Yayınlar & Eserler

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Modelling the future of HIV in Turkey: disease implications of improving prevention, diagnosis and treatment

JOURNAL OF THE INTERNATIONAL AIDS SOCIETY, cilt.23, ss.96-97, 2020 (SCI İndekslerine Giren Dergi) identifier

Rare Cytogenetic Anomalies in Two Pediatric Patients with Acute Leukemia

TURKISH JOURNAL OF HEMATOLOGY, cilt.37, sa.2, ss.132-133, 2020 (SCI İndekslerine Giren Dergi) identifier identifier identifier

A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2.

The Journal of rheumatology, cilt.47, sa.1, ss.117-125, 2020 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Vacuolization in Myeloid and Erythroid Precursors in a Child with Menkes Disease

Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.36, ss.203-204, 2019 (SCI İndekslerine Giren Dergi) identifier identifier

Molecular approaches to diagnose Diamond-Blackfan anemia: The EuroDBA experience.

European journal of medical genetics, cilt.61, ss.664-673, 2018 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, cilt.115, sa.20, ss.5241-5246, 2018 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias.

American journal of hematology, cilt.93, ss.672-682, 2018 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

A National Registry of Thalassemia in Turkey: Demographic and Disease Characteristics of Patients, Achievements, and Challenges in Prevention.

Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.35, ss.12-18, 2018 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like features.

The Journal of clinical investigation, cilt.127, ss.4090-4103, 2017 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Heavy metal levels in patients with ineffective erythropoiesis.

Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis, cilt.56, ss.539-543, 2017 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Predictors of Suboptimal Follow-up in Pediatric Cancer Survivors.

Journal of pediatric hematology/oncology, cilt.39, 2017 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Hypereosinophilic Syndrome: Hacettepe Experience

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, cilt.38, sa.7, ss.539-543, 2016 (SCI İndekslerine Giren Dergi) identifier identifier identifier

THE GLYCOCALYX AND TRAUMA: A REVIEW.

Shock (Augusta, Ga.), cilt.45, ss.338-48, 2016 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Serum Lipids in Turkish Patients with β-Thalassemia Major and β-Thalassemia Minor.

Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.33, ss.72-3, 2016 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotes.

British journal of haematology, cilt.172, ss.958-65, 2016 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Effects of blood transfusion on cytokine profile and pulmonary function in patients with thalassemia major.

The clinical respiratory journal, cilt.10, ss.153-62, 2016 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Neonates born to mothers with immune thrombocytopenic purpura: a single-center experience of 20 years

BLOOD COAGULATION & FIBRINOLYSIS, cilt.27, sa.1, ss.19-23, 2016 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense Mutations.

Pediatric blood & cancer, cilt.62, ss.2094-100, 2015 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Transcobalamin II Deficiency in Four Cases with Novel Mutations.

Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.32, ss.317-22, 2015 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

An Infant With Congenital Leukemia Cutis and AML-M5 With MLL Gene Rearrangement.

Journal of pediatric hematology/oncology, cilt.37, ss.566-7, 2015 (SCI Expanded İndekslerine Giren Dergi) identifier identifier

Case series of thromboembolic complications in childhood nephrotic syndrome: Hacettepe experience

Clinical and Experimental Nephrology, cilt.19, sa.3, ss.506-513, 2015 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

The Hematological and Molecular Spectrum of α-Thalassemias in Turkey: The Hacettepe Experience.

Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.32, ss.136-43, 2015 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Iron chelation with deferasirox in a patient with de-novo ferroportin mutation.

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 İndekslerine Giren Dergi) identifier identifier identifier

Molecular Analyses of Pyruvate Kinase Deficient Turkish Patients from a Single Center.

Pediatric hematology and oncology, cilt.32, ss.354-61, 2015 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Fanconi's Anemia Effect or Sickle Cell Anemia Effect: That is the Question.

Hemoglobin, cilt.39, ss.287-9, 2015 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Mean Platelet Volume can Predict Cerebrovascular Events in Patients with Sickle Cell Anemia.

