Eğitim Bilgileri
1989 - 1994
1989 - 1994Tıpta Yandal Uzmanlık
Hacettepe Üniversitesi, Çocuk Sağlığı Ve Hastalıkları Hematoloji Bilim Dalı, Türkiye
1981 - 1986
1981 - 1986Tıpta Uzmanlık
Hacettepe Üniversitesi, Çocuk Sağlığı Ve Hastalıkları, Türkiye
1975 - 1981
1975 - 1981Lisans
Hacettepe Üniversitesi, Tıp Fakültesi, Türkiye
Araştırma Alanları
Tıp
Sağlık Bilimleri
Dahili Tıp Bilimleri
Çocuk Sağlığı ve Hastalıkları
Pediatrik Hematoloji
Akademik Faaliyetlere Dayalı Araştırma Alanları
Avesis Araştırma Alanları
WoS Araştırma Alanları
Scopus Araştırma Alanları
Akademik Ünvanlar / Görevler
1981 - Devam Ediyor
1981 - Devam EdiyorProf. Dr.
Hacettepe Üniversitesi, Tıp Fakültesi (Türkçe), Dahili Tıp Bilimleri Bölümü
Yönetimsel Görevler
2016 - Devam Ediyor
2016 - Devam EdiyorBölüm Başkanı
Hacettepe Üniversitesi, Tıp Fakültesi
Akademi Dışı Deneyim
2001 - Devam Ediyor
2001 - Devam EdiyorProfesör
Hacettepe Üniversitesi, Profesör
Makaleler
2025
20251. Reply to Correspondence on "Retinal and Choroidal Circulation Impairments in Fanconi Anemia"
BEZCİ AYGÜN F., ALGEDİK TOKYÜREK M. Ö., Unal S., GÜMRÜK F., KADAYIFÇILAR S.
AMERICAN JOURNAL OF OPHTHALMOLOGY
, ss.259-260, 2025 (SCI-Expanded, Scopus)
2025
20252. Retinal and Choroidal Circulation Impairments in Fanconi Anemia
BEZCİ AYGÜN F., Tokyurek M. O. A., Unal S., GÜMRÜK F., KADAYIFÇILAR S.
AMERICAN JOURNAL OF OPHTHALMOLOGY
, ss.166-175, 2025 (SCI-Expanded, Scopus)
2025
20253. Etiologic spectrum and neurological outcomes in pediatric arterial ischemic stroke and cerebral sinovenous thrombosis: A 15-Year retrospective study at a tertiary hospital
BEKTAŞ H., GÖÇMEN R., Oguz K. K., Unal S., AYTAÇ EYÜPOĞLU Ş. S., Guemruek F., et al.
ACTA NEUROLOGICA BELGICA
, 2025 (SCI-Expanded, Scopus)
2024
20244. Alu-Mediated Deletion of FANCA in Turkish Families With Fanconi Anemia: Evidence of a Founder Effect
DURMAZ ÖZDİNÇ C. D., GÜMRÜK F., Celkan T., Unal S., ÇETİNKAYA A.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
, 2024 (SCI-Expanded, Scopus)
2024
20245. Associated Congenital Abnormalities and Physical Phenotype in Patients with Diamond-Blackfan Anemia May Be Overlooked
Soltanova G., ORAL N., GÜMRÜK F., ŞİMŞEK KİPER P. Ö., ÜNAL Ş.
TURKISH ARCHIVES OF PEDIATRICS
, cilt.59, sa.4, ss.364-369, 2024 (ESCI, Scopus, TRDizin)
2024
20246. Outcome of the Modified St. Jude Total XV Protocol in Turkish Children with Newly Diagnosed Acute Lymphoblastic Leukemia: A Single-Center Retrospective Analysis
YILMAZ H., AYTAÇ EYÜPOĞLU Ş. S., KUŞKONMAZ B. B., ÇETİNKAYA F. D., Unal S., GÜMRÜK F.
TURKISH JOURNAL OF HEMATOLOGY
, cilt.41, sa.3, ss.146-159, 2024 (SCI-Expanded, Scopus, TRDizin)
2024
20247. Single-center experience of four cases with iron-refractory iron deficiency anemia (IRIDA)
PARLAK KELEŞ G., Aksu M. D., GÜMRÜK F., ÜNAL Ş.
TURKISH JOURNAL OF PEDIATRICS
, cilt.66, sa.5, ss.658-665, 2024 (SCI-Expanded, Scopus, TRDizin)
2023
20238. Endocrine Disorders in Adult Beta-Thalassemia Patients: Insights from a Long-Term Follow-Up
Oğuz S. H., OKAY M., FEDAİ A. B., ÜNAL Ş., GÜMRÜK F., SAYINALP N., et al.
Endocrinology Research and Practice
, cilt.27, sa.4, ss.205-212, 2023 (Scopus, TRDizin)
2023
20239. A rare case of Klippel-Trenaunay syndrome presenting with chronic myeloid leukemia
COŞKUN Ç., AKSU T., GÜMRÜK F., ÜNAL Ş.
Turkish Journal of Pediatrics
, cilt.65, sa.1, ss.124-128, 2023 (SCI-Expanded, Scopus, TRDizin)
2022
202210. Oral health status of patients with inherited bone marrow failure syndromes
Ozler C. O., Mustuloglu S., Cemaloglu M., Dilek Turgut M., UZAMIŞ TEKÇİÇEK M., GÜMRÜK F., et al.
Pediatric Dental Journal
, cilt.32, sa.3, ss.151-159, 2022 (ESCI, Scopus)
2022
202211. First report of t(1;9)(q21;q34) in Fanconi anemia as a preceeding chromosomal aberration before leukemia development
BOZKURT S., ÜNAL Ş., GÜMRÜK F.
KUWAIT MEDICAL JOURNAL
, cilt.54, sa.1, ss.119-122, 2022 (SCI-Expanded)
2021
202112. Hematological involvement in pediatric systemic lupus erythematosus: A multi-center study
KAYA AKCA Ü., BATU AKAL E. D., PAÇ KISAARSLAN A., Poyrazoglu H., Ayaz N. A., Sozeri B., et al.
LUPUS
, cilt.30, sa.10, ss.1700-1708, 2021 (SCI-Expanded, Scopus)
2021
202113. Usage of Plasma Presepsin, C-Reactive Protein, Procalcitonin and Proadrenomedullin to Predict Bacteremia in Febril Neutropenia of Pediatric Hematological Malignancy Patients
Arikan K., Karadag-Oncel E., AYTAÇ EYÜPOĞLU Ş. S., ÇETİN M., CENGİZ A. B., GÜMRÜK F., et al.
LABORATORY MEDICINE
, cilt.52, sa.5, ss.477-484, 2021 (SCI-Expanded, Scopus)
2021
202114. Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy
Wong H. H., Seet S. H., Maier M., GÜREL A., Traspas R. M., Lee C., et al.
AMERICAN JOURNAL OF HUMAN GENETICS
, cilt.108, sa.7, ss.1301-1317, 2021 (SCI-Expanded, Scopus)
2021
202115. Hemophagocytosis in bone marrow aspirates in multisystem inflammatory syndrome in children
LAÇİNEL GÜRLEVİK S., AKSU T., ÖZEN S., KESİCİ S., GÜMRÜK F., ÖZSÜREKCİ Y.
PEDIATRIC BLOOD & CANCER
, cilt.68, sa.6, 2021 (SCI-Expanded, Scopus)
2021
202116. Proerythroblast Cells of Diamond-Blackfan Anemia Patients With RPS19 and CECR1 Mutations Have Similar Transcriptomic Signature
KARAOSMANOĞLU B., KURŞUNEL M. A., ÇETİNKAYA F. D., GÜMRÜK F., ESENDAĞLI G., ÜNAL Ş., et al.
FRONTIERS IN PHYSIOLOGY
, cilt.12, 2021 (SCI-Expanded, Scopus)
2021
202117. Transplacental hemophilia A and prophylactic treatment with intravenous immunoglobulin and recombinant factor VIIa in the newborn period: a case report
Gunel Karaburun I. E., Kayki G., AYTAÇ S. A., Celik H. T., GÜMRÜK F., Yigit Ş. S.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
, cilt.32, sa.2, ss.151-154, 2021 (SCI-Expanded, Scopus)
2020
202018. Acute promyelocytic leukemia in a child with reticulin fibrosis
AKSU T., KUŞKONMAZ B. B., ÜNAL Ş., Saglam A., GÜMRÜK F.
JOURNAL OF HEMATOPATHOLOGY
, cilt.13, sa.4, ss.269-273, 2020 (SCI-Expanded, Scopus)
2020
202019. Central nervous system lesions in Fanconi anemia: Experience from a research center for Fanconi anemia patients
AKSU T., GÜMRÜK F., Bayhan T., Coskun C., Oguz K. K., ÜNAL Ş.
PEDIATRIC BLOOD & CANCER
, cilt.67, sa.12, 2020 (SCI-Expanded, Scopus)
2020
202020. Comment on: Clinical, cytogenetic, and molecular analyses of 17 neonates with transient abnormal myelopoiesis and nonconstitutional trisomy 21
AKSU T., GÜMRÜK F., ÜNAL Ş.
PEDIATRIC BLOOD & CANCER
, cilt.67, sa.11, 2020 (SCI-Expanded, Scopus)
2020
202021. A case report of RAS-associated autoimmune lymphoproliferative disorder
COŞKUN Ç., GÜMRÜK F., CEMALOĞLU M., ORHAN M. F., TEZCAN F. İ., ÜNAL CANGÜL Ş.
Hematology, Transfusion and Cell Therapy , cilt.42, sa.1, ss.28-29, 2020 (ESCI, Scopus)
2020
202022. Comparison of Compliance of Different Iron Chelators Including Original and Bioequivalents of Deferasirox
AKSU T., Özbek N. Y., SÖKER M., Coşkun Ç., GÜZELKÜÇÜK Z., ÜZEL V. H., et al.
Acta Medica , cilt.51, sa.3, ss.38-43, 2020 (TRDizin)
2020
202023. Hemophagocytic Lymphohistiocytosis in Patients With Primary Immunodeficiency
Cetinkaya P. G., ÇAĞDAŞ AYVAZ D. N., GÜMRÜK F., Tezcan I.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.42, sa.6, 2020 (SCI-Expanded, Scopus)
2020
202024. Three patients with glucose-6 phosphatase catalytic subunit 3 deficiency
Cetinkaya P. G., Cagdas D. N., Arikoglu T., GÜMRÜK F., Tezcan I.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
, cilt.33, sa.7, ss.957-961, 2020 (SCI-Expanded, Scopus)
2020
202025. Autoinflammation in addition to combined immunodeficiency: SLC29A3 gene defect
Cagdas D. N., Surucu N., TAN Ç., ÖZGÜL R. K., Akkaya-Ulum Y. Z., Aydinoglu A. T., et al.
MOLECULAR IMMUNOLOGY
, cilt.121, ss.28-37, 2020 (SCI-Expanded, Scopus)
2020
202026. A rare form of congenital neutropenia: VPS45 deficiency
Karaatmaca B., Cagdas D. N., TAN Ç., Aytac Ş. S., Ozbek B., ÜNER A., et al.
