MD Tülin Tiraje Celkan is 28 year expert in Pediatric Hematology-Oncology . Currently after 28 year in Istanbul University Cerrahpasa Medical Faculty, she is working in Vadi Liv Hospital and also İstinye University. She was graduated from Istanbul University Medical Faculty in 1986. She completed her residency in Anadolu University in Eskisehir in 1991. For obligatory service she was in Şanlıurfa and Viranşehir between 1991-1994. Finally she began her fellowship program at Cerrahpasa Faculty december 1994, appointed as associate professor in 2003, and professor in 2009. She visited Amsterdam V...
MD Tülin Tiraje Celkan is 28 year expert in Pediatric Hematology-Oncology . Currently after 28 year in Istanbul University Cerrahpasa Medical Faculty, she is working in Vadi Liv Hospital and also İstinye University. She was graduated from Istanbul University Medical Faculty in 1986. She completed her residency in Anadolu University in Eskisehir in 1991. For obligatory service she was in Şanlıurfa and Viranşehir between 1991-1994. Finally she began her fellowship program at Cerrahpasa Faculty december 1994, appointed as associate professor in 2003, and professor in 2009. She visited Amsterdam Vu universty as a clinical observer in 1998. She was especially interested in different kind of bleeding and anemic patients and also leukemic and childdhood cancer patients. She has the largest patient cohort of plasminogen deficiency in the world. She has a large patient cohort of pediatric hemangiomas and AVM .
Articles
PTEN and AKT1 Variations in Childhood T-Cell Acute Lymphoblastic Leukemia
, 2020
Use of hyperbaric oxygen therapy of purpura fulminans in an extremely low birth weight preterm: A case report
, 2020
Safety of dabigatran etexilate for the secondary prevention of venous thromboembolism in children
, 2020
Adrenal masses in children: Imaging, surgical treatment and outcome
, 2020
Hepatosplenic Fungal Infections in Children With Leukemia. Risk Factors and Outcome: A Multicentric Study
, 2019
Cross-sectional study: long term follow-up care for pediatric cancer survivors in a developing country, Turkey: current status, challenges, and future perspectives
, 2020
Telemedicine Applications in a Tertiary Pediatric Hospital in Turkey During COVID-19 Pandemic
, 2021
Prognostic and clinical significance of expressions of P53, ERBB2, c-Kit and BCL2 in childhood medulloblastoma
, 2019
Congenital macrothrombocytopenia: is it misdiagnosed?
, 2018
High TUBB2A expression in childhood T-ALL is correlated with the clinical outcome
, 2020
Coagulation Disturbances in Patients with Argininemia
, 2018
Cross-sectional study: long term follow-up care for pediatric cancer survivors in a developing country, Turkey: current status, challenges, and future perspectives
, 2020
Evaluation of Alpha Thalassemia Mutations in Cases with Hypochromic Microcytic Anemia The İstanbul Perspective
, 2014
Telemedicine Applications in a Tertiary Pediatric Hospital in Turkey During COVID-19 Pandemic
, 2021
OUTCOMES OF ELTROMBOPAG TREATMENT AND DEVELOPMENT OF IRON DEFICIENCY IN CHILDREN WITH IMMUNE THROMBOCYTOPENIA IN TURKEY
, 2020
Adrenal masses in children: Imaging, surgical treatment and outcome
, 2020
Juvenile Myelomonocytic Leukemia in Turkey: A Retrospective Analysis of Sixty-five Patients
, 2018
Sirolimus Experience in Blue Rubber Bleb Nevus Syndrome
, 2018
Homozygous protein C deficiency presenting as neonatal purpura fulminans: management with fresh frozen plasma, low molecular weight heparin and protein C concentrate
, 2018
Five year old girl with tongue bleeding
, 2017
Ekstremite Yerleşimli Büyük Vasküler Anomaliler ve Seyri
, 2020
Wernicke s encephalopathy in a child with acute lymphoblastic leukemia
, 2016
Treatment of plasminogen deficiency patients with fresh frozen plasma.
, 2018
Adrenal masses in children: Imaging, surgical treatment and outcome
, 2020
Hemogram bize neler söyler?
