Search Results - "Aydogan, Gonul"
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Inherited human OX40 deficiency underlying classic Kaposi sarcoma of childhood
Published in The Journal of experimental medicine (26-08-2013)“…Kaposi sarcoma (KS), a human herpes virus 8 (HHV-8; also called KSHV)-induced endothelial tumor, develops only in a small fraction of individuals infected with…”
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2
Homozygous c.130–131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry
Published in Pediatric blood & cancer (01-10-2019)“…Background Severe congenital neutropenia is a rare disease, and autosomal dominantly inherited ELANE mutation is the most frequently observed genetic defect in…”
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3
Application of radioisotope synovectomy in the ankle joint in a child with congenital factor VII deficiency
Published in Turk Pediatri Arsivi (2020)Get full text
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4
Glucose 6 phosphate dehydrogenase deficiency: A single-center experience
Published in Turkish archives of pediatrics (01-05-2021)“…This study aims to evaluate the demographic information, clinical and laboratory findings of patients with glucose 6 phosphate dehydrogenase deficiency. We…”
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5
A National Registry of Thalassemia in Turkey: Demographic and Disease Characteristics of Patients, Achievements, and Challenges in Prevention
Published in Turkish journal of haematology (01-03-2018)“…The Turkish Society of Pediatric Hematology set up a National Hemoglobinopathy Registry to demonstrate the demographic and disease characteristics of patients…”
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6
Coexistence of early onset sarcoidosis and partial interferon-γ receptor 1 deficiency
Published in The Turkish journal of pediatrics (2016)“…Pediatric sarcoidosis comprises a spectrum of childhood granulomatous inflammatory conditions. Pathological hallmark of the disease is granuloma formation that…”
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7
Successful treatment of multiresistant Achromobacter xylosoxidans bacteremia in a child with acute myeloid leukemia
Published in Annals of Saudi medicine (01-03-2015)“…Achromobacter xylosoxidans is an aerobic gram-negative bacillus and important cause of bacteremia in immunocompromised patients. We describe a leukemia…”
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8
Cardiac T2 MRI assessment in patients with thalassaemia major and its effect on the preference of chelation therapy
Published in International journal of hematology (01-06-2014)“…The aim of the study is to assess the relationship between T2* magnetic resonance imaging (MRI) values and age, serum ferritin level, left ventricular ejection…”
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9
Upregulation of T-Cell-Specific Transcription Factor Expression in Pediatric T-Cell Acute Lymphoblastic Leukemia (T-ALL)
Published in Turkish journal of haematology (01-12-2012)“…T-cell acute lymphoblastic leukemia (T-ALL) is associated with recurrent chromosomal aberrations andabnormal ectopic gene expression during T-cell development…”
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10
Analysis of Chromosomal Aberrations and FLT3 gene Mutations in Childhood Acute Myelogenous Leukemia Patients
Published in Turkish journal of haematology (01-09-2012)“…To identify the well-known common translocations and FLT3 mutations in childhood acute myelogenousleukemia (AML) patients in Turkey. The study included 50…”
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11
Evaluation of PAX5 gene in the early stages of leukemic B cells in the childhood B cell acute lymphoblastic leukemia
Published in Leukemia research (01-01-2012)“…Abstract B-lineage acute lymphoblastic leukemia (B-ALL) is a common subtype of acute leukemia in children. PAX5 plays a central role in B-cell development and…”
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12
Acute renal failure caused by fungus balls in renal pelvises
Published in Pediatrics international (01-12-2009)Get full text
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13
Evaluation of Optical Coherence Tomography Findings and Choroidal Thickness in Beta-Thalassemia Major Patients Using Chelation Therapy
Published in Beyoglu eye journal (2022)“…This study aims to analyze the posterior segment of the eye in children with thalassemia major (TM) treated with chelation therapy. Forty-four patients…”
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14
The efficacy of magnetic resonance imaging and x-ray in the evaluation of response to radiosynovectomy in patients with hemophilic arthropathy
Published in Molecular imaging and radionuclide therapy (01-08-2011)“…We aimed to assess the role of Magnetic Resonance Imaging (MRI) and X-Ray in the evaluation of response to radiosynovectomy (RS) in patients with hemophilic…”
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15
Systemic onset juvenile idiopathic arthritis with macrophage activation syndrome and coronary artery dilatation misdiagnosed as Kawasaki disease
Published in Turkish journal of pediatrics (01-09-2015)“…Systemic onset juvenile idiopathic arthritis (SoJIA) is characterized by arthritis, fever and visceral organ involvement including hepatosplenomegaly,…”
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16
Anterior segment parameters and tear functions in patients with thalassemia major
Published in Inönü Üniversitesi Turgut Özal Tıp Merkezi dergisi (01-10-2019)“…Aim: To determine whether the biomicroscopic, topographic and biomechanical properties of the anterior segment and the tear function have changed in…”
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17
Adrenomedullin-A New Marker in Febrile Neutropenia: Comparison With CRP and Procalcitonin
Published in Pediatric hematology and oncology (03-10-2015)“…In this study, we aimed to determine serum adrenomedullin levels and compare them with levels of C-reactive protein (CRP) and procalcitonin (PCT). Cancer…”
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Comparison of anti-D immunoglobulin, methylprednisolone, or intravenous immunoglobulin therapy in newly diagnosed pediatric immune thrombocytopenic purpura
Published in Journal of thrombosis and thrombolysis (01-02-2013)“…This study aimed to evaluate the efficacy, cost, and effects of anti-D immunoglobulin (anti-D Ig), methylprednisolone, or intravenous immunoglobulin (IVIG)…”
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19
Long Term Outcome Following Splenectomy in Children
Published in Blood (29-11-2018)“…Aim: The aim of the study is to evaluate the efficacy, complications and long term results of splenectomy in children with hematologic diseases. Patients and…”
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How do we encounter rare factor deficiencies in children? Single-centre results from Turkey
Published in Blood coagulation & fibrinolysis (01-03-2015)“…BACKGROUNDRare factor deficiencies (RFDs) are autosomal recessively inherited coagulation factor deficiencies encountered at a frequency of between one in 500…”
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