نتایج جستجو برای: methylenetetrahydrofolate reductase

تعداد نتایج: 44947  

Journal: :iranian journal of neonatology 0
amin khaleghparast m.sc. of biology-genetics, tehran science and research branch of islamic azad university, tehran, iran sharif khaleghparast b.eng. of industrial engineering, iran university of science and technology (iust), tehran, iran hossein khaleghparast ph.d. of public law, tehran science and research branch of islamic azad university, tehran, iran

introduction: one factor known to cause thrombophilia in women with unexplained recurrent spontaneous abortion (rsa) is c677t polymorphism of methylenetetrahydrofolate reductase gene. this study aimed to determine the association between rsa and mthfr c677t polymorphism in iranian patients. methods: in this case-control study, 30 patients with previous history of two or more consecutive unexpla...

Journal: :فیض 0
بتول پورقیصری batool pourgheysari pathology and hematology department, shahrekord university of medical sciences, shahrekord, i. r. iran.شهرکرد، دانشگاه علوم پزشکی شهرکرد، گروه پاتولوژی عفت فرخی efat farrokhi مجتبی ساعدی mojtaba saedi

background: inherited thrombophilic gene polymorphisms have been related to the pathogenesis of venous thromboembolism and its outcomes. considering the scarcity of data on the frequency of the thrombophilic gene polymorphisms in iranian populations, the aim of this study was to assess such polymorphisms in healthy individuals. materials and methods: this cross-sectional study was performed on ...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

Journal: :journal of research in medical sciences 0
asghar ebadifar nazila ameli hamid reza khorramkhorshid koorosh kamali mehdi salehizeinabadi

background: we studied the role of maternal folic acid supplementation in modifying the effects of  methylenetetrahydrofolate reductase (mthfr c677t and a1298c) gene polymorphisms in iranian children with oral clefts. materials and methods: forty?seven newborn infants with orofacial cleft and their mothers were selected randomly. mothers were matched regarding dietary folate intake.the genotypi...

Journal: :Journal of Clinical Laboratory Analysis 2015

Journal: :journal of research in medical sciences 0
aydogan aydogdu cem haymana kamil baskoy ali h. durukan gokhan ozgur omer azal

we report a case of choroidal neovascularization (cnv) secondary to methylenetetrahydrofolate reductase (mthfr) gene mutation in a 20-year-old male patient with hypopituitarism. treatment with three consecutive injections of intravitreal ranibizumab (anti-vascular endothelial growth factor) resulted in significant improvement of the patient’s vision and the appearance of the macula. a search ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید