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Knowledge Level, Motivators and Barriers of Blood Donation Among Adults at Qatar University; A Cross-Sectional Survey
(Biomedical Sciences, 2020 , Professional Masters Project)
One out of every ten patients admitted to the hospital are in urgent
need of blood transfusion or blood products in Qatar. This study aims are (1) Assess the
level of knowledge towards blood donation and (2) Identify ...
Exploring the Genetic Causes of Non-syndromic Retinal Dystrophies in Qatar
(Genetic Counseling, 2023 , Professional Masters Project)
Background. Non-syndromic retinal dystrophies (RDs) are a set of degenerative retinal diseases that vary clinically and genetically. RDs comprise several overlapping disorders such as Leber congenital amaurosis (LCA) and ...
LABORATORIES PREPAREDNESS IN RESPONSE TO COVID 19 PANDEMIC IN QATAR STRATEGIC PLANNING AND EMERGENCY SUPPLY CHAIN MANAGEMENT
(Biomedical Sciences, 2022 , Professional Masters Project)
Introduction: the purpose of this study is to investigate the preparedness of laboratories
in Qatar on provisions of essential supplies in pandemic through assesses Supply Chain
Management capabilities and its resilience ...
QATAR NATIONAL EXPANDED METABOLIC NEWBORN SCREENING PROGRAM: INCIDENCE AND OUTCOMES
(Genetic Counseling, 2024 , Professional Masters Project)
Background: Newborn screening (NBS) is an essential public health strategy that aims to detect and diagnose inborn errors of metabolism (IEMs) in infants shortly after birth, typically through a minimally invasive heel ...
PRENATAL WHOLE EXOME SEQUENCING OF FETAL SONOGRAPHIC ABNORMALITIES IN QATAR: DIAGNOSTIC YIELD AND GENETIC FINDINGS
(Genetic Counseling, 2024 , Professional Masters Project)
Background: Fetal sonographic abnormalities at birth is estimated to be 2-3% of the global prevalence and are responsible for approximately 17%-42% of all perinatal deaths. Prenatal karyotype (KT) and chromosomal microarray ...
NONSYNDROMIC HEARING LOSS IN QATAR: THE GENETIC BASIS AND THE DIAGNOSTIC YIELD OF GENETIC TESTING
(Genetic Counseling, 2022 , Professional Masters Project)
Background: Hearing loss is the most predominant sensory defect worldwide with around 8% of cases occurring in children. Approximately 66% of childhood-onset hearing loss cases are attributed to genetic factors. The ...