SCANDINAVIAN JOURNAL OF IMMUNOLOGY
, cilt.91, sa.5, 2020 (SCI-Expanded, Scopus)
2020
202027. Hb H Disease Diagnosed During Adolescent Pregnancy
AKSU T., Coskun C., Kuskonmaz B. B., ÜNAL Ş., Aytac Ş. S., GÜMRÜK F.
HEMOGLOBIN
, cilt.44, sa.2, ss.137-138, 2020 (SCI-Expanded, Scopus)
2020
202028. A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2
Ozen S., Bilginer Y., Batu E., Taşkıran E., Özkara H. A., Ünal Ş., et al.
JOURNAL OF RHEUMATOLOGY
, cilt.47, sa.1, ss.117-125, 2020 (SCI-Expanded, Scopus)
2020
202029. Rare Cytogenetic Anomalies in Two Pediatric Patients with Acute Leukemia
Bozkurt S., ÜNAL Ş., Bayhan T., GÜMRÜK F., Cetin M.
TURKISH JOURNAL OF HEMATOLOGY
, cilt.37, sa.2, ss.132-133, 2020 (SCI-Expanded, Scopus, TRDizin)
2020
202030. The remarkable response to ponatinib therapy in a child with blastic phase of chronic myeloid leukemia
AKSU T., ÜNAL Ş., GÜMRÜK F.
Turkish Journal of Pediatrics
, cilt.62, sa.3, ss.479-481, 2020 (SCI-Expanded, Scopus, TRDizin)
2019
201931. Infant Acute Lymphoblastic Leukemia with Atypical Presentation
YAMAN BAJİN H. İ., YILDIZ Y., akın ş., AYTAÇ EYÜPOĞLU Ş. S., ÜNAL CANGÜL Ş., KUŞKONMAZ B. B., et al.
Acta Medica , cilt.50, sa.4, ss.57-59, 2019 (TRDizin)
2019
201932. Comparison of ferrous sulfate, polymaltose complex and iron-zinc in iron deficiency anemia
ÖZSÜREKCİ Y., ÜNAL Ş., ÇETİN M., GÜMRÜK F.
MINERVA PEDIATRICA
, cilt.71, sa.5, ss.449-454, 2019 (SCI-Expanded, Scopus)
2019
201933. A Spectrum of Clinical Findings from ALPS to CVID: Several Novel LRBA Defects
Cagdas D. N., Halaçlı S., Tan Ç., Lo B., Çetinkaya P., Esenboğa S., et al.
JOURNAL OF CLINICAL IMMUNOLOGY
, cilt.39, sa.7, ss.726-738, 2019 (SCI-Expanded, Scopus)
2019
201934. Fanconi anemia: a single center experience of a large cohort
KESİCİ S., ÜNAL Ş., Kuskonmaz B. B., Aytac Ş. S., Cetin M., GÜMRÜK F.
TURKISH JOURNAL OF PEDIATRICS
, cilt.61, sa.4, ss.477-484, 2019 (SCI-Expanded, Scopus, TRDizin)
2019
201935. Infant lymphoblastic leukemia: a single centers 10 year experience
Yaman-Bajin I., Aytac Ş. S., Kuskonmaz B. B., Uckan-Cetinkaya D., ÜNAL Ş., GÜMRÜK F., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.61, sa.3, ss.325-329, 2019 (SCI-Expanded, Scopus, TRDizin)
2019
201936. Fanconi anemia and ataxia telangiectasia in siblings who inherited unique combinations of novel FANCA and ATM null mutations
Balta G., Patiroglu T., Gumruk F.
Journal of Pediatric Hematology/Oncology
, cilt.41, sa.3, ss.243-246, 2019 (SCI-Expanded, Scopus)
2019
201937. Deferasirox in children with transfusion-dependent thalassemia or sickle cell anemia: A large cohort real-life experience from Turkey (REACH-THEM)
Antmen B., KARAKAŞ Z., Yesilipek M. A., KÜPESİZ O. A., Sasmaz I., Uygun V., et al.
EUROPEAN JOURNAL OF HAEMATOLOGY
, cilt.102, sa.2, ss.123-130, 2019 (SCI-Expanded, Scopus)
2019
201938. Vacuolization in myeloid and erythroid precursors in a child with menkes disease Menkes hastalıklı bir çocukta myeloid ve eritroid öncüllerde vaküolizasyon
Sayın S., Ünal Ş., Çetin M., Gümrük F.
Turkish Journal of Hematology
, cilt.36, sa.3, ss.203-204, 2019 (SCI-Expanded, Scopus, TRDizin)
2018
201839. Comparison of different types of twin pregnancies in terms of obstetric and perinatal outcomes: association of vanished twins with methylenetetrahydrofolate reductase (MTHFR) polymorphism(s)
Ozek M. A., Karaagaoglu E., Orgul G., GÜMRÜK F., YURDAKÖK M., BEKSAÇ M. S.
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
, cilt.35, sa.12, ss.2149-2154, 2018 (SCI-Expanded, Scopus)
2018
201840. Methylenetetrahydrofolate Reductase Polymorphisms and Pregnancy Outcome
TURĞAL M., GÜMRÜK F., Karaagaoglu E., BEKSAÇ M. S.
GEBURTSHILFE UND FRAUENHEILKUNDE
, cilt.78, sa.9, ss.871-878, 2018 (SCI-Expanded, Scopus)
2018
201841. Bone Marrow Mesenchymal Stem Cells Carrying FANCD2 Mutation Differ from the Other Fanconi Anemia Complementation Groups in Terms of TGF-beta 1 Production
CAGNAN I., GUNEL-OZCAN A., AERTS-KAYA F. S. F., Ameziane N., Kuskonmaz B., Dorsman J., et al.
STEM CELL REVIEWS AND REPORTS
, cilt.14, sa.3, ss.425-437, 2018 (SCI-Expanded, Scopus)
2018
201842. Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1
Seo A., Steinberg-Shemer O., Unal Ş., Casadei S., Walsh T., Gumruk F., et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
, cilt.115, sa.20, ss.5241-5246, 2018 (SCI-Expanded, Scopus)
2018
201843. Assessment of Peripheral Neuropathy in Patients with β-Thalassemia via Electrophysiological Study: Reevaluation in the Era of Iron Chelators
Bayhan T., Ünal Ş., Konuşkan B., Erdem O., Karabulut E., Gümrük F.
Hemoglobin
, cilt.42, sa.2, ss.113-116, 2018 (SCI-Expanded, Scopus)
2018
201844. The clinical and laboratory evaluation of familial hemophagocytic lymphohistiocytosis and the importance of hepatic and spinal cord involvement: a single center experience
Beken B., Aytac Ş. S., Balta G., Kuskonmaz B. B., Uckan D., Unal Ş., et al.
HAEMATOLOGICA
, cilt.103, sa.2, ss.231-236, 2018 (SCI-Expanded, Scopus)
2018
201845. Molecular genetic analysis of the F11 gene in 14 Turkish patients with factor XI deficiency: identification of novel and recurrent mutations and their inheritance within families
Colakoglu S., BAYHAN T., Tavil B., Keskin E. Y., Cakir V., GÜMRÜK F., et al.
BLOOD TRANSFUSION
, cilt.16, sa.1, ss.105-113, 2018 (SCI-Expanded, Scopus)
2018
201846. The prevalence of homozygous MTHFR polymorphism(s) in a Turkish university hospital population that necessitated MTHFR polymorphism investigation
GÜMRÜK F., ÖRGÜL G., Dogan O. A., TANAÇAN A., Karaagaoglu E., BEKSAÇ M. S.
ELECTRONIC JOURNAL OF GENERAL MEDICINE
, cilt.15, sa.4, 2018 (ESCI, Scopus)
2017
201747. Human Bocavirus: Can It Trigger Hemophagocytic Lymphohistiocytosis?
TANIR BAŞARANOĞLU S., AYKAÇ K., ÖZSÜREKCİ Y., Bajin I., Tavil B., GÜMRÜK F., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.39, sa.8, 2017 (SCI-Expanded, Scopus)
2017
201748. Tyrosine Kinase Inhibitor Responses in Pediatric CML Patients: Hacettepe Experience
Bajin I. Y., AYTAÇ S. A., KUŞKONMAZ B. B., ÜNAL S., Okur V., Cetinkaya D., et al.
PEDIATRIC BLOOD & CANCER
, cilt.64, 2017 (SCI-Expanded, Scopus)
2017
201749. Heavy metal levels in patients with ineffective erythropoiesis
Bayhan T., Ünal Ş., Çırak E., Erdem O., Akay C., Gürsel O., et al.
Transfusion and Apheresis Science
, cilt.56, sa.4, ss.539-543, 2017 (SCI-Expanded, Scopus)
2017
201750. Liver transplantation from a deceased donor with beta-thalassemia intermedia is not contraindicated: A case report
Gumus E., ABBASOĞLU O., Tanyel C., GÜMRÜK F., ÖZEN H., YÜCE A.
PEDIATRIC TRANSPLANTATION
, cilt.21, sa.3, 2017 (SCI-Expanded, Scopus)
2017
201751. The questioning for routine monthly monitoring of proteinuria in patients with β-thalassemia on deferasirox chelation
Bayhan T., Ünal Ş., Ünlü O., Küçüker H., Tutal A., Karabulut E., et al.
Hematology
, cilt.22, sa.4, ss.248-251, 2017 (SCI-Expanded, Scopus)
2016
201652. Hypereosinophilic Syndrome: Hacettepe Experience
Tavil B., Aytaç Ş. S., Unal Ş., Kuskonmaz B. B., Gumruk F., Cetin M.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.38, sa.7, ss.539-543, 2016 (SCI-Expanded, Scopus)
2016
201653. Macrophage activation syndrome in children with systemic juvenile idiopathic arthritis and systemic lupus erythematosus
AYTAC Ş. S., Batu E. D., ÜNAL Ş., BİLGİNER Y., ÇETİN M., TUNCER M., et al.
RHEUMATOLOGY INTERNATIONAL
, cilt.36, sa.10, ss.1421-1429, 2016 (SCI-Expanded, Scopus)
2016
201654. Severe Hypercalcemia in a Child With Acute Lymphoblastic Leukemia Relapse: Successful Management With Combination of Calcitonin and Bisphosphonate
Tagiyev A., DEMİRBİLEK H., Tavil B., Buyukyilmaz G., Gumruk F., Cetin M.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.38, sa.3, ss.232-234, 2016 (SCI-Expanded, Scopus)
2016
201655. Successful Outcome With Fludarabine-Based Conditioning Regimen for Hematopoietic Stem Cell Transplantation From Related Donor in Fanconi Anemia: A Single Center Experience From Turkey
Kuşkonmaz B. B., Ünal Ş., Bayhan T., Aytaç E., Tavil B., Çetin M., et al.
PEDIATRIC BLOOD & CANCER
, cilt.63, sa.4, ss.695-700, 2016 (SCI-Expanded, Scopus)
2016
201656. Sorafenib-induced Posterior Reversible Encephalopathy Syndrome in a Child With FLT3-ITD-positive Acute Myeloid Leukemia
Tavil B., Isgandarova F., Bayhan T., Unal Ş., Kuskonmaz B. B., Gumruk F., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.38, sa.3, ss.240-242, 2016 (SCI-Expanded, Scopus)
2016
201657. Effects of blood transfusion on cytokine profile and pulmonary function in patients with thalassemia major
Gülhan B., Yalçın E., Ünal Ş., Oğuz B., Özçelik U., Ersöz D., et al.
