Prof. Dr. Tülin Tıraje Celkan

Formation et spécialisation

• Lycée anatolien de Kadıköy, 1980
• Faculté de médecine d’Istanbul, 1986
• Université Anadolu — spécialisation en pédiatrie, 1986–1991
• Faculté de médecine de Cerrahpaşa, département de pédiatrie, unité d’hématologie et d’oncologie pédiatriques, janvier 1995–mai 2021

Expérience professionnelle

• Liv Hospital Ulus, 2021–Présent
• Faculté de médecine de Cerrahpaşa, unité d’hématologie et d’oncologie pédiatriques, 1995–2021
• Service public obligatoire dans les hôpitaux publics de Şanlıurfa et Viranşehir, 1991–1994
• Université VU — membre du corps enseignant invité, 1998

Adhésions professionnelles

• Société turque d’hématologie
• Société turque d’hématologie pédiatrique
• Société turque d’oncologie pédiatrique
• Société internationale d’oncologie pédiatrique (SIOP)
• SIOP Europe (SIOP-E)
• Association turque de pédiatrie
• Association médicale turque
• Association d’immunologie
• Association pour la protection des enfants malades

Prix et études sélectionnées

• Études de l’ADN dans les lymphomes de l’enfant — Prix de la meilleure étude sur le lymphome de la Société turque d’hématologie
• Suivi de patients atteints d’une tumeur de Wilms — Prix de la meilleure étude clinique de la Société turque d’oncologie pédiatrique
• Rôle des plaquettes dans la neutropénie fébrile — Prix de la meilleure présentation orale et étude de la Société turque d’hématologie pédiatrique

Recherche

• Études internationales sur les déficits rares en facteurs de coagulation
• Études internationales sur le déficit en plasminogène
• Direction de trois thèses sur les leucémies de l’enfant
• Direction de quatre thèses sur les anémies de l’enfant
• Direction de deux thèses sur les lymphomes de l’enfant
• 57 travaux de recherche

Publications et activités éditoriales

• Éditrice de deux ouvrages
• Éditrice adjointe de quatre publications
• Autrice de deux chapitres dans des ouvrages internationaux
• Autrice de chapitres dans de nombreux ouvrages
• 130 publications indexées dans PubMed
• Indicateur/citations Google Scholar : 2740

