Search Results - "Murat Söker"

Analysis of beta globin gene mutations in Diyarbakir by Tekeş, Selahaddin, Oral, Diclehan, Söker, Murat, Şimşek, Selda, Uzel, Veysiye Hülya, Çürük, Mehmet Akif

“…Abstract Objectives Hemoglobin disorders are quite heterogeneous in the Turkish population. Up to now, more than forty different beta thalassemia mutations and…”
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Evaluation of retinal nerve fiber layer and choroidal thickness with spectral domain optical coherence tomography in children with sickle cell anemia by Yılmaz, Kamil, Öncül, Hasan, Uzel, Hülya, Öncel, Kahraman, Yılmaz, E Deniz, Söker, Murat

“…The aim of this study is to examine the thickness of choroidal, macular and peripapillary retinal nerve fiber layer by spectral-domain optical coherence…”
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Evaluation of the relationship between splenic iron overload and liver, heart and muscle features evident on T2-weighted magnetic resonance imaging by Çetinçakmak, Mehmet Güli, Hattapoğlu, Salih, Söker, Murat, Ekici, Faysal, Yilmaz, Kamil, Göya, Cemil, Hamidi, Cihad

“…Splenic iron overload is the most common clinical condition in patients with thalassemia. However, few studies of the effects of splenectomy have been…”
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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 by Yılmaz Karapınar, Deniz, Patıroğlu, Türkan, Metin, Ayşe, Çalışkan, Ümran, Celkan, Tiraje, Yılmaz, Barış, Karakaş, Zeynep, Karapınar, Tuba H., Akıncı, Burcu, Özkınay, Ferda, Onay, Hüseyin, Yeşilipek, Mehmet Akif, Akar, Himmet Haluk, Tüysüz, Gülen, Tokgöz, Hüseyin, Özdemir, Gül Nihal, Aslan Kıykım, Ayça, Karaman, Serap, Kılınç, Yurdanur, Oymak, Yeşim, Küpesiz, Alphan, Olcay, Lale, Keskin Yıldırım, Zuhal, Aydoğan, Gönül, Gökçe, Müge, İleri, Talia, Aral, Yusuf Ziya, Bay, Ali, Atabay, Berna, Kaya, Zuhre, Söker, Murat, Özdemir Karadaş, Nihal, Özbek, Uğur, Özsait Selçuk, Bilge, Özdemir, Hamiyet Hekimci, Uygun, Vedat, Tezcan Karasu, Gülsün, Yılmaz, Şebnem

“…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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Bone mineral density in children with beta-thalassemia major in Diyarbakir by Pirinççioğlu, Ayfer Gözü, Akpolat, Veysi, Köksal, Orhan, Haspolat, Kenan, Söker, Murat

“…Abstract Bone mineral status has extensively been investigated in adult thalassemics but less in thalassemic children. This study involves measurements of the…”
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Evaluation of Hematological Parameters of Children Diagnosed with COVID-19: Single-Center Experience by Üzel, Veysiye Hülya, Yılmaz, Kamil, Şen, Velat, Aktar, Fesih, Karabel, Müsemma, Yolbaş, İlyas, Gözü Pirinççioğlu, Ayfer, Söker, Murat

“…Although many pediatric studies on children infected with coronavirus disease 2019 (COVID-19) have been published, the diagnosis, clinical symptoms, laboratory…”
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Urinary early kidney injury molecules in children with beta-thalassemia major by Şen, Velat, Ece, Aydın, Uluca, Ünal, Söker, Murat, Güneş, Ali, Kaplan, İbrahim, Tan, İlhan, Yel, Servet, Mete, Nuriye, Sahin, Cahit

“…The aim of this study was to investigate novel urinary biomarkers including N-acetyl-β-D-glucosaminidase (NAG), neutrophil gelatinase-associated lipocalin…”
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Deferasirox in children with transfusion‐dependent thalassemia or sickle cell anemia: A large cohort real‐life experience from Turkey (REACH‐THEM) by Antmen, Bulent, Karakaş, Zeynep, Yeşilipek, Mehmet Akif, Küpesiz, Osman Alphan, Şaşmaz, İlgen, Uygun, Vedat, Kurtoğlu, Erdal, Oktay, Gonul, Aydogan, Gonul, Akın, Mehmet, Salcioglu, Zafer, Vergin, Canan, Kazancı, Elif Güler, Ünal, Selma, Çalışkan, Ümran, Aral, Yusuf Ziya, Türkkan, Emine, Meral Güneş, Adalet, Tunç, Bahattin, Gümrük, Fatma, Ayhan, Aylin Canbolat, Söker, Murat, Koç, Ahmet, Oymak, Yeşim, Ertem, Mehmet, Timur, Çetin, Yıldırmak, Yıldız, İrken, Gülersu, Apak, Hilmi, Biner, Betül, Eren, Tuğba Gürleyen, Işık Balcı, Yasemin, Koçak, Ülker, Karasu, Gülsün, Akkaynak, Diyar, Patıroğlu, Türkan

“…Objectives To evaluate the long‐term efficacy and safety of deferasirox therapy in a large observational cohort of children with transfusion‐dependent…”
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Urinary Kidney Injury Molecules in Children with Iron-Deficiency Anemia by Güneş, Ali, Ece, Aydın, Aktar, Fesih, Tan, İlhan, Söker, Murat, Karabel, Duran, Balık, Hasan, Uluca, Ünal, Şen, Velat, Yolbaş, İlyas

