37 research outputs found

    Interstitial lung disease in children - genetic background and associated phenotypes

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    Interstitial lung disease in children represents a group of rare chronic respiratory disorders. There is growing evidence that mutations in the surfactant protein C gene play a role in the pathogenesis of certain forms of pediatric interstitial lung disease. Recently, mutations in the ABCA3 transporter were found as an underlying cause of fatal respiratory failure in neonates without surfactant protein B deficiency. Especially in familiar cases or in children of consanguineous parents, genetic diagnosis provides an useful tool to identify the underlying etiology of interstitial lung disease. The aim of this review is to summarize and to describe in detail the clinical features of hereditary interstitial lung disease in children. The knowledge of gene variants and associated phenotypes is crucial to identify relevant patients in clinical practice

    Synergism between particle-based multiplexing and microfluidics technologies may bring diagnostics closer to the patient

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    In the field of medical diagnostics there is a growing need for inexpensive, accurate, and quick high-throughput assays. On the one hand, recent progress in microfluidics technologies is expected to strongly support the development of miniaturized analytical devices, which will speed up (bio)analytical assays. On the other hand, a higher throughput can be obtained by the simultaneous screening of one sample for multiple targets (multiplexing) by means of encoded particle-based assays. Multiplexing at the macro level is now common in research labs and is expected to become part of clinical diagnostics. This review aims to debate on the “added value” we can expect from (bio)analysis with particles in microfluidic devices. Technologies to (a) decode, (b) analyze, and (c) manipulate the particles are described. Special emphasis is placed on the challenges of integrating currently existing detection platforms for encoded microparticles into microdevices and on promising microtechnologies that could be used to down-scale the detection units in order to obtain compact miniaturized particle-based multiplexing platforms

    Midrapidity antiproton-to-proton ratio from Au+Au collisions at root s(NN)=130 GeV (vol 86, pg 4778, 2001)

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    d̅ and 3He̅ Production in √sNN = 130 GeV Au+Au Collisions

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    A report on the first measurements of light antinucleus production in Au + Au collisions at the Relativistic Heavy-Ion Collider (RHIC) was presented. The production rates for d̄ and He were observed to be much larger than in lower energy nucleus-nucleus collisions. A little or no increase in the antinucleon freeze-out volume compared to CERN Super Proton Synchrotron (SPS) energy was indicated by a coalescence model analysis. The He freeze-out volume was indicated to be smaller than the d̄ freeze-out volume

    Erratum: Midrapidity antiproton-ti-proton ratio from Au + Au collisions at √S = 130 GeV (Phys. Rev. Lett. (2001) 86 (4778))

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    Erratum: Publisher's note - D̄ and He production in √s = 130 GeV Au + Au collisions (Physical Review Letters (2001) 87 (262301))

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    Pion interferometry of root s(NN)=130 GeV Au+Au collisions at RHIC

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    Two-pion correlation functions in An + Au collisions at roots(NN) = 130 GeV have been measured by the STAR (solenoidal tracker at RHIC) detector. The source size extracted by fitting the correlations grows with event multiplicity and decreases with transverse momentum. Anomalously large sizes or emission durations, which have been suggested as signals of quark-gluon plasma formation and rehadronization, are not observed. The Hanbury Brown-Twiss parameters display a weak energy dependence over a broad range in roots(NN)

    Reservoir Nanoagents for In-Situ Sensing and Intervention

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