Prof.Dr. ŞULE ÜNAL CANGÜL

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

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)

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)

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)

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) Sürdürülebilir Kalkınma

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)

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)

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)

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)

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)

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)

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)

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, ss.229-259, 2018 (SCI-Expanded)

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)

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) Sürdürülebilir Kalkınma

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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) Sürdürülebilir Kalkınma

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)

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) Sürdürülebilir Kalkınma

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)

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)

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)

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)

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) Sürdürülebilir Kalkınma

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)

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)

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)

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)

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)

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)

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, ss.317-22, 2015 (SCI-Expanded)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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) Sürdürülebilir Kalkınma

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

An unexpected parasitic cause of hypereosinophilia: fascioliasis.

Gökçe M., Sahiner Ü. M., Unal Ş., Parlakay A., Oncel I., Saçkesen C., et al.

The Turkish journal of pediatrics , cilt.53, sa.1, ss.111-3, 2011 (SCI-Expanded)

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)

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)

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)

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)

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)

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)

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)

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)

Hemophagocytosis associated with leukemia: a striking association with juvenile myelomonocytic leukemia.

Unal Ş., Cetin M., Kutlay N., Elmas S., Gumruk F., Tukun A., et al.

Annals of hematology , cilt.89, sa.4, ss.359-64, 2010 (SCI-Expanded)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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) Sürdürülebilir Kalkınma

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)

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, ss.537-41, 2008 (SCI-Expanded)

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)

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)

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)

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)

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)

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)

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)

Dysplasia and disorder of cell membrane entirety in iron-deficiency anemia

Yetgin S., Aslan D., Unal Ş., Tavil B., Kuşkonmaz B. B., Elmas S., et al.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , cilt.25, sa.6, ss.492-501, 2008 (SCI-Expanded)

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)

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)

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)

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)

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) Sürdürülebilir Kalkınma

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) Sürdürülebilir Kalkınma

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)

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)

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)

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)

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)

Autoimmune thrombocytopenic purpura after mumps infection.

Unal Ş., Yetgin S., Kara A., Kanra G.

The Turkish journal of pediatrics , cilt.47, ss.270-1, 2005 (SCI-Expanded)

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)

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)

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)

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)

Diğer Dergilerde Yayınlanan Makaleler

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)

Thalassemia

AKSU T., ÜNAL CANGÜL Ş.

Trends in pediatrics , cilt.2, sa.1, ss.1-7, 2021 (Scopus)

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)

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 (Hakemli Dergi)

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 (Hakemli Dergi)

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)

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)

Proceedings in Acta Medica

ÜNAL Ş., ER ÖZTAŞ Y., YAŞAR Ü.

Acta Medica , cilt.4, sa.1, 2015 (Hakemli Dergi)

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)

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)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

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

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

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

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

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

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

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

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

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

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

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

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