Eğitim Bilgileri
2005 - 2010
2005 - 2010Tıpta Yandal Uzmanlık
Hacettepe Üniversitesi, Çocuk Hematolojisi Ve Onkolojisi, Türkiye
1999 - 2005
1999 - 2005Tıpta Uzmanlık
Hacettepe Üniversitesi, Çocuk Sağlığı Ve Hastalıkları, Türkiye
1993 - 1999
1993 - 1999Lisans
Hacettepe Üniversitesi, Tıp Fakültesi (İngilizce), Türkiye
Yabancı Diller
C1 İleri
C1 İleriİngilizce
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
2017 - Devam Ediyor
2017 - Devam EdiyorProf. Dr.
Hacettepe Üniversitesi, Tıp Fakültesi (İngilizce), Dahili Tıp Bilimleri Bölümü
2011 - 2017
2011 - 2017Doç. Dr.
Hacettepe Üniversitesi, Tıp Fakültesi (İngilizce)
Akademi Dışı Deneyim
2010 - 2012
2010 - 2012DEVLET HİZMETİ YÜKÜMLÜLÜĞÜ, UZMAN
HATAY ANTAKYA DEVLET HASTANESİ, DEVLET HİZMETİ YÜKÜMLÜLÜĞÜ, UZMAN
Makaleler
2022
20221. 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
20222. Clinical Characteristics and Outcomes of COVID-19 in Turkish Patients with Hematological Malignancies
CİVRİZ BOZDAĞ S., CENGİZ SEVAL G., Hindilerden I. Y., Hindilerden F., ANDIÇ N., BAYDAR M., et al.
TURKISH JOURNAL OF HEMATOLOGY
, cilt.39, sa.1, ss.43-54, 2022 (SCI-Expanded, Scopus, TRDizin)
2021
20213. Thalassemia
AKSU T., ÜNAL CANGÜL Ş.
Trends in pediatrics
, cilt.2, sa.1, ss.1-7, 2021 (Scopus)
2020
20204. 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
20205. 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
20206. 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
20207. Modelling the future of HIV in Turkey: disease implications of improving prevention, diagnosis and treatment
Yaylali E., Gokengin D., Korten V., Tabak F., Unal S., Erdogan Z., et al.
JOURNAL OF THE INTERNATIONAL AIDS SOCIETY
, cilt.23, ss.96-97, 2020 (SCI-Expanded, Scopus)
2020
20208. 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
20209. TURKEY CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA REGISTRATION SYSTEM RESULTS
Albayrak C., Albayrak D., Oren H., Aksu T., Yarali N., Kacar D., et al.
HAEMOPHILIA
, cilt.26, ss.146-147, 2020 (SCI-Expanded, Scopus)
2020
202010. Outcomes of Eltrombopag Treatment and Development of Iron Deficiency in Children with Immune Thrombocytopenia in Turkey
Yozgat A. K., LEBLEBİSATAN G., Akbayram S., Ozel S. C., KARAKAŞ Z., ERDURAN E., et al.
TURKISH JOURNAL OF HEMATOLOGY
, cilt.37, sa.3, ss.139-144, 2020 (SCI-Expanded, Scopus, TRDizin)
2020
202011. 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
202012. 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)
2019
201913. 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
201914. Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein.
Russo R., Marra R., Andolfo I., De R., Rosato B., Manna F., et al.
Frontiers in physiology
, cilt.10, ss.621, 2019 (SCI-Expanded, Scopus)
2019
201915. Refugee children with beta-thalassemia in Turkey: Overview of demographic, socioeconomic, and medical characteristics.
Yazal E., Demir Y., Pekpak E., Akıncı B., Aktekin E., Bayram C., et al.
Pediatric blood & cancer
, cilt.66, 2019 (SCI-Expanded, Scopus)
2019
201916. 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
201817. Both Granulocytic and Non-Granulocytic Blood Cells Are Affected in Patients with Severe Congenital Neutropenia and Their Non-Neutropenic Family Members: An Evaluation of Morphology, Function, and Cell Death.
