Yazar "Albayrak, Canan" için listeleme
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Autosomal recessive osteopetrosis with a unique imaging finding: multiple encephaloceles
Saglam, Dilek; Bilgici, Meltem Ceyhan; Bekci, Tumay; Albayrak, Canan; Albayrak, Davut (Springer, 2017)Osteopetrosis is a hereditary form of sclerosing bone dysplasia with various radiological and clinical presentations. The autosomal recessive type, also known as malignant osteopetrosis, is the most severe type, with the ... -
Çocuklarda Akut Lenfoblastik Lösemi Tedavisinin Dental Gelişim Üzerine Etkisinin İncelenmesi
Avşar, Aysun; Yücel, Gül Seda; Albayrak, Canan (2016)Amaç: Çalışmanın amacı çocuklarda Akut Lenfoblastik Lösemi (ALL) tedavisinin dental yaş üzerine etkisini sağlıklı çocuklarla karşılaştırarak incelemektir. Yöntem: Ondokuz Mayıs Üniversitesi Pedodonti Anabilim Dalına tedavi ... -
Flow cytometric analysis of platelet surface glycoproteins in the diagnosis of thirty-two Turkish patients with Glanzmann thrombasthenia: A multicenter experience
Saraymen, Berkay; Muhtaroğlu, Sabahattin; Köker, Mustafa Yavuz; Sarper, Nazan; Zengin, Emine; Albayrak, Canan; Albayrak, Davut; Zülfikar, Bülent; Koç Şenol, Başak; Bentli, Esma; Yılmaz, Semih; Çetin, Aysun; Eser, Bülent; Çetin, Mustafa (TÜBİTAK, 2021)Background/aim: Glanzmann thrombasthenia (GT) is a rare autosomal recessively inherited bleeding disorder characterized by the quantitative (type 1 and type 2) or qualitative (type 3) deficiency in platelet membrane ... -
Good prediction of an anemic patient
Albayrak, Davut; Albayrak, Canan (Galenos Yayincilik, 2009)Anemias are a group of disease which draw the interest of by all clinicians as well as hematologists. An algorithm of anemia diagnosis by test parameters decreases the unuseful tests and prevents false diagnosis. Such ... -
Hematological disturbances in Down syndrome: single centre experience of thirteen years and review of the literature
Karakurt, Neslihan; Uslu, Ilker; Aygun, Canan; Albayrak, Canan (Turkish J Pediatrics, 2019)Neonates with Down syndrome (DS) may have hematological abnormalities such as polycythemia, thrombocytopenia and transient leukemia (TL). The primary objective of this study was to report the descriptive data of complete ... -
Invasive Fungal Infections in Children With Hematologic and Malignant Diseases
Ozsevik, Sevinc N.; Sensoy, Gulnar; Karli, Arzu; Albayrak, Canan; Dagdemir, Ayhan; Belet, Nursen; Albayrak, Davut (Lippincott Williams & Wilkins, 2015)Background: To evaluate the clinical feature and outcome of invasive fungal infections (IFI) in children with hematologic and malign diseases. Patients and Methods: The medical records of children with hematologic and ... -
Juvenile Myelomonocytic Leukemia in Turkey: A Retrospective Analysis of Sixty-five Patients
Tufekci, Ozlem; Kocak, Ulker; Kaya, Zuhre; Yenicesu, Idil; Albayrak, Canan; Albayrak, Davut; Evim, Melike Sezgin (Galenos Yayincilik, 2018)Objective: This study aimed to define the status of juvenile myelomonocytic leukemia (JMML) patients in Turkey in terms of time of diagnosis, clinical characteristics, mutational studies, clinical course, and treatment ... -
Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis
Walne, Amanda J.; Collopy, Laura; Cardoso, Shirleny; Ellison, Alicia; Plagnol, Vincent; Albayrak, Canan; Dokal, Inderjeet (Ferrata Storti Foundation, 2016)Dyskeratosis congenita is a highly pleotropic genetic disorder. This heterogeneity can lead to difficulties in making an accurate diagnosis and delays in appropriate management. The aim of this study was to determine the ... -
Myelofibrosis associated with rickets in a child with down syndrome
Albayrak, Canan; Albayrak, Davut; Kilinc, Ayse Ayzit; Kara, Cengiz (Wiley Periodicals, Inc, 2012)… -
Neonates born to mothers with immune thrombocytopenia: 11 years experience of a single academic center
Karakurt, Neslihan; Uslu, Ilker; Albayrak, Canan; Tomak, Leman; Ozyazici, Elif; Albayrak, Davut; Aygun, Canan (Lippincott Williams & Wilkins, 2018)A major problem associated with immune thrombocytopenic purpura (ITP) in pregnancy is neonatal thrombocytopenia. We analyzed newborns born to mothers with ITP and examined predictive factors for thrombocytopenia. This ... -
Once-weekly prophylaxis with glycoPEGylated recombinant factor VIII (N8-GP) in severe haemophilia A: Safety and efficacy results from pathfinder 2 (randomized phase III trial)
Curry, Nicola; Albayrak, Canan; Escobar, Miguel; Holme, Pal Andre; Kearney, Susan; Klamroth, Robert; Lentz, Steven R. (Wiley, 2019)Introduction Turoctocog alfa pegol (N8-GP) is a site-specific, 40 kDa glycoPEGylated recombinant factor VIII (FVIII) product with an extended half-life. The comprehensive main phase of the pivotal pathfinder 2 trial showed ... -
Pancytopenia As the Initial Manifestation of Brucellosis in Children
Karli, Arzu; Sensoy, Gulnar; Albayrak, Canan; Koken, Ozlem; Cirakli, Sevgi; Belet, Nursen; Albayrak, Davut (Mary Ann Liebert, Inc, 2015)Presenting with severe thrombocytopenia and pancytopenia is rare in children with brucellosis, and at the beginning it can be misdiagnosed as a hematological or a viral hemorrhagic disease. The follow-ups of 52 patients ... -
Red Cell Glucose 6-Phosphate Dehydrogenase Deficiency in the Northern Region of Turkey: Is G6PD Deficiency Exclusively a Male Disease?
Albayrak, Canan; Albayrak, Davut (Taylor & Francis Inc, 2015)Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked recessive genetic defect that can cause hemolytic crisis. However, this disease affects bothmales and females. In Turkey, the frequency of this enzyme ... -
Vitamin D levels in children with severe hemophilia A: an underappreciated deficiency
Albayrak, Canan; Albayrak, Davut (Lippincott Williams & Wilkins, 2015)Osteoporosis in hemophilic patients is a significant problem. The causes of osteoporosis in hemophilic patients are lack of adequate exercise, multiple hemorrhage and inflammation, and low vitamin D levels. The aim of this ... -
Vitamin D levels in patients with severe hemophilia A
Albayrak, Davut; Albayrak, Canan (Wiley-Blackwell, 2014)…