166 research outputs found

    Risk of latent tuberculosis infection among healthcare workers in Italy: a retrospective study with Quantiferon Test

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    OBJECTIVE. The latent tuberculosis infection (LTBI) is a state of persistent immune response to stimulation by Mycobacterium Tuberculosis antigens without clinical manifestation: the healthcare workers (HCWs) have a higher exposure risk so prevention is an important challenge for occupational medicine. The aim of our study is to evaluate the prevalence of LTBI among HCWs of the Foundation Policlinic “Tor Vergata”. METHODS. This is a retrospective study conducted by analyzing the clinical records of 825 HCWs of the PTV, from January 1st to December 31th 2016. To evaluate the TB infection we used the Quantiferon TB Gold interferon-gamma release assay. RESULTS. Our study underline the low prevalence of LTBI in the Italian healthcare workers. CONCLUSION. Although the LTBI status is not contagious, the diagnosis and the safety strategies require specific clinical and preventive considerations

    Variants in ATP6V0A1 cause progressive myoclonus epilepsy and developmental and epileptic encephalopathy

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    Bott et al. here reports that de novo and biallelic variants in ATP6V0A1 gene affect the ability of the V-ATPase complex to translocate protons and acidify the endolysosomal compartment in neurons, causing a severe neurological phenotype ranging from developmental and epileptic encephalopathy to progressive myoclonus epilepsy. The vacuolar H+-ATPase is a large multi-subunit proton pump, composed of an integral membrane V0 domain, involved in proton translocation, and a peripheral V1 domain, catalysing ATP hydrolysis. This complex is widely distributed on the membrane of various subcellular organelles, such as endosomes and lysosomes, and plays a critical role in cellular processes ranging from autophagy to protein trafficking and endocytosis. Variants in ATP6V0A1, the brain-enriched isoform in the V0 domain, have been recently associated with developmental delay and epilepsy in four individuals. Here, we identified 17 individuals from 14 unrelated families with both with new and previously characterized variants in this gene, representing the largest cohort to date. Five affected subjects with biallelic variants in this gene presented with a phenotype of early-onset progressive myoclonus epilepsy with ataxia, while 12 individuals carried de novo missense variants and showed severe developmental and epileptic encephalopathy. The R740Q mutation, which alone accounts for almost 50% of the mutations identified among our cases, leads to failure of lysosomal hydrolysis by directly impairing acidification of the endolysosomal compartment, causing autophagic dysfunction and severe developmental defect in Caenorhabditis elegans. Altogether, our findings further expand the neurological phenotype associated with variants in this gene and provide a direct link with endolysosomal acidification in the pathophysiology of ATP6V0A1-related conditions.Peer reviewe

    Comparative spectroscopic and thermo-optic study of Tm: LiLnF4 (Ln = Y, Gd, and Lu) crystals for highly-efficient microchip lasers at ~2 μm

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    We report on a detailed comparative study of the spectroscopic and thermo-optic properties of tetragonal Tm:LiLnF4 (Ln = Y, Gd, and Lu) crystals indicating their suitability for highly-efficient microchip lasers diode-pumped at ~791 nm and operating at ~1.91 μm. An a-cut 8 at.% Tm:LiYF4 micro-laser generated 3.1 W of linearly polarized output at 1904 nm with a slope efficiency of η = 72% and a laser threshold of only 0.24 W. The internal loss for this crystal is as low as 0.0011 cm-1. For 8 at.% Tm:LiGdF4 and 12 at.% Tm:LiLuF4 lasers, the output power reached ~2 W and η was 65% and 52%, respectively. The thermal lens in all Tm:LiLnF4 crystals is weak, positive and low-astigmatic. The potential for the Tm:LiLnF4 lasers to operate beyond ~2 μm due to a vibronic coupling has been proved. The Tm:LiYF4 vibronic laser generated 375 mW at 2026-2044 nm with η = 31%. The Tm:LiLnF4 crystals are very promising for passively Q-switched microchip lasers

    Educational Robotics and empowerment of executive cognitive processes: from typical development to special educational needs

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    This paper describes a new Educational Robotic (ER) approach aimed to empower higher cognitive functions in school-setting. As robot programming requires to mentally plan a complex sequence of actions before the motor act, ER may indeed promote several crucial cognitive processes underlying learning. The steps needed and the mental acts for robot programming may involve Executive Functions (EF), that are complex higher cognitive processes, particularly crucial in the early development, because they are the base for abstraction and logical reasoning, decision-making, sequential thinking, maintaining and updating information in memory and problem-solving. Recent studies attempting to attest with a scientific approach the effect of ER on executive functioning are described. They concern both classroom with typical development or special educational needs and rehabilitation environment for children with developmental disorder. Robotica Educativa e potenziamento dei processi cognitivi esecutivi: dallo sviluppo tipico ai bisogni educativi specialiIl presente lavoro descrive come la Robotica Educativa (RE) possa essere utilizzata per potenziare alcune funzioni cognitive di controllo. Le azioni necessarie e gli atti mentali per la programmazione di un robot implicano le Funzioni Esecutive (FE), processi cognitivi di alto ordine, particolarmente importanti durante lo sviluppo cognitivo perché coinvolti nel ragionamento logico e nell’astrazione, nel decision-making, nel pensiero sequenziale, nel problem-solving e nel mantenimento/ aggiornamento delle informazioni in memoria. Nell’articolo sono sintetizzati e discussi gli studi con cui abbiamo cercato di provare con metodi scientifici l’effetto della RE sulle FE, nel gruppo classe per bambini con sviluppo tipico o con bisogni educativi speciali, e in ambito riabilitativo per bambini con disturbo del neurosviluppo
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