Olcay L., Ünal Ş., Onay H., Erdemli E., Öztürk A., Billur D., et al.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.35, sa.4, ss.229-259, 2018 (SCI-Expanded, Scopus, TRDizin)
2018
201818. Molecular approaches to diagnose Diamond-Blackfan anemia: The EuroDBA experience.
Da C., O'Donohue M., van D., Albrecht K., Unal Ş., Ramenghi U., et al.
European journal of medical genetics
, cilt.61, ss.664-673, 2018 (SCI-Expanded, Scopus)
2018
201819. 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
201820. Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias.
Russo R., Andolfo I., Manna F., Gambale A., Marra R., Rosato B., et al.
American journal of hematology
, cilt.93, ss.672-682, 2018 (SCI-Expanded, Scopus)
2018
201821. MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia.
Germeshausen M., Ancliff P., Estrada J., Metzler M., Ponstingl E., Rütschle H., et al.
Blood advances
, cilt.2, ss.586-596, 2018 (SCI-Expanded, Scopus)
2018
201822. 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
201823. A National Registry of Thalassemia in Turkey: Demographic and Disease Characteristics of Patients, Achievements, and Challenges in Prevention.
Aydınok Y., Oymak Y., Atabay B., Aydoğan G., Yeşilipek A., Ünal S., et al.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.35, ss.12-18, 2018 (SCI-Expanded, Scopus, TRDizin)
2018
201824. 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)
2017
201725. Acute myeloid leukemia in a child with dedicator of cytokinesis 8 (DOCK8) deficiency
Kuşkonmaz B. B., Ayvaz D. N., Barış S., Ünal Ş., Tezcan İ., Uçkan D.
PEDIATRIC BLOOD & CANCER
, cilt.64, sa.12, 2017 (SCI-Expanded, Scopus)
2017
201726. Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like features.
Carapito R., Konantz M., Paillard C., Miao Z., Pichot A., Leduc M., et al.
The Journal of clinical investigation
, cilt.127, ss.4090-4103, 2017 (SCI-Expanded, Scopus)
2017
201727. 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
201728. Rapid lung magnetic resonance imaging in children with pulmonary infection: reply to Sodhi et al.
Ozcan H., Gormez A., Ozsurekci Y., Karakaya J., Oguz B., Unal Ş., et al.
Pediatric radiology
, cilt.47, ss.766, 2017 (SCI-Expanded, Scopus)
2017
201729. 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)
2017
201730. Predictors of Suboptimal Follow-up in Pediatric Cancer Survivors.
May L., Schwartz D., Frugé E., Laufman L., Holm S., Kamdar K., et al.
Journal of pediatric hematology/oncology
, cilt.39, 2017 (SCI-Expanded, Scopus)
2017
201731. Magnetic resonance imaging of pulmonary infection in immunocompromised children: comparison with multidetector computed tomography.
Ozcan H., Gormez A., Ozsurekci Y., Karakaya J., Oguz B., Unal Ş., et al.
Pediatric radiology
, cilt.47, ss.146-153, 2017 (SCI-Expanded, Scopus)
2016
201632. 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
201633. THE GLYCOCALYX AND TRAUMA: A REVIEW
Chignalia A., Yetimakman F., Christiaans S., Unal Ş., Bayrakci B., Wagener B., et al.
SHOCK
, cilt.45, sa.4, ss.338-348, 2016 (SCI-Expanded, Scopus)
2016
201634. 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
201635. 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
201636. 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
201637. 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
201638. 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
201639. Hypocholesterolemia A Neglected Laboratory Finding
ER ÖZTAŞ Y., ÜNAL CANGÜL Ş., YAŞAR Ü.
