Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Edip, Gali"'
Autor:
Selma Ünal, Gönül Oktay, Can Acıpayam, Gül İlhan, Edip Gali, Tiraje Celkan, Ali Bay, Barış Malbora, Nejat Akar, Yeşim Oymak, Tayfur Toptaş
Publikováno v:
Turkish Journal of Hematology, Vol 33, Iss 1, Pp 56-59 (2016)
The purpose of this study was to research the problem of hemoglobin H (HbH) disease, to reveal the distribution patterns among different health centers, and to emphasize the importance of this disease for Turkey. A total of 273 patients were included
Externí odkaz:
https://doaj.org/article/5d9b08ddbb78455291cce94aa1fc1176
Publikováno v:
Infectious Diseases in Clinical Practice. 15:167-170
Autor:
Fatih Yalçin, Taskin Duman, Tunzale Seydaliyeva, İsmet Melek, Ergün Seyfeli, Edip Gali, Ferit Akgül
Publikováno v:
Acta Haematologica. 118:1-6
Background: QT dispersion has been proposed to be a predictor of adverse outcomes in a variety of cardiac disease states. The objective of this study was to examine QT dispersion in patients with sickle cell disease (SCD) and to assess the effect of
Publikováno v:
Archives of Medical Research. 37:895-898
Background Transfusion-dependent patients are more prone to acquiring various transfusion-transmitted infections such as hepatitis B (HBV), hepatitis C (HCV) and human immunodeficiency virus (HIV). The aim of the study was to investigate the prevalen
Publikováno v:
The Tohoku Journal of Experimental Medicine. 209:135-140
Sickle cell disease (SCD) is a common form of hemoglobinopathy and is highly prevalent worldwide. Silent cerebral infarction, which represents infarction without clinical signs, is a risk factor for clinical stroke in patients with SCD. It is well kn
Publikováno v:
Journal of Medical Sciences. 5:61-63
Autor:
Ali, Balci, Sinem, Karazincir, Ozlem, Sangün, Edip, Gali, Turgay, Daplan, Cihangir, Cingiz, Ertuğrul, Eğilmez
Publikováno v:
Diagnostic and interventional radiology (Ankara, Turkey). 14(3)
The aim of this study was to evaluate the type and prevalence of abdominal ultrasonographic abnormalities in patients with sickle cell disease.A total of 102 patients with sickle cell disease at the Center of Hemoglobinopathy of the Antakya State Hos
Publikováno v:
Tuberkuloz ve toraks. 54(4)
Sickle cell anemia is a disease caused by production of abnormal hemoglobin. Infection, acute splenic sequestration crisis, aplastic crises, acute chest syndrome, stroke, cholelithiasis, renal disease and pain are the major complications. Unilateral
Background: Our aim is to determine comorbidities associated with pulmonary hypertension (PHT) in clinically stable sickle-cell disease (SCD) patients and to evaluate left ventricular (LV) and right ventricular (RV) function in those patients. Method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9c4d1cee3e1d082b338a4d3b20a212f
https://avesis.deu.edu.tr/publication/details/ee0f20ec-5a56-45a9-8d6d-a9529a602219/oai
https://avesis.deu.edu.tr/publication/details/ee0f20ec-5a56-45a9-8d6d-a9529a602219/oai
Right ventricular and pulmonary function in sickle cell disease patients with pulmonary hypertension
Publikováno v:
Pediatric cardiology. 27(4)
The effects of sickle cell disease (SCD) on right ventricular (RV) and pulmonary function in SCD patients with pulmonary hypertension is not well-known. The aim of this study was to investigate RV and pulmonary functions in patients suffering from SC