Search Results - "Salcioglu Zafer"
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Factor 8 Gene Mutation Spectrum of 270 Patients with Hemophilia A: Identification of 36 Novel Mutations
Published in Turkish journal of haematology (01-01-2020)“…Hemophilia A (HA) is the most severe X-linked inherited bleeding disorder caused by hemizygous mutations in the gene. The aim of this study is to determine the…”
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2
Congenital Factor Deficiencies in Children: A Report of a Single-Center Experience
Published in Clinical and applied thrombosis/hemostasis (01-09-2018)“…Congenital factor deficiencies (CFDs) refer to inherited deficiency of coagulation factors in the blood. A total of 481 patients with CFDs, who were diagnosed…”
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3
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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4
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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5
Mucoepidermoid Carcinoma of the Parotid Gland in Childhood Survivor of Acute Lymphoblastic Leukemia With Need of Radiotherapy for Treatment and Review of the Literature
Published in Pediatric hematology and oncology (01-05-2012)“…Diagnosis of secondary malignancies began with the increasing survival in childhood cancer. Children treated for acute lymphoblastic leukemia (ALL) have an…”
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Electrocardiographic markers for the early detection of cardiac disease in patients with beta-thalassemia major
Published in Jornal de pediatria (01-03-2010)“…To comparatively evaluate P-wave dispersion (PWD) in patients with beta-thalassemia major (TM) and healthy control subjects for the early prediction of…”
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7
Safety and efficacy of deferasirox in patients with transfusion-dependent thalassemia: A 4-year single-center experience
Published in Pediatric hematology and oncology (07-09-2021)“…This study was organized to determine the efficacy and safety of deferasirox (DFX) in reducing the SF of patients with transfusion-dependent thalassemia (TDT)…”
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Hematopoietic Stem Cell Transplantation and Results in Pediatric Patients with Thalassemia Major: Single-Center Study
Published in Turkish archives of pediatrics (01-09-2022)“…Objective: This study aimed to reveal whether patients with thalassemia major, who were followed up in our clinic, were given information about hematopoietic…”
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9
Marcadores eletrocardiográficos para detecção precoce de doença cardíaca em pacientes com talassemia beta maior
Published in Jornal de pediatria (01-04-2010)“…OBJETIVO: Analisar comparativamente a dispersão da onda P (DOP) em pacientes com talassemia beta maior (β-TM) e indivíduos saudáveis (controles) para a…”
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10
Application of radioisotope synovectomy in the ankle joint in a child with congenital factor VII deficiency
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11
A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndrome
Published in Turkish journal of pediatrics (2019)“…Odaman-Al I, Gezdirici A, Yıldız M, Ersoy G, Aydoğan G, Şalcıoğlu Z, Tahtakesen TN, Önal H, Küçükemre-Aydın B. A novel mutation in the SLC19A2 gene in a…”
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12
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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13
Autoimmune Markers in Children with Chronic Immune Thrombocytopenia
Published in Blood (29-11-2018)“…Introduction: Chronic immune thrombocytopenia (ITP) is defined as isolated thrombocytopenia lasting longer than 12 months. Rheumatologic diseases,…”
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14
A nation-wide survey of patients with homozygous familial hypercholesterolemia phenotype undergoing LDL-apheresis in Turkey (A-HIT 1 registry)
Published in Atherosclerosis (01-03-2018)“…Homozygous familial hypercholesterolemia (HoFH) is a genetic condition characterized by lethally high levels of low-density lipoprotein cholesterol (LDL-C)…”
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15
Causes of Hypochromic Microcytic Anemia in Children and Evaluation of Laboratory Parameters in the Differentiation
Published in Journal of pediatric hematology/oncology (01-05-2019)“…Most common causes of microcytic anemia in children are iron deficiency anemia (IDA) and thalassemia. Differentiation of these and detection of coexistence is…”
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16
A Pediatric Case of Idiopathic Hypereosinophilia Preceeding Precursor B-cell Lymphoblastic Lymphoma of Nasopharynx
Published in Journal of pediatric hematology/oncology (01-04-2020)Get full text
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Clinical management, psychosocial characteristics, and quality of life in patients with homozygous familial hypercholesterolemia undergoing LDL-apheresis in Turkey: Results of a nationwide survey (A-HIT1 registry)
Published in Journal of clinical lipidology (01-05-2019)“…Homozygous familial hypercholesterolemia (HoFH) is a rare, life-threatening inherited disease leading to early-onset atherosclerosis and associated morbidity…”
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What have we learned from Turkish familial hypercholesterolemia registries (A-HIT1 and A-HIT2)?
Published in Atherosclerosis (01-10-2018)“…Familial hypercholesterolemia (FH) is a common genetic disease of high-level cholesterol leading to premature atherosclerosis. One of the key aspects to…”
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a Pediatric Primary Renal Lymphoma Case Presenting with Acute Renal Failure Findings
Published in Blood (06-12-2014)“…▪ Lymphomatous involvement of the kidneys is a common manifestation of systemic non-Hodgkin’s lymphoma (NHL). In contrast, lymphoma originating within the…”
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20
Granulocyte Transfusion in Febrile Neutropenia
Published in Blood (03-12-2015)“…▪ Background: Over last 30 years cure rates are increasing among oncology patients. As the therapy intensifies, infectious complications become more common…”
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