151 results about "Selective excitation" patented technology

A lighting unit for producing flash light toward subjects in a photographic scene comprises an matrix array of light emitting elements arranged so as to have individual lighting fields different from one another, a selective excitation circuit for exciting selectively the light emitting elements so as to produce flash light, different in intensity as appropriate, in predetermined lighting patterns and an excitation/extinction circuit 250 for exciting or extinguishing the light emitting elements. A photographic equipment equipped with the lighting unit has directive switches or buttons for directing the lighting unit to select lighting pattern according to focal lengths, zoom rations, operation modes including a communication mode, and/or demands of pre-lighting,

A Discontinuous Positive Airway Pressure (DPAP) device and method of using the same for reducing sleep disordered breathing events, such as sleep apnea and snoring. The DPAP device provides selective excitation to the pharyngeal conduit or another muscle or cartilage along the respiratory path, a predetermined period of time before the end of the expiration stage, in order to prematurely reverse the respiratory cycle before the total collapse of the pharyngeal conduit, thus enabling the inhalation stage to reopen and refill the pharyngeal conduit.

Nucleic acid microparticles are sequenced by performing a sequencing reaction on the microparticles using one or more selectively exciting the microparticles in an excitation pattern, optically imaging the microparticles at a resolution insufficient to resolve individual microparticles, and processing the optical images of the microparticles using information on the excitation pattern to determine the presence or absence of the optical signature, which indicates the sequence information of the nucleic acid. An apparatus for optical excitation of the microparticles comprises an optical fiber delivering a first laser beam, and an interference pattern generation module coupled to the optical fiber. The interference pattern generation module splits the first laser beam into second and third laser beams and generates the excitation pattern for selectively exciting the microparticles by interference between the second and third laser beams.

A method for RARE magnetic resonance imaging comprising slice selective excitation of two or more slices and of one or more nuclei, followed by refocusing of these slices and application of gradient pulses which cause a diversion of the signal into spin echoes and stimulated echoes, is characterized by application of refocusing slice selective RF pulses, which are placed to fulfill the echo-spacing CPMG condition for each slice and by arrangement of gradient pulses which cause the phase accumulated by spins in each slice between two consecutive refocusing RF pulses corresponding to that slice to be equal, thus fulfilling the CPMG phase accumulation condition. Thereby, the obtainable signal can be increased and stabilized.

A synthetic aperture optics (SAO) imaging method minimizes the number of selective excitation patterns used to illuminate the imaging target, based on the objects' physical characteristics corresponding to spatial frequency content from the illuminated target and/or one or more parameters of the optical imaging system used for SAO. With the minimized number of selective excitation patterns, the time required to perform SAO is reduced dramatically, thereby allowing SAO to be used with DNA sequencing applications that require massive parallelization for cost reduction and high throughput. In addition, an SAO apparatus optimized to perform the SAO method is provided. The SAO apparatus includes a plurality of interference pattern generation modules that can be arranged in a half-ring shape.

An MRI apparatus obtains an ASL (Arterial Spin Labeling) image of a region to be imaged in a subject by performing a scan to the region to be imaged independently in a control mode and in a tag mode according to a pulse sequence based on an ASL technique. The pulse sequence includes a velocity-selective pulse, BVS (Band-limited Velocity-Selective)-pulse, that selectively excites magnetization spins in a blood flow passing through the region to be imaged and having a constant velocity range for the spins to undergo transition to transverse magnetization, and then performs excitation to cause the transverse magnetization to flip back to longitudinal magnetization. The velocity-selective pulse is formed in such a manner that the transverse magnetization excited in each of the control mode and the tag mode gives rise to a phase shift in an opposite polarity upon velocity-selective excitation.

A synthetic aperture optics (SAO) imaging method minimizes the number of selective excitation patterns used to illuminate the imaging target, based on the objects' physical characteristics corresponding to spatial frequency content from the illuminated target and/or one or more parameters of the optical imaging system used for SAO. With the minimized number of selective excitation patterns, the time required to perform SAO is reduced dramatically, thereby allowing SAO to be used with DNA sequencing applications that require massive parallelization for cost reduction and high throughput. In addition, an SAO apparatus optimized to perform the SAO method is provided. The SAO apparatus includes a plurality of interference pattern generation modules that can be arranged in a half-ring shape.

