Search Results - "AYDİN KÖKER, Sultan"

A Novel Frameshift Mutation in the FGA Gene (c.196 delT) Leading to Congenital Afibrinogenemia by Aydin Köker, Sultan, Köker, Alper, Neerman-Arbez, Marguerite, Ö. Tunçer, Gökçen, Akbas, Yilmaz, Kara, Tugce T., Coban, Yasemin

“…Congenital afibrinogenemia is characterized by the absence of fibrinogen. Congenital fibrinogen disorders result from several mutations in FGA, FGB, or FGG…”
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The Effects of Immunophenotyping with Flow Cytometry on Prognosis in Acute Lymphoblastic Leukemia by AYDİN KÖKER, Sultan, OYMAK, Yesim, VERGİN, Raziye, İNCE, Dilek, GENEL, Fearh

“…Background: The identification of immunophenotype subgroups is very important for the diagnosis and prognosis of acute lymphoblastic leukemia(ALL). Material…”
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Thrombotic Microangiopathy with Complement Factor H Gene Mutations Unassociated with Atypical Hemolytic Uremic Syndrome by Oymak, Yeşim, Karapınar, Tuba Hilkay, Ay, Yılmaz, Özcan, Esin, Müminoğlu, Neryal, Aydın Köker, Sultan, Töret, Ersin, Berdeli, Afig, Serdaroğlu, Erkin, Vergin, Canan

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Successful Management of l-Asparaginase–Associated Pancreatitis With Octreotide and Pegylated Asparaginase in 2 Patients With Acute Lymphoblastic Leukemia: Is There a Different Rare Warning Sign of Hypoglycemia for l-Asparaginase–Associated Pancreatitis? by Aydin Köker, Sultan, Oymak, Yeşim, Demirağ, Bengü, Karapinar, Tuba Hilkay, Koker, Alper, Genç, Sinan, Erdemir, Gülin, Vergin, Raziye Canan

“…l-Asparaginase (l-Asp) is a critical component of chemotherapy for acute lymphoblastic leukemia (ALL). However, toxic effects associated with l-Asp, such as…”
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Effect of pyridoxine plus pyridostigmine treatment on vincristine-induced peripheral neuropathy in pediatric patients with acute lymphoblastic leukemia: a single-center experience by Aydin Köker, Sultan, Gözmen, Salih, Demirağ, Bengü, Ünalp, Aycan, Karapinar, Tuba Hilkay, Oymak, Yeşim, Gürbüz, Gürkan, Öner, Ecem İpek, Vergin, Raziye Canan

“…Background Vincristine (VCR), which is a key component of chemotherapy, is important for survival. VCR is associated with a well-known side effect, including…”
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Comparison of Anemic and Non-anemic Iron-deficient Adolescents in Terms of Psychosocial Aspects and Quality of Life: A Case Control Study by Tekin, Uğur, Köker, Sultan Aydın, Uçar, Halit Necmi

“…Objective: In this study, anxiety levels, emotional and behavioral problems, self-esteem and quality of life (QoL) in adolescents with iron deficiency (ID) and…”
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Propionic acidemia: an extremely rare cause of hemophagocytic lymphohistiocytosis in an infant by Aydin Köker, Sultan, Yeşilbaş, Osman, Köker, Alper, Şevketoğlu, Esra

“…Hemophagocytic lymphohystiocytosis (HLH) may be primary (inherited/familial) or secondary to infections, malignancies, rheumatologic disorders, immune…”
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Evaluation of clinical findings and neurofibromatosis type 1 bright objects on brain magnetic resonance images of 60 Turkish patients with NF1 gene variants by Hazan, Filiz, Gürsoy, Semra, Unalp, Aycan, Yılmaz, Unsal, Demirağ, Bengü, Aydin Köker, Sultan, Ozyılmaz, Berk, Erdogan, Kadri Murat, Kalenderer, Önder, Erkuş, Serkan, Gürçınar, Müge, Tükün, Ajlan

“…Neurofibromatosis type 1 (NF1) is caused by mutations in the NF 1 gene. This retrospective study aims to evaluate the clinical manifestations and brain…”
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A Diagnosis that Is Probably Missed: Rubeola Lymphadenitis, an Epidemic that Causes a Renewed Alarm by POLAT ÜNAL, Sinem Eser, AYDİN KÖKER, Sultan, SÜREN, Dinç

“…Because Rubeola (measles) infection is not observed in our country after eradication and is especially on the agenda again after migrations, pathologists may…”
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A Rare Complication in a Child with Sickle Cell Anemia: Clavicular Osteomyelitis by Tural Kara, Tuğçe, Aydın Köker, Sultan, Öz Tuncer, Gökçen, Akbaş, Yılmaz, Çoban, Yasemin, Köker, Alper, Yeral, Hakan

