Browsing by Author "Ozcan, Alper"
Now showing items 1-7 of 7
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30 years of wilms tumor experience at one center in türkiye's central anatolia region
Akyol, Sefika; Odabas, Gul Pelin; Ozcan, Alper; Yilmaz, Ebru; Karaman, Zehra Filiz; Ozturk, Figen; Akgun, Huelya; Dogan, Ahmet Burak; Eroglu, Celalettin; Unal, Ekrem; Karakukcu, Musa (İstanbul Üniv., 2023)Objective: The current study aims to evaluate the clinical presentation, treatment, and follow-up of children with Wilms Tumor (WT) who had been admitted to Erciyes University, Faculty of Medicine Department of Pediatric ... -
Correction to: Dıaph1-deficiency is associated with major t, nk and ılc defects in humans
Azizoglu, Zehra Busra; Babayeva, Royala; Haskologlu, Zehra Sule; Acar, Mustafa Burak; Ayaz-Guner, Serife; Okus, Fatma Zehra; Alsavaf, Mohammad Bilal; Can, Salim; Basaran, Kemal Erdem; Canatan, Mehmed Fatih; Ozcan, Alper; Erkmen, Hasret; Leblebici, Can Berk; Yilmaz, Ebru; Karakukcu, Musa; Kose, Mehmet; Canoz, Ozlem; Özen, Ahmet; Karakoc-Aydiner, Elif; Ceylaner, Serdar; Gümüş, Gülsüm; Per, Huseyin; Gumus, Hakan; Canatan, Halit; Ozcan, Servet; Dogu, Figen; Ikinciogullari, Aydan; Unal, Ekrem; Baris, Safa; Eken, Ahmet (Springer, 2024)No Abstract -
DIAPH1-deficiency is associated with major t, nk and ılc defects in humans
Azizoglu, Zehra Busra; Babayeva, Royala; Haskologlu, Zehra Sule; Acar, Mustafa Burak; Ayaz-Guner, Serife; Okus, Fatma Zehra; Alsavaf, Mohammad Bilal; Can, Salim; Basaran, Kemal Erdem; Canatan, Mehmed Fatih; Ozcan, Alper; Erkmen, Hasret; Leblebici, Can Berk; Yilmaz, Ebru; Karakukcu, Musa; Kose, Mehmet; Canoz, Ozlem; Özen, Ahmet; Karakoc-Aydiner, Elif; Ceylaner, Serdar; Gümüş, Gülsüm; Per, Huseyin; Gumus, Hakan; Canatan, Halit; Ozcan, Servet; Dogu, Figen; Ikinciogullari, Aydan; Unal, Ekrem; Baris, Safa; Eken, Ahmet (Springer, December 2)Loss of function mutations in Diaphanous related formin 1 (DIAPH1) are associated with seizures, cortical blindness, and microcephaly syndrome (SCBMS) and are recently linked to combined immunodeficiency. However, the ... -
The effect of nivolumab in pediatric malignant tumors: A single center experience with nine children
Gok, Veysel; Aydin, Firdevs; Ozcan, Alper; Karaman, Zehra Filiz; Yilmaz, Ebru; Gorukmez, Orhan; Bisgin, Atil; Karakukcu, Musa; Patiroglu, Turkan; Unal, Ekrem (Akad Doktorlar Yayınevi, 2024)Nivolumab is an inhibitor of programmed cell death 1 (PD-1), which enables activated T cells to attack the tumor cells. Although the utilization of nivolumab in adulthood cancers is more common, experience in childhood has ... -
A Novel biallelic lck variant resulting in profound t-cell immune deficiency and review of the literature
Lanz, Anna-Lisa; Erdem, Serife; Ozcan, Alper; Ceylaner, Gulay; Cansever, Murat; Ceylaner, Serdar; Conca, Raffaele; Magg, Thomas; Acuto, Oreste; Latour, Sylvain; Klein, Christoph; Patiroglu, Turkan; Unal, Ekrem; Eken, Ahmet; Hauck, Fabian (Springer, 2024)No Abstract. -
Rare coagulation factor deficiencies: Multicenter experience with 188 cases
Gok, Veysel; Sahinoglu, Esra Pekpak; Tokgoz, Hueseyin; Mutlu, Fatma Turkan; Acipayam, Can; Karaman, Kamuran; Tuncel, Defne Ay; Oren, Ayse Ceyda; Simsek, Ayse; Arslan, Bilal; Unal, Hatice Beyza; Ozcan, Alper; Yilmaz, Ebru; Akbayram, Sinan; Karakukcu, Musa; Oner, Ahmet Fayik; Caliskan, Umran; Patiroglu, Turkan; Unal, Ekrem (İstanbul Üniv., 2024)Objective: Rare factor deficiencies are a group of autosomal recessive bleeding disorders (with the exception of dysfibrinogenemia), which are characterized by the deficiency or dysfunction of one or more coagulation factors ...
