Relevant bibliographies by topics / Gastrointestinal Imaging

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Gastrointestinal Imaging'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Gastrointestinal Imaging"

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Ferrett, C. G., and H. K. Bungay. "Imaging of the gastrointestinal tract." Imaging 18, no. 4 (December 2006): vi. http://dx.doi.org/10.1259/imaging/31481729.

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ANTHONY, S., and R. UBEROI. "CT imaging of acute gastrointestinal haemorrhage." Imaging 21, no. 1 (March 2009): 32–37. http://dx.doi.org/10.1259/imaging/29714526.

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Nolan, D. J. "Gastrointestinal Imaging." Clinical Radiology 39, no. 3 (January 1988): 332. http://dx.doi.org/10.1016/s0009-9260(88)80562-2.

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ANNAMALAI, G., N. MASSON, and I. ROBERTSON. "Acute gastrointestinal haemorrhage: investigation and treatment." Imaging 21, no. 2 (June 2009): 142–51. http://dx.doi.org/10.1259/imaging/29199389.

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Annamalai, G., and I. Robertson. "Acute gastrointestinal haemorrhage: investigation and treatment." Imaging 16, no. 3 (August 2004): 264–70. http://dx.doi.org/10.1259/imaging/41646236.

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Bramson, Robert T. "Pediatric Gastrointestinal Imaging." Radiology 175, no. 2 (May 1990): 478. http://dx.doi.org/10.1148/radiology.175.2.478.

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Cumming, William A., and Jonathan L. Williams. "Neonatal Gastrointestinal Imaging." Clinics in Perinatology 23, no. 2 (June 1996): 387–407. http://dx.doi.org/10.1016/s0095-5108(18)30248-3.

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Pickhardt, Perry J. "Radiologic Gastrointestinal Imaging." Gastroenterology Clinics of North America 47, no. 3 (September 2018): i. http://dx.doi.org/10.1016/s0889-8553(18)30048-7.

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&NA;. "GASTROINTESTINAL IMAGING COURSE." Critical Care Nursing Quarterly 10, no. 2 (September 1987): 91. http://dx.doi.org/10.1097/00002727-198709000-00017.

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Rao, Padma. "Neonatal gastrointestinal imaging." European Journal of Radiology 60, no. 2 (November 2006): 171–86. http://dx.doi.org/10.1016/j.ejrad.2006.07.021.

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Dissertations / Theses on the topic "Gastrointestinal Imaging"

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Pakzad, F. "Molecular imaging using positron emission tomography in gastrointestinal malignancy." Thesis, University College London (University of London), 2010. http://discovery.ucl.ac.uk/19224/.

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Positron Emission Tomography (PET) with 18F-FDG has emerged as a powerful tool in oncology. Furthermore, recent advent of PET/CT and novel tracers are continually expanding its role. This thesis investigates its application in two solid cancer models. In the diagnosing of primary pancreatic cancer, 18F-FDG PET/CT was shown to be more accurate than conventional CT. It did not add information to locoregional staging of disease but impacted management of patients with potentially operable tumours, by accurately confirming the presence / absence of metastases. In the pre-operative staging of patients with colorectal liver metastases (CLM), 18F- FDG PET/CT was also superior to CT in assessing extrahepatic disease, where it again impacted management. The accuracy of detecting hepatic disease was similar for both. Compared to PET alone, PET/CT improved the accuracy of lesions localization and interpretation. Next, the feasibility of imaging with the novel thymidine analogue tracer 18F-FLT was investigated. Overall, 18F-FLT PET was less accurate than 18F-FDG in detecting lesions in both cancer types, thus suggesting it to be an unsuitable tracer for routine diagnosis and staging. In the cohort of pancreatic cancer patients, 18F-FLT uptake (SUVs) were found to strongly correlate with the immunohistochemical proliferation marker, Ki-67 antigen. This supported 18F-FLT‟s potential role as a surrogate marker of proliferation. The prognostic implications of these require further investigation. Finally, an in vitro model was use to examine early changes in 18F-FLT uptake in response to treatment with cytotoxics. At 2 hours following pulse treatment with 5-fluorouracil, (and before changes in cell numbers and cell cycle phase were seen), a dose dependent increase in 18F-FLT uptake was seen. No change was observed with 18F-FDG nor following Cisplatin treatment. This adaptive response may have a role as an early predictor of response to 5-FU (and potentially other antimetabolites), which requires further investigation.
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Boulby, Philip Andrew. "The assessment of gastrointestinal physiology by echo-planar imaging." Thesis, University of Nottingham, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.267154.