Publications scientifiques

• Zülfikar B, Koç B, Şahin F, et al. Retrospective analysis of hemophilia B in Turkey: identifying main characteristics and treatment options. Research and Practice in Thrombosis and Haemostasis. 2024;8(7):102588. DOI: 10.1016/j.rpth.2024.102588. PMID: 39582809.
• Erbilgin Y, Firtina S, Kirat E, Khodzhaev K, Karakas Z, Ünüvar A, Ocak S, Celkan TT, et al. Status of IKZF1 Deletions in Diagnose and Relapsed Pediatric B-ALL Patients. Biochemical Genetics. 2026;64(1):152–167. DOI: 10.1007/s10528-024-11018-7. PMID: 39786526.
• Kılınç b., Durmaz B., Özel S. Ç., ocak s., CELKAN T. T. A Novel MPIG6B Gene Variant Identified in a Patient with Congenital Thrombocytopenia from Türkiye. Turkish Journal of Hematology , vol.43, no.3, pp.294-295, 2026.
• KARAKAŞ H., Eroglu A. G., AKYEL N. G., Cig G., Adaletli I., Ozdemir G. N., et al. Can biomarkers predict myocardial iron overload in children with thalassemia major?. CARDIOLOGY IN THE YOUNG , vol.33, pp.2203-2208, 2023.
• EROĞLU A. G., ULUĞ N., KARAKAŞ H., Yuksel E. K., AKYEL N. G., Cig G., et al. Evaluation of left ventricular function and myocardial deformation in children with beta-thalassemia major by real-time three-dimensional (four-dimensional) and speckle tracking echocardiography. ECHOCARDIOGRAPHY-A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES , vol.39, no.10, pp.1307-1315, 2022.
• KOCAMIŞ B., Baser D., Akcam B., Danielson J., Eltan S. B., Haliloglu Y., et al. Evolution and long-term outcomes of combined immunodeficiency due to CARMIL2 deficiency. ALLERGY , vol.77, no.3, pp.1004-1019, 2022.
• Erbilgin Y., Ng O. H., Can I., Firtina S., Kucukcankurt F., Karaman S., et al. Prognostic evidence of LEF1 isoforms in childhood acute lymphoblastic leukemia. INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY , vol.43, no.5, pp.1093-1103, 2021.
• Kacar A. G., KILINÇ OKTAY B., Ozel S., OCAK S., GÜNEŞ N., ULUDAĞ ALKAYA D., et al. Neurofibromatosis Type 1 in Children: A Single-Center Experience. TURKISH ARCHIVES OF PEDIATRICS , vol.56, no.4, pp.339-343, 2021.
• Celkan T. T., Fenercioglu S., Kacar A. G. A Peculiar Disease in a Young Woman Wanting to Get Pregnant. TURKISH JOURNAL OF HEMATOLOGY , vol.38, no.4, pp.333-334, 2021.
• CELKAN T. T. What does a hemogram say to us?. TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.55, no.2, pp.103-116, 2020.
• Cakir A. D., TURAN H., CELKAN T. T., ÇOMUNOĞLU N., ERCAN O., EVLİYAOĞLU S. O. An Unusual Presentation of Carney Complex. JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.12, no.1, pp.117-121, 2020.
• CELKAN T. T., Sunamak E. Accidental High-dose Intrathecal Treatment: Late Results of a Patient. TURKISH JOURNAL OF HEMATOLOGY , vol.37, no.1, pp.64-65, 2020.
• Kucukcankurt F., Erbilgin Y., Firtina S., Ng O. H., Karakas Z., CELKAN T. T., et al. PTEN and AKT1 Variations in Childhood T-Cell Acute Lymphoblastic Leukemia. TURKISH JOURNAL OF HEMATOLOGY , vol.37, no.2, pp.98-103, 2020.
• Kain Z. E., Ozcan G. G., Ozcan R., Emre S., CELKAN T. T., Comunoglu N. Role of immunohistochemistry on differential diagnosis of paediatric renal tumours: expression of Cyclin D1, PTEN, PDGFR-alfa and Beta-catenin. VIRCHOWS ARCHIV , vol.475, 2019.
• Erbilgin Y., Firtina S., Mercan S., Ng O. H., Karaman S., Tasar O., et al. Prognostic gene alterations and clonal changes in childhood B-ALL. LEUKEMIA RESEARCH , vol.83, 2019.
