Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Yonca, Egin"'
Autor:
Shatla, Hamed M., Tomoum, Hoda Y., Elsayed, Solaf M., Aly, Rasha H., Shatla, Rania H., Ismail, Mona A., El-Ghany, Naglaa A., Fakhry, Arsanios I., Abd Allah, Nasser A., Yonca, Egin, Nejat, Akar M.
Publikováno v:
In Pediatric Neurology August 2012 47(2):114-118
Publikováno v:
Experimental and Therapeutic Medicine
Deep vein thrombosis (DVT) is a type of venous thromboembolism and a clinically complex vascular disease. Oxidative stress serves a key role in the pathogenesis of numerous cardiovascular diseases, particularly in endothelial dysfunction-associated s
Publikováno v:
Turkish Journal of Hematology, Vol 25, Iss 03, Pp 133-135 (2008)
Objective: Protein Z (PZ) plays an enhancer role in coagulation as an anticoagulant. In this study G79A polymorphism was investigated in Turkish pediatric stroke patients. Material and Methods: Ninety-one pediatric stroke patients with cerebral ische
Externí odkaz:
https://doaj.org/article/75ba2e6a8a65499d81910505597a9175
Autor:
Fatoş Yalçınkaya, Fatma Semsa Cayci, Hafize Gökçe, Birsin Ozcakar, Yonca Egin, Mesiha Ekim, Nejat Akar
Publikováno v:
Pediatric Hematology and Oncology. 32:115-122
The pathogenesis of Henoch-Schönlein Purpura (HSP) has not been clearly defined. Inflammatory cytokines have been associated with HSP but there are only a few reports that have focused on coagulation. The endothelial protein C receptor (EPCR), which
Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 25(2)
Autor:
Sara M. Abdelhakam, Solaf M. Elsayed, Mohammad Sakr, Nejat Akar, Abdel Ghaffar Ty, Yonca Egin, Ezzat Elsobky, Yousuf S
Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 28(4)
Budd-Chiari syndrome is a multifactorial disease in which several prothrombotic disorders may predispose patients to the development of thrombosis at this uncommon location (hepatic veins). The aim of this study was to determine the prevalence and ch
Autor:
Yonca Egin, Mohammed A AboElAsrar, Mai Mohamed Mahmoud Saied, Ahmed Al-saeed Hamed, Nejat Akar
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 13, No 2 (2012); 139-145
In patients with type-I diabetes mellitus folate deficiency is associated with endothelial dysfunction. So, polymorphism in genes involved in folate metabolism may have a role in vascular disease. This study was designed to evaluate the relationship
Autor:
Naşit İğci, Ibrahim C. Haznedaroglu, Duygu Ozel-Demiralp, Nejat Akar, Beycan Ayhan, Yonca Egin
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis. 18:604-610
Ankaferd blood stopper (ABS) is a novel topical hemostatic agent of plant origin registered for the management of external hemorrhages, in Turkey. The ABS-induced formation of the protein network with vital erythroid aggregation covers the whole phys
Publikováno v:
Pteridines, Vol 23, Iss 1, Pp 14-21 (2012)
The C677T variant of methylenetetrahydrofolate reductase (MTHFR), a key enzyme in the remethylation of homocysteine (HCY) to methionine, is a frequent genetic cause of moderate hyperhomocysteinemia (HHCY) among individuals with cardiovascular disease
Autor:
Aydan Ongun, Sehsuvar Erturk, Nejat Akar, Yonca Egin, Cansin Tolunay, Kenan Keven, Irem Dincer, Sule Sengul, Mehmet Altan
Publikováno v:
Turkish Nephrology Dialysis Transplantation. 21:53-59
Vitamin D duzeyi ile kardiyovaskuler hastaliklar arasinda iliskiyi gosteren bircok calisma vardir. Vitamin D yetersizligi/eksikligi kronik bobrek hastaliklarinda ve bobrek nakli alicilarinda sik gozlenmekte ancak vitamin D duzeyi yaz ve kis aylarinda