Výsledky vyhledávání - Aktar, Fesih
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Serum Galectin-3 Levels in Children with Chronic Hepatitis B Infection and Inactive Hepatitis B Carriers Autor Uluca, Ünal, Şen, Velat, Ece, Aydın, Tan, İlhan, Karabel, Duran, Aktar, Fesih, Karabel, Müsemma, Balık, Hasan, Güneş, Ali
Vydáno 2015Text -
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Evaluation of Hematological Parameters of Children Diagnosed with COVID-19: Single-Center Experience Autor Üzel, Veysiye Hülya, Yılmaz, Kamil, Şen, Velat, Aktar, Fesih, Karabel, Müsemma, Yolbaş, İlyas, Pirinççioğlu, Ayfer Gözü, Söker, Murat
Vydáno 2021Text -
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Determining the Independent Risk Factors and Mortality Rate of Nosocomial Infections in Pediatric Patients Autor Aktar, Fesih, Tekin, Recep, Güneş, Ali, Ülgen, Cevat, Tan, İlhan, Ertuğrul, Sabahattin, Köşker, Muhammet, Balık, Hasan, Karabel, Duran, Yolbaş, Ilyas
Vydáno 2016Text -
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Assessment of epicardial adipose tissue thickness and the mean platelet volume in children with familial Mediterranean fever Autor Uluca, Ünal, Demir, Fikri, Ece, Aydın, Şen, Velat, Güneş, Ali, Aktar, Fesih, Tan, İlhan, Karabel, Duran, Yazgan, Ümitcan, Sabaz, Muhammed Nurullah
Vydáno 2015Text -
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METAP1 Mutation Is a Novel Candidate for Autosomal Recessive Intellectual Disability Autor Caglayan, Ahmet Okay, Aktar, Fesih, Bilguvar, Kaya, Baranoski, Jacob F., Akgumus, Gozde Tugce, Harmanci, Akdes Serin, Erson-Omay, Emine Zeynep, Yasuno, Katsuhito, Caksen, Huseyin, Gunel, Murat
Vydáno 2020Text -
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Protective effects of l-glutamine against toxicity of deltamethrin in the cerebral tissue Autor Varol, Sefer, Özdemir, Hasan Hüseyin, Çevik, Mehmet Uğur, Altun, Yaşar, Ibiloğlu, Ibrahim, Ekinci, Aysun, Ibiloğlu, Aslıhan Okan, Balduz, Metin, Arslan, Demet, Tekin, Recep, Aktar, Fesih, Aluçlu, Mehmet Ufuk
Vydáno 2016Text -
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Brain Malformations Associated with Knobloch Syndrome – Review of Literature, Expanding Clinical Spectrum and Identification of Novel Mutations Autor Caglayan, Ahmet Okay, Baranoski, Jacob F., Aktar, Fesih, Han, Wengi, Tuysuz, Beyhan, Guzel, Aslan, Guclu, Bulent, Kaymakcalan, Hande, Aktekin, Berrin, Akgumus, Gozde Tugce, Murray, Phillip B., Omay, E. Zeynep Erson, Caglar, Caner, Bakircioglu, Mehmet, Sakalar, Yildirim Bayezit, Guzel, Ebru, Demir, Nihat, Tuncer, Oguz, Senturk, Senem, Ekici, Baris, Minja, Frank J., Šestan, Nenad, Yasuno, Katsuhito, Bilguvar, Kaya, Caksen, Huseyin, Gunel, Murat
Vydáno 2014Text -
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CLP1 Founder Mutation Links tRNA Splicing and Maturation to Cerebellar Development and Neurodegeneration Autor Schaffer, Ashleigh E., Eggens, Veerle R.C., Caglayan, Ahmet Okay, Reuter, Miriam S., Scott, Eric, Coufal, Nicole G., Silhavy, Jennifer L., Xue, Yuanchao, Kayserili, Hulya, Yasuno, Katsuhito, Rosti, Rasim Ozgur, Abdellateef, Mostafa, Caglar, Caner, Kasher, Paul R., Cazemier, J. Leonie, Weterman, Marian A., Cantagrel, Vincent, Cai, Na, Zweier, Christiane, Altunoglu, Umut, Satkin, N. Bilge, Aktar, Fesih, Tuysuz, Beyhan, Yalcinkaya, Cengiz, Caksen, Huseyin, Bilguvar, Kaya, Fu, Xiang-Dong, Trotta, Christopher, Gabriel, Stacey, Reis, André, Gunel, Murat, Baas, Frank, Gleeson, Joseph G.
Vydáno 2014Text