• Albayrak C., Kavakli K., AR M. C., Albayrak D., KILINÇ Y., Baslar Z., et al. Haemophilia A genotype-phenotype analysis in Turkey. HAEMOPHILIA , vol.25, pp.63-64, 2019.
• Ocak S., ÖZKAN M. A., ÖZKAN F., Oz B., CELKAN T. T., APAK H. Prognostic and clinical significance of expressions of P53, ERBB2, c-Kit and BCL2 in childhood medulloblastoma. CUKUROVA MEDICAL JOURNAL , vol.44, no.1, pp.1-6, 2019.
• Özcan R., Karagöz A., Gökdemir E., Kendigelen P., Celkan T. T., Adaletli İ., et al. ÇOCUKLUK ÇAĞI TÜMÖRLERİNİN AKCİĞER METASTAZLARINA CERRAHİ YAKLAŞIM. ZEYNEP KAMİL TIP BÜLTENİ , vol.48, no.4, pp.131-134, 2017.
• Kavakli K., ZÜLFİKAR O. B., Ay Y., AYTAÇ S. A., CELKAN T. T., Salcioglu Z., et al. Turkish experience with low dose of immun tolerance treatment for inhibitor patients. JOURNAL OF THROMBOSIS AND HAEMOSTASIS , vol.14, pp.56, 2016.
• Celkan T. T., Özdemir N., Adaletli İ., Botanlioglu H., Kantarci F. OSTEONECROSIS : A COMPLICATION OF TREATING CHILDHOOD CANCER: A REPORT OF ZOLEDRONIC ACID THERAPY. PEDIATRIC BLOOD & CANCER , 2015.
• Karapinar D. Y., Patiroglu T., Metin A., Caliskan U., CELKAN T. T., YILMAZ B., et al. TURKISH NATIONAL SEVERE CONGENITAL NEUTROPENIA REGISTRY. HAEMATOLOGICA , vol.100, pp.11, 2015.
• Arcagök B. C., ÖZDEMİR G. N., Tekin A., ÖZCAN R., ELİÇEVİK M., ŞENYÜZ O. F., et al. Doğuştan afibrinojenemili hastada kendiliğinden gelis¸en dalak yırtılmas. Türk Pediatri Arşivi , vol.49, no.3, pp.247-249, 2014.
• Özdemir N., Çelik E., BAŞLAR Z., CELKAN T. T. A rare cause of thrombocyte dysfunction: Hermansky-pudlak syndrome Trombosit işlev bozukluǧunun nadir bir nedeni: Hermansky-pudlak sendromu. Turk Pediatri Arsivi , vol.49, no.2, pp.163-166, 2014.
• AKYAY A., Celkan T. T., ISKENDER G., TUKUN A., OGAN C., OLCAY L. Two Acute Myeloblastic Leukemia Cases Concomitant with Hemophagocytic Lymphohistiocytosis and Review of the Literature. ANNALS OF CLINICAL AND LABORATORY SCIENCE , vol.43, no.1, pp.85-90, 2013.
• Uzunaslan D., Saygin C., Gungor S., Hasiloglu Z., Ozdemir N., Celkan T. T. Novel use of propranolol for management of pain in children with vertebral hemangioma: report of two cases. CHILDS NERVOUS SYSTEM , vol.29, no.5, pp.855-860, 2013.
• Ercan T. E., Oztunc F., Celkan T., Bor M., Kizilkilic O., Vural M., et al. Macrocephaly-capillary malformation syndrome in a newborn with tetralogy of fallot and sagittal sinus thrombosis.. Journal of child neurology , vol.28, no.1, pp.115-9, 2013.
• Sayitoglu M., Erbilgin Y., Ng O. H., Yildiz I., Celkan T. T., Anak S., et al. Upregulation of T-Cell-Specific Transcription Factor Expression in Pediatric T-Cell Acute Lymphoblastic Leukemia (T-ALL). TURKISH JOURNAL OF HEMATOLOGY , vol.29, no.4, pp.325-333, 2012.
• Coskunpinar E., Anak S., Agaoglu L., Unuvar A., Devecioglu O., AYDOGAN G., et al. Analysis of Chromosomal Aberrations and FLT3 gene Mutations in Childhood Acute Myelogenous Leukemia Patients. TURKISH JOURNAL OF HEMATOLOGY , vol.29, no.3, pp.225-232, 2012.
• Ayhan A. C., Yildiz I., Yuzbasioglu S., Celkan T. T., Apak H., Ozkan A., et al. Erythrocyte membrane protein defects in hereditary spherocytosis patients in Turkish population. Hematology , vol.17, no.4, pp.232-236, 2012.