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Reese, George Edward. "Terahertz Pulsed Imaging of lower gastrointestinal mucosa : an in vitro study." Thesis, Imperial College London, 2015. http://hdl.handle.net/10044/1/26989.

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Medical imaging using Terahertz frequency radiation is in its infancy. Optical adjuncts to enhance the diagnostic precision of white light endoscopy are not new and almost all wavelengths of the electromagnetic spectrum have, at some point, been investigated to this end. The ultimate aim of an endoscopic technique is to identify 100% of mucosal lesions and to classify them with 100% specificity. Methods: This thesis examined the sensitivity and specificity of current technology to accurately identify colonic pathology using a diagnostic precision analysis of published data. The effect of biomaterials such as blood, mucus and faeces on Terahertz radiation was assessed using human tissue samples from health volunteers. The ability to discriminate pathological from normal colonic mucosa was assessed using terahertz radiation to interrogate excised samples of human colon. The physical nature of variation between pathological and normal colonic mucosa was assessed using histological markers in an attempt to identify the cause of terahertz radiation contrast. Results: Current technology has a sensitivity of 95% and a specificity of 78% in a non- inflamed colon. Terahertz pulsed imaging is a sensitive and specific technique for in vitro classification of colonic mucosal pathology. TPI may be a useful adjunct in the presence of inflamed mucosal tissue. Although there were too few data from the present study to quantify any potential benefit. The effects of blood, stool and mucus on TPI are similar but less pronounced than water. Immunohistochemical analysis has demonstrated an association between vascular and lymphatic density with neoplasia. This may be a mechanism for TPI discrimination of colonic pathology. TPI could in the future contribute to a minimally invasive method of in vivo diagnosis of colonic dysplasia or malignancy. Larger scale and in vivo trials of the technology are necessary to further investigate the potential clinical benefit.
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Hussein, Mahamoud Omar. "Magnetic resonance imaging and spectroscopy of fat emulsions in the gastrointestinal tract." Thesis, University of Nottingham, 2013. http://eprints.nottingham.ac.uk/13582/.

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The relationship between meal structure and composition can modulate gastrointestinal processing and the resulting sense of satiety. This applies also to the fat component of meals and particularly to the surface area available for digestion. The main hypothesis underpinning this thesis work was that fat emulsion droplet size has a profound effect on fat digestion and, in turn, on the gastrointestinal and satiety responses. To test this hypothesis two fat emulsion meal systems were used. They had exactly the same composition but a small (termed the Fine emulsion, with a droplet size of 400 nm) or a large (termed the Coarse emulsion, with a droplet size of 8 μm) emulsified fat droplet size. The two fat emulsion systems were manufactured and characterised using a range of bench techniques, in vitro digestion models and MRI techniques in vitro. The difference in microstructure caused different temporal creaming characteristics for the emulsions and different percentage hydrolysis profiles in a gastric digestion model in vitro. The Fine emulsion showed initial rapid hydrolysis whilst the Coarse emulsion showed an initial slow hydrolysis phase with the hydrolysis rate increasing at later stages. This indicated that there was indeed a droplet size effect on fat hydrolysis whereby the smaller droplet size with a larger surface area hydrolysed faster than a larger droplet size. The emulsions’ performance was finally tested in vivo in healthy volunteers using MRI in a series of pilot studies leading to a main physiological study. Creaming differences in the gastric lumen were addressed by redesigning the meals using a locust bean gum (LBG) thickener that made them stable throughout the gastric emptying process. A main three-way physiological and satiety study in healthy volunteers showed that a highly emulsified, intragastrically stable emulsion delayed gastric emptying, increased small bowel water content and reduced consumption of food at the end of the study day. Finally, magnetic resonance imaging, relaxometry and spectroscopy were further evaluated to assess fat emulsion parameters in vitro and in vivo in the gastric lumen. Main static magnetic field and droplet size effects on T2 relaxation times of the Fine and the Coarse emulsions were observed. There was reasonable correlation between m-DIXON and spectroscopy methods to quantify fat fraction both in vitro and in vivo. Differences in T2 relaxation times for different droplet sizes of 20% fat emulsions were detected in vitro. These changes were however difficult to separate from creaming effects in vivo with a view of drawing meaningful inferences on droplet sizes. The main conclusion from this work was that manipulating food microstructure especially intragastric stability and fat emulsion droplet size can influence human gastrointestinal physiology and satiety responses and that MRI and MRS provide unique non invasive insights into these processes. This improved knowledge could help designing foods with desired health-promoting characteristics which could help to fight the rising tide of obesity.
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Wilson, Kirsteen E. "Development of a novel magnetic moment imaging technique to assess gastrointestinal motility." Thesis, University of Strathclyde, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.443143.

