Abstract: A method for online authentication includes receiving membership authenticating information specific to members of a particular affiliation from the members and from one or more remote databases. The information is aggregated and stored in an aggregate database. An individual is authenticated, via a widget at least one of integrated into, and accessible by, at least one of a mobile application and a website of a provider of at least one of a particular program and a particular service, as a member of the particular affiliation based on a comparison of authenticating indicia provided online by the individual and the information stored in at least one of the aggregate database and the remote databases. Digital credentials are provided to the individual for access to the at least one of the particular program and the particular service when the individual is authenticated. The credentials include a unique identifier, a login and password.

Abstract: A colored glass article includes greater than or equal to 50 mol % and less than or equal to 80 mol % SiO2; greater than or equal to 7 mol % and less than or equal to 25 mol % Al2O3; greater than or equal to 1 mol % and less than or equal to 15 mol % B2O3; greater than or equal to 5 mol % and less than or equal to 20 mol % Li2O; greater than or equal to 0.5 mol % and less than or equal to 15 mol % Na2O; greater than 0 mol % and less than or equal to 1 mol % K2O; and greater than or equal to 1×10?6 mol % and less than or equal to 1 mol % Au. R2O—Al2O3 is greater than or equal to ?5 mol % and less than or equal to 7 mol %, R2O being the sum of Li2O, Na2O, and K2O.

Abstract: Systems and methods for threat evaluation and data collection are described herein. An example method may commence with collecting, by a wearable device, sensor data from one or more sensors installed on the wearable device. The wearable device may be worn by a user and be communicatively coupled to a central data portal and one or more external sources. The method may include receiving external sensor data from the one or more external sources. The method may continue with processing the sensor data and the external sensor data to evaluate a user state. The user state may be indicative of at least one physical threat to the user or at least one medical condition of the user. The method may further include transmitting the user state to the central data portal. The central data portal may be configured to process the user state for storage and visualization.

Abstract: A circuit for cooling is disclosed. The circuit uses a pulse generator in combination with a conductor. A cooling effect of the circuit on the conductor can be used and can be used in conjunction with a Carnot or Stirling engine. A resultant energy applied to a load is larger than the energy supplied by the pulse generator due to the absorption of external energy by the conductor.

Abstract: Antibody molecules that specifically bind to APRIL are disclosed. The antibody molecules can be used to treat, prevent, and/or diagnose disorders, such as IgA nephropathy.

Abstract: An image presentation system for an amusement park includes a first display with an opening extending therethrough, wherein at least a portion of the first display is viewable from a viewing area, a movable arm, wherein the movable arm is positioned within the opening, a second display supported by the movable arm and offset from the first display, wherein the second display conceals the opening from the viewing area, and a controller configured to provide a first image via the first display and a second image via the second display such that the second image comprises an image effect that accounts for the offset and coordinates with the first image to present as though the first image and the second image are a single image displayed by the first display.

Abstract: A storage apparatus has first and second bins with configurations that match. The bins have movable supports that enable the bins to be stacked on each other and attached to each other when employing the bins to store items in the bins and move the items from one area to another by moving the attached bins. The first and second bins are also nestable together to store the bins in a minimum of storage space when the bins are not in use.

Abstract: Medical devices including vascular access kits and related system and methods are disclosed. In some embodiments, a vascular access system may include a first conduit, a second conduit, and an expandable stent that is coupled to both the first and second conduits such that there is a continuous lumen between the first conduit and the second conduit. Methods of deploying the vascular access system within the body of a mammal, more particularly, a human patient are disclosed. Methods of bypassing a section of vasculature of a mammal, more particularly, a human patient are disclosed. The vascular access system, when implanted and assembled, may be a fully subcutaneous surgical implant.

Abstract: A medical appliance or prosthesis may comprise one or more layers of rotational spun nanofibers, including rotational spun polymers. The rotational spun material may comprise layers including layers of polytetrafluoroethylene (PTFE). Rotational spun nanofiber mats of certain porosities may permit tissue ingrowth into or attachment to the prosthesis. Additionally, one or more cuffs may be configured to allow tissue ingrowth to anchor the prosthesis.