• Kutlubay B., Ozdemir G. N., Tuysuz G., Apak H., Celkan T. Glanzmann thrombasthenia: Cerrahpasa Medical Faculty experience. TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.47, no.2, pp.104-106, 2012.
• PASAOGLU H. E., OZYALVACLI G., AKCETIN T. A., BOZKURT E., ELTUTAR K., Celkan T. T. A case of ligneous conjunctivitis. TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.47, no.2, pp.130-133, 2012.
• peyvandi f., palla r., Menegatti M., Siboni S. M., halimeh s., faeser b., et al. Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders. JOURNAL OF THROMBOSIS AND HAEMOSTASIS , vol.10, no.4, pp.615-621, 2012.
• Celkan T. T. Changes in chilhood ITP treatment and follow-up in 2011. TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.47, no.1, pp.8-16, 2012.
• Fisgin T., BALKAN C., Celkan T. T., KILINÇ Y., TURKER M., TIMUR C., et al. Rare Coagulation Disorders: A Retrospective Analysis of 156 Patients in Turkey. TURKISH JOURNAL OF HEMATOLOGY , vol.29, no.1, pp.48-54, 2012.
• Firtina S., Sayitoglu M., Hatirnaz O., Erbilgin Y., Oztunc C., Cinar S., et al. Evaluation of PAX5 gene in the early stages of leukemic B cells in the childhood B cell acute lymphoblastic leukemia. LEUKEMIA RESEARCH , vol.36, no.1, pp.87-92, 2012.
• Ozdemir G. N., Celik E., Bulut M., Uludag D., Ozcan R., Celkan T. Circumcision in children with bleeding diathesis. TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.46, no.4, pp.313-317, 2011.
• Ozdemir N., Yurt A., TURKAN E., Celkan T. T. Non-Hodgkin's lymphoma in a hemophilic patient with a traumatic hematoma. TURKISH JOURNAL OF HEMATOLOGY , vol.28, no.3, pp.237-238, 2011.
• Celkan T. T., Özdemir N. Reduced early prophylaxis of children with haemophilia in a developing country, Turkey. HAEMOPHILIA , vol.17, no.5, 2011.
• Ozdemir N., Celkan T. T., Kebudi R., Bor M., Yildiz I. Cytopenia associated with iron deficiency anemia and iron therapy: A report of two cases. TURKISH JOURNAL OF HEMATOLOGY , vol.28, no.3, pp.243-244, 2011.
• Celkan T. T. Daily and every other day use of iron prophylaxis in the first year of life. TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.46, no.2, pp.184, 2011.
• Celkan T. T., Ozdemir N., Bilgi Z., Oktay G., Apak H., Yildiz I. The effect of acute lymphoblastic leukemia treatment on mean cell volume of erytrocytes in children Çocukluk çaǧi akut lenfoblastik lösemisinde tedavinin ortalama eritrosit hacimleri üzerine etkisi. Turk Pediatri Arsivi , vol.46, no.2, pp.133-136, 2011.
• Fisgin T., PATIROĞLU T., Ozdemir A., Celkan T. T., Caliskan U., Ertem M., et al. Clinical and laboratory data of primary hemophagocytic lymphohistiocytosis: A retrospective review of the Turkish Histiocyte Study Group. TURKISH JOURNAL OF HEMATOLOGY , vol.27, no.4, pp.257-262, 2010.
• ATAOGLU E., DURU N. S., Celkan T. T., CIVILIBAL M., YAVUZ S. C., ELEVLI M., et al. Spontaneous intracranial bleeding in a neonate with congenital afibrinogenemia. BLOOD COAGULATION & FIBRINOLYSIS , vol.21, no.6, pp.592-594, 2010.
• VURAL S., ERDEM E., KARAMAN S., Celkan T. T., POLAT N., Dogan O. Malignancy-associated hemophagocytosis in children. TURKISH JOURNAL OF HEMATOLOGY , vol.27, no.1, pp.49-50, 2010.
• Celkan T. T. Aplastic anemia presenting as hemophagocytic lymphohistiocytosis. TURKISH JOURNAL OF HEMATOLOGY , vol.27, no.1, pp.38-42, 2010.
