Results 71 to 80 of about 66,696 (145)
Ultracold atoms in disordered potentials: elastic scattering time in the strong scattering regime
New Journal of Physics, 2019 We study the elastic scattering time ${\tau }_{{\rm{s}}}$ of ultracold atoms propagating in optical disordered potentials in the strong scattering regime, going beyond the recent work of Richard et al (2019 Phys. Rev. Lett. 122 100403).
Adrien Signoles +10 more
doaj +1 more source
In Vitro and In Vivo Amenability to Migalastat in Fabry Disease
Molecular Therapy: Methods & Clinical Development, 2020 Migalastat (1-deoxygalactonojirimycin) is approved for the treatment of Fabry disease (FD) in patients with an amenable mutation. Currently, there are at least 367 amenable and 711 non-amenable mutations known, based on an in vitro good laboratory ...
Malte Lenders +2 more
doaj +1 more source
New Journal of Physics, 2014 We demonstrate that different kinds of mesoscopic quantum states of light can be efficiently generated from a simple iterative scheme. These states exhibit strong non-classical features, and could be of great interest for many applications such as ...
Jean Etesse +3 more
doaj +1 more source
The frequency-dependent directivity of a planar Fabry-Perot polymer film ultrasound sensor [PDF]
, 2007 A model of the frequency-dependent directivity of a planar, optically-addressed, Fabry-Perot (FP), polymer film ultrasound sensor is described and validated against experimental directivity measurements made over a frequency range of 1 to 15 MHz and ...
Beard, PC, Cox, BT
core
On the diagnosis of Fabry's disease
Acta Dermato-Venereologica, 1975 Fabry's disease is a recessive X-linked inborn error of metabolism due to deficiency of the lysosomal enzyme alpha-galactosidase. The large variety of symptoms may make the diagnosis difficult. A severely afflicted female patient is presented. For several years she had been treated under the diagnosis polyarteritis nodosa until the characteristic ...
S, Wadskov +4 more
openaire +2 more sources
Best Practice & Research Clinical Endocrinology & Metabolism, 2015 Fabry disease is induced by a mutation in the alpha-galactosidase A gene, causing a deficiency of the enzyme alpha-galactosidase A. (1) The enzyme defect leads to progressive intracellular accumulation of globotriaosylceramide in lysosomes of various tissues and organs, including heart, kidney and nerve system.
Seydelmann, Nora +4 more
openaire +2 more sources
Self-seeding of a gain-switched integrated dual-laser source for the generation of highly wavelength-tunable picosecond optical pulses [PDF]
, 2004 The authors demonstrate the generation of nearly transform-limited optical pulses that are wavelength tunable over almost 50 nm. The wide tuning range is obtained by self-seeding a gain-switched source containing two Fabry-Perot lasers, and employing a ...
Anandarajah, Prince M. +3 more
core +2 more sources
Impact of ER stress and the unfolded protein response on Fabry disease
EBioMedicineSummary: Fabry disease (FD) is a lysosomal storage disorder caused by pathogenic missense and nonsense variants in the α-galactosidase A (GLA) gene, leading to absent or reduced enzyme activity.
Malte Lenders, Elisa Rudolph, Eva Brand
doaj +1 more source
Energy-resolved transport of ultracold atoms across the Anderson transition: theory and experiment
New Journal of PhysicsIn a recent experiment (Yu et al 2026 arXiv: https://arxiv.org/abs/2602.07654 ), energy-resolved measurements of an atomic matter wave spreading in a speckle potential enabled the direct observation of the three-dimensional Anderson transition.
Jean-Philippe Banon +9 more
doaj +1 more source