, 2020
Comparison of outcomes of children with acute lymphoblastic leukemia treated with BMF protocol across 2 decades
, 2020
High TUBB2A expression in childhood T-ALL is correlated with the clinical outcome
, 2020
Outcomes of eltrombopag treatment and development of iron deficiency in children with immune thrombocytopenia in Turkey İmmün trombositopenili çocuk hastalarda eltrombopag tedavisi ve tedaviye bağlı demir eksikliği
, 2020
Use of hyperbaric oxygen therapy of purpura fulminans in an extremely low birth weight preterm: A case report
, 2020
A novel combined treatment for plasminogen deficiency with lung involvement
, 2019
Accidental High Dose Intrathecal Treatment - Late Result of A Patient
, 2019
PTEN and AKT1 Variations in Childhood T-cell Acute Lymphoblastic Leukemia
, 2020
Posterior Reversible Encephalopathy Syndrome in Childhood Hematological/Oncological Diseases
, 2020
Frequency of ALK and GD2 Expression in Neuroblastoma
, 2019
Adrenal masses in children: Imaging, surgical treatment and outcome
, 2019
PTEN and AKT1 Variations in Childhood T-cell Acute Lymphoblastic Leukemia
, 2019
Association of the TLR4 and NOD2 Polymorphisms with Childhood Acute Lymphoblastic Leukemia
, 2018
All-Trans Retinoic Acid, Interferon-α and Zoledronic Acid (Zometa) in the Treatment of a Patient with Resistant Metastatic Osteosarcoma
, 2008
Homozygous c.130–131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry
, 2019
Posterior reversible encephalopathy syndrome in children with acute lymphoblastic leukemia: Experience of a single center using BFM protocols.
, 2019
Carney Complex: Unusual Presentation
, 2019
Langerhans Cell Histiocytosis: Single Center Experience of 25 Years.
, 2019
Accidental High Dose Intrathecal Treatment - Late Result of A Patient
, 2019
Ligneous gingivitis: Hard to diagnose and treat
, 2019
A novel combined treatment for plasminogen deficiency with lung involvement
, 2019
Pediatric Stroke
, 2019
Carney Complex: Unusual Presentation
, 2019
Use of a High-Purity Factor X Concentrate in Turkish Subjects with Hereditary Factor X Deficiency: Post Hoc Cohort Subanalysis of a Phase 3 Study
, 2018
Thrombosis in children: which test to whom, when and how much necessary?
, 2018
THE ANEMIA OF FAMILIAL MEDITERRANEAN FEVER DISEASE
, 2005
Juvenile Myelomonocytic Leukemia in Turkey: A Retrospective Analysis of 65 Patients
, 2017
Coagulation Disturbances in Patients with Argininemia
, 2018
Plasminogen deficiency
, 2017
Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency
, 2016
Hemoglobin H Disease In Turkey Experience From Eight Center
, 1900
The Association of TLR4 and NOD2 Polymorphisms with Childhood Acute Lymphoblastic Leukemia
, 2017
Prenatal unilateral cerebellar hypoplasia diagnosed as PHACE syndrome
, 2016
Pharmacokinetics of a high purity plasma derived factor X concentrate in subjects with moderate or severe hereditary factor X deficiency
, 2016
Efficacy safety and pharmacokinetics of a new high purity factor X concentrate in subjects with hereditary factor X deficiency
