background: temporal variation of stroke onset is suggested in some studies contained somewhat varieties. it is proposed that some predisposing changes occur in some ascertained times consequently resulted in stroke occurrence in some special times. objective: to determine the circadian and circaseptan variation of stroke onset. materials and methods: this cross sectional study was conducted fr...

Mutations in the ROMK1 potassium channel gene (KCNJ1) cause antenatal/neonatal Bartter syndrome type II (aBS II), a renal disorder that begins in utero, accounting for the polyhydramnios and premature delivery that is typical in affected infants, who develop massive renal salt wasting, hypokalaemic metabolic alkalosis, secondary hyperreninaemic hyperaldosteronism, hypercalciuria and nephrocalci...

Background: Temporal variation of stroke onset is suggested in some studies contained somewhat varieties. It is proposed that some predisposing changes occur in some ascertained times consequently resulted in stroke occurrence in some special times. Objective: To determine the circadian and circaseptan variation of stroke onset. Materials and Methods: This cross sectional study was conducted ...

Chartered Society of Massage and Medical Gymnastics, but she is recognised to have been an important motive-force in its progress and development, and she continued her untiring work on its behalf to the end of her life. Her work for midwives is also well known to all who have followed the progress of the movement to improve the standard of midwifery and the status of midwives. The memorial wil...

Background: Pityriasis rubra pilaris (PRP) is a rare skin disease characterized by follicular hyperkeratosis, perifollicular erythema with islands of normal skin scattered over the sheets of erythroderma, palmoplantar hyperkeratosis and pityriasis capitis with unknown etiology. Objective: This study has been done in order to determine the demographics, clinical and therapeutic aspects of PRP pa...

objective: type 1 diabetes mellitus (t1d) is an autoimmune and multifactorial disorder. subsequent analysis on human leukocyte antigen ( hla) region shows that hla-drb1 and -dqb1 genes have the strongest association with t1d. in this study, for the first time, we investigated the influence of gender on the hla-drb1 and -dqb1 association with type 1 diabetes mellitus in iranian patients in order...

drug therapy is a complex and important process and because of the importance of drug interactions, especially in in-patients, accompanying problems and obstacles would exist as a result of concomitant use of drugs in these patients. for this purpose 3130 prescription order forms from bou-ali hospital were collected and all potential drug interactions presentwere extracted and evaluated in term...