Books on the topic 'Laser blood flow meter'

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1

Fratkin, Randi D. Evaluation of a laser Doppler flowmeter to assess blood flow in primary anterior teeth. Ottawa: National Library of Canada, 1993.

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2

Cobb, Jonathan Edwin. An In-shoe laser Doppler sensor for assessing plantar blood flow in the diabetic foot. Poole: Bournemouth University, 2000.

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3

Ward, Geoffrey. Laser Doppler Flowmetry: Theoretical and in vitro models with red and green lasers. Oxford: Oxford Brookes University, 1995.

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4

ASME/JSME Fluids Engineering and Laser Anemometry Conference and Exhibition (1995 Hilton Head, S.C.). Bio-medical fluids engineering: Presented at the 1995 ASME/JSME Fluids Engineering and Laser Anemometry Conference and Exhibition, August 13-18, 1995, Hilton Head, South Carolina. New York, N.Y: American Society of Mechanical Engineers, 1995.

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5

Clements, B. Alyson. Low intensity laser therapy (LILT) and combined phototherapy/LILT: Effects upon blood flow and wound healing in humans. [s.l: The Author], 1997.

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6

P, Shepherd A., and Öberg P. Åke, eds. Laser-Doppler blood flowmetry. Boston: Kluwer Academic Publishers, 1990.

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7

Diagnostic Ultrasound And Blood Flow Measurements. Crc Pr I Llc, 2004.

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8

Shung, K. Kirk. Diagnostic Ultrasound: Imaging and Blood Flow Measurements. CRC, 2005.

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9

Shung, K. Kirk. Diagnostic Ultrasound: Imaging and Blood Flow Measurements, Second Edition. Taylor & Francis Group, 2015.

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10

Shung, K. Kirk. Diagnostic Ultrasound: Imaging and Blood Flow Measurements, Second Edition. CRC Press, 2017.

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11

Pierre, Péronneau, ed. Vélocimétrie Doppler: Applications en pharmacologie cardiovasculaire animale et clinique. Paris: Editions INSERM, 1991.

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12

(Editor), R. A. Gerbsch, and K. Ohba (Editor), eds. Bio-Medical Fluids Engineering: Presented at the 1995 Asme/Jsme Fluids Engineering and Laser Anemometry Conference and Exhibition, August 13-18, 1995, (Fed). American Society of Mechanical Engineers, 1995.

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13

McLaren, Grant Manson. Alterations of labyrinthine and cerebrospinal fluid volumes influence laser doppler measurements of cochlear blood flow in the rat. 1992.

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14

Schmidt, Jan Andre. Periodic Hemodynamics in Health and Disease (Medical Intelligence Unit). Landes Bioscience, 1996.

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15

Periodic Hemodynamics in Health and Disease (Medical Intelligence Unit). Landes Bioscience, 1996.

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16

Sklar, Larry A., ed. Flow Cytometry for Biotechnology. Oxford University Press, 2005. http://dx.doi.org/10.1093/oso/9780195183146.001.0001.

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Flow cytometry is a sensitive and quantitative platform for the measurement of particle fluorescence. In flow cytometry, the particles in a sample flow in single file through a focused laser beam at rates of hundreds to thousands of particles per second. During the time each particle is in the laser beam, on the order of ten microseconds, one or more fluorescent dyes associated with that particle are excited. The fluorescence emitted from each particle is collected through a microscope objective, spectrally filtered, and detected with photomultiplier tubes. Flow cytometry is uniquely capable of the precise and quantitative molecular analysis of genomic sequence information, interactions between purified biomolecules and cellular function. Combined with automated sample handling for increased sample throughput, these features make flow cytometry a versatile platform with applications at many stages of drug discovery. Traditionally, the particles studied are cells, especially blood cells; flow cytometry is used extensively in immunology. This volume shows how flow cytometry is integrated into modern biotechnology, dealing with issues of throughput, content, sensitivity, and high throughput informatics with applications in genomics, proteomics and protein-protein interactions, drug discovery, vaccine development, plant and reproductive biology, pharmacology and toxicology, cell-cell interactions and protein engineering.
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17

Kipnis, Eric, and Benoit Vallet. Tissue perfusion monitoring in the ICU. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0138.

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Resuscitation endpoints have shifted away from restoring normal values of routinely assessed haemodynamic parameters (central venous pressure, mean arterial pressure, cardiac output) towards optimizing parameters that reflect adequate tissue perfusion. Tissue perfusion-based endpoints have changed outcomes, particularly in sepsis. Tissue perfusion can be explored by monitoring the end result of perfusion, namely tissue oxygenation, metabolic markers, and tissue blood flow. Tissue oxygenation can be directly monitored locally through invasive electrodes or non-invasively using light absorbance (pulse oximetry (SpO2) or tissue (StO2)). Global oxygenation may be monitored in blood, either intermittently through blood gas analysis, or continuously with specialized catheters. Central venous saturation (ScvO2) indirectly assesses tissue oxygenation as the net balance between global O2 delivery and uptake, decreasing when delivery does not meet demand. Lactate, a by-product of anaerobic glycolysis, increases when oxygenation is inadequate, and can be measured either globally in blood, or locally in tissues by microdialysis. Likewise, CO2 (a by-product of cellular respiration) and PCO2 can be measured globally in blood or locally in accessible mucosal tissues (sublingual, gastric) by capnography or tonometry. Increasing PCO2 gradients, either tissue-to-arterial or venous-to-arterial, are due to inadequate perfusion. Metabolically, the oxidoreductive status of mitochondria can be assessed locally through NADH fluorescence, which increases in situations of inadequate oxygenation/perfusion. Finally, local tissue blood flow may be measured by laser-Doppler or visualized through intravital microscopic imaging. These perfusion/oxygenation resuscitation endpoints are increasingly used and studied in critical care.
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