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Relevant bibliographies by topics / Positron emission tomography

Academic literature on the topic 'Positron emission tomography'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 May 2024

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Journal articles on the topic "Positron emission tomography"

1

Kwee, Thomas C., Drew A. Torigian, and Abass Alavi. "Overview of Positron Emission Tomography, Hybrid Positron Emission Tomography Instrumentation, and Positron Emission Tomography Quantification." Journal of Thoracic Imaging 28, no. 1 (January 2013): 4–10. http://dx.doi.org/10.1097/rti.0b013e31827882d9.

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Even-Sapir, Einat, Eyal Mishani, Gideon Flusser, and Ur Metser. "18F-Fluoride Positron Emission Tomography and Positron Emission Tomography/Computed Tomography." Seminars in Nuclear Medicine 37, no. 6 (November 2007): 462–69. http://dx.doi.org/10.1053/j.semnuclmed.2007.07.002.

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Faisal, Arif. "Positron Emission Tomography." Jurnal Radiologi Indonesia 1, no. 2 (September 1, 2015): 121–30. http://dx.doi.org/10.33748/jradidn.v1i2.16.

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The aim of this study to evaluate the positron emission tomography (PET) scan technology and its role as a diagnostic tool in health care. New PET technology provide the integrated PET and CT or MRI scan have been applicated globally. In performing PET scan, a small amount of a radioactive substance (18F-FDG is widely used) is injected into a vein, and this substance is absorbed mainly by organs and tissues that use the most energy.The patients recieve internal radiation exposure from injected radiotracer and external radiation from CT component technology. PET and integrated PET seem to be used in oncology for diagnosis, tumor staging, evaluation after therapy and fnding recurrent cancer. An integrated PET/CT scan combines images from PET scan reveals any abnormal activity that might be going on tissues and organs inside the body, while a CT scan provides detailed pictures ofthere. In general, PET/CT can be considered similarly accurate to PET/MRI as whole-body staging approach. But PET/MRI will be indicated and performed superiorly to PET/CT that require high soft tissue contrast. The average specifc activity of 18F-FDG was equal to 3.5 to 4.3 MBq/kg. In PET/CT examination,the injected18F-FDG activity was on an average 300 MBq for adult patient, and by using TOF technology the average activity decreased to 250 MBq.The average e?ective dose related to whole body PET/CT was about 14.3 mSv (8.6 mSv due to CT scan, 5.7 mSv due to PET-FDG component). Another center reported the average e?ective dose was 4.4 mSv for PET component alone and totally 13.5 mSv for PET/CT examination. A PET technology and integrated PET with CT or MRI as new machine for diagnostic imaging can be used mainly for oncologic patients. The PET/MRI technology is superior to PET/CT in detecting soft tissue contrast of organs and tissues.

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Joseph, U. A. "Positron Emission Tomography." Journal of Nuclear Medicine 53, no. 6 (April 27, 2012): 1002–3. http://dx.doi.org/10.2967/jnumed.112.105403.

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Bell, M. R., and J. A. Rumberger. "Positron emission tomography." Circulation 82, no. 3 (September 1990): 1076–77. http://dx.doi.org/10.1161/circ.82.3.2393997.

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Ollinger, J. M., and J. A. Fessler. "Positron-emission tomography." IEEE Signal Processing Magazine 14, no. 1 (1997): 43–55. http://dx.doi.org/10.1109/79.560323.

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Kirsch, Murielle, Sarah Wannez, Aurore Thibaut, Steven Laureys, Jean François Brichant, and Vincent Bonhomme. "Positron Emission Tomography." International Anesthesiology Clinics 54, no. 1 (2016): 109–28. http://dx.doi.org/10.1097/aia.0000000000000090.

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Guerra, A. Del. "Positron Emission Tomography." Physica Scripta T19B (January 1, 1987): 481–86. http://dx.doi.org/10.1088/0031-8949/1987/t19b/026.

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Schelbert, H. R. "Positron emission tomography." Current Opinion in Cardiology 3, no. 6 (November 1988): 949. http://dx.doi.org/10.1097/00001573-198811000-00013.

