Search Results - Karaca, Neslihan Edeer
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CD4(+)CD25(+)Foxp3(+) T regulatory cells, Th1 (CCR5, IL-2, IFN-γ) and Th2 (CCR4, IL-4, Il-13) type chemokine receptors and intracellular cytokines in children with common variable... by Kutukculer, Necil, Azarsiz, Elif, Aksu, Guzide, Karaca, Neslihan Edeer
Published 2015Text -
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Interleukin-1 receptor antagonist deficiency with a novel mutation; late onset and successful treatment with canakinumab: a case report by Ulusoy, Ezgi, Karaca, Neslihan Edeer, El-Shanti, Hatem, Kilicoglu, Erhan, Aksu, Guzide, Kutukculer, Necil
Published 2015Text -
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Recurrent infections, neurologic signs, low serum uric acid levels, and lymphopenia in childhood: Purine nucleoside phosphorylase deficiency, an emergency for infants by Kütükçüler, Necil, Bölük, Ezgi, Tökmeci, Nazan, Karaca, Neslihan Edeer, Azarsız, Elif, Aksu, Güzide, Aykut, Ayça
Published 2020Text -
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X-linked agammaglobulinemia: investigation of clinical and laboratory findings, novel gene mutations and prevention of infective complications in long-term follow-up by Yıldırım, İlke, Topyıldız, Ezgi, Güven Bilgin, Raziye Burcu, Aykut, Ayça, Durmaz, Asude, Karaca, Neslihan Edeer, Aksu, Guzide, Kutukculer, Necil
Published 2021Text -
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Granulomatous skin lesions, severe scrotal and lower limb edema due to mycobacterial infections in a child with complete IFN–γ receptor–1 deficiency by Karaca, Neslihan Edeer, Boisson-Dupuis, Stephanie, Aksu, Güzide, Bustamante, Jacinta, Kandiloglu, Gulsen, Ozsan, Nazan, Hekimgil, Mine, Casanova, Jean-Laurent, Kutukculer, Necil
Published 2012Text -
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Familial inheritance and screening of first-degree relatives in common variable immunodeficiency and immunoglobulin A deficiency patients by Karaca, Neslihan Edeer, Severcan, Ezgi Ulusoy, Bilgin, Burcu Guven, Azarsiz, Elif, Akarcan, Sanem, Gunaydın, Nursen Cigerci, Gulez, Nesrin, Genel, Ferah, Aksu, Guzide, Kutukculer, Necil
Published 2018Text -
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Early Diagnosis and Hematopoietic Stem Cell Transplantation for IL10R Deficiency Leading to Very Early-Onset Inflammatory Bowel Disease Are Essential in Familial Cases by Karaca, Neslihan Edeer, Aksu, Guzide, Ulusoy, Ezgi, Aksoylar, Serap, Gozmen, Salih, Genel, Ferah, Akarcan, Sanem, Gulez, Nesrin, Hirschmugl, Tatjana, Kansoy, Savas, Boztug, Kaan, Kutukculer, Necil
Published 2016Text -
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Human immune disorder associated with homozygous hypomorphic mutation affecting MALT1B splice variant by Kutukculer, Necil, Seeholzer, Thomas, O’Neill, Thomas J., Graß, Carina, Aykut, Ayca, Karaca, Neslihan Edeer, Durmaz, Asude, Cogulu, Ozgur, Aksu, Guzide, Gehring, Torben, Gewies, Andreas, Krappmann, Daniel
Published 2021Text -
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Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency by Kiykim, Ayca, Ogulur, Ismail, Dursun, Esra, Charbonnier, Louis Marie, Nain, Ercan, Cekic, Sukru, Dogruel, Dilek, Karaca, Neslihan Edeer, Cogurlu, Mujde Tuba, Bilir, Ozlem Arman, Cansever, Murat, Kapakli, Hasan, Baser, Dilek, Kasap, Nurhan, Kutlug, Seyhan, Altintas, Derya Ufuk, Al-Shaibi, Ahmad, Agrebi, Nourhen, Kara, Manolya, Guven, Ayla, Somer, Ayper, Aydogmus, Cigdem, Ayaz, Nuray Aktay, Metin, Ayse, Aydogan, Metin, Uncuoglu, Aysen, Patiroglu, Turkan, Yildiran, Alisan, Guner, Sukru Nail, Keles, Sevgi, Reisli, Ismail, Aksu, Guzide, Kutukculer, Necil, Kilic, Sara S., Yilmaz, Mustafa, Karakoc-Aydiner, Elif, Lo, Bernice, Ozen, Ahmet, Chatila, Talal A., Baris, Safa
Published 2019Text