• Baris S., Ozdil M., Topal N., Dogru O., Ozdemir N., Sever L., et al. Acute promyelocytic leukemia treated with idarubicin complicated by focal segmental glomerulosclerosis. Journal of Pediatric Hematology/Oncology , vol.32, no.2, 2010.
• Erbilgin Y., Sayitoglu M., Hatirnaz O., Dogru O., AKCAY A., Tuysuz G., et al. Prognostic significance of NOTCH1 and FBXW7 mutations in pediatric T-ALL. DISEASE MARKERS , vol.28, no.6, pp.353-360, 2010.
• Baris S., Celkan T. T., Batar B., Guven M., Ozdil M., Ozkan A., et al. Association between genetic polymorphism in DNA repair genes and risk of B-cell lymphoma. Pediatric Hematology and Oncology , vol.26, no.6, pp.467-472, 2009.
• Aydemir Z., Ozdemir N., Celik N., Celkan T. T. ALCALIGENES XYLOSOXIDANS BACTEREMIA IN A PATIENT WITH ACUTE LYMPHOBLASTIC LEUKEMIA. MIKROBIYOLOJI BULTENI , vol.43, no.3, pp.481-485, 2009.
• Celkan T. T. Hereditary spherocytosis. TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.44, pp.27-34, 2009.
• Celkan T. T., Toptan H. H., Dogru O. Spurious thrombocytopenia. TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.44, no.2, pp.73-74, 2009.
• ONAL H., Baris S., Ozdil M., Yesil G., Altun G., Ozyilmaz I., et al. Thiamine-responsive megaloblastic anemia: early diagnosis may be effective in preventing deafness. TURKISH JOURNAL OF PEDIATRICS , vol.51, no.3, pp.301-304, 2009.
• Celkan T. T., Berrak S., KAZANCI E., Ozyurek E., ÜNAL Ş., Ucar C., et al. Malignancy-associated hemophagocytic lymphohistiocytosis in pediatric cases: a multicenter study from Turkey. TURKISH JOURNAL OF PEDIATRICS , vol.51, no.3, pp.207-213, 2009.
• Kantarcioglu A. S., Celkan T. T., YUCEL A., Mikami Y., Kurugoglu S., Mitani H., et al. Fatal Trichoderma harzianum infection in a leukemic pediatric patient. MEDICAL MYCOLOGY , vol.47, no.2, pp.207-215, 2009.
• Apak H., Ekici B., ALBAYRAM S., Erginoz E., Celkan T., Ozkan A., et al. The impact of low dose methotrexate on cerebral complications in acute lymphoblastic leukemia treatment Akut lenfoblastik lösemi tedavisinde düşük dozda metotreksatin beyin komplikasyonlarina etkisi. Turk Pediatri Arsivi , vol.44, no.2, pp.62-67, 2009.
• DURU N. S., Celkan T. T., CIVILIBAL M., OZBEK N. O., Basak A. N., ELEVLI M. Coinheritance of sickle cell anemia and hereditary spherocytosis. PEDIATRIC BLOOD & CANCER , vol.51, no.4, pp.560-563, 2008.
• Zhang S., Ma D., Wang X., Celkan T. T., Nordenskjoeld M., henter J., et al. Syntaxin-11 is expressed in primary human monocytes/macrophages and acts as a negative regulator of macrophage engulfment of apoptotic cells and IgG-opsonized target cells. BRITISH JOURNAL OF HAEMATOLOGY , vol.142, no.3, pp.469-479, 2008.
• KARAMAN S., YILDIZ İ., ERCAN O., BOLAYIRLI İ. M., CELKAN T. T., APAK H., et al. Çocukluk Çağı ALL’sinde Tedaviye Bağlı Endokrin Geç Yan Etkisi Olarak Tiroid Fonksiyonlarının Değerlendirilmesi. Türk Çocuk Hematoloji Dergisi , vol.2, pp.28-32, 2008.
• Unuvar A., Kavakli K., Baytan B., KAZANCI E., SAYLI T., Oren H., et al. Low-dose immune tolerance induction for paediatric haemophilia patients with factor VIII inhibitors. HAEMOPHILIA , vol.14, no.2, pp.315-322, 2008.
• Celkan T. T., Guven M., Batar B., Alhaj S. The difference between pre-B cell acute lymphoblastic leukemia and Burkitt lymphoma in relation to DNA damage repair gene polymorphisms in childhood. LEUKEMIA & LYMPHOMA , vol.49, no.8, pp.1638-1640, 2008.