Acta Medica , cilt.5, sa.1, ss.19-22, 2016 (Hakemli Dergi)
2016
201640. The European Hematology Association Roadmap for European Hematology Research: a consensus document.
Engert A., Balduini C., Brand A., Coiffier B., Cordonnier C., Döhner H., et al.
Haematologica
, cilt.101, ss.115-208, 2016 (SCI-Expanded, Scopus)
2016
201641. Achievements in the last year and the new targets
ER ÖZTAŞ Y., ÜNAL CANGÜL Ş., YAŞAR Ü.
Acta Medica , cilt.5, sa.1, ss.1, 2016 (Hakemli Dergi)
2016
201642. 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
201643. 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
201544. Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis.
Tesi B., Lagerstedt-Robinson K., Chiang S., Ben B., Abboud M., Belen B., et al.
Genome medicine
, cilt.7, ss.130, 2015 (SCI-Expanded, Scopus)
2015
201545. Transcobalamin II Deficiency in Four Cases with Novel Mutations.
Ünal Ş., Rupar T., Yetgin S., Yaralı N., Dursun A., Gürsel T., et al.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.32, sa.4, ss.317-22, 2015 (SCI-Expanded, Scopus, TRDizin)
2015
201546. 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
201547. Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense Mutations.
Tesi B., Chiang S., El-Ghoneimy D., Hussein A., Langenskiöld C., Wali R., et al.
Pediatric blood & cancer
, cilt.62, ss.2094-100, 2015 (SCI-Expanded, Scopus)
2015
201548. 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
201549. 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
201550. 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
201551. 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
201552. 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
201553. 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
201554. Proceedings in Acta Medica
ÜNAL Ş., ER ÖZTAŞ Y., YAŞAR Ü.
Acta Medica , cilt.4, sa.1, 2015 (Hakemli Dergi)
2015
201555. 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)
2015
201556. 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
201557. 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
201558. Mean Platelet Volume can Predict Cerebrovascular Events in Patients with Sickle Cell Anemia.
Celik T., Unal Ş., Ekinci O., Ozer C., Ilhan G., Oktay G., et al.
Pakistan journal of medical sciences
, cilt.31, ss.203-8, 2015 (SCI-Expanded, Scopus)
2015
201559. 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)
2014
201460. 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
201461. Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: definition of clinical and molecular spectrum and identification of new diagnostic scores.
Russo R., Gambale A., Langella C., Andolfo I., Unal Ş., Iolascon A.
American journal of hematology
, cilt.89, 2014 (SCI-Expanded, Scopus)
2014
201462. 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
201463. 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
201464. 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
201465. 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
201466. 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
201467. Kindlin-3-independent adhesion of neutrophils from patients with leukocyte adhesion deficiency type III
VAN DE VIJVER E., TOOL A. T. J., SANAL O., Cetin M., Unal S., Aytac Ş. S., et al.
Journal of Allergy and Clinical Immunology
, cilt.133, sa.4, ss.1215, 2014 (SCI-Expanded, Scopus)
2013
201368. 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
201369. Nocturnal enuresis in sickle cell disease and thalassemia major: associated factors in a clinical sample.
Ekinci O., Celik T., Ünal Ş., Oktay G., Toros F., Ozer C.
International journal of hematology
, cilt.98, ss.430-6, 2013 (SCI-Expanded, Scopus)
2013
201370. 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
201371. THROMBOPHILIC RISK FACTORS AND THE EFFICIENCY OF PROPHYLACTIC ANTICOAGULATION THERAPY IN CHILDREN WHO UNDERWENT RENAL TRANSPLANTATION
Tavil B., Aytac S., Gulhan B., Aki F., Unal S., Cetin M., et al.
HAEMATOLOGICA
, cilt.98, ss.753, 2013 (SCI-Expanded, Scopus)
2013
201372. 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
201373. Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine production.
Chiang S., Theorell J., Entesarian M., Meeths M., Mastafa M., Al-Herz W., et al.
