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Association between admission neutrophil to lymphocyte ratio and outcomes in patients with acute exacerbation of chronic obstructive pulmonary disease [Kronik obstrأ¼ktif akci?er hastal??? alevlenme olgular?nda ba?vuru n?trofil lenfosit oran? ile prognoz aras?ndaki ili?ki]
(2017)
Association between admission neutrophil to lymphocyte ratio and outcomes in patients with acute exacerbation of chronic obstructive pulmonary disease Introduction: The prognostic significance of neutrophil-to-lymphocyte ...
Association of ACE, VEGF and CCL2 gene polymorphisms with Henoch-Sch?nlein purpura and an evaluation of the possible interaction effects of these loci in HSP patients
(2017)
Background. Henoch-Sch?nlein purpura (HSP) is a multisystem, small vessel, leucocytoclastic vasculitis. It is predominantly a childhood vasculitis, rarely reported in adults. Studies have shown that several different genetic ...
Association of ?604G/A and ?501A/C Ghrelin and Obestatin Prepropeptide Gene Polymorphisms with Polycystic Ovary Syndrome
(2018)
Ghrelin hormone has an important role in a wide range of metabolic and non-metabolic processes. Polymorphisms of ghrelin gene could be associated with a large number of diseases. The aim of this study was to evaluate the ...
Association between the proportion of sclerotic glomeruli and serum creatinine in primary focal segmental glomerulosclerosis [Primer fokal glomerulosklerozda sklerotik glomerأ¼l yaygi{dotless}nli{dotless}?i{dotless} ile serum kreatinin i?li?kisi]
(2012)
Objective: To evaluate the possible correlation between the extent of sclerotic glomeruli and the level of serum creatinine and its clearance rate in patients with primary focal segmental glomerolusclerosis. Material and ...
Association between the FABP2 Ala54Thr, PPAR? Leu162/Val, and PPAR? intron7 polymorphisms and blood lipids ApoB and ApoCIII in hypertriglyceridemic subjects in Tehran
(2009)
Background: The alanine to threonine substitution at codon 54 in the FABP2 gene and PPAR? Val162 allele have been associated with hypertriglyceridemia. Objective: We sought to determine the prevalence of the Ala54Thr ...
Association between serum kalirin levels and the KALRN gene rs9289231 polymorphism in early-onset coronary artery diseas
(2018)
Background: Recently, rs9289231 genetic variations of kalirin (KALRN) have been introduced as potential genetic markers for coronary artery disease (CAD). However, the influence of KALRN single-nucleotide polymorphisms ...
Association between thrombophilia and repeated assisted reproductive technology failures
(2012)
Purpose: This study was performed to investigate the incidence of thrombophilic gene mutations in repeated assisted reproductive technology (ART) failures. Methods: The prevalence of mutated genes in the patients with a ...
Association between overweight and increased risk of acute myocardial infarction
(2008)
Objective: To assess relationship of obesity with occurrence of coronary artery disease (CAD) in Iranian patients. Methods: The CAD risk associated with obesity (body mass index ?25.0) was assessed in a case-control study ...
Beneficial role of antioxidants on clinical outcomes and erythrocyte antioxidant parameters in rheumatoid arthritis patients
(2014)
Background: This study aims to investigate the effect of antioxidants supplement on clinical outcomes and antioxidant parameters in rheumatoid arthritis (RA). Methods: The pre-post study was conducted on 40 female patients ...
Beliefs and practices of Iranian pregnant mothers regarding vitamins and minerals [Croyances et pratiques des femmes enceintes iraniennes au sujet des vitamines et des miné raux]
(2011)
The objective of this descriptive study was to examine the vitamin and mineral supplements safety beliefs and practices of Iranian pregnant women. Data were collected from 400 randomly chosen women. More than 50% of the ...