CLINICAL RESPIRATORY JOURNAL
, cilt.10, sa.2, ss.153-162, 2016 (SCI-Expanded, Scopus)
2016
201658. The genetic basis of asymptomatic codon 8 frame-shift (HBB: C25_26delAA) β0-thalassaemia homozygotes
Jiang Z., Luo H., Huang S., Farrell J., Davis L., Théberge R., et al.
British Journal of Haematology
, cilt.172, sa.6, ss.958-965, 2016 (SCI-Expanded, Scopus)
2016
201659. Foetal and neonatal intracranial haemorrhage in term newborn infants: Hacettepe University experience
Tavil B., Korkmaz A., Bayhan T., Aytaç Ş. S., Unal Ş., Kuskonmaz B. B., et al.
BLOOD COAGULATION & FIBRINOLYSIS
, cilt.27, sa.2, ss.163-168, 2016 (SCI-Expanded, Scopus)
2016
201660. Multiple Bone Cysts in Patient with Congenital Afibrinogenaemia
AYTAÇ S. A., KUŞKONMAZ B. B., ÇAĞLAR Ö., GÜMRÜK F., ÇETİN M.
HAEMOPHILIA
, cilt.22, ss.87-88, 2016 (SCI-Expanded, Scopus)
2016
201661. Hereditary Elliptocytosis with Pyropoikilocytosis
BAYHAN T., ÜNAL S., GÜMRÜK F.
TURKISH JOURNAL OF HEMATOLOGY
, cilt.33, sa.1, ss.86-87, 2016 (SCI-Expanded, Scopus, TRDizin)
2016
201662. The Feasibility of Magnetic Resonance Imaging for Quantification of Liver, Pancreas, Spleen, Vertebral Bone Marrow, and Renal Cortex R2*and Proton Density Fat Fraction in Transfusion-Related Iron Overload
İDİLMAN İ. S., GÜMRÜK F., HALİLOĞLU M., KARÇAALTINCABA M.
TURKISH JOURNAL OF HEMATOLOGY
, cilt.33, sa.1, ss.21-27, 2016 (SCI-Expanded, Scopus, TRDizin)
2016
201663. Serum lipids in Turkish patients with β-thalassemia major and β-thalassemia minor Türk β-talasemi majör ve β-talasemi minör hastalarının serum lipidleri
Işık B., Ünal Ş., Gümrük F.
Turkish Journal of Hematology
, cilt.33, sa.1, ss.72-73, 2016 (SCI-Expanded, Scopus, TRDizin)
2016
201664. Neonates born to mothers with immune thrombocytopenic purpura: a single-center experience of 20 years
Bayhan T., Tavil B., Korkmaz A., Ünal Ş., Hanalioğlu D., Yiğit Ş., et al.
BLOOD COAGULATION & FIBRINOLYSIS
, cilt.27, sa.1, ss.19-23, 2016 (SCI-Expanded, Scopus)
2015
201565. Immune Thrombocytopenic Purpura During Maintenance Phase of Acute Lymphoblastic Leukemia: A Rare Coexistence Requiring a High Degree of Suspicion, a Case Report and Review of the Literature.
Bayhan T., Ünal Ş., Gümrük F., Çetin M.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.32, sa.4, ss.363-6, 2015 (SCI-Expanded, Scopus, TRDizin)
2015
201566. OSTEOPOROSIS IN PATIENTS WITH ACUTE LYMPHOBLASTIC LEUKEMIA TREATED ON MODIFIED ST JUDE TOTAL XV THERAPY
AYTAÇ S. A., ÇETİN M., KUŞKONMAZ B. B., ÜNAL S., Tavil B., GÜMRÜK F.
PEDIATRIC BLOOD & CANCER
, cilt.62, 2015 (SCI-Expanded, Scopus)
2015
201567. An Infant With Congenital Leukemia Cutis and AML-M5 With MLL Gene Rearrangement.
Bayhan T., Çiki K., Tavil B., Gümrük F., Çetin M., Ünal Ş.
Journal of pediatric hematology/oncology
, cilt.37, sa.7, ss.566-7, 2015 (SCI-Expanded, Scopus)
2015
201568. Renal transplantation experience in a patient with factor V Leiden homozygous, MTHFR C677T heterozygous, and PAI heterozygous mutation
GÜLHAN B., Tavil B., GÜMRÜK F., AKI F. T., TOPALOĞLU R.
PEDIATRIC TRANSPLANTATION
, cilt.19, sa.5, 2015 (SCI-Expanded, Scopus)
2015
201569. Biochemical markers of glucose metabolism may be used to estimate the degree and progression of iron overload in the liver and pancreas of patients with β-thalassemia major.
Bas M., Gumruk F., Gonc N., Cetin M., Tuncer M., Hazırolan T., et al.
Annals of hematology
, cilt.94, sa.7, ss.1099-104, 2015 (SCI-Expanded, Scopus)
2015
201570. Risk of thrombosis in a cohort of pediatric acute lymphoblastic leukemia patients
ÜNAL S., GÜMRÜK F., Bayhan T., AYTAÇ S. A., Tavil B., KUŞKONMAZ B. B., et al.
JOURNAL OF THROMBOSIS AND HAEMOSTASIS
, cilt.13, ss.934, 2015 (SCI-Expanded, Scopus)
2015
201571. Case series of thromboembolic complications in childhood nephrotic syndrome: Hacettepe experience.
Tavil B., Kara F., Topaloglu R., Aytac Ş. S., Unal Ş., Kuskonmaz B. B., et al.
Clinical and experimental nephrology
, cilt.19, sa.3, ss.506-13, 2015 (SCI-Expanded, Scopus)
2015
201572. Basal cell carcinoma after treatment of childhood acute lymphoblastic leukemia and concise review of the literature.
Unal Ş., Cetin M., Gumruk F.
Pediatric dermatology
, cilt.32, sa.3, 2015 (SCI-Expanded, Scopus)
2015
201573. Iron chelation with deferasirox in a patient with de-novo ferroportin mutation.
Unal Ş., Piperno A., Gumruk F.
Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS)
, cilt.30, ss.1-3, 2015 (SCI-Expanded, Scopus)
2015
201574. Acute Megakaryoblastic Leukemia with t(1;22) Mimicking Neuroblastoma in an Infant.
Gökçe M., Aytaç Ş. S., Ünal Ş., Altan İ., Gümrük F., Çetin M.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.32, sa.1, ss.64-7, 2015 (SCI-Expanded, Scopus, TRDizin)
2015
201575. The first report of a homozygous codons 9/10 (+T) β-thalassemia mutation in a Turkish patient.
Unal Ş., Chui D., Luo H., Okur H., Oymak Y., Gumruk F.
Hemoglobin
, cilt.39, sa.1, ss.66-8, 2015 (SCI-Expanded, Scopus)
2015
201576. Fanconi's Anemia Effect or Sickle Cell Anemia Effect: That is the Question.
Unal Ş., Chui D., Gumruk F.
Hemoglobin
, cilt.39, sa.4, ss.287-9, 2015 (SCI-Expanded, Scopus)
2015
201577. Molecular Analyses of Pyruvate Kinase Deficient Turkish Patients from a Single Center.
Unal Ş., Gumruk F.
Pediatric hematology and oncology
, cilt.32, sa.5, ss.354-61, 2015 (SCI-Expanded, Scopus)
2015
201578. The hematological and molecular spectrum of α-thalassemias in Turkey: The hacettepe experience Türkiye’de alfa talasemilerin hematolojik ve moleküler spektrumu: Hacettepe deneyimi
Ünal Ş., Gümrük F.
Turkish Journal of Hematology
, cilt.32, sa.2, ss.136-143, 2015 (SCI-Expanded, Scopus, TRDizin)
2014
201479. THE OUTCOME OF PEDIATRIC ACUTE LYMPHOBLASTIC LEUKEMIA IN PATIENTS WHO PRESENTED WITH HYPERLEUKOCYTOSIS
ÜNAL S., ÖZSÜREKCİ Y., AYTAÇ S. A., KUŞKONMAZ B. B., Tavil B., TUNCER M., et al.
PEDIATRIC BLOOD & CANCER
, cilt.61, 2014 (SCI-Expanded, Scopus)
2014
201480. PEDIATRIC MYELODYSPLASTIC SYNDROME: EXPERIENCE FROM A SINGLE CENTER
ÇETİN M., ÜNAL S., Bayhan T., AYTAÇ S. A., KUŞKONMAZ B. B., Tavil B., et al.
PEDIATRIC BLOOD & CANCER
, cilt.61, 2014 (SCI-Expanded, Scopus)
2014
201481. the Effects of Deferasirox on Iron in Pituitary, Pancreas and Thyroid Glands: An Observational Case-Control Study
ÜNAL S., Bas M., HAZIROLAN T., TUNCER A. M., ÇETİN M., GÜMRÜK F.
BLOOD
, cilt.124, sa.21, 2014 (SCI-Expanded, Scopus)
2014
201482. Pediatric Myelodysplastic Syndrome: Experience from a Single Center
Cetin M., ÜNAL Ş., Bayhan T., Aytac Ş. S., KUŞKONMAZ B. B., Tavil B., et al.
BLOOD
, cilt.124, sa.21, 2014 (SCI-Expanded, Scopus)
2014
201483. Bleeding and non-bleeding phenotypes in patients with GGCX gene mutations.
Watzka M., Geisen C., Scheer M., Wieland R., Wiegering V., Dörner T., et al.
Thrombosis research
, cilt.134, sa.4, ss.856-65, 2014 (SCI-Expanded, Scopus)
2014
201484. Survey of Hfe Gene C282Y Mutation in Turkish Beta-Thalassemia Patients and Healthy Population: A Preliminary Study.
Unal S., Balta G., Gümrük F., Xu H.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.31, sa.3, ss.272-5, 2014 (SCI-Expanded, Scopus, TRDizin)
2014
201485. Thrombophilic Risk Factors And The Efficiency Of Prophylactic Anticoagulation Therapy In Children Who Underwent Renal Transplantation
GÜLHAN B., Tavil B., DÜZOVA A., ÖZALTIN F., ÖZEN S., TOPALOĞLU R., et al.
PEDIATRIC NEPHROLOGY
, cilt.29, sa.9, ss.1694, 2014 (SCI-Expanded, Scopus)
2014
201486. Number of erythrocyte transfusions is more predictive than serum ferritin in estimation of cardiac iron loading in pediatric patients with acute lymphoblastic leukemia.
ÜNAL Ş., ÇETİN M., HAZIROLAN T., Yildirim G., Meral A., Birbilen A., et al.
Leukemia research
, cilt.38, sa.8, ss.882-5, 2014 (SCI-Expanded, Scopus)
2014
201487. The relationship between hematological findings and coronary artery aneurysm in kawasaki disease.
Beken B., Unal Ş., Cetin M., Gümrük F.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.31, sa.2, ss.199-200, 2014 (SCI-Expanded, Scopus, TRDizin)
2014
201488. Lysosomal vesicles, giant granules, and erythrophagocytosis in chédiak-higashi syndrome.
Beken B., Unal Ş., Gümrük F.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.31, sa.2, ss.209-10, 2014 (SCI-Expanded, Scopus, TRDizin)
2014
201489. Successful hematopoietic stem cell transplantation in a patient with congenital dyserythropoietic anemia type II
Unal Ş., Russo R., Gumruk F., Kuskonmaz B. B., Cetin M., Sayli T., et al.