, 2016
Febrile neutropenia in children with acute lymphoblastic leukemia single center experience
, 2016
Syntaxin 11 is expressed in primary human monocytesmacrophages and acts as a negative regulator of macrophage engulfment of apoptotic cells and IgG opsonized target cells
, 2008
NAD P H quinone oxidoreductase 1 null genotype is not associated with pediatric de novo acute leukemia
, 2004
Coagulation factor activity and clinical bleeding severity in rare bleeding disorders results from the European Network of Rare Bleeding Disorders
, 2012
Approach to the patient with neutropenia in childhood
, 2015
A possible role for WNT5A hypermethylation in Pediatric Acute Lymphoblastic Leukemia
, 2015
Cytopenia associated with iron deficiency anemia and iron therapy A report of two cases
, 2011
Novel use of propranolol for management of pain in children with vertebral hemangioma report of two cases
, 2013
The difference between pre B cell acute lymphoblastic leukemia and Burkitt lymphoma in relation to DNA damage repair gene polymorphisms in childhood
, 2015
Childhood mastocytosis results of a single center
, 2015
The Role of Epstein Barr Virus LMP 1 Immunohistochemical Staining in Childhood Hodgkin Lymphoma
, 2015
Prognostic significance of NOTCH1 and FBXW7 mutations in pediatric T ALL
, 2010
A 17 year experience with ALL BFM protocol in acute lymphoblastic leukemia Prognostic predictors and interruptions during protocol
, 2014
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
, 2006
CONTROL OF BLEEDING ASSOCIATED WITH HEMOPHAGOCYTIC SYNDROME IN CHILDREN An Audit of the Clinical use of Recombinant Activated Factor VII
, 2007
Prevalence of Anemia and the Risk Factors Among Schoolchildren in Istanbul
, 2005
DNA repair gene XPD and XRCC1 polymorphisms and the risk of febrile neutropenia and mucositis in children with leukemia and lymphoma
, 2012
Tropisetron Navoban R in the Control of Nausea and Vomiting Induced by Combined Cancer Chemotherapy in Children
, 1999
Toxic Epidermal Necrolysis After the Use of High Dose Cytosine Arabinoside
, 2001
Thiamine responsive megaloblastic anemia early diagnosis may be effective in preventing deafnes
, 2009
Fatal Trichoderma harzianum infection in a leukemic pediatric patient
, 2009
Bacteremia in Childhood Cancer
, 2002
Is Familial Mediterranean Fever a thrombotic disease or not
, 2008
Late Effects of Childhood ALL Treatment on Body Mass Index and Serum Leptin Levels
, 2010
Radiological features in paediatric primary gastric MALT lymphoma and association with Helicobacter pylori
, 2002
Malignancy associated hemophagocytic lymphohistiocytosis in pediatric cases a multicenter study from Turkey
, 2009
Blue Rubber Bleb Nevus Syndrome Associated with Consumption Coagulopathy Treatment with Interferon
, 2004
Retinoblastoma in Turkey survival and clinical characteristics 1981â 2004
, 2006
Antibody Titers and Immune Response to Diphtheria Tetanus Pertussis and Measles Mumps Rubella Vaccination in Children Treated for Acute Lymphoblastic Leukemia
