BACKGROUND Metabolic syndrome (MetS) is a complex clustering cardiovascular risk factors such as abdominal obesity, hypertension, diabetes and dylipedemia. It has been a growing health problem in Iranian adults in recent decade. The objective of this article was to review the prevalence of MetS and the corresponding risk factors among Iranian adults. METHODS We conducted a systematic review t...

During more than the last four decades, Iran has been one of main interest areas not only in global political and strategic agenda but also cultural sphere as well. Most those interests focus on analyzing domestic economic situation addition to foreign policy Islamic Republic. However, observes a lack studies Iranian diaspora their culture, lifestyles, feelings comparative way. One such book wa...

In 1963, the United States Senate Permanent Subcommittee on Investigations received evidence alleging that US aid funds to Iran had been misappropriated and used bribe prominent American Iranian figures. Members of royal family high-profile businessmen diplomats were implicated in emerging corruption scandal. The allegations made by businessman self-proclaimed “World’s Best Dressed Man,” Khaiba...

There are wide individual differences in pharmacokinetic parameters of mycophenolate mofetil (MMF) among transplanted patients. Some studies have shown that single nucleotide polymorphisms (SNPs) of the Uridine Diphosphate Glucuronosyl Transferase1A9 (UGT1A9) are responsible for these differences in early days after transplantation. Therefore it was decided to evaluate the influence of UGT poly...

OBJECTIVES Takotsubo syndrome (TTS) is a reversible cause of heart failure rarely described in African-American patients. This study aimed to compare and contrast the clinical characteristics of TTS in African-American (AA) and non-African-American (NAA) patients. METHODS We retrospectively reviewed the charts of eight patients (four AA and four NAA) diagnosed with TTS, between June 2006 and ...

objective(s) primary or adult type hypolactasia, the most common enzyme deficiency in the world, is due to reduced lactase activity in the intestinal cell after weaning. lactase non-persistence is inherited as an autosomal recessive trait. a dna variant, single nucleotide polymorphism c/t−13910 which is located on 13910 base pairs (bp) upstream of the lactase gene (lct) at chromosome 2 has been...