Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Seyed Hamed Hosseini-Jangjou"'
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:
Seyed Hamed Hosseini-Jangjou, Farzad Ferdosian, Hossein Neamatzadeh, Mahmood Noorishadkam, Mohamad Hosein Lookzadeh, Seyed Reza Mirjalili, Zahra Nafei, Seyed Alireza Dastgheib
Publikováno v:
Fetal and Pediatric Pathology. 40:320-336
Background: Kawasaki Disease (KD) is a multifactorial condition at the junction of infectious diseases, immunology, rheumatology, and cardiology. The aim of this study is to derive a more precise e...
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:
Farzad, Ferdosian, Seyed Alireza, Dastgheib, Seyed Hamed, Hosseini-Jangjou, Zahra, Nafei, Mohamad Hosein, Lookzadeh, Mahmood, Noorishadkam, Seyed Reza, Mirjalili, Hossein, Neamatzadeh
Publikováno v:
Fetal and pediatric pathology. 40(4)
Kawasaki Disease (KD) is a multifactorial condition at the junction of infectious diseases, immunology, rheumatology, and cardiology. The aim of this study is to derive a more precise estimation of the association of TNF-α rs1800629, CASP3 rs7268923
Autor:
Reza Bahrami, Seyed Alireza Dastgheib, Abdolhamid Amooee, Hossein Neamatzadeh, E. Salehi, Jalal Sadeghizadeh-Yazdi, Majid Aflatoonian, Seyed Hamed Hosseini-Jangjou
Publikováno v:
Fetal and pediatric pathology. 40(3)
Hirschsprung's disease (HSCR) is a heterogeneous congenital malformation of the enteric nervous system with a complex genetic etiology. We investigated if there was an association between Neuregulin-1 (NRG1) rs7835688 G C, rs16879552 T C and rs243930