Two-dimensional and three-dimensional ultrasound imaging of suburethral slings

We report the case of a 46-year-old female who presented with a category IV pressure ulcer (PU) in the sacral region. Undermining of the PU was assessed with the aid of two-dimensional and three-dimensional ultrasound (3D-US).3D-US clearly visualized the wound in three directions and allowed determination of its volume. Our results show that volumetric analysis carried out with 3D-US enables the evaluation of wound morphology and thus better treatment of patients with PUs. The technique is simple and can be used routinely in daily wound management to assess the volume of the undermined wound.

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Intra- and inter-observer variability and reliability of prostate volume measurement via two-dimensional and three-dimensional ultrasound imaging

Ultrasound in Medicine & Biology ◽

10.1016/s0301-5629(98)00039-8 ◽

1998 ◽

Vol 24 (5) ◽

pp. 673-681 ◽

Cited By ~ 117

Author(s):

Shidong Tong ◽

H.Neale Cardinal ◽

Raymond F McLoughlin ◽

Dónal B Downey ◽

Aaron Fenster

Keyword(s):

Ultrasound Imaging ◽

Prostate Volume ◽

Three Dimensional ◽

Volume Measurement ◽

Observer Variability ◽

Two Dimensional ◽

Inter Observer Variability

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High Resolution Microscopy of Multi-Layered Biological Crystals

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s042482010005319x ◽

1982 ◽

Vol 40 ◽

pp. 80-83

Author(s):

H.A. Cohen ◽

T.W. Jeng ◽

W. Chiu

Keyword(s):

High Resolution ◽

Low Dose ◽

Three Dimensional ◽

Data Interpretation ◽

Two Dimensional ◽

Biological Objects ◽

Density Maps ◽

Density Map ◽

Complex Crystal ◽

High Resolution Microscopy

This tutorial will discuss the methodology of low dose electron diffraction and imaging of crystalline biological objects, the problems of data interpretation for two-dimensional projected density maps of glucose embedded protein crystals, the factors to be considered in combining tilt data from three-dimensional crystals, and finally, the prospects of achieving a high resolution three-dimensional density map of a biological crystal. This methodology will be illustrated using two proteins under investigation in our laboratory, the T4 DNA helix destabilizing protein gp32*I and the crotoxin complex crystal.

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Instrumentation For Quantitative Microscopy

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100078584 ◽

1977 ◽

Vol 35 ◽

pp. 206-209

Author(s):

B. Ralph ◽

A.R. Jones

Keyword(s):

Volume Fraction ◽

Three Dimensional ◽

Two Dimensional ◽

Automatic Data ◽

Phase Volume Fraction ◽

Statistical Confidence ◽

Resultant Data ◽

Automatic Data Collection ◽

Third Dimension ◽

Evolution Of Microstructure

In all fields of microscopy there is an increasing interest in the quantification of microstructure. This interest may stem from a desire to establish quality control parameters or may have a more fundamental requirement involving the derivation of parameters which partially or completely define the three dimensional nature of the microstructure. This latter categorey of study may arise from an interest in the evolution of microstructure or from a desire to generate detailed property/microstructure relationships. In the more fundamental studies some convolution of two-dimensional data into the third dimension (stereological analysis) will be necessary.In some cases the two-dimensional data may be acquired relatively easily without recourse to automatic data collection and further, it may prove possible to perform the data reduction and analysis relatively easily. In such cases the only recourse to machines may well be in establishing the statistical confidence of the resultant data. Such relatively straightforward studies tend to result from acquiring data on the whole assemblage of features making up the microstructure. In this field data mode, when parameters such as phase volume fraction, mean size etc. are sought, the main case for resorting to automation is in order to perform repetitive analyses since each analysis is relatively easily performed.

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