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A phase III, randomized, two-armed, double-blind, parallel, active controlled, and non-inferiority clinical trial to compare efficacy and safety of biosimilar adalimumab (CinnoRAآ®) to the reference product (Humiraآ®) in patients with active rheumatoid arthritis 

Jamshidi, A; Gharibdoost, F; Vojdanian, M; Soroosh, SG; Soroush, M; Ahmadzadeh, A; Nazarinia, MA; Mousavi, M; Karimzadeh, H; Shakibi, MR; Rezaieyazdi, Z; Sahebari, M; Hajiabbasi, A; Ebrahimi, AA; Mahjourian, N; Rashti, AM (2017)
Background: This study aimed to compare efficacy and safety of test-adalimumab (CinnoRAآ®, CinnaGen, Iran) to the innovator product (Humiraآ®, AbbVie, USA) in adult patients with active rheumatoid arthritis (RA). Methods: ...
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A randomized, double-blind, placebo-controlled study to evaluate the role of formoterol in the management of acute asthma 

Najafizadeh, K; Pour, HS; Ghadyanee, M; Shiehmorteza, M; Jamali, M; Majdzadeh, S (2007)
Aim: To evaluate the efficacy and tolerability of formoterol delivered by Aerolizer in the emergency department. Methods: A single-centre, double-blind, randomised, placebo-controlled, parallel group study was conducted ...
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A socio-cognitive inquiry of excessive mobile phone use 

Pourrazavi, S; Allahverdipour, H; Jafarabadi, MA; Matlabi, H (2014)
Objectives: The study examined the predictive ability of selected demographic and socio-psychological characteristics in explaining excessive mobile phone use (EMPU) behavior and problematic use in a sample of university ...
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Anatomical differences in the right and left renal arterial patterns 

Tarzamni, MK; Nezami, N; Rashid, RJ; Argani, H; Hajealioghli, P; Ghorashi, S (2008)
The aim of this study was to determine the pattern and character of the renal arteries in patients referred for preoperative or diagnostic evaluation of the renal or abdominal arteries by multi-detector computed tomography ...
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Association of UCP2 -866G>A polymorphism with nonalcoholic fatty liver disease in patients from North-West of Iran 

Mohseni, F; Farajnia, S; Farhangi, MA; Khoshbaten, M; Jafarabadi, M-A (2017)
Objective: To investigate the association of uncoupling protein-2 (UCP2) -866G>A gene polymorphism (rs659366) with nonalcoholic fatty liver disease (NAFLD). Methods: We performed a case-control study with a cohort of 75 ...
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An inverse relation between CagA+ strains of Helicobacter pylori infection and risk of erosive GERD 

Somi, MH; Fattahi, E; Fouladi, RF; Karimi, M; Bonyadi, R; Baballou, Z (2008)
Objective: The aim of this study is investigating the association of Helicobacter pylori (H. pylori) infection and its cytotoxic-associated gene A (cagA) strain with reflux esophagitis. Methods: In a case-control setting ...
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Apolipoprotein A polymorphysm predicts lipoprotein A concentration in renal transplant recipients 

Argani, H; Ghorbanihaghjo, A; Rashtchizadeh, N; Rahbaninobar, M (2005)
Increased serum lipoprotein(a) is an independent risk factor for atherosclerosis in renal transplant recipients. Higher levels may be due to genetic factors, for example, apolipoprotein A isoforms and/or environmental ...
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Association of endothelial nitric oxide synthase gene variants (-786 T>C, intron 4 b/a VNTR and 894 G>T) with idiopathic recurrent pregnancy loss: A case-control study with haplotype and in silico analysis 

Azani, A; Hosseinzadeh, A; Azadkhah, R; Zonouzi, AAP; Zonouzi, AP; Aftabi, Y; Khani, H; Heidary, L; Danaii, S; Bargahi, N; Pouladi, N; Hosseini, SM (2017)
Objective(s) Many lines of evidence suggest that reduced production of nitric oxide (NO) due to single nucleotide polymorphisms in endothelial nitric oxide synthase (eNOS) gene may affect the implantation and maintenance ...
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Association of P53 (?16ins-Pro) Haplotype with the Decreased Risk of Differentiated Thyroid Carcinoma in Iranian-Azeri Patients 

Dehghan, R; Hosseinpour Feizi, MA; Pouladi, N; Babaei, E; Montazeri, V; Fakhrjoo, A; Sedaei, A; Azarfam, P; Nemati, M (2015)
Association of P53 polymorphisms with the increased risk of various cancers has been investigated in numerous studies. However, the results were conflicting and no polymorphism has been determined as a definite risk factor. ...
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A single nucleotide polymorphism in the FOXP3 gene associated wit] behcet's disease in an Iranian population 

Hosseini, A; Shanehbandi, D; Estiar, MA; Gholizadeh, S; Khabbazi, A; Khodadadi, H; Sakhinia, E; Babaloo, Z (2015)
Background: Behcet's Disease (BD) is a rare autoimmune disease that involves the dysfunction of regulatory T cells. FOXP3 is a key transcription factor in the development and function of Treg cells. Recent studies have ...
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AuthorArgani, H (6)Farhangi, MA (5)Goldust, M (5)Ghojazadeh, M (4)Babaloo, Z (3)Dastgiri, S (3)Ebrahimi, AA (3)Farajnia, S (3)Farzadi, L (3)Ghaffari, S (3)... View MoreSubject
adult (111)
controlled study (111)
Female (111)
female (111)
human (111)
Humans (111)Adult (89)Male (85)male (85)Middle Aged (69)... View MoreDate Issued2010 - 2018 (74)2004 - 2009 (37)Has File(s)No (63)Yes (48)

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