Publications by authors named "M A Mosrati"
Given consumers', environmental and sustainability apprehensions, the meat industry investigated the natural colorant resources. As proof, betalain, peels (OSP) pigment, is premeditated in the meat industry. Here, OSP betalains were qualitatively profiled using UPLC-MS/MS, and 7 metabolites were identified: 6 betacyanins and a betaxanthin (arginine-betaxanthin).
View Article and Find Full Text PDFBackground: In Tunisia, the number of cardiac implantable electronic devices (CIEDs) is increasing, owing to the increase in patient life expectancy and expanding indications. Despite their life-saving potential and a significant reduction in population morbidity and mortality, their increased numbers have been associated with the development of multiple early and late complications related to vascular access, pockets, leads, or patient characteristics.
Objective: The study aims to identify the rate, type, and predictors of complications occurring within the first year after CIED implantation.
Unlabelled: Introduction-Aim: The third cycle of medical studies (TCMS) lasts 3 years for the specialty of family medicine (FM) in Tunisia. The members of the FM committee of the Faculty of Medicine of Monastir (FMM) aimed to detail the learning objectives (LO) of residents in FM.
Method: We used the Delphi method in 2 rounds including a group of experts called FM Learning Objectives Writing Group (FMLOWG) at the FMM.
Deep analysis of the LRTOMTc.242G>A variant in non-syndromic hearing loss North African patients and the Berber population: Implications for genetic diagnosis and genealogical studies.
Mol Genet Genomic Med
October 2021
Article Synopsis
- Autosomal recessive non-syndromic hearing loss (ARNSHL) is a common genetic cause of hearing impairment, especially in North Africa due to many consanguineous marriages.
- The study focused on the LRTOMT c.242G>A variant, found in 5.02% of Tunisian and 2.94% of Libyan deaf patients, indicating its relevance in those populations.
- The variant has a common origin linked to the Berber population, estimated to be between 2025 and 3425 years old, suggesting it can serve as a biomarker for deafness and as a tool for tracing Berber ancestry.
Hereditary hearing impairment (HI) is a common disease with the highest incidence among sensory defects. Several genes have been identified to affect stereocilia structure causing HI, including the unconventional myosin3A. Interestingly, we noticed that variants in gene have been previously found to cause variable HI onset and severity.
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