adult-onset still’s disease (aosd) is a rare systemic inflammatory disorder of unknown etiology. there is not currently any specific serological markers for aosd , and  diagnosis still relying on the exclusion of other likely diagnoses. yamaguchi’s criteria are used as a diagnostic criterion which contains negative serologic markers for other collagen vascular diseases including systemic lupus ...

this survey-study carried out among 360 randomly selected farmers living in drought-prone areas of fars province, iran, set out to investigate the perceptions and psychologi-cal coping strategies of farmers when facing drought. results showed that farmers per-ceived drought as a threat to all of their resources (material, conditions, personal, social and energies) and used emotion-focused and r...

summary: adult-onset still’s disease (aosd) is a rare systemic inflammatory disorder of unknown etiology. it is characterized by high grade fever, skin rash, arthritis, leukocytosis, increased esr, crp and liver enzyme levels and high levels of ferritin. the treatment of aosd includes nsaids, steroids, and disease-modifying antirheumatic drugs (dmards). recently biologic agents have been used f...

conclusions sexual activity in last week of pregnancy might be associated with the onset of labor. therefore, in the absence of complications in term pregnancy, sexual activity can be considered as a natural way to prevent post term pregnancy. background pregnancy is one of the most critical periods in women's lives. sexual relationships change in this period. monitoring of uterine contractions...

the organic deposition particularly asphaltenes has many detrimental effects on the oil industries, such as plugging in pipelines, wellbore and facilities and subsequently, considerable reduction in well productivity.asphaltenes are the most polar fractions, which they have been dispersed as colloidal clusters in crude oil. the accumulation of these clusters lead to the flocculation of colloids...

Background: Tyrosinemia type 1 is an autosomal recessive metabolic disorder, which typically affects liver and kidneys. It is caused by a defect in fumarylacetoacetate hydrolase or fumarylacetoacetase (FAH) enzyme, the final enzyme in the tyrosine degradation pathway. The disease typically manifests as early onset type in early infancy with acute hepatic crisis with hepatomegaly and bleeding te...

objective ullrich congenital muscular dystrophy is a rather severe type of congenital muscular dystrophy with early onset features related to motor development. in general it is inherited in autosomal recessive principles, however in the western world mostly seen with de novo dominant mutations in the collagen vi genes. milder form of the condition is the bethlem myopathy. there may be overlap ...