Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mohammadamin Ghadyani"'
Autor:
Hossein Neamatzadeh, Mohammadamin Ghadyani, Hamideh Shajari, Seyed Hamed Hosseini-Jangjou, Reza Bahrami, Seyed Alireza Dastgheib
Publikováno v:
World Journal of Peri & Neonatology.
Background: Retinopathy of prematurity (ROP) is an important cause of preventable blindness in children. The aim of this study was to examine the association of the polymorphisms at Factor V Leiden (FVL) and methylene tetrahydrofolate reductase (MTHF
Autor:
Mahmood Noorishadkam, Hossein Neamatzadeh, Reza Bahrami, Elahe Akbarian, Maryam Saeida-Ardekani, Zahra Zare, Seyed Hamed Hosseini-Jangjou, Mohammadamin Ghadyani
Publikováno v:
World Journal of Peri & Neonatology.
Background: Retinopathy of prematurity (ROP) is a major cause of blindness in newborn infants worldwide. It is well known that neovascularization of the retina is prominent in the proliferative stages of ROP. It is suggested that vascular endothelial
Autor:
Elnaz Sheikhpour, Sahel Khajehnoori, Hossein Neamatzadeh, Mohammadamin Ghadyani, Seyed Alireza Dastgheib, Seyed Sajjad Tabei, Fatemeh Asadian, Mohamad Hossein Antikchi
Publikováno v:
Journal of gastrointestinal cancer. 53(1)
Genetic polymorphisms play an important role in the development of colorectal cancer (CRC). Functional variants in the epidermal growth factor (EGF), survivin, and Ephrin A1 (EFNA1) genes have been previously reported to play a potential role in susc
Autor:
Elnaz Sheikhpour, Hossein Neamatzadeh, Masoud Mehdinezhad-Yazdi, Mohammadamin Ghadyani, Ahmad Hashemzehi, Mohammadreza Sobhan, Seyed Alireza Dastgheib, Masoud Zare-Shehneh
Publikováno v:
SSRN Electronic Journal.
Background: The associations of Matrilin-3 (MATN3) and Adiponectin (ADIPOQ) polymorphisms with knee osteoarthritis (OA) risk have been reported, but it is currently the conclusions have been divergent. Methods: We carried out this case-control study