, 2005
DNA repair gene XPD and XRCC1 polymorphisms and the risk of childhood acute lymphoblastic leukemia
, 2009
Osseous presentation of Hodgkin s disease a case report and review of the literature
, 2007
Reports
IKZF1 Deletions at Diagnose and Relapse of Childhood B-ALL - ERBİLGİN YÜCEL,FIRTINA SİNEM,HATIRNAZ NG Özden,CELKAN TÜLİN TIRAJE,KARAKAŞ ZEYNEP,ANAK SENİYE SEMA,SARPER NAZAN,ZENGİN EMİNE,EŞKAZAN AHMET EMRE,SAYİTOĞLU MÜGE,ÖZBEK UĞUR
T-akut lenfoblastik lösemi (T-ALL) Hastalarında Yüksek TUBB2A Gen Anlatımı ve siRNA Aracılı Modülasyonu - Khodzhaev Khusan,HATIRNAZ NG ÖZDEN,TUĞCU DENİZ,Ng Yuk Yin,ERBİLGİN YÜCEL,CELKAN TÜLİN TIRAJE,KARAMAN SERAP,SARPER NAZAN,Aydoğan Gönül,Timur Çetin,SAYİTOĞLU MÜGE
Determination of Zinc Finger Protein 384 (ZNF384) Gene Fusion in Childhood Acute Lymphoblastic Leukemia Patients - Sudutan Tuğçe, ERBİLGİN YÜCEL, HATIRNAZ NG ÖZDEN, KARAKAŞ ZEYNEP, SARPER NAZAN, CELKAN TÜLİN TIRAJE, TİMUR ÇETİN, Aydoğan Gönül, SAYİTOĞLU MÜGE
IKZF1 Deletions at Diagnose and Relapse of Childhood B-ALL - ERBİLGİN YÜCEL,Fırtına Sinem,HATIRNAZ NG ÖZDEN,CELKAN TÜLİN TIRAJE,KARAKAŞ ZEYNEP,ANAK SENİYE SEMA,ZENGİN EMİNE,SARPER NAZAN,Eşkazan Emre,SAYİTOĞLU MÜGE,ÖZBEK UĞUR
Pharmacokinetic-guided prophylaxis based on bayesian model with myPKFiT (R) in hemophilia A: Turkish experience - BALKAN CAN,ALBAYRAK CANAN,özbek namık,KAYA ZÜHRE,şsşmaz ilgen,CELKAN TÜLİN TIRAJE,KARAMAN SERAP,kavaklı kaan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - ALBAYRAK CANAN,kavaklı kaan,ar cem,albayrak davut,CELKAN TÜLİN TIRAJE,timur çetin,BAŞLAR ZAFER,hande çağlayan
Haemophilia A genotype-phenotype analysis in Turkey - albayarak canan,kavaklı kaan,özbek namık,CELKAN TÜLİN TIRAJE,ar cem,çağlayan hande
Haemophilia A genotype-phenotype analysis in Turkey - albayarak canan,kavaklı kaan,özbek namık,CELKAN TÜLİN TIRAJE,ar cem,çağlayan hande
Haemophilia A genotype-phenotype analysis in Turkey - albayarak canan,kavaklı kaan,özbek namık,CELKAN TÜLİN TIRAJE,ar cem,çağlayan hande
Pharmacokinetic-guided prophylaxis based on bayesian model with my PKFİT in hemophilia A: Turkish experience - BALKAN CAN,ALBAYRAK CANAN,ÖZBEK NAMUK YAŞAR,KAYA ZÜHRE,ŞAŞMAZ HATİCE İLGEN,CELKAN TÜLİN TIRAJE,YAĞCI M,KARAMAN SERAP,ERDURAN EROL,ŞAHİN FAHRİ,ÖZDEMİR GN,PATIROĞLU TÜRKAN,OYMAK YEŞİM,TÜRKKAN EMİNE,SEZGİN EVİM MELİKE,GÜLEN H,AY Y,OKAN V,AKSU S,İLERİ DİLBER TALİA,ANDIÇ N,YILMAZ B,ALBAYRAK D,ÖREN HALE,KÜPESİZ OSMAN ALPHAN,ZENGİN EMİNE,SÖKER MURAT,AR C,KAVAKLI RAMAZAN KAAN
Bilateral Wilms tümörü tedavi sonuçları çok merkezli çalışma - KEBUDİ REJİN,TUĞCU DENİZ,AKICI FERHAN,CELKAN TÜLİN TIRAJE,VURAL SEMA,TOKUÇ AYŞE GÜLNUR,AYDOĞAN GÖNÜL,KARAKAŞ ZEYNEP,ZÜLFİKAR OSMAN BÜLENT,BÜYÜKKAPU BAY SEMA,İRİBAŞ AYÇA,GÜN SOYSAL FERYAL,ADALETLİ İBRAHİM,KURUĞOĞLU SEBUH,BİLGİÇ MEBRURE BİLGE,DARENDELİLER MEHMET EMİN