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Basford, Peter John. "Advanced endoscopic imaging in the gastrointestinal tract : improving the view of neoplasia." Thesis, University of Portsmouth, 2015. https://researchportal.port.ac.uk/portal/en/theses/advanced-endoscopic-imaging-in-the-gastrointestinal-tract(14c0150e-ea3d-4e3d-8438-f7defe159f9c).html.

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Gastrointestinal endoscopy is a vital tool for the detection and treatment of early neoplasia in the upper and lower gastrointestinal tracts. Survival from gastrointestinal cancer is largely dependent on the stage at diagnosis – thus detection of early lesions, or better still treatment of pre-cancerous lesions is vital to improve outcomes. The world of endoscopy is changing rapidly with the development of dye-based and digital enhancement techniques with the aim of improving the detection and characterisation of neoplastic lesions. This thesis reviews the development of all the main advanced imaging techniques and comprehensively reviews the evidence for the use of these in the colon. Chapter 4 describes the development of a new classification system for characterising small colonic polyps using the Pentax i-Scan digital enhancement system. Chapter 5 describes a prospective cohort study using i-Scan for the in-vivo characterisation of small colonic polyps in 87 patients. No differences in the accuracy of polyp characterisation between high-definition white light endoscopy, i-Scan and chromoendoscopy were found when performed by an expert endoscopist. All 3 modalities met the ASGE criteria for management based on optical diagnosis. Chapter 6 describes a retrospective study looking at factors influencing polyp and adenoma detection in a large UK Bowel cancer screening cohort. Endoscope definition (standard vs high definition) was examined in particular. In this group of patients, endoscope definition was found to have no impact on any outcome measure, but endoscopist and bowel preparation were consistent predictors of key quality outcomes. Chapter 7 describes a randomised controlled clinical trial recruiting 126 patients of a pre-endoscopy drink containing water, n-acetyl cysteine and simeticone. This was shown to significantly improve mucosal visibility compared to water alone, or no preparation, and also significantly reduced the need for procedural fluid flushes. Chapters 8 & 9 describes two studies examining the baseline performance and impact of training modules on the accuracy of colonic lesion and polyp characterisation amongst non-endoscopists and endoscopists with varying degrees of experience. Baseline performance of experienced endoscopists was found to be no different to that of inexperienced endoscopists and novices in both studies, but training improved accuracy in all groups. These studies highlight the need for training in lesion characterisation to become part of the formal training programme for all endoscopists.
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Desouza, Nandita Maria. "The clinical applications of internal receiver coils in magnetic resonance imaging." Thesis, University of Newcastle Upon Tyne, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307919.

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Liang, Kaicheng. "Development and investigation of devices for ultrahigh speed gastrointestinal Optical Coherence Tomography imaging." Thesis, Massachusetts Institute of Technology, 2018. http://hdl.handle.net/1721.1/118085.

