Search Results - "KÜPESİZ, OSMAN ALPHAN"

Psychopathology in pediatric bone marrow transplantation survivors and their mothers by Adanir, Aslı Sürer, Taşkiran, Gülseren, Osman Alphan Küpesiz, Özatalay, Esin

“…Background Bone marrow transplantation (BMT) is used to treat various hematologic, oncologic and metabolic diseases. While the treatment is lifesaving, it is…”
Get full text

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…”
Get full text

Therapeutic apheresis: is it safe in children with kidney disease? by Kalenderoğlu, Muhammed Doğukan, Çomak, Elif, Aksoy, Gülşah Kaya, Bilge, Uğur, Küpesiz, Osman Alphan, Koyun, Mustafa, Akman, Sema

“…Background Therapeutic apheresis (TA) is already used to treat various diseases in the field of nephrology. The aim of this study was to evaluate the frequency…”
Get full text

Decreased Serum Levels of Sphingomyelins and Ceramides in Sickle Cell Disease Patients by Aslan, Mutay, Kıraç, Ebru, Kaya, Sabriye, Özcan, Filiz, Salim, Ozan, Küpesiz, Osman Alphan

“…Limited data are available on the serum levels of different sphingomyelin (CerPCho) and ceramide (CER) species in sickle‐cell disease (SCD). This study was…”
Get full text

TCIRG1 and SNX10 gene mutations in the patients with autosomal recessive osteopetrosis by Koçak, Gamze, Güzel, Banu Nur, Mıhçı, Ercan, Küpesiz, Osman Alphan, Yalçın, Koray, Manguoğlu, Ayşe Esra

“…Autosomal recessive osteopetrosis (ARO) is a rare genetic bone disease characterized by dense and fragile bone, caused by a defect in osteoclasts responsible…”
Get full text

Follow‐up of human adenovirus viral load in pediatric hematopoietic stem cell transplant recipients by Peker, Bilal Olcay, Tüysüz Kintrup, Gülen, Sağlık, İmran, Can Sarınoğlu, Rabia, Güler, Elif, Mutlu, Derya, Küpesiz, Osman Alphan, Çolak, Dilek

“…Background The spectrum of human adenovirus (HAdV)–related disease is broad, and the virus acts on many organs and systems in hematopoietic stem cell…”
Get full text

Investigation of Torque Teno Virus (TTV) DNA as an immunological and virological marker in pediatric hematopoietic stem cell transplantation (HSCT) patients by Peker, Bilal Olcay, Daloğlu, Aylin Erman, Görzer, Irene, Puchhammer-Stöckl, Elisabeth, Parkan, Ömür Mustafa, Akbaş, Hilal, Kintrup, Gülen Tüysüz, Mutlu, Derya, Küpesiz, Osman Alphan, Çolak, Dilek

“…High viral loads are observed in Torque Teno Virus (TTV) infection after hematopoietic stem cell transplantation (HSCT). We aimed to analyze the kinetics of…”
Get full text

Investigation of Ganciclovir Resistance in Cytomegalovirus Isolates by Phenotypic and Genotypic Methods by Sarınoğlu, Rabia Can, Çolak, Dilek, Küpesiz, Osman Alphan, Kuşkucu, Mert Ahmet, Yalçın, Koray, Sağlık, İmran, Mutlu, Derya, Midilli, Kenan, Peker, Bilal Olcay, Özhak, Betil, Özkul, Aykut, Foldes, Kataline

“…Ganciclovir-resistant cytomegalovirus (CMV) strains are reported following long-term antiviral agent use, especially for immune-suppressive patients. In this…”
Get full text

Specific Granule Deficiency Due To Novel Homozygote SMARCD2 Variant by Kihtir, Zeynep, Çelik, Kıymet, Tayfun Küpesiz, Funda, Küpesiz, Osman Alphan, Kocacik Uygun, Dilara Fatma, Arayici, Sema, Ongun, Hakan, Acarbulut, İpek, Sağlam, Celal, Ceylaner, Gülay, Bingöl, Ayşen

“…Specific granule deficiency (SGD) is a rare immunodeficiency associated with gene variants. It can cause severe recurrent infections and is lethal without…”
Get more information

Clinical Characteristics and Treatment Outcomes of Patients with Malignant Extracranial Germ Cell Tumors: A 20-Year Single-Center Experience by Tayfun Küpesiz, Funda, Tüysüz, Gülen, Akınel, Ayşe Nur, Tekneci, Ayşegül, Sivrice, Ayşe Çiğdem, Melikoglu, Mustafa, Pestereli, Hadice Elif, Küpesiz, Osman Alphan, Güler, Elif

Get full text

Retrospective analysis of hemophilia B in Turkey: identifying main characteristics and treatment options by Zülfikar, Bülent, Koç, Başak, Şahin, Fahri, Şaşmaz, Hatice İlgen, Kavaklı, Kaan, Balkan, Can, Antmen, Ali Bülent, Akbayram, Sinan, Güvenç, Birol, Okan, Vahap, Türkkan, Emine, Albayrak, Canan, Albayrak, Davut, Sarper, Nazan, Celkan, Tülin Tiraje, Ayyıldız, Orhan, Aksu, Salih, Patıroğlu, Türkan, Şalcıoğlu, Zafer, Güneş, Adalet Meral, Torun, Yasemin Altuner, Çalışkan, Ümran, Tokgöz, Hüseyin, Ay, Yılmaz, Özdemir, Gül Nihal, Sönmez, Mehmet, Ünal, Ekrem, Öner, Ahmet Fayik, Güler, Nil, Küpesiz, Osman Alphan, Ören, Hale, Karaman, Serap, Ünüvar, Ayşegül, Dağlı, Mehmet, Demir, Ahmet Muzaffer, Söker, Murat, Alioğlu, Bülent, Kaya, Zühre, Ayhan, Aylin Canbolat, Bıçakçı, Zafer, Aral, Yusuf Ziya, Ar, Muhlis Cem