Blood
, cilt.121, ss.1345-56, 2013 (SCI-Expanded, Scopus)
2012
201274. Medical management of moyamoya disease and recurrent stroke in an infant with Majewski osteodysplastic primordial dwarfism type II (MOPD II).
Kılıç E., Utine E., Unal Ş., Haliloğlu G., Oğuz K., Cetin M., et al.
European journal of pediatrics
, cilt.171, ss.1567-71, 2012 (SCI-Expanded, Scopus)
2012
201275. Psychiatric problems in children and adolescents with sickle cell disease, based on parent and teacher reports.
Ekinci O., Celik T., Unal Ş., Ozer C.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.29, ss.259-64, 2012 (SCI-Expanded, Scopus, TRDizin)
2012
201276. 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
201277. 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
201278. Observational study comparing long-term safety and efficacy of Deferasirox with Desferrioxamine therapy in chelation-naïve children with transfusional iron overload.
Aydinok Y., Unal Ş., Oymak Y., Vergin C., Türker Z., Yildiz D., et al.
European journal of haematology
, cilt.88, ss.431-8, 2012 (SCI-Expanded, Scopus)
2012
201279. Hematologically important mutations: Leukocyte adhesion deficiency (first update)
van de Vijver E., Maddalena A., Sanal O., Holland S. M., Uzel G., Madkaikar M., et al.
BLOOD CELLS MOLECULES AND DISEASES
, cilt.48, sa.1, ss.53-61, 2012 (SCI-Expanded, Scopus)
2012
201280. 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
201181. 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
201182. 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
201183. Mild to fatal course of pandemic influenza H1N1 in children with acute leukaemia.
Sule U., Muge G., Selin A., Murat T., Mualla C., Fatma G.
British journal of haematology
, cilt.152, ss.492-3, 2011 (SCI-Expanded, Scopus)
2011
201184. 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
201085. 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
201086. 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
201087. 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
201088. 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
201089. 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
201090. Assessment of clinical and laboratory presentations of familial hemophagocytic lymphohistiocytosis patients with homozygous W374X mutation.
Balta G., Okur H., Unal Ş., Yarali N., Gunes A., Unal S., et al.
Leukemia research
, cilt.34, ss.1012-7, 2010 (SCI-Expanded, Scopus)
2010
201091. 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
201092. 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
201093. 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
201094. 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)
2010
201095. 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)
2009
200996. Depletion of innate immunity or bone marrow suppresion by viral infection ?
Özsoylu Ş., Ünal Ş.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.26, ss.158, 2009 (SCI-Expanded, Scopus, TRDizin)
2009
200997. Hypertrichosis: the possible side effect of cyclosporin in an infant with hemophagocytic lymphohistiocytosis receiving HLH-2004 chemotherapy protocol.
Akgül S., Balcı Y., Ünal Ş., Alikaşifoğlu A., Gürgey A.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.26, ss.154-6, 2009 (SCI-Expanded, Scopus, TRDizin)
2009
200998. Mild clinical phenotype and subtle radiographic findings in an infant with cartilage-hair hypoplasia.
Türkkani-Asal G., Alanay Y., Turul-Ozgür T., Zenker M., Thiel C., Rauch A., et al.
The Turkish journal of pediatrics
, cilt.51, ss.493-6, 2009 (SCI-Expanded, Scopus)
2009
200999. Disease causing nature of homozygous missense, p.A523D, alteration in the perforin gene.
Oner A., Okur H., Balta G., Unal Ş., Deger I., Akarsu N., et al.
Leukemia research
, cilt.33, 2009 (SCI-Expanded, Scopus)
2009
2009100. 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
2009101. 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
2009102. LAD-1/variant syndrome is caused by mutations in FERMT3.
Kuijpers T., van d., Weterman M., de B., Tool A., van d., et al.
Blood
, cilt.113, ss.4740-6, 2009 (SCI-Expanded, Scopus)
2009
2009103. Malignancy-associated hemophagocytic lymphohistiocytosis in pediatric cases: a multicenter study from Turkey.
Celkan T., Berrak S., Kazanci E., Ozyürek E., Unal Ş., Uçar C., et al.