CENTRAL NERVOUS SYSTEM FUNGAL INFECTIONS IN CHILDREN WITH LEUKEMIA:RISK FACTORS AND OUTCOME: A MULTICENTRIC STUDY - KARAMAN SERAP,KEBUDİ REJİN,KIZILOCAK HANDE,KARAKAŞ ZEYNEP,SEZGİN EVİM MELİKE,KAYA ZÜHRE,YARALI NEŞE,ÇALIŞKAN ÜMRAN,ŞAHİN KARAGÜN BARBAROS,YILMAZ ŞEBNEM,YILMAZ KARAPINAR DENİZ,ÜNAL EKREM,MERAL GÜNEŞ ADALET,KOÇAK ÜLKER,CELKAN TÜLİN TIRAJE
Lösemi ve Kemik İliği Nakli Yapılan Olgularda Santral Sinir Sistemi Fungal Enfeksiyonla - KARAMAN SERAP,KEBUDİ REJİN,KIZILOCAK HANDE,KARAKAŞ ZEYNEP,SEZGİN EVİM MELİKE,KAYA ZÜHRE,YARALI NEŞE,ÇALIŞKAN ÜMRAN,YILMAZ ŞEBNEM,YILMAZ KARAPINAR DENİZ,ÜNAL EKREM,MERAL GÜNEŞ ADALET,GÜZELKÜÇÜK ZELİHA,KOÇAK ÜLKER,CELKAN TÜLİN TIRAJE
DESMOID TYPE FIBROMATOSIS OF MANDIBLE: ACASE REPORT - KUZU ŞEHRİ BURCU,TEVETOĞLU FIRAT,YENER HAYDAR MURAT,CELKAN TÜLİN TIRAJE,ADA RECEP MEHMET
Yenidoğanın nadir bir tümörü: özofagogastrik bölgeden kaynaklanan teratom - özcan rahşan,şenol emre,KURUĞOĞLU SEBUH,TÜTÜNCÜ AYŞE ÇİĞDEM,CELKAN TÜLİN TIRAJE,TEKANT GONCA AYŞE
JUVENILE MYELOMONOCYTIC LEUKEMIA IN TURKEY: A RETROSPECTIVE ANALYSIS OF 65 PATIENT. - TÜFEKÇİ ÖZLEM,KOÇAK ÜLKER,KAYA ZÜHRE,YENİCESU İDİL,ALBAYRAK CANAN,ALBAYRAK DAVUT,BENGOA ŞEBNEM,PATIROĞLU TÜRKAN,karakükçü musa,ÜNAL EKREM,ünal ince elif,İLERİ DİLBER TALİA,ERTEM MEHMET,CELKAN TÜLİN TIRAJE,ÖZDEMİR GÜL NİHAL,kaçar dilek,yaralı neşe,ÖZBEK NAMIK,KÜPESİZ OSMAN ALPHAN,karapınar tuba,VERGİN CANAN,ÇALIŞKAN ÜMRAN,TOKGÖZ HÜSEYİN,SEZGİN Evim Melike,BAYTAN BİROL,GÜNEŞ ADALET MERAL,YILMAZ KARAPINAR DENİZ,KARAMAN SERAP,UYGUN VEDAT,KARASU GÜLSÜN,YEŞİLİPEK MEHMET AKİF,KOÇ AHMET,ERDURAN EROL,ATABAY BERNA,ÖNİZ HALDUN,ÖREN HALE
PTEN AND AKT1 GENE VARIATIONS IN CHILDHOODT-ALL PATIENTS - Küçükcankurt Fulya,HATIRNAZ NG ÖZDEN,ERBİLGİN YÜCEL,ÖZBEK UĞUR,KARAKAŞ ZEYNEP,CELKAN TÜLİN TIRAJE,SAYİTOĞLU MÜGE
Juvenile Myelomonocytic Leukemia in Turkey: A Retrospective Analysis of 65 Patient - TÜFEKÇİ ÖZLEM,KOÇAK ÜLKER,KAYA ZÜHRE,YENİCESU İDİL,ALBAYRAK CANAN,ALBAYRAK DAVUT,BENGOA ŞEBNEM,PATIROĞLU TÜRKAN,KARAKÜKCÜ MUSA,ÜNAL EKREM,İNCE EU,İLERİ DİLBER TALİA,ERTEM MEHMET,CELKAN TÜLİN TIRAJE,ÖZDEMİR GÜL NİHAL,SARPER NAZAN,KAÇAR DE,YARALI NEŞE,ÖZBEK NAMIK,KÜPESİZ ALPHAN,KARAPINAR TE,VERGİN CANAN,ÇALIŞKAN ÜMRAN,TOKGÖZ HÜSEYİN,SEZGİN EVİM MELİKE,BAYTAN BİROL,MERAL GÜNEŞ ADALET,YILMAZ KARAPINAR DENİZ,KARAMAN SERAP,UYGUN VEDAT,KARASU GÜLSÜN,YEŞİLİPEK MEHMET AKİF,KOÇ AHMET,ERDURAN EROL,ATABAY BERNA,ÖNİZ HALDUN,ÖREN HALE
Infection and Hemophagocytic Syndrome Single Center Experience - ÖZDEMİR GÜL NİHAL,KOÇ BEGÜM ŞİRİN,VAROL FATİH,CELKAN TÜLİN TIRAJE,APAK HİLMİ
Pituitary Stalk Thickening and Diabetes Insipidus Proceeding to Langerhans Cell Histiocytosis - KIZILOCAK KUMKUMOĞLU HANDE,ÖZDEMİR GÜL NİHAL,CELKAN TÜLİN TIRAJE
Hodgkin s Disease 1975 2012 Long Term Results of a Single Center - CELKAN TÜLİN TIRAJE,ÖZDEMİR GÜL NİHAL,akı hilal,APAK HİLMİ,ÖZKAN MUSTAFA ALP,metin hallaç,ADALETLİ İBRAHİM,özcan rahşan,ergen arzu,inci yıldız
Surgical Interventions In Patients With Factor VII Deficiency - KOÇ ŞENOL SAYİME BAŞAK,ÖZDEMİR GÜL NİHAL,CELKAN TÜLİN TIRAJE,ZÜLFİKAR OSMAN BÜLENT
Intracranial Bleeding In Patients With Factor Deficiencies - ÖZDEMİR GÜL NİHAL,CELKAN TÜLİN TIRAJE
