Zobrazeno 1 - 10
of 117
pro vyhledávání: '"Cigdem Altay"'
Autor:
Sule Unal, Mualla Cetin, Aytemiz Gurgey, Gunay Balta, Didem Efendioglu, Eren Cimen, Cigdem Altay, Fatma Gumruk, Hamza Okur
Publikováno v:
Turkish Journal of Hematology, Vol 28, Iss 02, Pp 125-130 (2011)
Numerous acquired etiological factors, such as infections, malignancies, and collagen tissue disorders, are involved in the development of acquired hemophagocytic lymphohistiocytosis (AHLH). Not everyone with the same etiological factors developments
Autor:
Fatma Gumruk, Özgür Özyüncü, Nur Çakar, Sezcan Mumusoglu, Aytemiz Gurgey, Cigdem Altay, M. Sinan Beksaç
Publikováno v:
Pediatric Hematology and Oncology. 28:51-55
Between 1983 and 2008, prenatal diagnostic procedures for identifying hemoglobinopathies were performed in 947 at-risk fetuses. Seventy-six percent of the fetuses were at risk for beta-thalassemia major and 16% for sickle cell anemia; only a small pe
Autor:
Kudret Aytemir, Aytemiz Gurgey, Cigdem Altay, Ali Oto, Giray Kabakci, Nasih Nazli, Lale Tokgozoglu, Orhan Onalan, Gunay Balta
Publikováno v:
Journal of Thrombosis and Thrombolysis. 26:211-217
A case control study was conducted to test the hypothesis that plasminogen activator inhibitor type-1 (PAI-1) 4G/5G gene polymorphism confers an increased risk for myocardial infarction (MI) in patients with known coronary atherosclerosis.One hundred
Autor:
Turgay Coşkun, Cigdem Altay, Aytemiz Gurgey, Fatma Gumruk, Betul Tavil, Hatice Sivri, Ayşegül Tokatlı, Emel Ozyurek, Ali Dursun
Publikováno v:
Journal of Inherited Metabolic Disease. 29:607-611
Early detection and therapy of haematological abnormalities and/or diseases may improve the prognosis of metabolic disorders. Accordingly, we aimed to evaluate the frequency and types of haematological abnormalities in children[-31pc] with various in
Autor:
Zhongyuan Li, Essam A.R. Ismail, Albert de la Chapelle, James D. Perko, Ralph Gräsbeck, Stephan M. Tanner, Laurence Faivre, Mualla Cetin, Zekiye Yurtsever, C. Öner, Cigdem Altay, Karen L. David
Publikováno v:
Proceedings of the National Academy of Sciences. 102:4130-4133
Hereditary juvenile megaloblastic anemia due to vitamin B 12 (cobalamin) deficiency is caused by intestinal malabsorption of cobalamin. In Imerslund–Gräsbeck syndrome (IGS), cobalamin absorption is completely abolished and not corrected by the adm
Publikováno v:
Blood Coagulation & Fibrinolysis. 15:657-662
A total of 360 pediatric patients aged 1 month to 18 years were diagnosed as having thrombosis between January 1998 and April 2003. Of these patients, those aged 11-18 years (n = 131) were regarded as adolescents and the rest as children. The proport
Autor:
M. Mert Sozen, Ç. Karaaslan, C. Öner, R. Öner, Cigdem Altay, Fatma Gumruk, M.A. Özdemir, Aytemiz Gurgey
Publikováno v:
American Journal of Hematology. 76:378-382
A boy presented at age 4 years with severe congenital hemolytic anemia characterized by highly elevated reticulocyte count (30-50%) and prominent basophilic stippling. Hb had been 4 g/dL at age 7 months. The patient was on a monthly transfusion regim
Publikováno v:
Blood. 102:1900-1903
Pyrimidine 5′ nucleotidase-I (P5N-I) deficiency is a rare autosomal recessive disorder associated with hemolytic anemia, marked basophilic stippling, and accumulation of high concentrations of pyrimidine nucleotides within the erythrocyte. Recently
Autor:
Nazmiye Yüksek, Gunay Balta, Gönül Hiçsönmez, Emel Ozyurek, Aytemiz Gurgey, Cigdem Altay, Ulya Ertem
Publikováno v:
American Journal of Hematology. 73:154-160
The role of methylenetetrahydrofolate reductase (MTHFR C677T), glutathione S-transferases (GSTM1 and GSTT1 null, GSTP1 Ile105Val), and cytochromes p450 (CYP1A1*2A) genotypes in the etiology of childhood leukemia was simultaneously investigated. 144 T
Publikováno v:
American Journal of Hematology. 71:275-278
Recently, measurement of serum alpha-fetoprotein (sAFP) was introduced as a preliminary test for diagnosis of Fanconi's anemia (FA). In the present study, sAFP levels were measured in order to determine its sensitivity and specificity in 33 Turkish F