Abdulla Bashein
YOU?
Author Swipe
View article: Correlation between maternal and fetal umbilical cord blood lead concentrations in Libya
Correlation between maternal and fetal umbilical cord blood lead concentrations in Libya Open
Background: People are exposed to lead from car exhaust fumes (leaded petrol), lead-based paints, plumbing systems, cigarette smoking, contaminated soil and dust, foods grown in polluted areas, and water sources. Among the vulnerable subpo…
View article: Association of venous thromboembolism and myocardial infarction with Factor V Leiden and Factor II gene mutations among Libyan patients
Association of venous thromboembolism and myocardial infarction with Factor V Leiden and Factor II gene mutations among Libyan patients Open
Factor V Leiden G1691A (FVL) and Factor II prothrombin G20210A (PGM) mutations are the leading causes of thrombophilia. In this study, we have investigated the prevalence of the FVL G1691A and PGM G20210A single nucleotide polymorphisms (S…
View article: The Impact of CYP2C9 and VKORC1 Polymorphism in Patient’s Response to Warfarin and Acenocoumarol
The Impact of CYP2C9 and VKORC1 Polymorphism in Patient’s Response to Warfarin and Acenocoumarol Open
Warfarin is commonly prescribed as oral anticoagulant medication for Libyan patients, the wide inter-individual variation between the patients in their response to oral anticoagulants is attributed to genetics factors, mainly polymorphisms…
View article: Detection of CTX-M-15 Among Uropathogenic Escherichia coli Isolated from Five Major Hospitals in Tripoli, Libya
Detection of CTX-M-15 Among Uropathogenic Escherichia coli Isolated from Five Major Hospitals in Tripoli, Libya Open
The isolation of MDR ESBL-producing uropathogens expressing the CTX-M-15 gene will limit the choices clinicians have to treat their patients with UTIs. Continued surveillance and implementation of efficient infection control measures are r…
View article: Development of hydrolysis probe real-time polymerase chain reaction and high-resolution melting analysis protocols for screening of e280k and c.1055del.g mutations in phenylalanine hydroxylase gene
Development of hydrolysis probe real-time polymerase chain reaction and high-resolution melting analysis protocols for screening of e280k and c.1055del.g mutations in phenylalanine hydroxylase gene Open
Background: Phenylketonuria (PKU) is one of the most common inborn errors of amino acids metabolism. It is an autosomal recessive disease that is caused by mutations in phenylalanine hydroxylase (PAH) gene. In the North Africa and Eastern …
View article: PHENOTYPIC AND GENOTYPIC INVESTIGATION OF OXA23 AND OXA51 CARBAPENEMASES PRODUCING ACINETOBACTER BAUMANNII IN TRIPOLI HOSPITALS
PHENOTYPIC AND GENOTYPIC INVESTIGATION OF OXA23 AND OXA51 CARBAPENEMASES PRODUCING ACINETOBACTER BAUMANNII IN TRIPOLI HOSPITALS Open
Acinetobacter baumannii is an opportunistic pathogen causing various nosocomial infections. The aim of this study was tocharacterize the molecular support of carbapenem-resistant A. baumannii clinical isolates recovered from four hospitals…