PEDIATRIC TRANSPLANTATION
, cilt.18, sa.4, 2014 (SCI-Expanded, Scopus)
2014
201490. An infant presented with deficiencies of vitamin K dependent factors due to an inherited novel mutation in GGCX gene
ÜNAL S., Khaniyev S., Watzka M., Oldenburg J., GÜMRÜK F.
HAEMOPHILIA
, cilt.20, ss.105, 2014 (SCI-Expanded, Scopus)
2014
201491. Sea-blue histiocytes in the bone marrow of a boy with severe congenital neutropenia associated with G6PC3 mutation
Tavil B., Cetin M., Gumruk F.
BRITISH JOURNAL OF HAEMATOLOGY
, cilt.165, sa.4, ss.426, 2014 (SCI-Expanded, Scopus)
2014
201492. A Novel Mutation in Protein C Gene (PROC) Causing Severe Phenotype in Neonatal Period
Unal Ş., Gumruk F., Yigit Ş., Tuncer M., Tavil B., Cil O., et al.
PEDIATRIC BLOOD & CANCER
, cilt.61, sa.4, ss.763-764, 2014 (SCI-Expanded, Scopus)
2014
201493. Metamizole-Induced Bicytopenia Reversed by G-CSF and IVIG Treatment in a Child
Tavil B., Cetin M., Gumruk F., ÇAĞDAŞ AYVAZ D. N., CENGİZ A. B.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.31, sa.2, ss.117-119, 2014 (SCI-Expanded, Scopus)
2014
201494. Congenital thrombotic thrombocytopenic purpura with novel mutations in three unrelated Turkish children.
Metin A., Unal Ş., Gümrük F., Palla R., Cairo A., Underwood M., et al.
Pediatric blood & cancer
, cilt.61, sa.3, ss.558-61, 2014 (SCI-Expanded, Scopus)
2014
201495. Striking Hematological Abnormalities in Patients With Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPD II): A Potential Role of Pericentrin in Hematopoiesis
ÜNAL Ş., Alanay Y., ÇETİN M., Boduroglu K., Utine E., CORMİER-DAİRE V., et al.
PEDIATRIC BLOOD & CANCER
, cilt.61, sa.2, ss.302-305, 2014 (SCI-Expanded, Scopus)
2013
201396. Atypical combined immunodeficiency due to Artemis defect: a case presenting as hyperimmunoglobulin M syndrome and with LGLL.
Bajin İ., Ayvaz D. N., Ünal Ş., Özgür T., Çetin M., Gümrük F., et al.
Molecular immunology
, cilt.56, sa.4, ss.354-7, 2013 (SCI-Expanded, Scopus)
2013
201397. IMPROVED OUTCOME IN HIGH RISK GROUP PATIENTS WITH HIGH DOSE METHYLPREDNISOLONE DURING INDUCTION OF MODIFIED ST JUDE TOTAL XIIIA
ÜNAL S., Gurgey A., Yetgin S., GÜMRÜK F., TUNCER M., AYTAÇ S. A., et al.
PEDIATRIC BLOOD & CANCER
, cilt.60, ss.70, 2013 (SCI-Expanded, Scopus)
2013
201398. CONTRIBUTORY RISK FACTORS FOR DEVELOPMENT OF THROMBOSIS IN CHILDRENWITH NEPHROTIC SYNDROME
KaraEroglu F., Tavil B., ÖZALTIN F., BEŞBAŞ N., ÖZEN S., ÇETİN M., et al.
PEDIATRIC NEPHROLOGY
, cilt.28, sa.8, ss.1584, 2013 (SCI-Expanded, Scopus)
2013
201399. Recurrent macrophage activation syndrome associated with heterozygous perforin W374X gene mutation in a child with systemic juvenile idiopathic arthritis.
Unal Ş., Balta G., Okur H., Aytac Ş. S., Cetin M., Gumruk F., et al.
Journal of pediatric hematology/oncology
, cilt.35, sa.5, 2013 (SCI-Expanded, Scopus)
2013
2013100. Glucose-6-phosphate dehydrogenase deficiency in neonatal hyperbilirubinaemia: Hacettepe experence
Celik H., Günbey C., Unal Ş., Gümrük F., Yurdakök M.
JOURNAL OF PAEDIATRICS AND CHILD HEALTH
, cilt.49, sa.5, ss.399-402, 2013 (SCI-Expanded, Scopus)
2013
2013101. Double trouble: Duchenne muscular dystrophy and hemophilia
Gokce M., Gumruk F., Haliloglu G., Serdaroglu E., Caglayan H.
PEDIATRIC BLOOD & CANCER
, cilt.60, sa.3, ss.525, 2013 (SCI-Expanded, Scopus)
2013
2013102. Dysfunctional uterine bleeding in adolescent girls and evaluation of their response to treatment.
Başaran H. Ö., AKGÜL S., Oksuz-Kanbur N., GÜMRÜK F., ÇETİN M., DERMAN O.
The Turkish journal of pediatrics
, cilt.55, sa.2, ss.186-9, 2013 (SCI-Expanded, Scopus)
2012
2012103. Intracerebral metastasis in pediatric acute lymphoblastic leukemia: A rare presentation
Gokce M., Aytac Ş. S., Altan I., ÜNAL Ş., Tuncer M., GÜMRÜK F., et al.
Journal of Pediatric Neurosciences
, cilt.7, sa.3, ss.208-210, 2012 (SCI-Expanded, Scopus)
2012
2012104. Hematological features of pediatric systemic lupus erythematosus: suggesting management strategies in children
Gokce M., Bilginer Y., Besbas N., Ozaltin F., Cetin M., Gumruk F., et al.
LUPUS
, cilt.21, sa.8, ss.878-884, 2012 (SCI-Expanded, Scopus)
2012
2012105. RECURRENT PEDIATRIC THROMBOSIS: INFLUENCE AND UNDERLYING OR COEXISTING FACTORS
Gokce M., Altan I., ÜNAL S., KUŞKONMAZ B. B., AYTAÇ S. A., ÇETİN M., et al.
HAEMATOLOGICA
, cilt.97, ss.192, 2012 (SCI-Expanded, Scopus)
2012
2012106. Recurrent pediatric thrombosis: the effect of underlying and/or coexisting factors.
Gokce M., Altan I., Unal Ş., Kuskonmaz B. B., Aytac Ş. S., Cetin M., et al.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
, cilt.23, sa.5, ss.434-9, 2012 (SCI-Expanded, Scopus)
2012
2012107. Acute lymphoblastic leukaemia in a child with systemic lupus erythematosus
Gokce M., Bulus D., Bilginer Y., Gumruk F., Besbas N., Cetin M.
LUPUS
, cilt.21, sa.8, ss.910-913, 2012 (SCI-Expanded, Scopus)
2012
2012108. Is Swine-origin Influenza a Predisposing Factor for Deep Vein Thrombosis?
Gökçe M., Unal Ş., Aytaç Ş. S., Kara A., Ceyhan M., Tuncer M., et al.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.29, sa.2, ss.174-6, 2012 (SCI-Expanded, Scopus, TRDizin)
2012
2012109. Secondary hemophagocytosis in 3 patients with organic acidemia involving propionate metabolism.
Gokce M., Unal O., Hismi B., Gumruk F., Coskun T., Balta G., et al.
Pediatric hematology and oncology
, cilt.29, sa.1, ss.92-8, 2012 (SCI-Expanded, Scopus)
2012
2012110. A rare metabolic complication of acute lymphoblastic leukemia in childhood: lactic acidosis
Gökçe M., Unal Ş., Gülşen H., Başaran O., Cetin M., Gümrük F., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.54, sa.1, ss.61-63, 2012 (SCI-Expanded, Scopus)
2011
2011111. NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet alpha-granules
Gunay-Aygun M., Falik-Zaccai T. C., Vilboux T., Zivony-Elboum Y., Gumruk F., Cetin M., et al.
NATURE GENETICS
, cilt.43, sa.8, ss.732-734, 2011 (SCI-Expanded, Scopus)
2011
2011112. The frequency of A91V in the perforin gene and the effect of tumor necrosis factor-α promoter polymorphism on acquired hemophagocytic lymphohistiocytosis.
Okur H., Ünal Ş., Balta G., Efendioğlu D., Çimen E., Çetin M., et al.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.28, sa.2, ss.125-30, 2011 (SCI-Expanded, Scopus, TRDizin)
2011
2011113. The effects of deferasirox on renal, cardiac and hepatic iron load in patients with β-thalassemia major: preliminary results.
Unal Ş., Hazirolan T., Eldem G., Gumruk F.
Pediatric hematology and oncology
, cilt.28, sa.3, ss.217-21, 2011 (SCI-Expanded, Scopus)
2011
2011114. Prenatal Diagnosis of Hemoglobinopathies in Hacettepe University, Turkey
BEKSAÇ M. S., GÜMRÜK F., Gurgey A., Cakar N., MÜMÜŞOĞLU S., ÖZYÜNCÜ Ö., et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.28, sa.1, ss.51-55, 2011 (SCI-Expanded, Scopus)
2011
2011115. An unexpected parasitic cause of hypereosinophilia: fascioliasis
Gökçe M., Sahiner Ü. M., Unal Ş., Parlakay A., Oncel İ. H., Saçkesen C., et al.
TURKISH JOURNAL OF PEDIATRICS
, sa.1, ss.111-113, 2011 (SCI-Expanded, Scopus)
2010
2010116. Autoimmune hemolytic anemia and giant cell hepatitis: Report of three infants
Ünal Ş., Kuşkonmaz B. B., Balamtekin N., Baysoy G., Aytaç E., Orhan D., et al.
TURKISH JOURNAL OF HEMATOLOGY
, cilt.27, sa.4, ss.308-313, 2010 (SCI-Expanded, Scopus, TRDizin)
2010
2010117. Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p
Gunay-Aygun M., Zivony-Elboum Y., Gumruk F., Geiger D., Cetin M., Khayat M., et al.
BLOOD
, cilt.116, sa.23, ss.4990-5001, 2010 (SCI-Expanded, Scopus)
2010
2010118. Hematological consequences of pandemic influenza H1N1 infection: a single center experience
Unal Ş., Gökçe M., Aytaç-Elmas Ş. S., Karabulut E., Altan I., Ozkaya-Parlakay A., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.52, sa.6, ss.570-575, 2010 (SCI-Expanded, Scopus)
2010
2010119. Thiamine-responsive megaloblastic anemia syndrome
Bay A., KESKİN M., Hizli S., Uygun H., Dai A., GÜMRÜK F.
INTERNATIONAL JOURNAL OF HEMATOLOGY
, cilt.92, sa.3, ss.524-526, 2010 (SCI-Expanded, Scopus)
2010
2010120. Fludarabine, cytarabine, granulocyte colony-stimulating factor, and idarubicin (FLAG-IDA) for the treatment of children with poor-prognosis acute leukemia: the Hacettepe experience.
