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Department of Medical Imaging Technology, Manipal College of Health Professions, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.

Introduction: Magnetic resonance imaging (MRI) is essential for brain imaging, but conventional methods rely on qualitative contrast, are time-intensive, and prone to variability. Magnetic resonance finger printing (MRF) addresses these limitations by enabling fast, simultaneous mapping of multiple tissue properties like T1, T2. Using dynamic acquisition parameters and a precomputed signal dictionary, MRF provides robust, qualitative maps, improving diagnostic precision and expanding clinical and research applications in brain imaging.

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Background: Anatomical variations of the recurrent motor branch (RMB) are at risk of injury during carpal tunnel release procedures. Previous studies have visualized the RMB using ultrasound (US) and magnetic resonance imaging (MRI) but have not compared the imaging capabilities of the two. Previous investigations have overlooked two specific types of carpal tunnel syndrome (CTS): simultaneous compression of the median nerve and the RMB and isolated compression of the latter.

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Defect-Engineered Luminescent Nanozyme with Enhanced Phosphohydrolase Activity for Degradation and Dual-Mode Detection of Paraoxon.

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The excessive use of organophosphorus pesticides poses a substantial threat to both human health and the environment. Consequently, there is an urgent need for new methods that can quickly degrade and sensitively detect these compounds. A versatile nanozyme based on the biomimetic principle is an effective strategy to solve this problem.

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