Abstract: A storage apparatus has first and second bins with configurations that match. The bins have movable supports that enable the bins to be stacked on each other and attached to each other when employing the bins to store items in the bins and move the items from one area to another by moving the attached bins. The first and second bins are also nestable together to store the bins in a minimum of storage space when the bins are not in use.

Abstract: A medical appliance or prosthesis may comprise one or more layers of electrospun nanofibers, including electrospun polymers. The electrospun material may comprise layers including layers of polytetrafluoroethylene (PTFE). Electrospun nanofiber mats of certain porosities may permit tissue ingrowth into or attachment to the prosthesis.

Abstract: A stent or other prosthesis may be formed by coating a single continuous wire scaffold with a polymer coating. The polymer coating may consist of layers of electrospun polytetrafluoroethylene (PTFE). Electrospun PTFE of certain porosities may permit endothelial cell growth within the prosthesis.

Abstract: An embolic filter balloon is disclosed. The embolic filter balloon may comprise an inflatable balloon portion. Further, the inflatable balloon portion may be coupled to a filter member. The embolic filter balloon may be disposed in a body lumen. In some embodiments, the embolic filter balloon may be configured such that when the inflatable balloon portion is at least partially inflated the filter member extends at least partially across the body lumen. Such a configuration may allow the embolic filter balloon, when deployed, to filter particles greater than a predetermined size from a fluid in the body lumen.

Abstract: Medical devices and related method for improving blood flow to regions of a patient are described herein. Some medical devices may include a first graft portion, a second graft portion, and a catheter portion disposed between the first graft portion and the second graft portion. The medical device may be implanted into a patient to establish a non-natural flow path.

Abstract: A medical appliance or prosthesis may comprise one or more layers of rotational spun nanofibers, including rotational spun polymers. The rotational spun material may comprise layers including layers of polytetrafluoroethylene (PTFE). Rotational spun nanofiber mats of certain porosities may permit tissue ingrowth into or attachment to the prosthesis. Additionally, one or more cuffs may be configured to allow tissue ingrowth to anchor the prosthesis.

Abstract: Medical devices including vascular access kits and related system and methods are disclosed. In some embodiments, a vascular access system may include a first conduit, a second conduit, and an expandable stent that is coupled to both the first and second conduits such that there is a continuous lumen between the first conduit and the second conduit. Methods of deploying the vascular access system within the body of a mammal, more particularly, a human patient are disclosed. Methods of bypassing a section of vasculature of a mammal, more particularly, a human patient are disclosed. The vascular access system, when implanted and assembled, may be a fully subcutaneous surgical implant.

Abstract: Medical appliances including reinforcing bands and radiopaque marker bands are disclosed. In some embodiments, bands may comprise two or more material layers. A first layer may control the mechanical properties of a multilayered marking band, and a second layer may exhibit greater radiopacity than the first layer. Bands may also comprise a single layer.

Abstract: A medical appliance or prosthesis may comprise one or more layers of electrospun nanofibers, including electrospun polymers. The electrospun material may comprise layers including layers of polytetrafluoroethylene (PTFE). Electrospun nanofiber mats of certain porosities may permit tissue ingrowth into or attachment to the prosthesis.

Abstract: A model visualization system analyzes model behavior to identify clusters of data instances with similar behavior. For a selected feature, data instances are modified to set the selected feature to different values evaluated by a model to determine corresponding model outputs. The feature values and outputs may be visualized in an instance-feature variation plot. The instance-feature variation plots for the different data instances may be clustered to identify latent differences in behavior of the model with respect to different data instances when varying the selected feature. The number of clusters for the clustering may be automatically determined, and the clusters may be further explored by identifying another feature which may explain the different behavior of the model for the clusters, or by identifying outlier data instances in the clusters.

Abstract: Medical devices including vascular access kits and methods of using the kit are disclosed. In some embodiments, a conduit is measured using an outside diameter measurement apparatus to determine if the conduit is compatible with a connector such that there is a continual lumen between the conduit and the connector. In some embodiments, various outside diameter measurement devices and the methods of their use are disclosed. In some embodiments, the methods of connecting a conduit, and in some embodiments a strain relief structure, to a connector are described.