The Turkish journal of pediatrics
, cilt.51, ss.207-13, 2009 (SCI-Expanded, Scopus)
2009
2009104. Transient depletion of innate immunity in varicella infections in otherwise healthy children.
Erdemli N., Ünal Ş., Okur H., Seçmeer G., Kara A., Gürgey A.
Turkish journal of haematology : official journal of Turkish Society of Haematology
, cilt.26, ss.12-6, 2009 (SCI-Expanded, Scopus, TRDizin)
2009
2009105. 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
2009106. Successful treatment with gemtuzumab ozogamicin monotherapy in a pediatric patient with resistant relapse of acute myeloid leukemia
Unal Ş., Cakir M., Kuşkonmaz B. B., Cetin M., Tuncer A.
TURKISH JOURNAL OF PEDIATRICS
, cilt.51, sa.1, ss.69-71, 2009 (SCI-Expanded, Scopus)
2008
2008107. Neonatal Primary Hemophagocytic Lymphohistiocytosis in Turkish Children
Gurgey A., Unal Ş., Okur H., Orhan D., Yurdakok M.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, cilt.30, sa.12, ss.871-876, 2008 (SCI-Expanded, Scopus)
2008
2008108. 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
2008109. The prognostic impact of myeloid antigen expression in pediatric acute lymphoblastic leukemia patients.
Unal Ş., Cetin M., Tuncer A., Gümrük F., Yetgin S.
The Turkish journal of pediatrics
, cilt.50, sa.6, ss.533-6, 2008 (SCI-Expanded, Scopus)
2008
2008110. The absence of peripheral blood blasts at diagnosis may predict CNS involvement or CNS relapse in pediatric acute lymphoblastic leukemia patients.
Unal Ş., Tuncer A., Cetin M., Yetgin S.
The Turkish journal of pediatrics
, cilt.50, sa.6, ss.537-41, 2008 (SCI-Expanded, Scopus)
2008
2008111. Lymphocytic vacuolization in sialic acid storage disease
Kuskonmaz B. B., Unal Ş., Cördükcü E., Aydin H., Coskun T., Gurgey A., et al.
AMERICAN JOURNAL OF HEMATOLOGY
, cilt.83, sa.10, ss.821, 2008 (SCI-Expanded, Scopus)
2008
2008112. 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
2008113. Clinical and molecular aspects of Turkish familial hemophagocytic lymphohistiocytosis patients with perforin mutations
Okur H., Balta G., Akarsu N., Oner A., Patiroglu T., Bay A., et al.
LEUKEMIA RESEARCH
, cilt.32, sa.6, ss.972-975, 2008 (SCI-Expanded, Scopus)
2008
2008114. The rapid correction of hypercalcemia at presentation of acute lymphoblastic leukemia using high-dose methylprednisolone
Unal Ş., Durmaz E., Erkoçoğlu M., Bayrakçi B., Bircan O., Alikaşifoğlu A., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.50, sa.2, ss.171-175, 2008 (SCI-Expanded, Scopus)
2008
2008115. 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
2008116. Weekly long-term intravenous immunoglobulin for refractory parvovirus B19 and Epstein-Barr virus-induced immune thrombocytopenic purpura
Tavil B., Unal Ş., Aytaç-Elmas Ş. S., Yetgin S.
TURKISH JOURNAL OF PEDIATRICS
, cilt.50, sa.1, ss.74-77, 2008 (SCI-Expanded, Scopus)
2008
2008117. Foamy histiocytes in a patient with visceral leishmaniasis after treatment with liposomal amphotericin B.
Tavil B., Seçmeer G., Ozen H., Cengiz A., Unal Ş., Gürgey A.
