Search Results - "Canatan, D"

I21 Hemoglobinopathy prevention program in Turkey by Canatan, D

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Haemoglobinopathy Prevention Program in Turkey by Canatan, D.

“…Thalassemia and abnormal haemoglobins are a serious health problem in Turkey. Very important steps for toward preventing thalassemia have been taken in Turkey…”
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Molecular analysis of beta-thalassemia and sickle cell anemia in Antalya by Keser, I, Sanlioglu, A D, Manguoglu, E, Guzeloglu Kayisli, O, Nal, N, Sargin, F, Yesilipek, A, Simsek, M, Mendilcioglu, I, Canatan, D, Luleci, G

“…We have studied 918 chromosomes for mutations leading to beta-thalassemia and sickle cell anemia, which are the two most frequently found monogenic disorders…”
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TT virus infection and genotype distribution in blood donors and a group of patients from Turkey by ERENSOY, S, SAYINER, A. A, TÜRKOGLU, S, CANATAN, D, AKARCA, U. S, SERTÖZ, R, ÖZACAR, T, BATUR, Y, BADUR, S, BILGIC, A

“…TT virus (TTV) DNA has been found in a large proportion of patients with different forms of non-A-G hepatitis, however the clinical importance is unclear. We…”
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Molecular pathology of haemophilia A in Turkish patients: identification of 36 independent mutations by Ti̇mur, A. A., Gürgey, A., Aktugˇlu, G., Kavakli, K., Canatan, D., Olek, K., Çagˇlayan, S. H.

“…Haemophilia A is an X‐linked recessive bleeding disorder caused by heterogeneous mutations in the factor VIII gene. In an attempt to reveal the molecular…”
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Continuous desferrioxamine infusion by an infusor in thalassaemia major by CANATAN, D, TEMIMHAN, N, DINCER, N, ÖZSANCAK, A, OGUZ, N, TEMIMHAN, M

“…Chelation therapy with desferrioxamine (DFO) can be an important problem for patients with thalassaemia major (TM). In an effort to find a solution to this…”
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Post-splenectomy thrombosis and haemolytic anaemias by Kemahli, S, Canatan, D, Cin, S, Uysal, Z, Akar, N, Arcasoy, A

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EVALUATION OF OSTEOPOROSIS IN THALASSEMIA BY QUANTITATIVE COMPUTED TOMOGRAPHY: Is It Reliable? by Akpek, Sergin, Canatan, Duran, Araç, Mehmet, Ilgit, Erhan T.

“…This study was conducted to quantify the degree of osteoporosis in thalassemic patients by single energy quantitative computed tomography (SEQCT) and to test…”
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DDAVP shortens bleeding time in Bernard-Soulier syndrome by Kemahli, S, Canatan, D, Uysal, Z, Akar, N, Cin, S, Arcasoy, A

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GM-CSF in the treatment of Fanconi's anaemia by Kemahli, S, Canatan, D, Uysal, Z, Akar, N, Cin, S, Arcasoy, A

“…We have used recombinant human (rh) GM-CSF in two 12-year-old Fanconi's aplastic anaemia patients. They had not received any previous therapy except blood…”
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Natural Inhibitors and Lipids in Patients with Sickle Cell Disease by Canatan, D, Oğuz, N, Özsancak, A, Aslan, İ, Bengü, A, Gürman, A, Sarıca, B

“…Microvascular occlusion in sickle cell disease (SCD) is a multifactorial process. Disordered coagulation may play a role in the pathogenesis of vaso occlusive…”
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A Data-Mining Approach for Investigating Social and Economic Geographical Dynamics of \beta-Thalassemia's Spread by Akay, A., Dragomir, A., Yardimci, A., Canatan, D., Yesilipek, A., Pogue, B.W.

“…beta-Thalassemia is an anemic genetic disorder that remains a major global health issue, especially in the globalized era where public health, economics, and…”
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Hemoglobinopathy control program in Turkey by Canatan, Duran, Kose, M Rifat, Ustundag, Munip, Haznedaroglu, Dilek, Ozbas, Sema

“…Hemoglobinopathies are a very important health problem in Turkey. To date many studies have been performed but there has been no national hemoglobinopathy…”
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Psychosocial burden of β-thalassaemia major in Antalya, south Turkey by Canatan, Duran, Ratip, Siret, Kaptan, Saniye, Cosan, Rüya

“…β-thalassaemia is a recessively inherited blood disorder characterised by chronic anaemia. It requires monthly blood transfusions and regular iron chelation…”
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Fluorosis and its hematological effects by Eren, Erdal, Özturk, Mustafa, Mumcu, Ethem Faruk, Canatan, Duran

“…Although it has been reported that fluoride ingestion has no influence on various indices of hematopoiesis, some research has been published that excessive…”
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β-Thalassemia major associated with Down syndrome by Keser, İbrahim, Canatan, D, Güzeloglu-Kayişli, Ö, Coşan, R, Lüleci, G

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Iron Chelation Therapy with Deferasirox (Exjade®, ICL670) or Deferoxamine Is Effective in Reducing Iron Overload in Patients with Advanced Fibrosis and Cirrhosis by Angelucci, E., Turlin, B., Canatan, D., Mangiagli, A., De Sanctis, V., Meddeb, B., Rose, C., Soulieres, D., Cunningham, M., Gattermann, N., Ressayre-Djaffer, C., Rabault, B., Ford, J.

“…Introduction: Although the direct measurement of iron from a liver biopsy is the reference standard method to determine liver iron concentration (LIC), results…”
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Antioxidant capacity of G-6-PD-deficient erythrocytes by Bilmen, Süreyya, Aksu, T.Aslan, Gümüşlü, Saadet, Korgun, Dijle Kipmen, Canatan, Duran

“…Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency is the most common human enzymopathy. In this research, we studied two groups consisting of 30 male…”
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SOFT TISSUE DENSITY VARIATIONS IN THALASSEMIA MAJOR: A Possible Pitfall in Lumbar Bone Mineral Density Measurements by Dual-Energy X-Ray Absorptiometry by Y ld z, Mustafa, Canatan, Duran

“…Osteoporosis is common in patients with thalassemia major. A 16-year-old patient with thalassemia major was referred for evaluation of osteoporosis. The…”
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Deferasirox (Exjade®, ICL670) Demonstrates Iron Chelating Efficacy Related to Transfusional Iron Intake in Pediatric Patients by Kattamis, C., Kilinc, Y., Fattoum, S., Ferster, A., Gallisai, D., Maggio, A., Dresse, M.F., Klingebiel, T., Bourantas, K., Canatan, D., Maseruka, H., Gathmann, I., Ford, J.

“…Chelation therapy is the conventional treatment for transfusional iron overload, which leads to complications in the heart, liver and endocrine glands. A…”
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