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Thesis: Ph. D., Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, 2018.
Cataloged from PDF version of thesis.
Includes bibliographical references (pages 139-149).
Diseases of the gastrointestinal (GI) tract are typically diagnosed by random biopsy of tissue, which samples only a small area and often misses focal neoplasias. Existing endoscopic visualization tools including white light endoscopy, narrowband imaging and confocal laser endomicroscopy have enabled in vivo assessment to guide biopsies, but suffer from technical limitations and have demonstrated suboptimal sensitivity and specificity to neoplasia. Optical Coherence Tomography (OCT) can generate in vivo, 3-dimensional microscopic imaging. Recent efforts in ultrahigh-speed OCT systems for endoscopic applications have shown promise, but devices had limited fields of view and imprecise beam scanning mechanisms, limiting image quality and coverage. This thesis develops a wide range of new fiber optic devices that substantially extend OCT capabilities in the GI tract, either by greatly increasing field of view for wide field mapping of entire luminal organs, or achieving high precision 2-D beam scanning with compact actuators for in vivo microscopy. Piezoelectrically actuated fiber scanning devices enable forward viewing for focal inspection, while micromotor actuators combined with pneumatic or piezoelectric mechanisms enclosed in tethered capsules generate side viewing over large areas. The work also advances the emerging paradigm of gastrointestinal screening without use of sedation, which promises to lower costs of screening and improve access for a broader population. Design, fabrication and benchtop evaluation of devices, as well as pre-clinical and clinical imaging protocols are reported. Results from validation studies in living swine, and human patients in collaboration with the Veterans Affairs Boston Healthcare System are discussed. The thesis work demonstrates new imaging modalities for in vivo detection and diagnosis of GI pathology that could have important applications in disease screening, surveillance, and therapeutic procedures.
by Kaicheng Liang.
Ph. D.
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Barberio, Manuel. "Real-time intraoperative quantitative assessment of gastrointestinal tract perfusion using hyperspectral imaging (HSI)." Thesis, Strasbourg, 2019. http://www.theses.fr/2019STRAJ120.

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La fistule anastomotique (FA) est une complication grave de la chirurgie. Une perfusion locale adéquate est fondamentale pour réduire le risque de FA. Cependant, les critères cliniques ne sont pas fiables pour évaluer la perfusion intestinale. À cet égard, l'angiographie par fluorescence (AF) a été explorée. Malgré des résultats prometteurs dans les essais cliniques, l'évaluation de l'AF est subjective, d'où l'incertitude quant à son efficacité. L'AF quantitative a déjà été introduite. Cependant, elle est limitée par la nécessité d'injecter un fluorophore. L'imagerie hyperspectrale (HSI) est une technique d'imagerie optique prometteuse couplant un spectroscope à une caméra photo, permettant une analyse quantitative des tissus en temps réel et sans contraste. L'utilisation intraopératoire de l'HSI est limitée par la présence d'images statiques. Nous avons développé la hyperspectral-based enhanced reality (HYPER), pour permettre une évaluation précise de la perfusion intraopératoire. Cette thèse décrit les étapes du développement et de la validation d'HYPER
Anastomotic leak (AL) is a severe complication in surgery. Adequate local perfusion is fundamental to promote anastomotic healing, reducing the risk of AL. However, clinical criteria are unreliable to evaluate bowel perfusion. Consequently, a tool allowing to objectively detect intestinal viability intraoperatively is desirable. In this regard, fluorescence angiography (FA) has been explored. In spite of promising results in clinical trials, FA assessment is subjective, hence the efficacy of FA is unclear. Quantitative FA has been previously introduced. However, it is limited by the need of injecting a fluorophore. Hyperspectral imaging (HSI) is a promising optical imaging technique coupling a spectroscope with a photo camera, allowing for a contrast-free, real-time, and quantitative tissue analysis. The intraoperative usability of HSI is limited by the presence of static images. We developed hyperspectral-based enhanced reality (HYPER), to allow for precise intraoperative perfusion assessment. This thesis describes the steps of the development and validation of HYPER
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Alwafi, Reem. "Development of optical coherence tomography endoscopy for gynaecological and gastrointestinal studies and peritoneal membrane imaging." Thesis, University of Manchester, 2012. https://www.research.manchester.ac.uk/portal/en/theses/development-of-optical-coherence-tomography-endoscopy-for-gynaecological-and-gastrointestinal-studies-and-peritoneal-membrane-imaging(8254ec5d-549d-413a-a048-7d773e28dc79).html.