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Berger, A. "Positron emission tomography." BMJ 326, no. 7404 (June 26, 2003): 1449. http://dx.doi.org/10.1136/bmj.326.7404.1449.

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Dissertations / Theses on the topic "Positron emission tomography"

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Andrews, Thomasin Catharine. "Positron emission tomographic [tomography] studies in Huntingdon's disease." Thesis, University of London, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.271604.

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Strother, S. C. (Steven Charles) 1955. "Quantitation in positron emission tomography." Thesis, McGill University, 1986. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=72815.

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Wills, A. J. "Positron emission tomography studies of tremor." Thesis, Queen Mary, University of London, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297290.

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Bailey, Dale L. "Quantification in 3D positron emission tomography." Thesis, University of Surrey, 1996. http://epubs.surrey.ac.uk/770395/.

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Acquisition and reconstruction of data in three-dimensional positron emission tomography (3D PET) was introduced in 1990 almost 20 years after the first PET scanners were developed. 3D PET offers a significant sensitivity improvement over conventional, sliceoriented 2D PET, but at the cost of a three-fold increase in acceptance of scattered events. In addition, processing time is increased and new methods for applying corrections such as for photon attenuation, calibration, and detector/geometry normalisation are required. 3D PET raised concerns that the high quantitative accuracy that was possible with 2D PET (with its moderate sensitivity) would not be matched in 3D, primarily because of the greatly increased scattered photon component in the measured data. The aim of this thesis was to develop methods that enable quantitatively accurate measurements with 3D PET. A technique to correct for scattered photons prior to reconstruction has been developed, implemented and assessed. A device for normalising the data for detector efficiency and the geometry of the cylindrical detector system has been developed, and the factors affecting reconstruction investigated. A new approach to calibration of the reconstructed data to produce images of activity concentration which is independent of scatter has been implemented. Finally, the techniques have been applied to data from brain scans of human subjects. Evaluation of images reconstructed from 3D PET demonstrates that the methodology developed in this work produces data accurate to within 10% of the true activity concentration in an object with reasonably homogeneous density. 3D PET is shown to be as accurate as 2D PET, but with a sensitivity advantage that improves signal-to-noise by approximately a factor of three in the human brain and slightly less in other regions of the body.

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Shu, Chengyi Jenny. "Positron emission tomography of immune responses." Diss., Restricted to subscribing institutions, 2008. http://proquest.umi.com/pqdweb?did=1679380111&sid=1&Fmt=2&clientId=1564&RQT=309&VName=PQD.

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Palmer, Matthew Rex. "Noise propagation in quantitative positron emission tomography." Thesis, University of British Columbia, 1985. http://hdl.handle.net/2429/25131.

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Image noise in Positron Emission Tomography (PET) is the result of statistical fluctuation in projection data. The variance properties of images obtained with the UBC/TRIUMF PETT VI tomograph are studied by analytical methods, computer simulations, and phantom experiments. The PETT VI image reconstruction algorithm is described and analyzed for noise propagation properties. Procedures for estimating both point-wise (pixel) and region of interest (ROI) variances are developed: these include the effects of corrections for non-uniform sampling, detector efficiency variation, object self-attenuation and random coincidences. The analytical expression for image-plane variance is used in computer simulations to isolate the effects of the various data corrections: It is shown that the image precision is degraded due to non-uniform sampling of the projections. The RMS noise is found to be increased by 9% due to the wobble motion employed in PETT VI. Analytical predictions for both pixel and ROI variances are verified with phantom experiments. The average error between measured and predicted ROI variances due to noise in emission data for a set of seven regions placed on a 20 cm cylindrical phantom is 9.5%. Images showing variance distributions due to noise in emission data and due to noise in transmission data are produced from human subject brain scan data collected by the UBC/TRIUMF PET group. The maximum ratio of image variance due to noise in transmission data to that due to noise in emission data is calculated as 2.6 for a typical FDG study, and 0.082 for a typical fluorodopa study. Total RMS noise varies between 0.4% and 11.6% for a typical set of ROI's placed on mid-brain slices reconstructed from these data sets. Procedures are suggested for improving the statistical accuracy of quantitative PET measurements.
Applied Science, Faculty of
Electrical and Computer Engineering, Department of
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Sayeed, Abdul. "Positron emission tomography analysis of Alzheimer's disease." Thesis, University of Surrey, 2001. http://epubs.surrey.ac.uk/842834/.

