Publications by authors named "K Ghedira"

Maurotoxin (MTX) is a 34-residue peptide from venom. It is reticulated by four disulfide bridges with a unique arrangement compared to other scorpion toxins that target potassium (K) channels. Structure-activity relationship studies have not been well performed for this toxin family.

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Cranial retained surgical sponges, known as "gossypiboma" or "textiloma", represent a rare but potentially severe complication following surgical procedures. While it is infrequent, it poses a significant risk, particularly in delicate surgical settings such as neurosurgery. The inadvertent retention of cotton balls or surgical gauzes may cause localized inflammation, infection, abscess, or neurologic sequelae.

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Article Synopsis
  • The Genome Tunisia Project is a two-phase initiative (2022-2035) aimed at sequencing the Tunisian Genome and advancing personalized medicine in Tunisia, a diverse North African country affected by human migration patterns from various continents.
  • A multidisciplinary team of Tunisian experts is focused on addressing key priorities, such as determining the reference genome sequence, enhancing education and awareness, and improving infrastructure for personalized medicine integration.
  • The project involves collaboration among various stakeholders, including healthcare providers and policymakers, and aims to boost research and innovation in genomics while improving healthcare practices in the region.
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Background: The advent of high-throughput technologies, including cutting-edge sequencing devices, has revolutionized biomedical data generation and processing. Nevertheless, big data applications require novel hardware and software for parallel computing and management to handle the ever-growing data size and analysis complexity. On-premise, high-performance computing (HPC) is increasingly used in biomedical research for big data stewardship.

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Ataxia Telangiectasia (AT) is a rare multisystemic neurodegenerative disease caused by biallelic mutations in the ATM gene. Few clinical studies on AT disease have been conducted in Tunisia, however, the mutational landscape is still undefined. Our aim is to determine the clinical and genetic spectrum of AT Tunisian patients and to explore the potential underlying mechanism of variant pathogenicity.

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