The Turkish journal of pediatrics
, cilt.50, ss.67-9, 2008 (SCI-Expanded, Scopus)
2008
2008118. Dysplasia and disorder of cell membrane entirety in iron-deficiency anemia
Yetgin S., Aslan D., Unal Ş., Tavil B., Kuşkonmaz B. B., Elmas Ş. S., et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, cilt.25, sa.6, ss.492-501, 2008 (SCI-Expanded, Scopus)
2007
2007119. Case reports of successful therapeutic plasma exchange in severe amitriptyline poisoning
Bayrakci B., Unal Ş., Erkocoglu M., Güngör H., Aksu S.
THERAPEUTIC APHERESIS AND DIALYSIS
, cilt.11, sa.6, ss.452-454, 2007 (SCI-Expanded, Scopus)
2007
2007120. Favorable outcome with allogeneic hematopoietic stem cell transplantation in pediatric acquired aplastic anemia patients.
Unal Ş., Cetin M., Tavil B., Calişkan N., Yetgin S., Uçkan D.
Pediatric transplantation
, cilt.11, sa.7, ss.788-91, 2007 (SCI-Expanded, Scopus)
2007
2007121. Allogeneic hematopoietic stem cell transplantation in pediatric chronic myelogenous leukemia cases: Hacettepe experience.
Unal Ş., Fidan G., Tavil B., Cetin M., Cetinkaya D.
Pediatric transplantation
, cilt.11, sa.6, ss.645-9, 2007 (SCI-Expanded, Scopus)
2007
2007122. 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
2007123. 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
, cilt.37, sa.7, ss.498-502, 2007 (SCI-Expanded, Scopus)
2007
2007124. Successful treatment of propafenone, digoxin and warfarin overdosage with plasma exchange therapy and rifampicin
Unal Ş., Bayrakci B., Yasar U., Karagoz T.
CLINICAL DRUG INVESTIGATION
, cilt.27, sa.7, ss.505-508, 2007 (SCI-Expanded, Scopus)
2006
2006125. 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
2006126. 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
, cilt.30, sa.5, ss.537-541, 2006 (SCI-Expanded, Scopus)
2005
2005127. Focal segmental glomerulosclerosis associated with mitochondrial cytopathy: Report of two cases with special emphasis on podocytes
Gucer S., Talim B., Asan E., Korkusuz P., Ozen S., Unal Ş., et al.
PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
, cilt.8, sa.6, ss.710-717, 2005 (SCI-Expanded, Scopus)
2005
2005128. Answer to hypotonia: a simple hemogram.
Kanra G., Cetin M., Unal Ş., Haliloglu G., Akça T., Akalan N., et al.
Journal of child neurology
, cilt.20, ss.930-1, 2005 (SCI-Expanded, Scopus)
2005
2005129. Autoimmune thrombocytopenic purpura after mumps infection.
Unal Ş., Yetgin S., Kara A., Kanra G.
The Turkish journal of pediatrics
, cilt.47, sa.3, ss.270-1, 2005 (SCI-Expanded, Scopus)
2005
2005130. Four-month-old infant with focal segmental glomerulosclerosis and mitochondrial DNA deletion
Unal S., Kalkanoglu H., Kocaefe C., Gueer S., Ozen S., TURANLI G., et al.
JOURNAL OF CHILD NEUROLOGY
, cilt.20, sa.1, ss.83-84, 2005 (SCI-Expanded, Scopus)
2001
2001131. Acute gastric dilatation complicating the use of mydriatics in a preterm newborn
SARICI S., YURDAKOK M., Unal S.
PEDIATRIC RADIOLOGY
, cilt.31, sa.8, ss.581-583, 2001 (SCI-Expanded, Scopus)
2000
2000132. Evaluation of surveillance methods for detecting hospital infections at a Turkish university hospital
Babur Y., Cetinkaya Y., Hayran M., Akova M., Sayek I., Unal S.