CLINICAL MANIFESTATIONS AND TREATMENT OUTCOME OF FANCONI ANEMIA RESULTS OF A SINGLE CENTER - KOÇ ŞENOL SAYİME BAŞAK,ÖZDEMİR GÜL NİHAL,KOÇ BEGÜM ŞİRİN,DİKME GÜRCAN,APAK HİLMİ,CELKAN TÜLİN TIRAJE
CHRONIC IMMUNE THROMBOCYTOPENIA IN CHILDHOOD EVALUATION OF THE DATA OVER 30 YEARS BASED ON THE REVISED CRITERIA OF INTERNATIONAL WORKING GROUP - KOÇ BEGÜM ŞİRİN,ÖZDEMİR GÜL NİHAL,APAK HİLMİ,CELKAN TÜLİN TIRAJE,inci yıldız
LANGERHANS CELL HISTIOCYTOSIS ONE CENTER EXPERIENCE - ÖZDEMİR GÜL NİHAL,CELKAN TÜLİN TIRAJE,gülen tüysüz,APAK HİLMİ,ADALETLİ İBRAHİM,metin hallaç,hız murat,DERVİŞOĞLU SERGÜLEN,inci yıldız
MIFAMURTIDE L MTP PE IN CHILDREN WITH OSTEOSARCOMA THE TURKISH EXPERIENCE - KEBUDİ REJİN,neriman sarı,KANTAR MEHMET,ÇAKIR FATMA BETÜL,GÜLER ELİF,nur olgun,CELKAN TÜLİN TIRAJE,vural sema,GÖRGÜN ÖMER NAFİ HALİL,ÇETİNGÜL NAZAN,inci ilhan
OSTEONECROSIS A COMPLICATION OF TREATING CHILDHOOD CANCER A REPORT OF ZOLEDRONIC ACID THERAPY - CELKAN TÜLİN TIRAJE,ÖZDEMİR GÜL NİHAL,ADALETLİ İBRAHİM,BOTANLIOĞLU HÜSEYİN,KANTARCI FATİH
TWO CASES OF SYSTEMIC TROMBOSIS AS A COMPLICATION OF INTRAARTERIAL CHEMOTHERAPY FOR RETINOBLASTOMA - CELKAN TÜLİN TIRAJE,ÖZDEMİR GÜL NİHAL,KIZILKILIÇ OSMAN,SARICI AHMET MURAT
Books
çocuk hematolojionkolojide olgular – galenos
hematolojide destek tedaviler – galenos
çocuk hematolojide olgularla tromboz – galenos
çocuk hematolojide olgularla tromboz – galenos
Çocuk Hematolojide Olgularla tromboz – galenos
çocuk hematolojide olgularla tromboz – galenos
Kemik İliği Yetersizlikleri – creative commons
çocuk hematolojide olgularla tromboz – galenos
çocuk hematolojide olgularla tromboz – galenos
çocuk hematolojide olgularla tromboz – galenos
Çocuk Hematoloji-Onkolojide Olgular – GALENOS YAYINEVİ
çocuk hematoloji onkolojide olgular – galenos
çocuk hematoloji onkolojide olgular – galenos
çocuk hematoloji onkolojide olgular – galenos
çocuk hematoloji onkoloji olgular – galenos
çocuk hematoloji onkolojide olgular – galenos
çocuk hematoloji onkolojide olgular – galenos
çocuk hematoloji onkolojide olgular – galenos
çocuk hematoloji-onkolojide olgular – galenos
çocuk hematoloji onkolojide olgular – galenos
çocuk hematoloji-onkolojide olgular – galenos
çocuk hematoloji onkolojide olgular – galenos
çocuk hematoloji-onkolojide olgular – galenos
çocuk hematoloji onkolojide olgular – galenos
çocuk hematoloji onkolojide olgular – galenos
çocuk hematoloji-onkoloji olgular – galenos
çocuk hematoloji-onkoloji – galenos
çocuk hematoloji-onkoloji olgular – galenos
çocuk hematoloji- onkoloji olgular – galenos
ÇOCUK HEMATOLOİ-ONKOLOJİDE OLGULAR – GALENOS YAYINEVİ
Çocuk Hematoloji Onkolojide Olgular – Galenos Yayınevi
Çocuk Hematoloji Onkolojide Olgular – Galenos Yayın evi
Çocuk Hematoloji Onkolojide Olgular – Galenos Yayınevi
Çocukluk Çağı Lösemilerinin Geç Komplikasyonları – creative commons
pediatri – güneş tıp evi
pediatri – güneş tıp evi
LÖSEMİLER – galenoz
Pediatrinin Esasları – istanbul tıp kitapevleri
hematolog nadir hstalıklar – galenos
Awards
lenfoproliferatif hastalıklar serbest bildiri ödülü – 2007