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Alzheimer's Disease (AD) is a major concern for the elderly population, currently affecting over 670,000 people in the UK. With the continual increase in the age of the population the problem is expected to rise. There is no known cure to the condition and a definite diagnosis cannot be made in life. Clinical diagnosis is considered to be approximately 80% - 90% accurate, sometimes taking up to a year to assess. Early detection could aid in the care and possible development of better treatments or even a cure. AD has been shown to alter the structure and global texture of the brain. Studies using Magnetic Resonance imaging (MRI) and Computerised Tomography (CT) have been used to detect these changes with some success by some researchers. Positron Emission Tomography (PET) imaging is a functional imaging modality and in theory before structural changes are evident functional changes should be apparent. Therefore we utilise PET images for this study. This thesis will exploit the fact that AD alters the global texture of the brain. Texture features extracted from fluoro-deoxy-glucose (FDG) PET images and sinograms of the brain will be used. Most texture feature extraction methods fail, due to poor signal to noise ratio so we will use a novel texture feature extraction method known as the Trace transform - triple features, which can extract features directly from raw data acquired by PET scanners. Classifiers will be used to aid in the separation of the two groups, namely AD patients and normal controls. The Trace transform - triple feature method has proven its potential as a good feature extraction technique. It enabled us to achieve classification accuracy of up to 93% on raw sinogram data using a combination of five features. This result is very good compared with the clinical accuracy of 80% reported by most researcher. It is comparable to results obtained by Kippenhan et al [52, 53, 51, 50], who used regional metabolic activity using PET and a neural network classifier. Monomial features extracted from images achieved accuracies as high as 87%. These features are good discriminators, however, they suffer from lack of scaling invariance. This is problematic as brain sizes do vary considerably. The use of registration and extraction of regional information failed to produce fruitful results. This is principally due to poor registration. The registration failed primarily because a very small cross section of the brain was available. Also the effect of AD alters the structure of the brain. Since the registration relies on matching structure, it becomes questionable whether one can actually register automatically a very degraded AD brain. Gender and age are crucial to the progress of Alzheimer's disease. Age and gender matching is not sufficient to get the best results. This thesis has shown that performance gains of up to 11% can be attained by simply incorporating age and/or gender into the classification model. However, the maximum classification accuracy was not improved any further.

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Andrée, Bengt. "Positron emission tomography in serotonergic drug development /." Stockholm, 2001. http://diss.kib.ki.se/2001/91-628-4779-1/.

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Spinelli, Antonello Enrico. "Quantitative dynamic imaging using positron emission tomography." Thesis, Institute of Cancer Research (University Of London), 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.406697.

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Prevett, Martin Charles. "Positron emission tomography in idiopathic generalised epilepsy." Thesis, University of Southampton, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296348.

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Books on the topic "Positron emission tomography"

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Valk, Peter E., Dominique Delbeke, Dale L. Bailey, David W. Townsend, and Michael N. Maisey, eds. Positron Emission Tomography. London: Springer London, 2006. http://dx.doi.org/10.1007/1-84628-187-3.

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Juweid, Malik E., and Otto S. Hoekstra, eds. Positron Emission Tomography. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-062-1.

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Bailey, Dale L., David W. Townsend, Peter E. Valk, and Michael N. Maisey, eds. Positron Emission Tomography. London: Springer-Verlag, 2005. http://dx.doi.org/10.1007/b136169.

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Granov, Anatoliy, Leonid Tiutin, and Thomas Schwarz, eds. Positron Emission Tomography. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-21120-1.

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Das, Birendra Kishore, ed. Positron Emission Tomography. New Delhi: Springer India, 2015. http://dx.doi.org/10.1007/978-81-322-2098-5.

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Positron emission tomography. New York: Humana Press, 2011.

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1933-, Reivich Martin, and Alavi Abass, eds. Positron emission tomography. New York: A.R. Liss, 1985.

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Granov, A. M., L. A. Tiutin, and Schwarz Thomas. Positron emission tomography. Heidelberg: Springer, 2013.

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Witney, Timothy H., and Adam J. Shuhendler, eds. Positron Emission Tomography. New York, NY: Springer US, 2024. http://dx.doi.org/10.1007/978-1-0716-3499-8.

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Schwaiger, Markus, ed. Cardiac Positron Emission Tomography. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-1233-8.

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Book chapters on the topic "Positron emission tomography"

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Granov, Anatoliy, Leonid Tiutin, and Thomas Schwarz. "The Physical Basis of Positron Emission Tomography." In Positron Emission Tomography, 3–24. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-21120-1_1.

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Granov, Anatoliy, Leonid Tiutin, and Thomas Schwarz. "Pancreatic Cancer." In Positron Emission Tomography, 127–37. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-21120-1_10.

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Granov, Anatoliy, Leonid Tiutin, and Thomas Schwarz. "Kidney Cancer." In Positron Emission Tomography, 139–47. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-21120-1_11.

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Granov, Anatoliy, Leonid Tiutin, and Thomas Schwarz. "Ovarian Cancer." In Positron Emission Tomography, 149–52. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-21120-1_12.

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Granov, Anatoliy, Leonid Tiutin, and Thomas Schwarz. "Cervical and Endometrial Cancers." In Positron Emission Tomography, 153–61. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-21120-1_13.

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Granov, Anatoliy, Leonid Tiutin, and Thomas Schwarz. "Prostate Cancer." In Positron Emission Tomography, 163–74. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-21120-1_14.

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Granov, Anatoliy, Leonid Tiutin, and Thomas Schwarz. "Testicular Cancer." In Positron Emission Tomography, 175–81. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-21120-1_15.

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Granov, Anatoliy, Leonid Tiutin, and Thomas Schwarz. "Lymphoproliferative Diseases." In Positron Emission Tomography, 183–93. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-21120-1_16.

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Granov, Anatoliy, Leonid Tiutin, and Thomas Schwarz. "Skin Melanoma." In Positron Emission Tomography, 195–201. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-21120-1_17.

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Granov, Anatoliy, Leonid Tiutin, and Thomas Schwarz. "Musculoskeletal Tumors." In Positron Emission Tomography, 203–10. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-21120-1_18.

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Conference papers on the topic "Positron emission tomography"

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Townsend, D. W. "Positron Emission Tomography." In Diagnostic Imaging Applications, edited by Edwin S. Beckenbach. SPIE, 1985. http://dx.doi.org/10.1117/12.945130.

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Bodvarsson, Bjarni, Lars Kai Hansen, Claus Svarer, and Gitte Knudsen. "NMF on Positron Emission Tomography." In 2007 IEEE International Conference on Acoustics, Speech, and Signal Processing. IEEE, 2007. http://dx.doi.org/10.1109/icassp.2007.366678.

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Hart, Hiram, Alan Schoenfeld, and Zhengrong Liang. "Four Planar Positron Emission Tomography." In 31st Annual Technical Symposium, edited by Andrew G. Tescher. SPIE, 1988. http://dx.doi.org/10.1117/12.942128.

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Mair, Bernard A., Murali Rao, and J. M. M. Anderson. "Semi-infinite positron emission tomography." In SPIE's 1995 International Symposium on Optical Science, Engineering, and Instrumentation, edited by Randall L. Barbour, Mark J. Carvlin, and Michael A. Fiddy. SPIE, 1995. http://dx.doi.org/10.1117/12.224179.

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Lemesios, Christos, Loizos Koutsantonis, and Costas N. Papanicolas. "RISE: Tomographic Image Reconstruction in Positron Emission Tomography." In 2019 IEEE Nuclear Science Symposium and Medical Imaging Conference (NSS/MIC). IEEE, 2019. http://dx.doi.org/10.1109/nss/mic42101.2019.9060020.

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Kambali, Imam, and Hari Suryanto. "Cancer Imaging Using Positron Emission Tomography/Computed Tomography." In 2020 International Seminar on Intelligent Technology and Its Applications (ISITIA). IEEE, 2020. http://dx.doi.org/10.1109/isitia49792.2020.9163740.

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Guerra, Pedro, Juan E. Ortuno, George Kontaxakis, Maria J. Ledesma, Juan J. Vaquero, Manuel Desco, and Andres Santos. "Digital timing in positron emission tomography." In 2006 IEEE Nuclear Science Symposium Conference Record. IEEE, 2006. http://dx.doi.org/10.1109/nssmic.2006.354272.

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Eriksson, L., D. Townsend, M. Conti, M. Eriksson, C. Bohm, H. Rothfuss, M. Schmand, M. E. Casey, and Bernard Bendriem. "Future instrumentation in positron emission tomography." In 2006 IEEE Nuclear Science Symposium Conference Record. IEEE, 2006. http://dx.doi.org/10.1109/nssmic.2006.354427.

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Wernick, Miles N., and Chin-Tu Chen. "Super-resolution in positron emission tomography." In Optical Engineering Midwest 1992, edited by Robert J. Heaston. SPIE, 1992. http://dx.doi.org/10.1117/12.130955.

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Fullerton, PhD, Gary D. "Positron emission tomography and radiation oncology." In MEDICAL PHYSICS: Fifth Mexican Symposium. AIP, 2001. http://dx.doi.org/10.1063/1.1420465.

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Reports on the topic "Positron emission tomography"

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Welch, M. J. Positron Emission Tomography (PET). Office of Scientific and Technical Information (OSTI), January 1990. http://dx.doi.org/10.2172/6869838.

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Wadas, Thaddeus J. Imaging Prostate Cancer with Positron Emission Tomography. Fort Belvoir, VA: Defense Technical Information Center, July 2014. http://dx.doi.org/10.21236/ada608223.

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Conti, M., and V. Perez-Mendez. Amorphous silicon detectors in positron emission tomography. Office of Scientific and Technical Information (OSTI), December 1989. http://dx.doi.org/10.2172/7256541.

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Drukier, A. Positron Emission Tomography with improved spatial resolution. Office of Scientific and Technical Information (OSTI), April 1990. http://dx.doi.org/10.2172/6854157.

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Hall, William J. Positron Emission Tomography Studies of Top-Down Processing,. Fort Belvoir, VA: Defense Technical Information Center, January 1995. http://dx.doi.org/10.21236/ada298838.

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Alpert, Nathaniel M. Cognition in the Brain: Investigations Using Positron Emission Tomography. Fort Belvoir, VA: Defense Technical Information Center, July 1992. http://dx.doi.org/10.21236/ada254280.

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Budinger, T. F., S. E. Derenzo, R. H. Huesman, W. J. Jagust, and P. E. Valk. High-resolution PET (positron emission tomography) for medical science studies. Office of Scientific and Technical Information (OSTI), September 1989. http://dx.doi.org/10.2172/5473405.

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Cheung, Nai-Kong V., Shakeel Modak, Yukang Lin, Hongfen Guo, Pat Zanzonico, John Chung, Yuting Zuo, et al. Pharmacokinetics of Genetically Engineered Antibody Forms Using Positron Emission Tomography. Office of Scientific and Technical Information (OSTI), August 2004. http://dx.doi.org/10.2172/828873.

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Correia, John A. A Novel High Resolution Positron Emission Tomography System for Measurement of Bone Metabolism. Fort Belvoir, VA: Defense Technical Information Center, September 2001. http://dx.doi.org/10.21236/ada400560.

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Kuhl, D. E. New techniques for positron emission tomography in the study of human neurological disorders. Office of Scientific and Technical Information (OSTI), July 1992. http://dx.doi.org/10.2172/10154585.

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