Browsing by Author "Kiykim, Ayca"
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Correction to: primary antibody deficiencies in Turkey: molecular and clinical aspects
Fırtına, Sinem; Ng, Yuk Yin; Ng, Ozden H.; Kiykim, Ayca; Yücel Özek, Esra; Kara, Manolya; Kaya, Ayşenur (Springer, 2021)The original published version of this article contained a mistake in one of the affiliations. The correct affiliation of author Manolya Kara (7) should read: Istinye University Faculty of Medicine, VM MedicalPark Pendik ... -
Humoral and cellular immunity to SARS-COV-2 vaccination with BNT162B2 MRNA vaccine in pediatric kidney transplant and dialysis patients
Gulmez, Ruveyda; Ozbey, Dogukan; Agbas, Ayse; Aksu, Bagdagul; Yildiz, Nurdan; Uckardes, Diana; Saygili, Seha; Yildirim, Zeynep Yuruk; Tasdemir, Mehmet; Kiykim, Ayca; Cokugras, Haluk; Canpolat, Nur; Nayir, Ahmet; Kocazeybek, Bekir S.; Caliskan, Salim (Springer, 2022)Humoral And Cellular Immunity To Sars-Cov-2 Vaccination With Bnt162b2 Mrna Vaccine In Pediatric Kidney Transplant And Dialysis Patients -
ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patients
Eken, Ahmet; Cansever, Murat; Okus, Fatma Zehra; Erdem, Serife; Nain, Ercan; Azizoglu, Zehra Busra; Haliloglu, Yesim; Karakukcu, Musa; Ozcan, Alper; Devecioglu, Omer; Aksu, Guzide; Arikan Ayyildiz, Zeynep; Topal, Erdem; Karakoc Aydiner, Elif; Kiykim, Ayca; Metin, Ayse; Erol Cipe, Funda; Kaya, Aysenur; Artac, Hasibe; Reisli, Ismail; Guner, Sukru N.; Uygun, Vedat; Tezcan Karasu, Gulsun; Doenmez Altuntas, Hamiyet; Canatan, Halit; Oukka, Mohamed; Ozen, Ahmet; Chatila, Talal A.; Keles, Sevgi; Baris, Safa; Unal, Ekrem; Patiroglu, Turkan (Wiley, 2020)BackgroundDedicator of cytokinesis 8 (DOCK8) deficiency is the main cause of the autosomal recessive hyper-IgE syndrome (HIES). We previously reported the selective loss of group 3 innate lymphoid cell (ILC) number and ... -
Lymphoma predisposing gene in an extended family: CD70 signaling defect
Khodzhaev, Khusan; Bay, Sema Buyukkapu; Kebudi, Rejin; Altindirek, Didem; Kaya, Aysenur; Erbilgin, Yucel; Ng, Ozden Hatirnaz; Kiykim, Ayca; Erol Cipe, Funda; Sen Zengin, Feride; Firtina, Sinem; Ng, Yuk Yin; Aksoy, Basak Adakli; Sayitoglu, Muge (Springer/Plenum Publishers, 2020)Genome-wide sequencing studies in pediatric cancer cohorts indicate that about 10% of patients have germline mutations within cancer predisposition genes. Within this group, primary immune deficiencies take the priority ... -
Novel frameshift autosomal recessive loss-of-function mutation in SMARCD2 encoding a chromatin remodeling factor mediates granulopoiesis
Yucel, Esra Ozek; Karakus, Ibrahim Serhat; Krolo, Ana; Kiykim, Ayca; Heredia, Raul Jimenez; Tamay, Zeynep; Erol Cipe, Funda; Karakoc-Aydiner, Elif; Ozen, Ahmet; Karaman, Serap; Boztug, Kaan; Baris, Safa (2021)Purpose: Recently, a new form of congenital neutropenia that is caused by germline biallelic loss-of-function mutations in the SMARCD2 gene was described in four patients. Given the rarity of the condition, the clinical ... -
Primary antibody deficiencies in Turkey: molecular and clinical aspects
Fırtına, Sinem; Ng, Yuk Yin; Ng, Ozden H.; Kiykim, Ayca; Yucel Ozek, Esra; Kara, Manolya (Springer Link, 2021)Primary antibody deficiencies (PAD) are the most common subtype of primary immunodeficiencies, characterized by increased susceptibility to infections and autoimmunity, allergy, or malignancy predisposition. PAD syndromes ... -
A set of clinical and laboratory markers differentiates hyper-IgE syndrome from severe atopic dermatitis
Kasap, Nurhan; Celik. Velat; Isik, Sakine; Cennetoglu, Pakize; Kiykim, Ayca; Bilgic Eltan, Sevgi; Nain, Ercan; Ogulur, Ismail; Baser, Dilek; Akkelle, Emre; Celiksoy, Mehmet Halil; Kocamis, Burcu; Erol Cipe, Funda; Yucelten, Ayse Deniz; Karakoc Aydiner, Elif; Ozen, Ahmet; Baris, Safa (Elsevier Inc., 2021)Hyper-IgE syndrome (HIES) patients may share many features observed in severe atopic dermatitis (SAD), making a diagnostic dilemma for physicians. Determining clinical and laboratory markers that distinguish both disorders ...