• Bryceson Y. T., rudd E., Zheng C., edner J., ma D., Wood S. M., et al. Defective cytotoxic lymphocyte degranulation in syntaxin-11-deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients. BLOOD , vol.110, no.6, pp.1906-1915, 2007.
• Doğru Ö., Celkan T. T., DEMİR T. Hematological and biochemical changes in volatile substance abusing street children in Istanbul. Turk J Hematol , vol.24, pp.52-56, 2007.
• KOESEOGLU R. D., SENAYLI A., BICAKCI U., ONUK-FILIZ N., SEZER T., Celkan T. T. Osseous presentation of Hodgkin's disease: a case report and review of the literature. TURKISH JOURNAL OF PEDIATRICS , vol.49, no.2, pp.218-222, 2007.
• Celkan T. T., ALHAJ S., CIVILIBAL M., Elicevik M. Control of bleeding associated with hemophagocytic syndrome in children: An audit of the clinical use of recombinant activated factor VII. PEDIATRIC HEMATOLOGY AND ONCOLOGY , vol.24, no.2, pp.117-121, 2007.
• Celkan T. T., OZKAN A., Apak H., YILDIZ I. Antiviral prophylaxis with continuous low dose acyclovir in childhood cancer. Leukemia and Lymphoma , vol.47, no.7, pp.1418-1420, 2006.
• BERBER E., Fidanci I. D., UN C., EL-MAARRI O., AKTUGLU G., GURGEY A., et al. Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N. HAEMOPHILIA , vol.12, no.4, pp.398-400, 2006.
• Celkan T. T., CELIK M., KASAPCOPUR O., OZKAN A., APAK H., OCAK S., et al. The anemia of familial Mediterranean fever disease. PEDIATRIC HEMATOLOGY AND ONCOLOGY , vol.22, no.8, pp.657-665, 2005.
• ERCAN T., SOYCAN L., APAK H., Celkan T. T., OZKAN A., AKDENIZLI E., et al. Antibody titers and immune response to diphtheria-tetanus-pertussis and measles-mumps-rubelia vaccination in children treated for acute lymphoblastic leukemia. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , vol.27, no.5, pp.273-277, 2005.
• KARAMAN S., CELKAN T. T., KURUĞOĞLU S., CANPOLAT A., KIYKIM E., ÖZKAN M. A., et al. Wilms Kemoterapisi ve Asit. Turkish Journal of Oncology , vol.20, no.2, pp.79-83, 2005.
• SIRMA S. Ö., AGAOGLU L., YILDIZ i., CAYLI D., HORGUSLUOGLU L., ANAK S., et al. NAD(P)H : quinone oxidoreductase 1 null genotype is not associated with pediatric de novo acute leukemia. PEDIATRIC BLOOD & CANCER , vol.43, no.5, pp.568-570, 2004.
• APAK H., Celkan T. T., OZKAN A., YILDIZ i., AYDEMIR E. H., OZDIL S., et al. Blue rubber bleb nevus syndrome associated with consumption coagulopathy: treatment with interferon. DERMATOLOGY , vol.208, no.4, pp.345-348, 2004.
• APAK H., Celkan T. T., OZKAN A., YUKSEL L., BILGI Z., YILDIZ i. Severe factor X deficiency treated with heparin-added prothrombin complex concentrate. ANNALS OF HEMATOLOGY , vol.82, no.11, pp.710-711, 2003.
• Celkan T. T., OZKAN A., APAK H., DIREN S., Can G., YUKSEL L., et al. Bacteremia in childhood cancer. JOURNAL OF TROPICAL PEDIATRICS , vol.48, no.6, pp.373-377, 2002.
• Kurugoglu S., Mihmanli I., Celkan T. T., Aki H., Aksoy H., Korman U. Radiological features in paediatric primary gastric MALT lymphoma and association with Helicobacter pylori. Pediatric Radiology , vol.32, no.2, pp.82-87, 2002.
• OZKAN A., APAK H., Celkan T. T., YUKSEL L., YILDIZ i. Toxic epidermal necrolysis after the use of high-dose cytosine arabinoside. PEDIATRIC DERMATOLOGY , vol.18, no.1, pp.38-40, 2001.