Tavil B., Aytac Ş. S., Balci Y., Unal Ş., Kuskonmaz B. B., Yetgin S., et al.
Pediatric hematology and oncology
, cilt.27, sa.7, ss.517-28, 2010 (SCI-Expanded, Scopus)
2010
2010121. Deferasirox in iron-overloaded patients with transfusion-dependent myelodysplastic syndromes: Results from the large 1-year EPIC study
Gattermann N., Finelli C., Della Porta M., Fenaux P., Ganser A., Guerci-Bresler A., et al.
Leukemia Research
, cilt.34, sa.9, ss.1143-1150, 2010 (SCI-Expanded, Scopus)
2010
2010122. Deferasirox use after hematopoietic stem cell transplantation in pediatric patients with beta-thalassemia major: preliminary results.
Unal Ş., Kuskonmaz B. B., Hazirolan T., Eldem G., Aytac Ş. S., Cetin M., et al.
Pediatric hematology and oncology
, cilt.27, sa.6, ss.482-9, 2010 (SCI-Expanded, Scopus)
2010
2010123. Acral erythema with bullous formation: A side effect of chemotherapy in a child with acute lymphoblastic leukemia
Aytac Ş. S., GÜMRÜK F., ÇETİN M., Tuncer M., YETGİN S.
Turkish Journal of Pediatrics
, cilt.52, sa.2, ss.211-214, 2010 (SCI-Expanded, Scopus)
2010
2010124. Antihyperlipidemic Agents Cause a Decrease in von Willebrand Factor Levels in Pediatric Patients with Familial Hyperlipidemia
Yalçin S. S., Güneş B., Unal Ş., Gümrük F., Coşkun T.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
, cilt.23, sa.8, ss.765-771, 2010 (SCI-Expanded, Scopus)
2010
2010125. Measles, mumps, and rubella antibody status and response to immunization in children after therapy for acute lymphoblastic leukemia
Aytac Ş. S., YALÇIN Ş., Cetin M., Yetgin S., GÜMRÜK F., Tuncer M., et al.
Pediatric Hematology and Oncology
, cilt.27, sa.5, ss.333-343, 2010 (SCI-Expanded, Scopus)
2010
2010126. Stanozolol treatment for successful prevention of attacks of severe primary cryofibrinogenemia.
ÜNAL Ş., KARA F., Ozen S., ORHAN D., TUNCER M., GÜMRÜK F.
Pediatric blood & cancer
, cilt.55, ss.174-6, 2010 (SCI-Expanded, Scopus)
2010
2010127. Anemia and Neutropenic Fever with High Dose Diazoxide Treatment in a Case with Hyperinsulinism Due to Munchausen by Proxy
Ozon A., DEMİRBİLEK H., ERTUĞRUL A., ÜNAL S., GÜMRÜK F., KANDEMİR N.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
, cilt.23, sa.7, ss.719-723, 2010 (SCI-Expanded, Scopus)
2010
2010128. An unusual presentation of pediatric acute lymphoblastic leukemia with parotid gland involvement and dactylitis
Ünal Ş., Kuşkonmaz B. B., Balcı Y., Cengiz B., Tuncer M., Gürgey A., et al.
TURKISH JOURNAL OF HEMATOLOGY
, cilt.27, sa.2, ss.117-119, 2010 (SCI-Expanded, Scopus, TRDizin)
2010
2010129. Chronic Recurrent Multifocal Osteomyelitis as the First Presentation of Acute Lymphoblastic Leukemia in a 2-year-old Boy
Tavil B., Secmeer G., Balci Y. I., Tezer H., Aksoy C., Alan S., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.32, sa.4, 2010 (SCI-Expanded, Scopus)
2010
2010130. Molecular analysis of Chanarin-Dorfman syndrome (CDS) patients: Identification of novel mutations in the ABHD5 gene
EMRE S., Unver N., EVANS S., YÜZBAŞIOĞLU A., GÜRAKAN F., GÜMRÜK F., et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS
, cilt.53, sa.3, ss.141-144, 2010 (SCI-Expanded, Scopus)
2010
2010131. Hemophagocytosis associated with leukemia: a striking association with juvenile myelomonocytic leukemia.
Unal Ş., Cetin M., Kutlay N., Elmas Ş. S., Gumruk F., Tukun A., et al.
Annals of hematology
, cilt.89, sa.4, ss.359-64, 2010 (SCI-Expanded, Scopus)
2010
2010132. The efficacy of tissue Doppler imaging in predicting myocardial iron load in patients with beta-thalassemia major: correlation with T2*cardiovascular magnetic resonance
AYPAR E., ALEHAN D., HAZIROLAN T., Gumruk F.
INTERNATIONAL JOURNAL OF CARDIOVASCULAR IMAGING
, cilt.26, sa.4, ss.413-421, 2010 (SCI-Expanded, Scopus)
2010
2010133. Dual-echo TFE MRI for the assessment of myocardial iron overload in beta-thalassemia major patients.
Hazirolan T., Eldem G., Unal Ş., Akpinar B., Gümrük F., Alibek S., et al.
Diagnostic and interventional radiology (Ankara, Turkey)
, cilt.16, sa.1, ss.59-62, 2010 (SCI-Expanded, Scopus)
2010
2010134. Early detection of pulmonary fungal infection by CT scan in pediatric ALL patients under chemotherapy or in post-transplantation period with primary complaint of chest pain
Ünal Ş., Kuşkonmaz B. B., Tavil B., Aytaç E., Uçkan Ç., Çetin M., et al.
TURKISH JOURNAL OF HEMATOLOGY
, cilt.27, sa.1, ss.34-37, 2010 (SCI-Expanded, Scopus, TRDizin)
2009
2009135. A novel mutation in a family with DNA ligase IV deficiency syndrome.
Unal Ş., Cerosaletti K., Uckan-Cetinkaya D., Cetin M., Gumruk F.
Pediatric blood & cancer
, cilt.53, sa.3, ss.482-4, 2009 (SCI-Expanded, Scopus)
2009
2009136. Wilms Tumor, AML and Medulloblastoma in a Child With Cancer Prone Syndrome of Total Premature Chromatid Separation and Fanconi Anemia
Sari N., AKYÜZ C., Aktas D., GÜMRÜK F., ORHAN D., ALİKAŞİFOĞLU M., et al.
PEDIATRIC BLOOD & CANCER
, cilt.53, sa.2, ss.208-210, 2009 (SCI-Expanded, Scopus)
2009
2009137. Serum Erythropoietin Levels in Pediatric Hematologic Disorders and Impact of Recombinant Human Erythropoietin Use.
Çetin M., Ünal Ş., Gümrük F., Gürgey A., Altay Ç.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.26, sa.2, ss.72-6, 2009 (Scopus, TRDizin)
2009
2009138. Brilliant cresyl blue staining for screening hemoglobin H disease: Reticulocyte smear.
Kulaç İ., Ünal Ş., Gümrük F.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.26, sa.1, ss.45, 2009 (Scopus, TRDizin)
2009
2009139. PARVOVIRUS B19-INDUCED PERSISTENT PURE RED CELL APLASIA IN A CHILD WITH T-CELL IMMUNODEFICIENCY
Tavil B., Sanal O., Turul T., Yel L., Gurgey A., Gumruk F.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.26, sa.2, ss.63-68, 2009 (SCI-Expanded, Scopus)
2009
2009140. Pulmonary thromboembolism in childhood: A single-center experience from Turkey
Tavil B., Kuskonmaz B. B., Kiper N., Cetin M., Gumruk F., Gurgey A.
HEART & LUNG
, cilt.38, sa.1, ss.56-65, 2009 (SCI-Expanded, Scopus)
2008
2008141. Value of Dual Energy Computed Tomography for detection of myocardial iron deposition in Thalassaemia patients: initial experience.
Hazirolan T., Akpinar B., Unal Ş., Gümrük F., Haliloglu M., Alibek S.
European journal of radiology
, cilt.68, sa.3, ss.442-5, 2008 (SCI-Expanded, Scopus)
2008
2008142. Significance of fetal hemoglobin values in detection of heterozygotes in fanconi anemia: reevaluation of fetal hemoglobin values by a sensitive method.
Gumruk F., Tavil B., Balta G., Unal S., Gurgey A.
Journal of pediatric hematology/oncology
, cilt.30, sa.12, ss.896-9, 2008 (SCI-Expanded, Scopus)
2008
2008143. The prognostic impact of myeloid antigen expression in pediatric acute lymphoblastic leukemia patients.
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The Turkish journal of pediatrics
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2008
2008144. Two new cases with Pearson syndrome and review of Hacettepe experience.
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The Turkish journal of pediatrics
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2008
2008145. Central nervous system involvement in Turkish children with primary hemophagocytic lymphohistiocytosis.
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Journal of child neurology
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2008
2008146. Hyperimmunoglobulinemia D and periodic fever syndrome; treatment with etanercept and follow-up
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CLINICAL RHEUMATOLOGY
, cilt.27, sa.10, ss.1317-1320, 2008 (SCI-Expanded, Scopus)
2008
2008147. Lymphocytic vacuolization in sialic acid storage disease
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AMERICAN JOURNAL OF HEMATOLOGY
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2008
2008148. Nonstroke arterial thrombosis in children: Hacettepe experience.
Balci Y., Unal Ş., Gumruk F., Cetin M., Ozkutlu S., Gurgey A.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
, cilt.19, sa.6, ss.519-24, 2008 (SCI-Expanded, Scopus)
2008
2008149. Congenital coagulation factor deficiencies: Hacettepe experience
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HAEMOPHILIA
, cilt.14, ss.12-13, 2008 (SCI-Expanded, Scopus)
2008
2008150. Pearson syndrome associated with hemophagocytic syndrome in a child
GÜMRÜK F., KUŞKONMAZ B. B., COŞKUN T.
Turkish Journal of Hematology
, cilt.25, sa.1, ss.54-55, 2008 (SCI-Expanded, Scopus, TRDizin)
2008
2008151. CD-34 selected hematopoetic stem cell transplantation from HLA identical family members for fanconi anemia
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PEDIATRIC BLOOD & CANCER
, cilt.50, sa.5, ss.1065-1067, 2008 (SCI-Expanded, Scopus)
2008
2008152. Evaluation of cardiovascular complications with Tc-99m tetrofosmin gated myocardial perfusion scintigraphy in patients with thalassernia major
Gedik G. K., Caglar M., ÜNAL S., Gumruk F.
REVISTA ESPANOLA DE MEDICINA NUCLEAR
, cilt.27, sa.3, ss.191-198, 2008 (SCI-Expanded, Scopus)
2008
2008153. Red cell glucose-6-phosphate dehydrogenase deficiency in Turkey.
Altay Ç., Gümrük F.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.25, sa.1, ss.1-7, 2008 (Scopus, TRDizin)
2008
2008154. Severe Henoch-Schönlein purpura in a thalassemic patient under deferiprone treatment.
Unal Ş., Gücer S., Kale G., Besbas N., Ozen S., Gümrük F.