“…The aim of this study was to investigate the urine levels of human kidney injury molecule-1 (KIM-1), neutrophil gelatinase-associated lipocalin (NGAL),…”
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Clinical Characteristics and Outcomes of Cancer Cases Among Syrian Refugees From Southern Turkey by Kutluk, Tezer, Sahin, Berksoy, Kirazli, Meral, Ahmed, Fahad, Aydin, Sinem, Yesil Çinkir, Havva, Sezgin, Gülay, Bayram, Ibrahim, Ebinç, Senar, Isikdogan, Abdurrahman, Sasmaz, Ilgen, Okan, Vahap, Ilhan, Gül, Ören, Ayse Ceyda, Akbayram, Sinan, Harputluoglu, Hakan, Ural, Cihan, Ayyildiz, Orhan, Aktas, Gökmen, Uçar, Mehmet Ali, Güvenç, Birol, Köse, Dogan, Acipayam, Can, Güncan, Sabri, Erçolak, Vehbi, Berber, Ilhami, Akdeniz, Aydan, Akyay, Arzu, Üzel, Veysiye Hülya, Söker, Murat, Sengelen, Meltem, Yalçin, Suayib, Sullivan, Richard

“…Cancer was a common noncommunicable disease in Syria before the present conflict and is now a major disease burden among 3.6 million Syrian refugees in Turkey…”
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Hereditary Spherocytosis: Evaluation of 68 Children by Konca, Çapan, Söker, Murat, Tas, Mehmet Ali, Yildirim, Ruken

“…To determine the clinical and hematologic features of 68 children with hereditary spherocytosis (HS). In this retrospective study, we analyzed recorded…”
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Outcomes of Eltrombopag Treatment and Development of Iron Deficiency in Children with Immune Thrombocytopenia in Turkey by Koca Yozgat, Ayça, Leblebisatan, Göksel, Akbayram, Sinan, Çınar Özel, Simge, Karakaş, Zeynep, Erduran, Erol, Yılmaz, Şebnem, Koçak, Ülker, Ünal, Şule, Özdemir, Gül Nihal, Albayrak, Meryem, Zengin, Emine, Oymak, Yeşim, Bör, Özcan, Çakmaklı, Hasan Fatih, Söker, Murat, Gürlek Gökçebay, Dilek, Tokgöz, Hüseyin, Malbora, Barış, Karaman, Serap, Celkan, Tiraje, Şaşmaz, İlgen, Yaralı, Neşe, Ören, Hale, Ünüvar, Ayşegül, Özbek, Namık Yaşar

“…Immune thrombocytopenia (ITP) is a rare autoimmune disease and hematologic disorder characterized by reduced platelet counts that can result in significant…”
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Central Nervous System Tuberculosis in Children: A Review of 214 Cases by Yaramis, Ahmet, Gurkan, Fuat, Elevli, Murat, Soker, Murat, Haspolat, Kenan, Kirbas, Gokhan, Tas, M. Ali

“…To study the clinical, laboratory, and treatment features observed in pediatric patients with tuberculous meningitis in Turkey. Study Design. Retrospective…”
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Cardiac Tamponade may be the First Symptom of Leukemia by Karabel, Müsemma, Söker, Murat, Kelekçi, Selvi, Karabel, Duran, Yel, Servet, Bilici, Meki

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A rare cause of recurrent oral lesions: chediak-higashi syndrome by Karabel, Müsemma, Kelekçi, Selvi, Sen, Velat, Karabel, Duran, Aliosmanoğlu, Ciğdem, Söker, Murat

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The effects of pomegranate and carvacrol on methotrexate-induced bone marrow toxicity in rats by Şen, Velat, Bozkurt, Mehtap, Söker, Sevda, Ece, Aydın, Güneş, Ali, Uluca, Ünal, Söker, Murat, Yel, Servet, Kaplan, İbrahim

“…The aim of this study was to evaluate the effects of pomegranate (PMG) extract and carvacrol (CARV) on methotrexate (MTX)-induced oxidative stress and bone…”
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The Clinical Findings and Prophylactic Treatment in Children with Factor X Deficiency by Karabel, Müsemma, Söker, Murat, Y ld r m, Aysen Türedi, Oymak, Ye im, Kelekçi, Selvi, Karabel, Duran

“…Factor X (FX) is the component of both extrinsic and intrinsic coagulation cascade and is the first enzyme of the common pathway which results in thrombus…”
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Assessment of thyroid function in children aged 1-13 years with Beta-thalassemia major by Pirinççioğlu, Ayfer Gözü, Deniz, Turgay, Gökalp, Deniz, Beyazit, Nurcan, Haspolat, Kenan, Söker, Murat

“…Hypothyroidism usually appears in the second decade of life and is thought to be associated with iron overload in patients with thalassemia major. This study…”
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Urinary levels of early kidney injury molecules in children with vitamin B12 deficiency by Güneş, Ali, Aktar, Fesih, Tan, İlhan, Söker, Murat, Uluca, Ünal, Balık, Hasan, Mete, Nuriye

“…The aim of this study was to investigate urine early kidney injury molecules, including human kidney injury molecule-1 (KIM-1), liver-type fatty-acid binding…”
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Mutation Analysis of Beta-Thalassemia Major Patients and Their Parents in Diyarbakir Province, Turkey by POLAT, Cemal

“…Objectives: In this study, beta-Thalassemia Major (BTM) diagnosed patients and their parents were subjected to DNA sequencing in order to confirm their…”
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