Communications scientifiques

• FIRTINA S., ERBİLGİN Y., TAŞAR O., MERCAN S., HATIRNAZ N. Ö., şişko s., et al. Çocukluk Çağı B-All Hastalarında Tanı Ve Nüks Anındaki Moleküler Değişimlerin Dinamiği. 43. Ulusal hematoloji kongresi, Turkey, 1 - 04 November 2017,.
• HATIRNAZ N. Ö., FIRTINA S., AKGÜN E., TAKA E., ERBİLGİN Y., CELKAN T. T., et al. Çocukluk Çağı B-All Gelişiminde Kanonik Olmayan Wnt Yolağı Prognoz ve Sağ Kalım İle İlişkili Olabilir. 43. Ulusal hematoloji kongresi, Turkey, 1 - 04 November 2017,.
• ERBİLGİN Y., FIRTINA S., khodzhaev k., HATIRNAZ N. Ö., KARAKAŞ Z., CELKAN T. T., et al. Çocukluk Çağı B-ALL Hastalarında IKZF1 Delesyonlarının Araştırılması. 43. Ulusal hematoloji kongresi, Turkey, 1 - 04 November 2017,.
• Şahin H., KURU R. D., ÇIRAKOĞLU A., YILMAZ Ş., ARGÜDEN Y., AR M. C., et al. Down Sendromu hastalarında görülen hematolojik malignitelerin retrospektif olarak değerlendirilmesi. XV.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 26 - 29 October 2017, pp.343,.
• ERBİLGİN Y., işlek b., FIRTINA S., HATIRNAZ N. Ö., İNAL A., DOĞAN P., et al. Gene-expression patterns in relapsed B-cell acute lymphoblastic leukemia and potential therapeutic targets. ESHG, 21 - 24 May 2016,.
• ERBİLGİN Y., FIRTINA S., HATIRNAZ N. Ö., KARAKAŞ Z., CELKAN T. T., SARPER N., et al. Prognostic significance of IKZF1 deletions in Childhood B-ALL. 10th Biennal of Childhood Leukemia Symposium, 24 April 2016,.
• ERBİLGİN Y., HATIRNAZ N. Ö., FIRTINA S., CELKAN T. T., ANAK S. S., KARAKAŞ Z., et al. Çocukluk Çağı Nüks Akut Lösemide Genom Boyu Metilasyon Analizleri. 40. Ulusal Hematoloji Kongresi, Turkey, 22 - 25 October 2014,.
• KÜÇÜKCANKURT F., ERBİLGİN Y., CAN İ., HATIRNAZ N. Ö., MERCAN S., şişko s., et al. Pediatrik ALL Hastalarında LEF1 Mutasyon Analizi. 40. Ulusal Hematoloji Kongresi, Turkey, 22 - 25 October 2014,.
• ÖZDEMİR G., CELKAN T. T., İSKELELİ M. G., KAFADAR A. Lignöz konjonktivit:Tip 1 plazminojen eksikliği:2 olgu sunumu.. 7.Ulusal Pediatrik Hematoloji Kongresi, Ankara, Turkey, 24 - 27 June 2014, pp.55,.
• ERBİLGİN Y., HATIRNAZ N. Ö., FIRTINA S., CELKAN T. T., ANAK S. S., KARAKAŞ Z., et al. Epigenetic profile of early relapsed Childhood ALL. European Society of Human Genetics, 31 May - 03 June 2014,.
• PEHLİVAN E., CANPOLAT N., ÇALIŞKAN S., SEVER F. L., CELKAN T. T. Adjusting The Dose of LMWH in Thrombosis of The Patients with Nephrological Disorders. 7th Annual Congress of the European Association for Hemophilia and Allied Disorders, Brussels, Belgium, 26 - 28 February 2014, vol.20, pp.18-91,.
• FIRTINA S., ERBİLGİN Y., HATIRNAZ N. Ö., CAN İ., KARAKAŞ Z., CELKAN T. T., et al. Derin Dizi Analizi ile Pediatrik Akut Lenfoblastik Lösemi Hastalarında TP53 Gen Mutasyonlarının Saptanması ve Prognostik Önemi. 39. Ulusal Hematoloji Kongresi, Turkey, 23 - 26 October 2013,.
• ERBİLGİN Y., HATIRNAZ N. Ö., FIRTINA S., CELKAN T. T., ANAK S. S., KARAKAŞ Z., et al. Çocuk Çağı Nüks Akut Lösemi Hastalarının Genetik ve Epigenetik Karakterizasyonu. 39. Ulusal Hematoloji Kongresi, Turkey, 23 - 26 October 2013,.