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In the medical field, the detection and diagnosis of diseases continue to improve. Developments in diagnostic techniques have helped to improve treatment in the early stages and avoid many risks to patients. One relatively new diagnostic technique is optical coherence tomography (OCT), which is used in many medical applications to perform internal microstructure imaging of the human body at high resolution (typically 10 micro metre), at high speed and in real time. OCT is non-invasive and can be used as a contact or non-contact technique to obtain an image. In medicine, there are many applications that involve OCT, such as in ophthalmology, gastroenterology, cardiology and oncology. This work demonstrates the design, development and implementation of a high resolution swept laser OCT system for the imaging and diagnosis of tissues in laboratory and clinical experiments. It reports an investigation to measure the thickness of the peritoneal membrane and the use of optical imaging contrast agents such as gold nanorods. There is also an account of the design of an endoscope-catheter fast scanning OCT system for biomedical studies of the gastrointestinal tract and gynaecological areas. These results were achieved by using a swept tuneable laser source with a very high tuning speed of 16 kHz over a wide range of wavelengths: 1260 nm to 1390 nm. The laser sweeps across 110 nm at a 16 kHz repetition rate. The real axial line speed is limited by the source that is used in the OCT system. The axial resolution of the system is 7 µm and its transverse resolution is 15 µm. The bandwidth of the source is up to DeltaGamma = 110 nm, centred at Gamma0 = 1325 nm, and the coherent length is 7 µm. On the sample arm of the interferometer, the swept laser OCT technique is combined with an optical probe and endoscope in order to develop a novel diagnostic imaging device to visualize tissue in vivo for animal and human experimental trials.
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Books on the topic "Gastrointestinal Imaging"

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Gastrointestinal imaging. Stuttgart: Thieme, 2008.

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Pediatric gastrointestinal imaging. Toronto: B.C. Decker, 1989.

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Specialty imaging: Gastrointestinal oncology. Salt Lake City, UT: Amirsys, 2011.

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P, Cole Thomas, and Feczko Peter J, eds. Gastrointestinal imaging: Case review. 2nd ed. Philadelphia, PA: Mosby/Elsevier, 2007.

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Stringer, David A., and Paul Babyn. Pediatric gastrointestinal imaging and intervention. 2nd ed. Hamilton, Ont: B.C. Decker, 2000.

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Imaging of gastrointestinal tract tumors. Berlin: Springer-Verlag, 1990.

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Bruneton, Jean-Noël. Imaging of Gastrointestinal Tract Tumors. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-83825-5.

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Mayo Clinic gastrointestinal imaging review. Boca Raton, Fla: Mayo Clinic Scientific Press, 2005.

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L, Eisenberg Ronald, ed. Gastrointestinal radiology companion: Imaging fundamentals. Philadelphia: Lippincott Williams & Wilkins, 1999.

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S, Levine Marc, ed. High-yield imaging. Philadephia, PA: Saunders/Elsevier, 2010.

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Book chapters on the topic "Gastrointestinal Imaging"

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Lee, Susanna I., and James H. Thrall. "Gastrointestinal Imaging." In Choosing the Correct Radiologic Test, 47–122. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-15772-1_4.

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Huq, Samantha, Marco Molina, and Charan K. Singh. "Gastrointestinal Imaging." In Clinical Gastroenterology, 1–8. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-91316-2_1.

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Wang, Gary X., Mark A. Anderson, Lauren Uzdienski, and Susanna I. Lee. "Gastrointestinal Imaging." In Choosing the Correct Radiologic Test, 167–258. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-65185-5_5.

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de Lutio di Castelguidone, Elisabetta, Vincenza Granata, Roberto Carbone, Francesca Iacobellis, Sergio Venanzio Setola, and Antonella Petrillo. "Gastrointestinal Tumors." In Geriatric Imaging, 817–51. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-35579-0_31.

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Donnelly, Lane F. "Gastrointestinal." In Pediatric Imaging, 86–124. Elsevier, 2009. http://dx.doi.org/10.1016/b978-1-4160-5907-3.00005-2.

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"Gastrointestinal Imaging." In Primer of Diagnostic Imaging, 115–203. Elsevier, 2011. http://dx.doi.org/10.1016/b978-0-323-06538-2.00003-2.

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Sharma, Raju, and Ankur Goyal. "Gastrointestinal Imaging." In Textbook of Surgical Gastroenterology (2 Volumes), 7. Jaypee Brothers Medical Publishers (P) Ltd., 2016. http://dx.doi.org/10.5005/jp/books/12748_3.

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Jhala, Khushboo, Junzi Shi, Cory Robinson-Weiss, Fiona E. Malone, Ellen X. Sun, and Shanna A. Matalon. "Gastrointestinal Imaging." In Core Radiology, 95–228. 2nd ed. Cambridge University Press, 2021. http://dx.doi.org/10.1017/9781108966450.004.