CLINICAL INFECTIOUS DISEASES
, cilt.31, sa.1, ss.282, 2000 (SCI-Expanded, Scopus)
2000
2000133. Adrenocortical carcinoma associated with adrenogenital syndrome in a child
Varan A., Unal S., Ruacan S., Vidinlisan S.
MEDICAL AND PEDIATRIC ONCOLOGY
, cilt.35, sa.1, ss.88-90, 2000 (SCI-Expanded)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler
2023
20231. GINS4 deficiency - an immunodeficiency syndrome with complex developmental aberrations
Nieke J., Meino R., Smiers F., ÜNAL CANGÜL Ş., Klein C.
56th Annual Conference of the European-Society-of-Human-Genetics (ESHG), Glasgow, İngiltere, 10 - 13 Haziran 2023, ss.452, (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. Occurence of acute myeloid leukemia after primary hepatic carcinoma in a patient who had liver transplantation
COŞKUN Ç., ÜNAL CANGÜL Ş., ÜNER A., AKSU T., AYTAÇ EYÜPOĞLU Ş. S., KUŞKONMAZ B. B., et al.
XIth Eurasian Hematology Oncology, 21 Ekim 2020, cilt.42, ss.72-73, (Özet Bildiri)
2020
20204. 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
20195. The Outcome of Modified St. Jude Total XV Protocol in Turkish Children with Newly Diagnosed Acute Lymphoblastic Leukemia
KÖSE H., AYTAÇ EYÜPOĞLU Ş. S., KUŞKONMAZ B. B., UÇKAN ÇETİNMKAYA D., ÜNAL CANGÜL Ş., GÜMRÜK F., et al.
61th ASH Annuan Meeting, 7 - 10 Aralık 2019
2019
20196. 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
20197. Muscle strength is associated with activities and participation level in children with acute lymphoblastic leukemia undergoing consolidation therapy
Kabak V. Y., Ipek F., Dogan M., Uysal S. A., Unal S., Duger T.
10th Eurasian Hematology Oncology Congress, İstanbul, Türkiye, 8 - 11 Ekim 2019, cilt.85, (Özet Bildiri)
2019
20198. Wait and watch, or test for anti-granulocyte antibody
Coskun C., Gumruk F., Unal S.
10th Eurasian Hematology Oncology Congress, İstanbul, Türkiye, 8 - 11 Ekim 2019, cilt.85, (Özet Bildiri)
2019
20199. 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)
2019
201910. AB0574 A MONOGENIC DISEASE WITH WIDE RANGE OF SYMPTOMS: DEFICIENCY OF ADENOSINE DEAMINASE 2
BATU AKAL E. D., TAŞKIRAN Z. E., TEZCAN F. İ., ÖZKARA H. A., ÇAĞDAŞ AYVAZ D. N., ÖZEN S., et al.
Annual European Congress of Rheumatology (EULAR), Madrid, İspanya, 12 - 15 Haziran 2019, cilt.78, ss.1748, (Tam Metin Bildiri)
2018
201811. 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)
2017
201712. 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
201713. 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)
2016
201614. A Rare Cause of EBV related Familial HLH CD27 Deficiency
ÜNAL CANGÜL Ş., GÜMRÜK F., TEZCAN F. İ., ÇAĞDAŞ AYVAZ D. N., ÇETİN M.
ESID 2016, 21 - 24 Eylül 2016, (Özet Bildiri)
2016
201615. 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
201616. 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
201617. Pediatrik hematopoietik kök hücre nakli sonrasında görülen dirençli sitopenilerin rituksimab ile tedavi sonuçları
AKSU T., KUŞKONMAZ B. B., OKUR F. V., ÜNAL CANGÜL Ş., ÇETİNKAYA F. D.
9. Ulusal Kemik İliği Transplantasyonu ve Kök Hücre Tedavileri Kongresi, 03 Mart 2016, (Özet Bildiri)
2015
201518. 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)
2005
200519. Mitokondriyal sitopati ile ilişkili fokal segmental glomeruloskleroz Podosit ince yapısı ağırlıklı iki olgu sunumu
GÜÇER K. Ş., TALİM B., AŞAN E., KORKUSUZ P., ÖZEN S., ÜNAL Ş.