• ERBİLGİN Y., HATIRNAZ N. Ö., FIRTINA S., CELKAN T. T., ANAK S. S., KARAKAŞ Z., et al. Whole genome methylation profile of relapsed childhood leukemia, Translating Epigenomes into Function: a Next-Generation Challenge for Human Disease. FEBS Workshop, 13 - 16 October 2013,.
• ERBİLGİN Y., HATIRNAZ N. Ö., CELKAN T. T., FIRTINA S., CAN İ., ÜNÜVAR A., et al. Çocukluk Çağı Nüks ALL Hastalarında Tüm Genom SNP Array Analizi. 9. Ulusal Pediatrik Hematoloji Kongresi, Turkey, 24 - 28 May 2013,.
• FIRTINA S., CAN İ., HATIRNAZ N. Ö., ERBİLGİN Y., KARAKAŞ Z., CELKAN T. T., et al. Yeni nesil dizileme yöntemi ile tanı ve nüks akut lösemi hastalarında Tp53 Mutasyonlarının araştırılması. 9. Ulusal Pediatrik Hematoloji Kongresi, Turkey, 24 - 28 May 2013,.
• CANPOLAT N., SEVER F. L., CELKAN T. T., LAÇİNEL GÜRLEVİK S., TAŞDEMİR M., KESER A., et al. Enoxaparin Dosing in Pediatric Hemodialysis Patients. 50th ERA-EDTA Congress, İstanbul, Turkey, 18 - 21 May 2013, vol.28, pp.519,.
• TAŞAR O., FIRTINA S., CELKAN T. T., ANAK S. S., aydoğan g., DEVECİOĞLU Ö., et al. B Hücreli Akut Lenfoblastik Lösemide WNT Ligand-Reseptör Aktivasyonu. 38. Türk Hematoloji Derneği, Turkey, 31 October - 03 November 2012,.
• FIRTINA S., ERBİLGİN Y., HATIRNAZ N. Ö., AĞAOĞLU L., CELKAN T. T., ÖZGÜVEN A. A., et al. Çocukluk Çağı B-ALL Hastalarında WNT sinyal İleti Yolağının İncelenmesi. 38. Türk Hematoloji Derneği, Turkey, 31 October - 03 November 2012,.
• ERBİLGİN Y., SAYİTOĞLU M., HATIRNAZ N. Ö., FIRTINA S., ÖZGÜVEN A. A., AĞAOĞLU L., et al. Çocukluk Çağı Nüks Akut Lösemi Hastalarında Tüm Genom Analizleri Ön Bulgular. 38. Ulusal Hematoloji Kongresi, Turkey, 31 October - 03 November 2012,.
• CAN İ., FIRTINA S., TATONYAN S., SAYİTOĞLU M., UZ B., CELKAN T. T., et al. LEF1 Geninin İzoformlarının Dengesi Hematolojik Malignitelerde Farklılık Gösteriyor ve Bu Farklılık Malignitelerin Patolojilerinde Önemli Rol Oynayabilir. 38. Türk Hematoloji Derneği, Turkey, 31 October - 03 November 2012,.
• FIRTINA S., SAYİTOĞLU M., HATIRNAZ N. Ö., ERBİLGİN Y., ÖZTUNÇ C., ÇINAR S., et al. Evaluation of PAX5 gene in the early stages of leukemic B cells in the childhood B cell acute lymphoblastic leukemia. Molecular Immunology Immunogenetics Congress, 27 - 29 April 2012,.
• GÜVEN M., Batar B., CELKAN T. T., Özdemir N., GÜVEN G., Yosunkaya E., et al. The role of glutathione S-transferase M1, T1 and P1 gene polymorphisms in susceptibility to childhood acute lymphoblastic leukemia. Joint International Conferance of the African and Southern African Societies of Human Genetics, Cape Town, South Africa, 6 - 09 March 2011, pp.111,.
• YILDIZ İ., KARAMAN S., ERCAN O., CELKAN T. T., APAK H., ÖZKAN A., et al. Late Effects of Childhood Acute Lymphoblastic Leukemia Treatment on Gonadal Function in Female Survivors. 38th Annual Conference of the International Society of Paediatric Oncology SIOP, Switzerland, pp.490,.
• KARAMAN S., ERCAN O., YILDIZ İ., CELKAN T. T., APAK H., ÖZKAN A., et al. Çocukluk Çağı ALL’sinde Tedaviye Bağlı Endokrin Geç Yan Etkilerden Vücut Kitle İndeksi(BMI) Leptin Düzeyleri ve Obezitenin Değerlendirilmesi. 6. Ulusal Pediatrik Hematoloji Kongresi, Bursa, Turkey, 22 - 26 May 2006, pp.113,.