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Harger, Beverly L., Lisa E. Hoffman, and Richard Arkless. "Gastrointestinal Diseases." In Clinical Imaging, 1308–26. Elsevier, 2014. http://dx.doi.org/10.1016/b978-0-323-08495-6.00030-0.

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Schindera, Sebastian T., and William M. Thompson. "Gastrointestinal Lipomas." In Cancer Imaging, 395–97. Elsevier, 2008. http://dx.doi.org/10.1016/b978-012374212-4.50112-7.

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Conference papers on the topic "Gastrointestinal Imaging"

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Park, Jae Myung. "Molecular imaging of gastrointestinal tumors (Conference Presentation)." In 17th International Photodynamic Association World Congress, edited by Tayyaba Hasan. SPIE, 2019. http://dx.doi.org/10.1117/12.2525894.

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Wang, Thomas D. "Clinical Molecular Imaging in the Gastrointestinal Tract." In Biomedical Optics. Washington, D.C.: OSA, 2008. http://dx.doi.org/10.1364/biomed.2008.bsuf4.

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Chen, Xiaodong, Zhi Xu, Hongbo Xie, Dongqing Chen, and Daoyin Yu. "Autofluorescence endoscopy for detecting gastrointestinal cancer." In International Workshop on Photonics and Imaging in Biology and Medicine, edited by Qingming Luo, Britton Chance, and Valery V. Tuchin. SPIE, 2002. http://dx.doi.org/10.1117/12.462524.

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Chen, Yu, Paul R. Herz, Pei-Lin Hsiung, Aaron D. Aguirre, Karl Schneider, James G. Fujimoto, Hiroshi Mashimo, et al. "Ultrahigh-resolution endoscopic optical coherence tomography for gastrointestinal imaging." In Biomedical Optics 2005, edited by Valery V. Tuchin, Joseph A. Izatt, and James G. Fujimoto. SPIE, 2005. http://dx.doi.org/10.1117/12.592609.

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Strupler, Mathias, Martin Poinsinet de Sivry-Houle, Xavier Attendu, Caroline Boudoux, Nicolas Godbout, Camille Crunelle, Joanie Urbain, Chloe Turrell, and Billie Maubois. "Towards combined optical coherence tomography and hyper-spectral imaging for gastrointestinal endoscopy." In Multimodal Biomedical Imaging XIII, edited by Fred S. Azar and Xavier Intes. SPIE, 2018. http://dx.doi.org/10.1117/12.2288772.

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Sagstetter, Ann M., Jon J. Camp, Matthew S. Lurken, Joseph H. Szurszewski, Gianrico Farrugia, Simon J. Gibbons, and Richard A. Robb. "Computer aided classification of cell nuclei in the gastrointestinal tract by volume and principal axis." In Medical Imaging, edited by Maryellen L. Giger and Nico Karssemeijer. SPIE, 2007. http://dx.doi.org/10.1117/12.710274.

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Kim, Christopher Y. "Reevaluation of JPEG image compression to digitalized gastrointestinal endoscopic color images: a pilot study." In Medical Imaging '99, edited by Seong K. Mun and Yongmin Kim. SPIE, 1999. http://dx.doi.org/10.1117/12.349453.

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Publicover, Nelson G., Terence K. Smith, and Randel J. Stevens. "Fluorescence imaging of the propagation of excitability in gastrointestinal muscles." In BiOS '99 International Biomedical Optics Symposium, edited by Darryl J. Bornhop, Christopher H. Contag, and Eva M. Sevick-Muraca. SPIE, 1999. http://dx.doi.org/10.1117/12.351010.

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Georgakopoulos, Spiros V., Dimitris K. Iakovidis, Michael Vasilakakis, Vassilis P. Plagianakos, and Anastasios Koulaouzidis. "Weakly-supervised Convolutional learning for detection of inflammatory gastrointestinal lesions." In 2016 IEEE International Conference on Imaging Systems and Techniques (IST). IEEE, 2016. http://dx.doi.org/10.1109/ist.2016.7738279.

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VM, Murukeshan, N. Sujatha, Ong L. S, and Seah L. K. "Imaging considerations in a fiber optic system for the gastrointestinal endoscopy." In European Conference on Biomedical Optics. Washington, D.C.: OSA, 2003. http://dx.doi.org/10.1364/ecbo.2003.5143_170.

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