17. Ulusal Elektronmikroskobi kongresi. Uluslararası katılımlı, Türkiye, 22 - 24 Haziran 2005, (Özet Bildiri)
Kitaplar
2023
20231. Nötropeninin Nadir Bir Nedeni: Bileşik Heterozigot Mutasyonu Olan Shwachman-Diamond Sendromu
AKSU T., AKARSU A. N., ÜNAL CANGÜL Ş.
Olgularla Kemik İliği Yetmezlikleri, Şule Ünal Cangül, Didem Atay, Turan Bayhan, Yusuf Ziya Aral, Editör, Galenos Yayın Evi, ss.171-173, 2023
2023
20232. CTC1 Mutasyonu İlişkili İzole Kalıtsal Kemik İliği Yetmezliği Olgusu
AKSU T., ÜNAL CANGÜL Ş.
Olgularla Kemik İliği Yetmezlikleri, Şule Ünal Cangül, Didem Atay, Turan Bayhan, Yusuf Ziya Aral, Editör, Galenos Yayın Evi, ss.59-61, 2023
2023
20233. 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
20214. Hemoglobinopatiler
AKSU T., ÜNAL CANGÜL Ş.
Pediatri, Zülfikar Akelma, Editör, Ankara Nobel Tıp Kitabevleri Ltd. Şti., Ankara, ss.949-954, 2021
Desteklenen Projeler
2020 - 2024
2020 - 2024Primer ve Sekonder Hemofagositik Lenfohistiositozun Tanısında T ve NK HücreFonksiyonlarının ve Biyobelirteçlerin Rolü
Dernek (STK)
Aksu T. (Yürütücü), Aytaç Eyüpoğlu Ş. S., Alpdündar Bulut E., Çetinkaya F. D., Ünal Cangül Ş.
2015 - 2020
2015 - 2020Rotasyonel tromboelastografi ROTEM cihazı kullanılarak çocuklarda santral venöz kateterlerde tromboz gelişimi riskinin öngörülebilirliğinin belirlenmesi
Yükseköğretim Kurumları Destekli Proje , BAP Diğer
GÜMRÜK F. (Yürütücü), BAYHAN T., ÜNAL Ş., ÇETİN M.
2017 - 2019
2017 - 2019Hacettepe Üniversitesi Tıp Fakültesi Dergisi Acta Medica'nın Yapılandırılması
Yükseköğretim Kurumları Destekli Proje , BAP Diğer
KARAKOÇ D. (Yürütücü), YORGUN H., ÜNAL CANGÜL Ş., ER ÖZTAŞ Y., ESENDAĞLI G., KONAŞ E., et al.
2015 - 2017
2015 - 2017Kafa Travması Olan ve Olmayan Ağır Travmalı Pediatrik Hastalarda Koagulopatinin Değerlendirilmesi
Yükseköğretim Kurumları Destekli Proje , BAP Diğer
BAYRAKCİ B. (Yürütücü), GÜMRÜK F., ÇETİN M., ÜNAL Ş., KESİCİ S., TEKŞAM Ö., et al.
2015 - 2015
2015 - 2015Diamond Blackfan anemili hastalarda yüksek çözünürlüklü dizileme yöntemi ile genom boyu analizi
Yükseköğretim Kurumları Destekli Proje , BAP Diğer
ÜNAL CANGÜL Ş. (Yürütücü), ÇETİN M., AKARSU A. N., GÜMRÜK F., TAŞKIRAN Z. E., BAYHAN T.
Bilimsel Dergilerdeki Faaliyetler
2018 - Devam Ediyor
2018 - Devam EdiyorTurkish Journal Of Pediatrics
Editör
2014 - Devam Ediyor
2014 - Devam Ediyor