Now showing items 1371-1379 of 1379
Comparison of technetium-99m IgG with technetium-99m red blood cells labeling in cardiac blood-pool scintigraphy: A preliminary study
This first clinical prospective study was conducted to use of technetium-99m immunoglobulin G (99mTc-IgG) as compared with autologous 99mTc-red blood cells (RBC) in gated blood pool ventriculography. We studied 12 patients ...
Comparison of effectiveness of lovastatin and gemfibrozil on HDL-C level in diabetic type 2 patients
Background: Diabetes mellitus is the most common human metabolic disease. Chronic hyperglycemia and carbohydrate metabolism disorder accompany with plasma lipid and lipoprotein disorder. Cardiovascular disease is one of ...
Novel missense mutation at codon 2774 (C.8321 G>A) p.S2774n of APC gene in a denovo case of familial adenomatous polyposis
Familial adenomatous polyposis (FAP) is an autosomal dominant inherited disease caused by germline mutation in Adenomatous Polyposis Coli (APC) gene. FAP accounts less than 1% of all colorectal cancers incidence. Patients ...
New insights into HLA class I association to Behط£آ§et's syndrome in Iranian Azari patients
Behط£آ§et's syndrome (BS) is a chronic recurrent inflammatory disorder characterized by oral and genital ulcers and ocular inflammation. BS has a complex genetic etiology. To evaluate the influence of human leukocyte antigen ...
Molecular Study of Deletional and Nondeletional Mutations on the ?-Globin Locus in the Azeri Population of Northwestern Iran
The aim of this study was to determine the molecular spectrum and frequency of deletional and nondeletional ?-thalassemia (?-thal) mutations and the genotype-phenotype correlation in common mutations in the Azeri population ...
Necessity of an integrated road traffic injuries surveillance system: A community-based study
Objectives: A prerequisite to improving the situation of traffic accidents and injury prevention is to set up a road traffic accident and victim information system (RTAVIS), which does not exist in Iran. The objective of ...
Molecular spectrum of ?-thalassemia mutations in Northwestern Iran
?-Thalassemia (?-thal) is a hereditary autosomal disorder with decreased or absent ?-globin chain synthesis. This study was designed to identify the common and rare ?-thal mutations in the Azerbaijan provinces, Northwestern ...
Crimean - Congo haemorrhagic fever presenting as thrombotic microangiopathy and acute renal failure
[No abstract available]
Neurocognitive effects of phenobarbital discontinuation in epileptic children
Purpose. Phenobarbital (PB) is the most widely used antiepileptic drug in the world, but its possible deleterious cognitive and behavioral side effects remain an important concern among physicians and patients. We therefore ...