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Träfflista för sökning "WFRF:(Sutherland M.) srt2:(1995-1999)"

Sökning: WFRF:(Sutherland M.) > (1995-1999)

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  • Escobar Kvitting, John-Peder, 1976-, et al. (författare)
  • How accurate is visual assessment of synchronicity in myocardial motion? An in vitro study with computer-simulated regional delay in myocardial motion : clinical implications for rest and stress echocardiography studies
  • 1999
  • Ingår i: Journal of the American Society of Echocardiography. - 0894-7317 .- 1097-6795. ; 12:9, s. 698-705
  • Tidskriftsartikel (refereegranskat)abstract
    • Asynchronicity in echocardiographic images is normally assessed visually. No prior quantitative studies have determined the limitations of this approach. To quantify visual recognition of myocardial asynchronicity in echocardiographic images, computer-simulated delay phantom loops were generated from a 3.3 MHz digital image data from a normal left ventricular short-axis heart cycle acquired at 55 frames per second. Six expert observers visually assessed 30 abnormal and 3 normal loops with differing computer-induced delay patterns on 3 occasions and in this optimally simulated environment could recognize only single delays of 89 ms or more. This was improved to 71 ms or more by use of side-by-side (normal versus abnormal) comparative review. Thus visual assessment of clinically important regional delay in rest or stress echo images is limited.
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  • Strotmann, Jörg M., et al. (författare)
  • Anatomic M-mode echocardiography : a new approach to assess regional myocardial function - A comparative in vivo and in vitro study of both fundamental and second harmonic imaging modes
  • 1999
  • Ingår i: Journal of the American Society of Echocardiography. - 0894-7317 .- 1097-6795. ; 12:5, s. 300-307
  • Tidskriftsartikel (refereegranskat)abstract
    • Objective: To evaluate the accuracy of anatomic M-mode echocardiography (AMM).Methods: Eight phantoms were rotated on a device at different insonation depths (IDs) in a water beaker. They were insonated with different transducer frequencies in fundamental imaging (FI) and second harmonic imaging (SHI), and the diameters were assessed with conventional M-mode echocardiography (CMM) and AMM with the applied angle correction (AC) after rotation. In addition, left ventricular wall dimensions were measured with CMM and AMM in FI and SHI in 10 volunteers.Results: AC had the greatest effect on the measurement error in AMM followed by ID (AC: R2 = 0.295, ID: R2 = 0.268; P < .0001). SHI improved the accuracy, and a difference no longer existed between CMM and AMM with an AC up to 60 degrees. In vivo the limit of agreement between AMM and CMM was -1.7 to +1.8 mm in SHI.Conclusion: Within its limitations (AC < 60 degrees; ID < 20 cm), AMM could be a robust tool in clinical practice.
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  • Tamás, Markus J., 1970, et al. (författare)
  • Fps1p controls the accumulation and release of the compatible solute glycerol in yeast osmoregulation.
  • 1999
  • Ingår i: Molecular microbiology. - 0950-382X .- 1365-2958. ; 4, s. 1087-104
  • Tidskriftsartikel (refereegranskat)abstract
    • The accumulation of compatible solutes, such as glycerol, in the yeast Saccharomyces cerevisiae, is a ubiquitous mechanism in cellular osmoregulation. Here, we demonstrate that yeast cells control glycerol accumulation in part via a regulated, Fps1p-mediated export of glycerol. Fps1p is a member of the MIP family of channel proteins most closely related to the bacterial glycerol facilitators. The protein is localized in the plasma membrane. The physiological role of Fps1p appears to be glycerol export rather than uptake. Fps1 delta mutants are sensitive to hypo-osmotic shock, demonstrating that osmolyte export is required for recovery from a sudden drop in external osmolarity. In wild-type cells, the glycerol transport rate is decreased by hyperosmotic shock and increased by hypo-osmotic shock on a subminute time scale. This regulation seems to be independent of the known yeast osmosensing HOG and PKC signalling pathways. Mutants lacking the unique hydrophilic N-terminal domain of Fps1p, or certain parts thereof, fail to reduce the glycerol transport rate after a hyperosmotic shock. Yeast cells carrying these constructs constitutively release glycerol and show a dominant hyperosmosensitivity, but compensate for glycerol loss after prolonged incubation by glycerol overproduction. Fps1p may be an example of a more widespread class of regulators of osmoadaptation, which control the cellular content and release of compatible solutes.
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  • Wilkenshoff, Ursula M., et al. (författare)
  • Regional mean systolic myocardial velocity estimation by real-time color Doppler Myocardial Imaging: A new technique for quantifying regional systolic function
  • 1998
  • Ingår i: Journal of the American Society of Echocardiography. - : Elsevier BV. - 0894-7317 .- 1097-6795. ; 11:7, s. 683-692
  • Tidskriftsartikel (refereegranskat)abstract
    • A new color Doppler myocardial imaging (CDMI) system with high spatial and temporal resolution and novel postprocessing modalities has been developed that could allow quantifiable stress echocardiography. The purpose of this study was to determine whether regional myocardial systolic velocities could be accurately and reproducibly measured both at rest and during bicycle ergometry by using CDMI. Thirty normal subjects were examined with CDMI at rest, and peak mean systolic myocardial velocities (MSV) were measured for 34 predetermined left ventricular myocardial segments. Interobserver variability and intraobserver variability were established for all segments. Submaximal bicycle ergometry was performed in 20 normal subjects by using standardized weight-related increases in workload. MSV were measured at each step of exercise for 16 left ventricular stress echo segments. At rest, a base-apex gradient in regional MSV was recorded with highest longitudinal shortening velocities at the base. A similar pattern was noted for circumferential shortening MSV. Measurements were predictable and highly reproducible with low interobserver and intraobserver variability for 26 of 34 segments. Reproducibility was poor for basal anteroseptal segments in all views and mid anterior, anteroseptal, and septal segments in the short-axis views. During exercise, mid and basal segments of all walls showed a significant increase of MSV between each workload step and for apical segments between alternate steps. The resting base-apex velocity gradient observed at rest remained in all walls throughout ergometry. Thus a CDMI system with improved spatial and temporal resolution and postprocessing analysis modalities provided reproducible and accurate quantification of segmental left ventricular circumferential and longitudinal contraction both at rest and during exercise.
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