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Late diagnosis of leukocyte adhesion deficiency type II and Bombay blood type in a child: a rare case report by Yaman, Yöntem, Köker, Sultan Aydin, Ayhan, Fahri Yüce, Genel, Ferah, Acıpayam, Can, Oymak, Yeşim, Tuğrul Sarıbeyoğlu, Ebru, Vergin, Canan Raziye

“…Leukocyte adhesion deficiency type II (LAD II) is a rare, autosomal, recessive inherited immunodeficiency disease that induces frequent and recurrent…”
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An Unusual Presentation of T-Cell Lymphoblastic Lymphoma with Isolated Renal Involvement by Gül Şiraz, Ülkü, Kayadibi, Yasemin, Köksoy, Adem Yasin, Koker, Alper, Aydın Köker, Sultan, Tekin, Emine

“…The clinical presentation of Non-Hodgkin lymphoma (NHL) is frequently associated with the involvement of the abdomen and mediastinal lymphadenopathies, but…”
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Idiopathic Pulmonary Hemosiderosis Mimicking Iron Deficiency Anemia: A Delayed Diagnosis? by Koker, Sultan Aydin, Gözmen, Salih, Oymak, Yeşim, Karapinar, Tuba Hilkay, Can, Demet, Genç, Sinan, Vergin, Raziye Canan

“…Idiopathic pulmonary hemosiderosis (IPH) is an uncommon chronic disorder in children. It is characterized by recurrent pulmonary hemorrhage and may result in…”
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Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report by Katipoğlu, Nagehan, Karapinar, Tuba H, Demir, Korean, Aydin Köker, Sultan, Nalbantoğlu, Özlem, Ay, Yılmaz, Korkmaz, Hüseyin A, Oymak, Yeşim, Yıldız, Melek, Tunç, Selma, Hazan, Filiz, Vergin, Canan, Ozkan, Behzat

“…Thiamine-responsive megaloblastic anemia syndrome (TRMA), also known as Rogers syndrome, is characterized by megaloblastic anemia, sensorineural hearing loss,…”
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Eltrombopag Add-on Treatment in a Child With Fanconi Aplastic Anemia Awaiting Hematopoietic Stem Cell Transplantation by Aydin Koker, Sultan, Çalişkan Polat, Arzu

“…Fanconi aplastic anemia (FAA) is a rare inherited bone marrow failure disorder characterized by congenital defects and pancytopenia. Hematopoietic stem cell…”
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The Evaluation of Taking Iron Supplements in Children Aged 6 Months-2 Years by Hilkay Karapınar, Tuba, Bildik, Olgay, Aydın Köker, Sultan, Töret, Ersin, Oymak, Yeşim, Ay, Yılmaz, Demirağ, Bengü, Vergin, Canan

“…Aim: In spite of special supplemental programs for infants, iron deficiency anemia remains relatively common, depending on ethnicity and socioeconomic status…”
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Irritability and Perceived Expressed Emotion in Adolescents With Iron Deficiency and Iron Deficiency Anemia: A Case-Control Study by Uçar, Halit Necmi, Aydin Köker, Sultan, Tekin, Uğur

“…The objective of this study was to assess the difference in irritability and perceived expressed emotion (EE) between adolescents with iron deficiency (ID) or…”
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Serum Zonulin Levels in Pediatric Migraine by Öz Tunçer, Gökçen, Akbaş, Yılmaz, Köker, Alper, Aydın Köker, Sultan, Tural Kara, Tuğçe, Çoban, Yasemin, Kömüroğlu, Ahmet Ufuk

“…Migraine is a complex neurogenic inflammatory disorder. There are strong neuronal, endocrine, and immunologic connections between the brain and…”
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Identification of a Novel Mutation in the SEC23B Gene Associated With Congenital Dyserythropoietic Anemia Type II Through the Use of Next-generation Sequencing Panel in an Undiagnosed Case of Nonimmune Hereditary Hemolytic Anemia by Aydin Koker, Sultan, Karapinar, Tuba H, Oymak, Yeşim, Bianchi, Paola, Fermo, Elisa, Gozmen, Salih, Vergin, Canan

“…Congenital dyserythropoietic anemias (CDAs) are rare hereditary blood disorders characterized by ineffective erythropoiesis, hemolysis, and erythroblast…”
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Akut Lenfoblastik Lösemide Flow Sitometri ile İmmünofenotiplemenin Prognoz Üzerine Etkileri by Sultan Aydi̇n Köker, Raziye Vergi̇n, Yesim Oymak, Dilek İnce, Fearh Genel

“…Giriş: Akut lenfoblastik löseminin (ALL) tanı ve prognozu için immünofenotip alt gruplarının tanımlanması çok önemlidir. Gereç ve Yöntem: Çalışmaya TR-ALL 2000…”
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