The Cardiac Imaging System

2001 ◽  
pp. 1-8
Author(s):  
Steven Kelly
Keyword(s):  
Cardiac Imaging ◽  
Imaging System

scholarly journals High-Resolution High-Speed Panoramic Cardiac Imaging System

2008 ◽  
Vol 55 (3) ◽  
pp. 1241-1243 ◽  
Author(s):  
D.W. Evertson ◽  
M.R. Holcomb ◽  
M.D.C. Eames ◽  
M.-A. Bray ◽  
V.Y. Sidorov ◽  
...  
Keyword(s):  
High Resolution ◽  
Cardiac Imaging ◽  
High Speed ◽  
Imaging System

scholarly journals A STUDY ON A MULTI-MODALITY IMAGING SYSTEM IN A TERTIARY CARE HOSPITAL: A CASE ON CARDIAC IMAGING.

2017 ◽  
Vol 5 (2) ◽  
pp. 976-980
Author(s):  
FirasA. Ghomraoui ◽  
◽  
AbdullahA. Alhallali ◽  
Nasriah Zakaria. ◽  
◽  
...  
Keyword(s):  
Cardiac Imaging ◽  
Imaging System ◽  
Tertiary Care Hospital ◽  
Tertiary Care ◽  
Care Hospital

A transputer based three-dimensional dynamic cardiac imaging system

1993 ◽  
Vol 38 (4) ◽  
pp. 491-501
Author(s):  
A J Lomax ◽  
M Y Norton ◽  
P G B Ross ◽  
P E Undrill
Keyword(s):  
Cardiac Imaging ◽  
Imaging System ◽  
Three Dimensional

Diagnostic accuracy of an ultrasonic multiple transducer cardiac imaging system

1975 ◽  
Vol 90 (3) ◽  
pp. 329-334
Author(s):  
Richard L. Popp ◽  
Owen R. Brown ◽  
Donald C. Harrison
Keyword(s):  
Diagnostic Accuracy ◽  
Cardiac Imaging ◽  
Imaging System

New Aspects in the Design of Electron Optical Magnification Systems

1972 ◽  
Vol 30 ◽  
pp. 606-607
Author(s):  
Willem H.J. Andersen
Keyword(s):  
Electron Microscope ◽  
Imaging System ◽  
Chromatic Aberration ◽  
Research Tool ◽  
Energy Losses ◽  
Objective Lens ◽  
Theoretical Limit ◽  
Optical Magnification ◽  
Chromatic Aberrations ◽  
High Degree

Electron microscope design, and particularly the design of the imaging system, has reached a high degree of perfection. Present objective lenses perform up to their theoretical limit, while the whole imaging system, consisting of three or four lenses, provides very wide ranges of magnification and diffraction camera length with virtually no distortion of the image. Evolution of the electron microscope in to a routine research tool in which objects of steadily increasing thickness are investigated, has made it necessary for the designer to pay special attention to the chromatic aberrations of the magnification system (as distinct from the chromatic aberration of the objective lens). These chromatic aberrations cause edge un-sharpness of the image due to electrons which have suffered energy losses in the object.There exist two kinds of chromatic aberration of the magnification system; the chromatic change of magnification, characterized by the coefficient Cm, and the chromatic change of rotation given by Cp.

Some Quantification Problems in Parallel EELS Images

1990 ◽  
Vol 48 (2) ◽  
pp. 36-37
Author(s):  
G. Botton ◽  
G. L’Espérance ◽  
M.D. Ball ◽  
C.E. Gallerneault
Keyword(s):  
Electron Microscope ◽  
Imaging System ◽  
Signal To Noise Ratio ◽  
Scanning Transmission Electron Microscope ◽  
Acquisition Time ◽  
Thickness Variation ◽  
Transmission Electron ◽  
Distribution Of Elements ◽  
Scanning Transmission ◽  
Present Distribution

The recently developed parallel electron energy loss spectrometers (PEELS) have led to a significant reduction in spectrum acquisition time making EELS more useful in many applications in material science. Dwell times as short as 50 msec per spectrum with a PEELS coupled to a scanning transmission electron microscope (STEM), can make quantitative EEL images accessible. These images would present distribution of elements with the high spatial resolution inherent to EELS. The aim of this paper is to briefly investigate the effect of acquisition time per pixel on the signal to noise ratio (SNR), the effect of thickness variation and crystallography and finally the energy stability of spectra when acquired in the scanning mode during long periods of time.The configuration of the imaging system is the following: a Gatan PEELS is coupled to a CM30 (TEM/STEM) electron microscope, the control of the spectrometer and microscope is performed through a LINK AN10-85S MCA which is interfaced to a IBM RT 125 (running under AIX) via a DR11W line.

Multi-mode light microscopy of microtubule assembly dynamics and chromosome movement in vivo and In vitro

1996 ◽  
Vol 54 ◽  
pp. 730-731
Author(s):  
E. D. Salmon ◽  
J. C. Waters ◽  
C. Waterman-Storer
Keyword(s):  
Imaging System ◽  
Ccd Camera ◽  
Transmitted Light ◽  
Microtubule Assembly ◽  
Live Cells ◽  
Optical Efficiency ◽  
Multiple Band ◽  
Multi Mode

We have developed a multi-mode digital imaging system which acquires images with a cooled CCD camera (Figure 1). A multiple band pass dichromatic mirror and robotically controlled filter wheels provide wavelength selection for epi-fluorescence. Shutters select illumination either by epi-fluorescence or by transmitted light for phase contrast or DIC. Many of our experiments involve investigations of spindle assembly dynamics and chromosome movements in live cells or unfixed reconstituted preparations in vitro in which photodamage and phototoxicity are major concerns. As a consequence, a major factor in the design was optical efficiency: achieving the highest image quality with the least number of illumination photons. This principle applies to both epi-fluorescence and transmitted light imaging modes. In living cells and extracts, microtubules are visualized using X-rhodamine labeled tubulin. Photoactivation of C2CF-fluorescein labeled tubulin is used to locally mark microtubules in studies of microtubule dynamics and translocation. Chromosomes are labeled with DAPI or Hoechst DNA intercalating dyes.

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