American journal of hematology
, cilt.83, sa.2, ss.165-6, 2008 (SCI-Expanded, Scopus)
2008
2008155. Interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α) levels and IL-6, TNF-polymorphisms in children with thrombosis
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Journal of Pediatric Hematology/Oncology
, cilt.30, sa.1, ss.26-31, 2008 (SCI-Expanded, Scopus)
2007
2007156. Diaphragmatic mesothelial cyst in a child with Fanconi aplastic anemia
Balci Y. I., Tavil B., AKINCI D., KARÇAALTINCABA M., Guemruek F.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.29, sa.12, ss.860-861, 2007 (SCI-Expanded, Scopus)
2007
2007157. The validity of pallor as a clinical sign of anemia in cases with beta-thalassemia
YALÇIN S. S., Uenal S., Guemruek F., Yurdakoek K.
TURKISH JOURNAL OF PEDIATRICS
, cilt.49, sa.4, ss.408-412, 2007 (SCI-Expanded, Scopus)
2007
2007158. Pulmonary tuberculosis presenting with pancytopaenia, haemophagocytosis and foamy histiocytes in an infant.
Tavil B., Caliskan U., Unal Ş., Gumruk F.
The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease
, cilt.11, sa.8, ss.931-2, 2007 (SCI-Expanded, Scopus)
2007
2007159. Evaluation of the children with beta-thalassemia in terms of their self-concept, behavioral, and parental attitudes
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JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.29, sa.8, ss.523-528, 2007 (SCI-Expanded, Scopus)
2007
2007160. The rate of hepatitis B and C virus infections and the importance of HBV vaccination in children with acute lymphoblastic leukemia.
Tavil B., Cetin M., Tuncer M., Gumruk F., Yuce A., Demir H., et al.
Hepatology research : the official journal of the Japan Society of Hepatology
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2007
2007161. Anti phospholipid antibodies in Turkish children with thrombosis
Tavil B., Ozyurek E., Gumruk F., Cetin M., Gurgey A.
BLOOD COAGULATION & FIBRINOLYSIS
, cilt.18, sa.4, ss.347-352, 2007 (SCI-Expanded, Scopus)
2007
2007162. Oral and dental findings in children with Fanconi anemia.
Tekcicek M., Tavil B., Cakar A., Pinar A., Unal S., Gumruk F.
Pediatric dentistry
, cilt.29, sa.3, ss.248-52, 2007 (SCI-Expanded)
2007
2007163. A case of interleukin-12 receptor beta-1 deficiency with recurrent leishmaniasis
Sanal O., Turkkani G., Gumruk F., Yel L., Secmeer G., Tezcan I., et al.
PEDIATRIC INFECTIOUS DISEASE JOURNAL
, cilt.26, sa.4, ss.366-368, 2007 (SCI-Expanded, Scopus)
2006
2006164. Haematological findings in children with inborn errors of metabolism
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JOURNAL OF INHERITED METABOLIC DISEASE
, cilt.29, sa.5, ss.607-611, 2006 (SCI-Expanded, Scopus)
2006
2006165. Fanconi anemia patient with bilaterally hypoplastic scapula and unilateral winging associated with scoliosis and rib abnormality.
Unal Ş., Gumruk F.
Journal of pediatric hematology/oncology
, cilt.28, sa.9, ss.616-7, 2006 (SCI-Expanded, Scopus)
2006
2006166. Hemophagocytic syndrome and acute liver failure associated with ethylene glycol ingestion: A case report
Kuskonmaz B. B., Duzova A., Kanbur N. O., Gurakan F., Gumruk F., Gurgey A.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.23, sa.5, ss.427-432, 2006 (SCI-Expanded, Scopus)
2006
2006167. Transfusion-transmitted virus prevalance in Turkish patients with thalassemia
Ozyurek E., ERGÜNAY K., Kuskonmaz B. B., ÜNAL S., Cetin M., Ustacelebi S., et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.23, sa.4, ss.347-353, 2006 (SCI-Expanded, Scopus)
2006
2006168. The neurologic complications in pediatric acute lymphoblastic leukemia patients excluding leukemic infiltration
Kuskonmaz B. B., Unal Ş., Gumruk F., Cetin M., Tuncer A., Gurgey A.
LEUKEMIA RESEARCH
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2006
2006169. Diamond-Blackfan anemia associated with beta-thalassemia trait
Tavil B., Cetin M., Kuskonmaz B. B., Gumruk F.
AMERICAN JOURNAL OF HEMATOLOGY
, cilt.81, sa.3, ss.214-215, 2006 (SCI-Expanded, Scopus)
2005
2005170. Secondary hemophagocytic lymphohistiocytosis in Turkish children
Gurgey A., Secmeer G., Tavil B., Ceyhan M., Kushkonmaz B. B., Cengiz B., et al.
PEDIATRIC INFECTIOUS DISEASE JOURNAL
, cilt.24, sa.12, ss.1116-1117, 2005 (SCI-Expanded, Scopus)
2005
2005171. Bone mineral density and serum bone turnover markers in survivors of childhood acute lymphoblastic leukemia: Comparison of megadose methylprednisolone and conventional-dose prednisolone treatments
Alikasifoglu A., Yetgin S., Cetin M., Tuncer M., Gumruk F., Gurgey A., et al.
AMERICAN JOURNAL OF HEMATOLOGY
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2005
2005172. Atypical presentation of spondylitis in a case with sickle cell disease
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TURKISH JOURNAL OF PEDIATRICS
, cilt.47, sa.4, ss.369-372, 2005 (SCI-Expanded, Scopus)
2005
2005173. Genital ulcers after treatment with all-trans-retinoic acid in a child with acute promyelocytic leukemia
ÜNAL S., Gumruk F., Cetin M., Hicsonmez G.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.22, sa.5, ss.357-359, 2005 (SCI-Expanded, Scopus)
2005
2005174. Prothrombin G20210A mutation in Turkish children with thrombosis and the frequency of prothrombin C20209T
Gurgey A., ÜNAL S., Okur H., Duru F., Gumruk F.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.22, sa.4, ss.309-314, 2005 (SCI-Expanded, Scopus)
2005
2005175. The Frequency of Hepatitis B, Hepatitis C and Hepatitis G Virus in Patients with Beta-Thalassemia Major Who Receive Frequent Blood Transfusion
Sanli C., ALBAYRAK M., Nakipoglu F., GÜMRÜK F.
VIRAL HEPATIT DERGISI-VIRAL HEPATITIS JOURNAL
, cilt.10, sa.3, ss.150-157, 2005 (ESCI, TRDizin)
2004
2004176. A child with vitamin B12 deficiency presenting with pancytopenia and hyperpigmentation
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JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.26, sa.12, ss.834-836, 2004 (SCI-Expanded, Scopus)
2004
2004177. Analysis of some clinical and laboratory aspects of adolescent patients with thrombosis.
Gurgey A., Balta G., Gumruk F., Altay C.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
, cilt.15, sa.8, ss.657-62, 2004 (SCI-Expanded, Scopus)
2004
2004178. Five Fanconi anemia patients with unusual organ pathologies
ÜNAL S., Ozbek N., Kara A., Alikasifoglu M., Gumruk F.
AMERICAN JOURNAL OF HEMATOLOGY
, cilt.77, sa.1, ss.50-54, 2004 (SCI-Expanded, Scopus)
2004
2004179. Severe hemolytic anemia associated with Hb Volga [beta27(B9)Ala-->Asp]: GCC-->GAC at codon 27 in a Turkish family.
Sözen M., Karaaslan C., Oner R., Gümrük F., Ozdemir M., Altay C., et al.
American journal of hematology
, cilt.76, sa.4, ss.378-82, 2004 (SCI-Expanded, Scopus)
2004
2004180. Clinical and laboratory evaluation of Turkish children with thrombosis for homozygous factor V G1691A mutation.
Unal S., Balta G., Duru F., Gumruk F., Altay C., Gurgey A.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
, cilt.15, sa.4, ss.343-6, 2004 (SCI-Expanded, Scopus)
2004
2004181. Hemophagocytic syndrome associated with visceral leishmaniasis.
Koçak N., Eren M., Yüce A., Gümrük F.
Indian pediatrics
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2004
2004182. Efficacy of daily and weekly iron supplementation on iron status in exclusively breast-fed infants.
Yurdakok K., Temiz F., Yalcin S. S., Gumruk F.
Journal of pediatric hematology/oncology
, cilt.26, sa.5, ss.284-8, 2004 (SCI-Expanded, Scopus)
2004
2004183. Acute lymphoblastic leukemia in infants
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TURKISH JOURNAL OF PEDIATRICS
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2004
2004184. The prognosis and survival of childhood acute lymphoblastic leukemia with central nervous system relapse
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PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.21, sa.3, ss.279-289, 2004 (SCI-Expanded, Scopus)
2003
2003185. Acute lymphoblastic leukemia as a second malignant neoplasm in a child with medulloblastoma
Caglar K., ÜNAL S., Cetinkaya A., Gumruk F., Yetgin S.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.20, sa.7, ss.535-537, 2003 (SCI-Expanded, Scopus)
2003
2003186. Molecular characterization of Turkish patients with pyrimidine 5 ' nucleotidase-I deficiency
Balta G., GUMRUK F., AKARSU N., GURGEY A., ALTAY C.
BLOOD
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2003
2003187. Use of recombinant factor VIIa for bleeding in children with Glanzmann thrombasthenia.
Caglar K., Cetinkaya A., Aytac Ş. S., Gumruk F., Gurgey A.
Pediatric hematology and oncology
, cilt.20, sa.6, ss.435-8, 2003 (SCI-Expanded, Scopus)
2003
2003188. The effect of hydroxyurea on the coagulation system in sickle cell anemia and beta-thalassemia intermedia patients: A preliminary study
Koc A., Gumruk F., Gurgey A.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.20, sa.6, ss.429-434, 2003 (SCI-Expanded, Scopus)
2003
2003189. Primary hemophagocytic lymphohistiocytosis in Turkish children
Gurgey A., Gogus S., Ozyurek E., Aslan D., Gumruk F., Cetin M., et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
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2003
2003190. Agranulocytosis: A Rare Complication of Infectious Mononucleosis and Recovery After IVIG Therapy.
Ölmez A., Gümrük F., Ceyhan M., Tezcan İ.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.20, sa.2, ss.91-3, 2003 (Scopus)
2003
2003191. Thrombosis in children with cardiac pathology: Frequency of factor V Leiden and prothrombin G20210A mutations
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PEDIATRIC CARDIOLOGY
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2003
2003192. Benefit of high-dose methylprednisolone in comparison with conventional-dose prednisolone during remission induction therapy in childhood acute lymphoblastic leukemia for long-term follow-up
Yetgin S., Tuncer M., Cetin M., Gumruk F., Yenicesu I., Tunc B., et al.
LEUKEMIA
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2002
2002193. Serum alpha-fetoprotein level in Fanconi's anemia: Evaluation of 33 Turkish patients
Aslan D., Gumruk F., Alikasifoglu M., Altay C.