“…Hemophilia B (HB), an X-linked recessive inherited bleeding disorder, exhibits a high prevalence among males. To present the first national cohort of persons…”
Get full text

Investigating the physiological role of S199A and S199D mutants of PHF6 protein in T-cell acute lymphoblastic leukemia by ERDOĞAN, GÖKÇE, ÖZEŞ, OSMAN NİDAİ, KÜPESİZ, OSMAN ALPHAN, YOLDAŞ, ŞÜKRAN BURÇAK

Get full text

P-95 - Decreased circulating sphingomyelins and ceramides in sickle cell disease patients by Aslan, Mutay, Kıraç, Ebru, Kaya, Sabriye, Özcan, Filiz, Salim, Ozan, Küpesiz, Osman Alphan

“…This study aimed to identify levels of C16-C24 sphingomyelin (CerPCho) and C16-C24 ceramide (CER) in serum obtained from SCD patients and controls. Circulating…”
Get full text

Decreased circulating sphingomyelins and ceramides in sickle cell disease patients by Aslan, Mutay, Kıraç, Ebru, Kaya, Sabriye, Özcan, Filiz, Salim, Ozan, Küpesiz, Osman Alphan

Get full text

Alterations of panoramic radiomorphometric indices in children and adolescents with beta-thalassemia major: A fractal analysis study by Yagmur, B, Tercanli-Alkis, H, Tayfun-Kupesiz, F, Karayilmaz, H, Kupesiz, O-A

“…Beta-thalassemia major is an inherited disorder that can cause bone deformity and loss of bone mineral density. The objective of this study is to evaluate the…”
Get full text

Investigation of Alpha Globin Gene Mutations by Complementary Methods in Antalya by Keser, Ibrahim, Mercan, Tugba Karaman, Bilgen, Türker, Kupesiz, Osman Alphan, Arikan, Yunus, Canatan, Duran

“…Alpha (a) thalassemia is one of the hemoglobinopaties that is inherited by autosomal recessive mode. It is caused by mutations on alpha-1 and alpha-2 globin…”
Get full text

Clinical Characteristics and Treatment Outcomes of Patients with Malignant Extracranial Germ Cell Tumors: A 20-Year Single-Center Experience/Ekstrakraniyal Malign Germ Hucreli Tumor Tanili Hastalarin Klinik Ozellikleri ve Tedavi Sonuclari; 20 Yillik Tek Merkez Deneyimi by Kupesiz, Funda Tayfun, Tuysuz, Gulen, Akinel, Ayse Nur, Tekneci, Aysegul, Sivrice, Ayse Cigdem, Melikoglu, Mustafa, Pestereli, Hadice Elif, Kupesiz, Osman Alphan, Guler, Elif

“…Introduction: Germ cell tumors account for 2-3% of all pediatric tumors. The aim of this study was to evaluate the clinical features and treatment outcomes of…”
Get full text

Factor 8 Gene Mutation Spectrum of 270 Patients with Hemophilia A: Identification of 36 Novel Mutations by Atik, Tahir, Işık, Esra, Onay, Hüseyin, Akgün, Bilçağ, Shamsali, Moharram, Kavaklı, Kaan, Evim, Melike, Tüysüz, Gülen, Özbek, Namık Yaşar, Şahin, Fahri, Salcıoğlu, Zafer, Albayrak, Canan, Oymak, Yeşim, Ünal, Ekrem, Belen, Fatma Burcu, Yılmaz Keskin, Ebru, Balkan, Can, Baytan, Birol, Küpesiz, Alphan, Culha, Vildan, Tahtakesen Güçer, Tuba Nur, Güneş, Adalet Meral, Özkınay, Ferda

“…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…”
Get full text

The Impact of HEAD-US Scoring System for Observing the Protective Effect of Prophylaxis in Hemophilia Patients: A Prospective, Multicenter, Observational Study by Kavaklı, Kaan, Özbek, Süha Süreyya, Antmen, Ali Bülent, Şahin, Fahri, Aytaç, Şevkiye Selin, Küpesiz, Alphan, Zülfikar, Bülent, Sönmez, Mehmet, Çalışkan, Ümran, Balkan, Can, Akbaş, Tuğana, Arpacı, Taner, Tamsel, İpek, Seber, Turgut, Oğuz, Berna, Çevikol, Can, Bulakçı, Mesut, Koşucu, Polat, Aydoğdu, Demet, Şaşmaz, İlgen, Tüysüz, Gülen, Koç, Başak, Tokgöz, Hüseyin, Mehrekula, Zuhal, Özkan, Burcu

“…To observe preventive effect of prophylactic treatment on joint health in people with hemophilia (PwH) and to investigate the importance of integration of…”
Get full text

Investigation of Ganciclovir Resistance in Cytomegalovirus Isolates by Phenotypic and Genotypic Methods by Sarınoğlu, Rabia Can, Çolak, Dilek, Küpesiz, Osman Alphan, Kuşkucu, Mert Ahmet, Yalçın, Koray, Sağlık, İmran, Mutlu, Derya, Midilli, Kenan, Peker, Bilal Olcay, Özhak, Betil, Özkul, Aykut, Foldes, Kataline

Get full text