Pakistan journal of medical sciences, cilt.31, ss.203-8, 2015 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Bleeding and non-bleeding phenotypes in patients with GGCX gene mutations.

Thrombosis research, cilt.134, ss.856-65, 2014 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

The relationship between hematological findings and coronary artery aneurysm in kawasaki disease.

Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.31, ss.199-200, 2014 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Lysosomal vesicles, giant granules, and erythrophagocytosis in chédiak-higashi syndrome.

Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.31, ss.209-10, 2014 (SCI İndekslerine Giren Dergi) identifier identifier

A novel mutation in protein C gene (PROC) causing severe phenotype in neonatal period.

Pediatric blood & cancer, cilt.61, ss.763-4, 2014 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Congenital thrombotic thrombocytopenic purpura with novel mutations in three unrelated Turkish children.

Pediatric blood & cancer, cilt.61, ss.558-61, 2014 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Kindlin-3-independent adhesion of neutrophils from patients with leukocyte adhesion deficiency type III

Journal of Allergy and Clinical Immunology, cilt.133, sa.4, ss.1215, 2014 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Nocturnal enuresis in sickle cell disease and thalassemia major: associated factors in a clinical sample.

International journal of hematology, cilt.98, ss.430-6, 2013 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Glucose-6-phosphate dehydrogenase deficiency in neonatal hyperbilirubinaemia: Hacettepe experence

JOURNAL OF PAEDIATRICS AND CHILD HEALTH, cilt.49, sa.5, ss.399-402, 2013 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Psychiatric problems in children and adolescents with sickle cell disease, based on parent and teacher reports.

Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.29, ss.259-64, 2012 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Recurrent pediatric thrombosis: The effect of underlying and/or coexisting factors

Blood Coagulation and Fibrinolysis, cilt.23, sa.5, ss.434-439, 2012 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Hematologically important mutations: Leukocyte adhesion deficiency (first update)

BLOOD CELLS MOLECULES AND DISEASES, cilt.48, sa.1, ss.53-61, 2012 (SCI İndekslerine Giren Dergi) identifier identifier identifier

A rare metabolic complication of acute lymphoblastic leukemia in childhood: lactic acidosis

TURKISH JOURNAL OF PEDIATRICS, cilt.54, sa.1, ss.61-63, 2012 (SCI İndekslerine Giren Dergi) identifier identifier identifier

The frequency of A91V in the perforin gene and the effect of tumor necrosis factor-α promoter polymorphism on acquired hemophagocytic lymphohistiocytosis.

Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.28, ss.125-30, 2011 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Mild to fatal course of pandemic influenza H1N1 in children with acute leukaemia.

British journal of haematology, cilt.152, ss.492-3, 2011 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

An unexpected parasitic cause of hypereosinophilia: fascioliasis.

The Turkish journal of pediatrics, cilt.53, ss.111-3, 2011 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Autoimmune hemolytic anemia and giant cell hepatitis: Report of three infants

TURKISH JOURNAL OF HEMATOLOGY, cilt.27, sa.4, ss.308-313, 2010 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Dual-echo TFE MRI for the assessment of myocardial iron overload in beta-thalassemia major patients.

Diagnostic and interventional radiology (Ankara, Turkey), cilt.16, ss.59-62, 2010 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Depletion of innate immunity or bone marrow suppresion by viral infection ?

Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.26, ss.158, 2009 (SCI Expanded İndekslerine Giren Dergi) identifier

Hypertrichosis: the possible side effect of cyclosporin in an infant with hemophagocytic lymphohistiocytosis receiving HLH-2004 chemotherapy protocol.

Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.26, ss.154-6, 2009 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Mild clinical phenotype and subtle radiographic findings in an infant with cartilage-hair hypoplasia.

The Turkish journal of pediatrics, cilt.51, ss.493-6, 2009 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

A novel mutation in a family with DNA ligase IV deficiency syndrome.

Pediatric blood & cancer, cilt.53, ss.482-4, 2009 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Serum Erythropoietin Levels in Pediatric Hematologic Disorders and Impact of Recombinant Human Erythropoietin Use.

Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.26, ss.72-6, 2009 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

LAD-1/variant syndrome is caused by mutations in FERMT3.

Blood, cilt.113, ss.4740-6, 2009 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Malignancy-associated hemophagocytic lymphohistiocytosis in pediatric cases: a multicenter study from Turkey.

The Turkish journal of pediatrics, cilt.51, ss.207-13, 2009 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Brilliant cresyl blue staining for screening hemoglobin H disease: Reticulocyte smear.

Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.26, ss.45, 2009 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Transient depletion of innate immunity in varicella infections in otherwise healthy children.

Turkish journal of haematology : official journal of Turkish Society of Haematology, cilt.26, ss.12-6, 2009 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Neonatal Primary Hemophagocytic Lymphohistiocytosis in Turkish Children

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, cilt.30, sa.12, ss.871-876, 2008 (SCI İndekslerine Giren Dergi) identifier identifier identifier

The prognostic impact of myeloid antigen expression in pediatric acute lymphoblastic leukemia patients.

The Turkish journal of pediatrics, cilt.50, ss.533-6, 2008 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Lymphocytic vacuolization in sialic acid storage disease

AMERICAN JOURNAL OF HEMATOLOGY, cilt.83, sa.10, ss.821, 2008 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Nonstroke arterial thrombosis in children: Hacettepe experience.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, cilt.19, ss.519-24, 2008 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Severe Henoch-Schönlein purpura in a thalassemic patient under deferiprone treatment.

American journal of hematology, cilt.83, ss.165-6, 2008 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

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

PEDIATRIC HEMATOLOGY AND ONCOLOGY, cilt.25, sa.6, ss.492-501, 2008 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Case reports of successful therapeutic plasma exchange in severe amitriptyline poisoning.

Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy, cilt.11, ss.452-4, 2007 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Pulmonary tuberculosis presenting with pancytopaenia, haemophagocytosis and foamy histiocytes in an infant.

The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease, cilt.11, ss.931-2, 2007 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Fanconi anemia patient with bilaterally hypoplastic scapula and unilateral winging associated with scoliosis and rib abnormality.

Journal of pediatric hematology/oncology, cilt.28, ss.616-7, 2006 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Answer to hypotonia: a simple hemogram.

Journal of child neurology, cilt.20, ss.930-1, 2005 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

Autoimmune thrombocytopenic purpura after mumps infection.

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

Four-month-old infant with focal segmental glomerulosclerosis and mitochondrial DNA deletion

JOURNAL OF CHILD NEUROLOGY, cilt.20, sa.1, ss.83-84, 2005 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Acute gastric dilatation complicating the use of mydriatics in a preterm newborn

PEDIATRIC RADIOLOGY, cilt.31, sa.8, ss.581-583, 2001 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Adrenocortical carcinoma associated with adrenogenital syndrome in a child

MEDICAL AND PEDIATRIC ONCOLOGY, cilt.35, sa.1, ss.88-90, 2000 (SCI İndekslerine Giren Dergi) identifier

Diğer Dergilerde Yayınlanan Makaleler

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference: Interactive e-Posters

European Society of Human Genetics Virtual Conference, June 6-9, 2020., 6 - 09 Haziran 2020, cilt.28, ss.302

Wait and watch, or test for anti-granulocyte antibody

10th Eurasian Hematology Oncology Congress, İstanbul, Türkiye, 8 - 11 Ekim 2019, cilt.85 identifier

Cranial MRI findings of Patients with fanconi Anemia

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

Annual European Congress of Rheumatology (EULAR), Madrid, İspanya, 12 - 15 Haziran 2019, cilt.78, ss.1748 identifier

Tyrosine Kinase Inhibitor Responses in Pediatric CML Patients: Hacettepe Experience

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

Childhood leukemia in an ETV6-related Thrombocytopenia family.

49th Congress of the International Society of Pediatric Oncology (SIOP), Washington, Kiribati, 12 - 15 Ekim 2017, cilt.64, ss.192