AMERICAN JOURNAL OF HEMATOLOGY
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2002
2002194. Mutations in coagulation factor XIII A gene in three Turkish patients: two novel mutations and a known insertion
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BRITISH JOURNAL OF HAEMATOLOGY
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2002
2002195. The prevalence and molecular basis of beta-thalassemia in Isparta province and region.
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The Turkish journal of pediatrics
, cilt.44, sa.1, ss.18-20, 2002 (SCI-Expanded, Scopus)
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2002196. Importance of RDW value in differential diagnosis of hypochrome anemias
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AMERICAN JOURNAL OF HEMATOLOGY
, cilt.69, sa.1, ss.31-33, 2002 (SCI-Expanded, Scopus)
2001
2001197. Severe hemolytic anemia after repair of primum septal defect and cleft mitral valve
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Turkish Journal of Pediatrics
, cilt.43, sa.4, ss.329-331, 2001 (SCI-Expanded, Scopus, TRDizin)
2001
2001198. Beta-Thalassemia Mutations in the East of Turkey.
Öner A. F., Özer R., Üner A., Arslan Ş., Gümrük F.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.18, sa.4, ss.239-41, 2001 (Scopus, TRDizin)
2001
2001199. Homozygosity for Hb E-Saskatoon [β22(B4)Glu → Lys] in a Turkish patient
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Hemoglobin
, cilt.25, sa.4, ss.409-415, 2001 (SCI-Expanded, Scopus)
2001
2001200. βB-Thalassaemia intermedia in a Turkish girl: Homozygosity for G→A substitution at +22 relative to the β-globin cap site
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British Journal of Haematology
, cilt.115, sa.1, ss.90-94, 2001 (SCI-Expanded, Scopus)
2001
2001201. Acute tumour lysis syndrome following a single-dose corticosteroid in children with acute lymphoblastic leukaemia
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EUROPEAN JOURNAL OF HAEMATOLOGY
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2001
2001202. Severe beta-thalassemia in frameshift codon 6 (-A) homozygotes: Effects of haplotype on phenotype
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HEMOGLOBIN
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2000
2000203. Triosephosphate isomerase deficiency with elevated sweat chloride test: report of a case.
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The Turkish journal of pediatrics
, cilt.42, sa.4, ss.319-21, 2000 (SCI-Expanded, Scopus, TRDizin)
2000
2000204. Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Turkey.
Oner R., Gümrük F., Acar C., Oner C., Gürgey A., Altay C.
Haematologica
, cilt.85, sa.3, ss.320-1, 2000 (SCI-Expanded, Scopus)
2000
2000205. Platelet release defect in a child with Ehlers-Danlos syndrome
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PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.17, sa.2, ss.193-194, 2000 (SCI-Expanded, Scopus)
2000
2000206. Beta-thalassemia intermedia associated with homozygosity for the -87 (C-->T) mutation in a Turkish family.
Gumruk F., Mergen H., Oner R., Ozcebe O., Sayinalp N., Oner C., et al.
Hemoglobin
, cilt.24, sa.1, ss.23-9, 2000 (SCI-Expanded, Scopus)
2000
2000207. Molecular analysis of Turkish beta-thalassemia heterozygotes with normal Hb A(2) levels
Oner R., Birben E., Acar C., Oner C., Kara A., Gumruk F., et al.
HEMOGLOBIN
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2000
2000208. Pyoderma gangrenosum in a child with myelodysplastic syndrome
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American Journal of Pediatric Hematology/Oncology
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1999209. Autoimmune hemolytic anemia with warm antibodies in children: retrospective analysis of 51 cases.
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The Turkish journal of pediatrics
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1999210. Changes of hemostatic factors in patients with hemoglobinopathies.
Oner A. F., Gürgey A., Okur H., Kirazli S., Gümrük F., Altay C.
The Turkish journal of pediatrics
, cilt.41, sa.3, ss.323-7, 1999 (SCI-Expanded, Scopus, TRDizin)
1999
1999211. A warm antibody mediated acute hemolytic anemia with reticulocytopenia in a four-month-old girl requiring immunosuppressive therapy
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TURKISH JOURNAL OF PEDIATRICS
, cilt.41, sa.2, ss.239-244, 1999 (SCI-Expanded, Scopus, TRDizin)
1999
1999212. Beta thalassaemia: A report of 20 children
Onur Ö., Sivri A., GÜMRÜK F., Altay Ç.
Clinical Rheumatology
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1998
1998213. Anaemia and thrombocytopenia due to haemophagocytosis in a 7-month-old boy with galactosialidosis
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Journal of Inherited Metabolic Disease
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1998
1998214. A comparison of the effect of high-dose methylprednisolone with conventional-dose prednisolone in acute lymphoblastic leukemia patients with randomization.
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Leukemia research
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1998
1998215. A case of hypereosinophilic syndrome associated with factor V Leiden mutation and thrombosis [1]
GÜMRÜK F., GÜRGEY A., Altay Ç.
British Journal of Haematology
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1998
1998216. Effect of alpha-gene numbers on the expression of beta-thalassemia intermedia, beta-thalassemia and (delta beta)(0)-thalassemia traits
Altay C., Oner C., Oner R., Gumruk F., Mergen H., Gurgey A.
HUMAN HEREDITY
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1998
1998217. Dramatic resolution of pleural effusion in children with chronic myelomonocytic leukemia following short-course high-dose methylprednisolone
HİÇSÖNMEZ G., ÇETİN M., Tunç B., TUNCER A., GÜMRÜK F., Yenicesu I.
Leukemia and Lymphoma
, cilt.29, sa.5-6, ss.617-623, 1998 (SCI-Expanded, Scopus)
1998
1998218. Hb H disease with homozygosity for red cell G6PD deficiency in a Turkish female
Oner C., Oner R., Birben E., Balkan H., Gumruk F., Gurgey A., et al.
HEMOGLOBIN
, cilt.22, sa.2, ss.157-160, 1998 (SCI-Expanded, Scopus)
1997
1997219. Serum erythropoietin in children with iron deficiency anemia.
Cetin M., Gürgey A., Gümrük F., Altay C.
The Turkish journal of pediatrics
, cilt.39, sa.4, ss.459-64, 1997 (Scopus)
1997
1997220. Genotype-phenotype analysis in HbS-beta-thalassemia
Altay C., Oner C., Oner R., Mesci L., Balkan H., Tuzmen S., et al.
HUMAN HEREDITY
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1997
1997221. Compound heterozygosity for hemoglobin Knossos [alpha 2 beta 2 27 (B9) Ala-Ser] and IVS I-1 mutation.
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The Turkish journal of pediatrics
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1997
1997222. The molecular basis of Hb H disease in Turkey
Oner C., Gurgey A., Oner R., Balkan H., Gumruk F., Baysal E., et al.
HEMOGLOBIN
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1996
1996223. A Novel (Δβ)°-Thalassemia due to a ∼30-kb Deletion Observed in a Turkish Family
öner R., öner C., ERDEM G., Balkan H., ÖZDAĞ SEVGİLİ H., Erkan M., et al.
Acta Haematologica
, cilt.96, sa.4, ss.232-236, 1996 (Scopus)
1996
1996224. Prenatal diagnosis of hemoglobinopathies in Turkey: Hacettepe experience
GÜRGEY A., Beksaç S., GÜMRÜK F., Çakar N., Mesçi L., Altay S., et al.
Pediatric Hematology and Oncology
, cilt.13, sa.2, ss.163-166, 1996 (Scopus)
1996
1996225. Serum TNF-alpha, gamma-INF, G-CSF and GM-CSF levels in neutropenic children with acute leukemia treated with short-course, high-dose methylprednisolone
TUNCER A. M., HİÇSÖNMEZ G., GÜMRÜK F., Sayli T., Güler E., ÇETİN M., et al.
Leukemia Research
, cilt.20, sa.3, ss.265-269, 1996 (Scopus)
1996
1996226. Treatment of hemophilic pseudotumor with low-dose radiotherapy.
Ozbek N., Unsal M., Kara A., Gumruk F., Gurgey A.
The Turkish journal of pediatrics
, cilt.38, sa.1, ss.91-4, 1996 (Scopus)
1995
1995227. The effect of high-dose methylprednisolone on CD34-positive bone marrow cells in the children with acute myeloblastic leukemia.
Tuncer A. M., Hiçsönmez G., Gümrük F., Albayrak D., Duru F., Güzel E., et al.
The Turkish journal of pediatrics
, cilt.37, sa.4, ss.345-9, 1995 (Scopus)
1995
1995228. Bernard-Soulier-like functional platelet defect in myelodysplastic syndrome and in acute myeloblastic leukemia associated with trilineage myelodysplasia.
Hiçsönmez G., Gümrük F., Cetin M., Ozbek N., Tuncer M., Gürsel T.
The Turkish journal of pediatrics
, cilt.37, sa.4, ss.425-9, 1995 (Scopus)
1995
1995229. Familial selective vitamin b12 malabsorption (imerslund-grasbeck syndrome) in a pool of turkish patients
Altay C., ÇETİN M., GÜMRÜK F., Irken G., YETGİN S., Laleli Y.
Pediatric Hematology and Oncology
, cilt.12, sa.1, ss.19-28, 1995 (Scopus)
1995
1995230. Congenital hypoplastic anemia in six patients: Unusual association of short proximal phalanges with mild anemia
ÇETİN M., Kara A., GÜRGEY A., GÜMRÜK F., Irken G., YETGİN S., et al.
Pediatric Hematology and Oncology
, cilt.12, sa.2, ss.153-158, 1995 (Scopus)
1995
1995231. Pyridoxine-responsive sideroblastic anemia in four children
Altay Ç., Gumriik F.
Pediatric Hematology and Oncology
, cilt.12, sa.2, ss.205-208, 1995 (Scopus)
1994
1994232. Vacuolated white blood cells in thalassemia major.
Duru F., Gümrük F., Gürgey A.
The Turkish journal of pediatrics
, cilt.36, sa.3, ss.255-8, 1994 (Scopus)
1994
1994233. Convulsion after blood transfusion in four p-thalassemia intermedia patients
GÜRGEY A., Kalaya Ó., Giimriik F., ÇETİN M., Altay C.
Pediatric Hematology and Oncology
, cilt.11, sa.5, ss.549-552, 1994 (Scopus)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler
2021
20211. TİP III VON WİLLEBRAND HASTALIĞI OLAN ÇOCUKLARDA UZUN SÜRELİ PROFİLAKSİ PROFİLAKSİ VERELİM Mİ? VERMEYELİM Mİ?
Coşkun Ç., AKSU T., GÜMRÜK F., AYTAÇ EYÜPOĞLU Ş. S.
7. Hemofili Vakalarla Eğitim Sempozyumu (HEVES), 18 - 20 Şubat 2021, (Özet Bildiri)
2020
20202. Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference: Interactive e-Posters
GÜREL A., ÜNAL CANGÜL Ş., Yaralı N., ŞİMŞEK KİPER P. Ö., CEYLANER S., Bilir O. A., et al.
European Society of Human Genetics Virtual Conference, June 6-9, 2020., 6 - 09 Haziran 2020, cilt.28, ss.302, (Tam Metin Bildiri)
2020
20203. Klippel–Trenaunay syndrome associated with chronic myeloid leukemia
Coşkun Ç., AKSU T., GÜMRÜK F., ÜNAL CANGÜL Ş.
XIth Eurasian Hematology Oncology, Türkiye, 21 - 24 Ekim 2020, (Özet Bildiri)
2019
20194. Pyruvate Kinase Deficiency Cases Mimicking Congenital Dyserythropoietic Anemia
ÜNAL CANGÜL Ş., AKSU T., Coşkun Ç., GÜMRÜK F.
