic bone marrow transplantation von TEZCAN, I, XU, W, DESNICK, R. J, GURGEY, A, TUNCER, M, CETIN, M, ÖNER, C, YETGIN, S, ERSOY, F, AIZENCANG, G, ASTRIN, K. H

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Impaired IgG antibody production to pneumococcal polysaccharides in patients with ataxia-telangiectasia von SANAL, O, ERSOY, F, ZEGERS, B. J. M, YEL, L, TEZCAN, I, METIN, A, ÖZYÜREK, H, GARIBOGLU, S, FIKRIG, S, BERKEL, A. I, RIJKERS, G. T

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Serum Zinc and Alkaline Phosphatase Values in Pediatric Bone Marrow Transplantation Patients von Uckan, D., Cetin, M., Dincer, N., Kalkan, G., Tuncer, M., Tezcan, I.

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