A magnetic resonance imaging method and apparatus includes a navigator region defined within the subject by selective excitation. Blood flow is measured within the selected region using the principles of phase contrast MR angiography. A cardiac cycle plot is constructed from Fourier transformed data that represents measured velocity of blood flow through the navigator region as a function of time. On the basis of the cardiac cycle plot and the navigator measurements, data acquisition is synchronized or gated to portions of the cardiac cycle.

A piezoelectric motor has an actuator 26 which drives a slider 24. The actuator has a rectangular steel core of square cross-section with an axially projection driving tip 28. A ceramic piezoelectric element 40 is bonded to each of the four faces of the core. Each piezoelectric element has four quadrants covered by quadrant electrodes 40a-40d on one side and a common or earth electrode on the other side contacting the core which electrically joins the common electrodes. By selective excitation of corresponding diagonally opposite quadrants of opposite piezoelectric elements, the actuator is made to drive the tip in either the X direction or the Y direction. The preferred slider is a spherical ball held captive within arms extending from a housing of the actuator. The driving tip is pressed against the ball by a preload spring 34 acting on the actuator. Operation of the actuator causes the ball 24 to rotate about an X axis or about a Y axis producing a two dimensional movement from a single motor and single actuator.

In a method and apparatus for the correction of artifacts in magnetic resonance images (MR) acquired with an MR pulse sequence in which gradients are switched simultaneously during the radiation of at least one non-selective excitation pulse, measurement data acquired with the pulse sequence in k-space are loaded into a processor, in which a perturbation matrix is determined on the basis of spatial and k-space point data of the acquired measurement data and the gradients used during the excitation. A corrected image is calculated from the acquired measurement data in k-space and the perturbation matrix, with the calculation of the corrected image including a matrix inversion of the perturbation matrix. The corrected image is then stored or displayed.

The invention discloses a method for selectively exciting diffraction levels on the basis of metasurface complex amplitude modulation, and belongs to the field of micro-nano optics. The structure sizes of nano rectangular columns of metasurfaces are changed to obtain amplitudes and dynamic phase information of target light fields, and azimuth angles theta of the nano rectangular columns of the metasurfaces are determined, and accordingly phases of the target light fields can be modulated; the amplitudes and the phase information are combined with one another, and accordingly complex amplitudescan be arbitrarily regulated and controlled in a single pixel; the periods of the metasurfaces are determined, Fourier levels corresponding to all the selected diffraction levels are superimposed, accordingly, complex amplitude information of various unit structures of the metasurfaces can be set, and the spatial propagation diffraction levels can be selectively excited. The method has the advantages that amplitude values of the target light fields can be processed by stages, and the phases of the target light fields can be continuously changed; the metasurface design and processing complexity can be lowered by the aid of the method, and the method can be widely applied to the fields of light field shaping, laser parallel processing, micro-nano optical detection and the like.

The invention relates to an RF based spatially selective excitation in MRI. Herein a method for slice selection is provided in an MRI process, the method involves controlling a transmit array by adding low flip angle RF pulses interspersed between refocusing pulses that are used to move a k-space weighting function with respect to one or more B l fields used to deposit energy according to a desired k-space weighting function. The low flip angle pulses deposit energy so that an envelope traced by the low flip angle pulses in the k-space weighting function is related to a desired spatially excited region of the sample volume, for example by a Fourier transform, if the phase encoding directions are linear axes that coordinatize the sample volume, and the Bl fields have linear phase gradients.

A nanobioprocessor for protein and cell therapy comprises a selectively coated quantum dot having selected band gap energies, characteristic absorption, emission spectra and outer coatings for therapy and diagnostic purposes in biophotonics and nanomedicine, and an electromagnetic radiation and detector source configured to remotely heat and/or selectively excite the quantum dot to associate with target specific misfolded or anomalous proteins, diseased cells and tissue.