61ND ASH ANNUAL MEETING AND EXPOSITION, Amerika Birleşik Devletleri, 7 - 10 Aralık 2019, (Özet Bildiri)
2019
20195. Cranial MRI findings of Patients with fanconi Anemia
AKSU T., GÜMRÜK F., KARLI OĞUZ H. K., BAYHAN T., coşkun ç., ÜNAL CANGÜL Ş.
31st Annual Fanconi anemia research fund scientific symposium, Chicago, Amerika Birleşik Devletleri, 19 - 22 Eylül 2019, (Tam Metin Bildiri)
2018
20186. Influence of Paroxysmal Nocturnal Hemoglobinuria Clone Positivity on Outcome of Childhood Acquired Aplastic Anemia: A Multicenter Center Study
ÜNAL CANGÜL Ş., YILMAZ KARAPINAR D., Erdem A. Y., Yarali H. N., Ozdemir H. H., GÜMRÜK F., et al.
60th Annual Meeting of the American-Society-of-Hematology (ASH), California, Amerika Birleşik Devletleri, 1 - 04 Aralık 2018, cilt.132, (Özet Bildiri)
2018
20187. Transplacental Hemophilia a and Prophylactic Treatment with Recombinant FVIIa in the Newborn Period
Aytac Ş. S., Celik T., YİĞİT Ş., GÜMRÜK F.
60th Annual Meeting of the American-Society-of-Hematology (ASH), California, Amerika Birleşik Devletleri, 1 - 04 Aralık 2018, cilt.132, (Özet Bildiri)
2017
20178. Childhood leukemia in an ETV6-related Thrombocytopenia family.
YAMAN BAJİN H. İ., AYTAÇ EYÜPOĞLU Ş. S., KUŞKONMAZ B. B., ÜNAL CANGÜL Ş., OKUR F. V., ÇETİNKAYA F. D., et al.
49th Congress of the International Society of Pediatric Oncology (SIOP), Washington, Kiribati, 12 - 15 Ekim 2017, cilt.64, ss.192, (Özet Bildiri)
2017
20179. Tyrosine Kinase Inhibitor Responses in Pediatric CML Patients: Hacettepe Experience
YAMAN BAJİN H. İ., AYTAÇ EYÜPOĞLU Ş. S., KUŞKONMAZ B. B., ÜNAL CANGÜL Ş., OKUR F. V., ÇETİNKAYA F. D., et al.
49th Congress of the International Society of Paediatric Oncology (SIOP) Washington, DC, USA October 12–15, 2017, Washington, Kiribati, 12 - 15 Ekim 2017, cilt.64, ss.202, (Özet Bildiri)
2017
201710. Galactosemia Presenting withAfibrinogenemia
GÜMRÜK F., YAMAN BAJİN H. İ., AYTAÇ EYÜPOĞLU Ş. S., ÇELİK H. T., YİĞİT Ş., TOKATLI A., et al.
XXVI Congress of the International Society on Thrombosis and Haemostasis, July 8–13, 2017, Berlin, Almanya, 8 Haziran - 13 Temmuz 2017, cilt.1, ss.648, (Özet Bildiri)
2016
201611. Long-Term Outcome of Deferasirox Chelation in Patients with Thalassemia Major
ÜNAL S., Kalkan N., ÇETİN M., GÜMRÜK F.
58th Annual Meeting and Exposition of the American-Society-of-Hematology (ASH), California, Amerika Birleşik Devletleri, 3 - 06 Aralık 2016, cilt.128, (Özet Bildiri)
2016
201612. A Homozygous Germ Line Nonsense Mutation in BRCA1 Leading Fanconi Anemia and Neuroblastoma
Mehmet D., ÜNAL S., GÜMRÜK F., Akarsu N. A.
58th Annual Meeting and Exposition of the American-Society-of-Hematology (ASH), California, Amerika Birleşik Devletleri, 3 - 06 Aralık 2016, cilt.128, (Özet Bildiri)
2016
201613. A rare cause of EBV related familial CD27 deficiency
ÜNAL CANGÜL Ş., GÜMRÜK F., TEZCAN F. İ., ÇAĞDAŞ AYVAZ D. N., ÇETİN M.
17 ESİD, 20 - 24 Eylül 2016, (Özet Bildiri)
2016
201614. The Absence of Somatic Defects in Fanconi Anemia is Not Indicative for the Absence of Bone Marrow Failure
ALTAN İ., ÜNAL CANGÜL Ş., BAYHAN T., ÜTİNE G. E., GÜMRÜK F.
Fanconi Anemia Research FundScientific Symposium September 15-18, Bellevue, Washington, USA, 15 - 18 Eylül 2016, (Özet Bildiri)
2016
201615. Use of alternative or supportive care products among hematology patients in a pediatric hematology outpatient clinic.
ÜNAL S., Bayhan T., Gumruk F., Cetin M.
Annual Meeting of the American-Society-of-Clinical-Oncology (ASCO), Illinois, Amerika Birleşik Devletleri, 3 - 07 Haziran 2016, cilt.34, (Özet Bildiri)
2016
201616. Osteosarcoma Associated Acquired Isolated Factor VII Deficiency
YAMAN BAJİN H. İ., AYTAÇ EYÜPOĞLU Ş. S., AYDIN G. B., VARAN A., ÇETİN M., GÜMRÜK F., et al.
9th Annual Congress of the European Association for Haemophilia and Allied Disorders 2016, 3 - 05 Şubat 2016, cilt.22, ss.19-111, (Özet Bildiri)
2015
201517. Serum Heavy Metal Levels in Patients with Ineffective Erythropoiesis and the Effect of Chelation on Heavy Metal Levels
BAYHAN T., ÜNAL S., Cirak E., Erdem O., Akay C., Eker I., et al.
57th Annual Meeting of the American-Society-of-Hematology, Florida, Amerika Birleşik Devletleri, 5 - 08 Aralık 2015, cilt.126, (Özet Bildiri)
2015
201518. The concomitant use of milk thistle in pediatric acute lymphoblastic leukemia for the prevention and treatment chemotherapy related hepatotoxicities.
ÜNAL S., BAYHAN T., Tavil B., GÜMRÜK F., ÇETİN M.
Annual Meeting of the American-Society-of-Clinical-Oncology (ASCO) / Clinical Science Symposium on Predicting and Improving Adverse Outcomes in Older Adults with Cancer, Illinois, Amerika Birleşik Devletleri, 29 Mayıs - 02 Haziran 2015, cilt.33, (Özet Bildiri)
2015
201519. Hematopoietic stem cell transplantation in patients with genetic hemophagocytic lymphohistiocytosis
KUŞKONMAZ B. B., AYTAÇ EYÜPOĞLU Ş. S., ÇAĞDAŞ AYVAZ D. N., BAYHAN T., TAVİL E. B., ÜNAL Ş., et al.
41 st Annual Meeting of the European Society for Blood and Marrow Transplantation, 22-25 March 2015, İstanbul, Turkey, 22 - 25 Mart 2015, (Özet Bildiri)
2015
201520. Hematopoietic stem cell transplantation in patient with genetic hemophagocytic lymphohistiocytosis
BARIŞ K., AYTAÇ EYÜPOĞLU Ş. S., ÇAĞDAŞ AYVAZ D. N., BAYHAN T., TAVİL E. B., SULE U., et al.
41st EBMTANNual Meeting,İstanbul, Turkey, 22 - 25 Mart 2015, (Özet Bildiri)
2014
201421. The Use of Biochemical Parameters Instead of MRI for the Prediction of Pancreatic Iron Loading Among Patients with beta- Thalassemia Major
Bas M., GÜMRÜK F., HAZIROLAN T., TUNCER A. M., ÇETİN M., ÜNAL S.
56th Annual Meeting of the American-Society-of-Hematology, San-Francisco, Kostarika, 6 - 09 Aralık 2014, cilt.124, (Özet Bildiri)
2014
201422. Twice Daily Use of Deferasirox Is More Effective in Decreasing Serum Ferritin
GÜMRÜK F., ÜNAL S., BAYHAN T., HAZIROLAN T., TUNCER A. M., ÇETİN M.
56th Annual Meeting of the American-Society-of-Hematology, San-Francisco, Kostarika, 6 - 09 Aralık 2014, cilt.124, (Özet Bildiri)
2014
201423. Assessment of HbF QTLs Affecting Disease Severity and Genetic Analysis in Patients Homozygous for Codon 8 (-AA) beta(0)-Thalassemia Mutation
Jiang Z., Huang S., Luo H. Y., Akar N., Basak A. N., Al-Allawi N., et al.
56th Annual Meeting of the American-Society-of-Hematology, San-Francisco, Kostarika, 6 - 09 Aralık 2014, cilt.124, (Özet Bildiri)
2007
200724. Molecular characterization of a prototype family harboring two genomic instability disorders: Ataxia telangiectasia and fanconi anemia
BALTA G., PATIROĞLU T., GÜMRÜK F., Sanal O., GÜRGEY A., Altay C.
49th Annual Meeting of the American-Society-of-Hematology, Georgia, Amerika Birleşik Devletleri, 8 - 11 Aralık 2007, cilt.110, (Özet Bildiri)
2007
200725. Successful hematopoietic stem cell transplantation in a patient with a novel DNA ligase IV mutation
ÜNAL S., Cerosaletti K., TEKİN M., ÇETİN M., Uckan-Cetinkaya D., GÜMRÜK F.
49th Annual Meeting of the American-Society-of-Hematology, Georgia, Amerika Birleşik Devletleri, 8 - 11 Aralık 2007, cilt.110, (Özet Bildiri)
2006
200626. Pyrimidine 5' nucleotidase-1 (P5N-1) deficiency associated with 4 novel mutations in 5 new Turkish families: Genotype-phenotype analysis.
Balta G., Gurgey A., Gumruk F., Buyukasik Y., Beksac M., Altay C.
48th Annual Meeting of the American-Society-of-Hematology, Florida, Amerika Birleşik Devletleri, 9 - 12 Aralık 2006, cilt.108, (Özet Bildiri)
2006
200627. Mesenchymal stem cell studies in children with inherited diseases: A proposal for identification of candidate diseases for mesenchymal stem cell therapies (Pedi-Stem Project).
ÇETİNKAYA F. D., Kılıç E., AERTS KAYA F. S. F., ÇETİN M., GÜMRÜK F., CAN A., et al.
ISCT annual meeting 2006, 4 - 07 Mayıs 2006, cilt.8, ss.241, (Özet Bildiri)
Kitaplar
2023
20231. Diamond-Blackfan Anemisi ile İlişkili Osteosarkom Olgusu
Coşkun Ç., AKSU T., GÜMRÜK F., ÜNAL CANGÜL Ş.
Olgularla Kemik İliği Yetmezlikleri, Şule Ünal Cangül, Didem Atay, Turan Bayhan, Yusuf Ziya Aral, Editör, Galenos Yayın Evi, ss.24-25, 2023
2021
20212. Fanconi Anemisi
AKSU T., GÜMRÜK F.
Kalıtsal Anemiler, Özcan Bör, Hüseyin Gülen, Şule Ünal, Editör, Galenos Yayınevi, İstanbul, ss.152-160, 2021
Desteklenen Projeler
2015 - 2020
2015 - 2020