Relevant bibliographies by topics / Spectroscoping imaging

Academic literature on the topic 'Spectroscoping imaging'

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Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Spectroscoping imaging"

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Zhu Jiacheng, 朱嘉诚, 陆伟奇 Lu Weiqi, 赵知诚 Zhao Zhicheng, 陈新华 Chen Xinhua, and 沈为民 Shen Weimin. "静止轨道中波红外成像光谱仪分光成像系统." Acta Optica Sinica 41, no. 11 (2021): 1122001. http://dx.doi.org/10.3788/aos202141.1122001.

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Lewis, E. Neil, and Ira W. Levin. "Vibrational Spectroscopic Microscopy: Raman, Near-Infrared and Mid-Infrared Imaging Techniques." Microscopy and Microanalysis 1, no. 1 (February 1995): 35–46. http://dx.doi.org/10.1017/s1431927695110351.

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New instrumental approaches for performing vibrational Raman, near-infrared and mid-infrared spectroscopic imaging microscopy are described. The instruments integrate imaging quality filters such as acousto-optic tunable filters (AOTFs), with visible charge-coupled device (CCD) and infrared focal-plane array detectors. These systems are used in conjunction with infinity-corrected, refractive microscopes for operation in the visible and near-infrared spectral regions and with Cassegrainian reflective optics for operation in the mid-infrared spectral interval. Chemically specific images at moderate spectral resolution (2 nm) and high spatial resolution (1 μm) can be collected rapidly and noninvasively. Image data are presented containing 128 × 128 pixels, although significantly larger format images can be collected in approximately the same time. The instruments can be readily configured for both absorption and reflectance spectroscopies. We present Raman emission images of polystyrene microspheres and a lipid/amino acid mixture and near-infrared images of onion epidermis and a hydrated phospholipid dispersion. Images generated from mid-infrared spectral data are presented for a KBr disk containing nonhomogeneous domains of lipid and for 50-μm slices of monkey cerebellum. These are the first results illustrating the use of infrared focal-plane array detectors as chemically specific spectroscopic imaging devices and demonstrating their application in biomolecular areas. Extensions and future applications of the various vibrational spectroscopic imaging techniques are discussed.
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P. Engler, R. L. Barbour, J. H. Gibson, M. S. Hazle, D. G. Cameron, and R. H. Duff. "Imaging With Spectroscopic Data." Advances in X-ray Analysis 31 (1987): 69–75. http://dx.doi.org/10.1154/s0376030800021856.

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Spectroscopic data from a var iety of analyt ical techniques such as x-ray diffraction (XRD), infrared (IR) and Raman spectroscopies, secondary ion mass spectrometry (SIMS) and energy dispersive X-ray analysis (EDX) can be obtained from small areas of samples (< 1 mm2) through the use of microscope sampling accessories. If provisions are made to scan or translate the sample, then a spectrum that is characteristic of each region of interest can be obtained. Alternatively, selective area detectors eliminate the requirement for scanning the sample. Extract ion of information about a specific energy band from each spectrum allows elucidat ion of the spatial distribution of the feature giving rise to that band. For example, the distribution of a compound could be imaged by extracting the intensity of an IR band or XRD peak due to that compound. Peak posit ion and peak width are other parameters that can be extracted as a function of posit ion. Similarly, elemental distributions could be obtained using SIMS and EDX.
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Catala, Claude, Jacques Baudrand, Torsten Böhm, and Bernard H. Foing. "The Musicos Project: Multi-Site Continuous Spectroscopy." International Astronomical Union Colloquium 137 (1993): 662–64. http://dx.doi.org/10.1017/s0252921100018601.

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Many scientific programs, most of them linked to stellar physics (such as asteroseismology, stellar rotational modulation, surface structures, Doppler imaging, Zeeman-Doppler imaging, variable stellar winds) require a continuous spectroscopic coverage during several days.MUSICOS (for MUlti-SIte COntinuous Spectroscopy) is an international project for setting up a network of high resolution spectrometers coupled to telescopes of the 2m class, well distributed around the world, and partly dedicated to continuous spectroscopy.The strategy to reach this objective was defined during two workshops organized at Paris-Meudon Observatory in 1988 and 1990, and consists of three steps: 1) organize multi-site spectroscopie campaigns using resident instruments on various telescopes around the world and transportable fiber-fed spectrographs where adequate spectroscopie equipment is not available; 2) design and develop a cross-dispersed echelle spectrograph, well suited for the scientific programs that require multi-site observations; 3) propose this MUSICOS spectrograph for duplication at several collaborating sites.
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Voronine, Dmitri V., Zhenrong Zhang, Alexei V. Sokolov, and Marlan O. Scully. "Surface-enhanced FAST CARS: en route to quantum nano-biophotonics." Nanophotonics 7, no. 3 (February 23, 2018): 523–48. http://dx.doi.org/10.1515/nanoph-2017-0066.

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AbstractQuantum nano-biophotonics as the science of nanoscale light-matter interactions in biological systems requires developing new spectroscopic tools for addressing the challenges of detecting and disentangling weak congested optical signals. Nanoscale bio-imaging addresses the challenge of the detection of weak resonant signals from a few target biomolecules in the presence of the nonresonant background from many undesired molecules. In addition, the imaging must be performed rapidly to capture the dynamics of biological processes in living cells and tissues. Label-free non-invasive spectroscopic techniques are required to minimize the external perturbation effects on biological systems. Various approaches were developed to satisfy these requirements by increasing the selectivity and sensitivity of biomolecular detection. Coherent anti-Stokes Raman scattering (CARS) and surface-enhanced Raman scattering (SERS) spectroscopies provide many orders of magnitude enhancement of chemically specific Raman signals. Femtosecond adaptive spectroscopic techniques for CARS (FAST CARS) were developed to suppress the nonresonant background and optimize the efficiency of the coherent optical signals. This perspective focuses on the application of these techniques to nanoscale bio-imaging, discussing their advantages and limitations as well as the promising opportunities and challenges of the combined coherence and surface enhancements in surface-enhanced coherent anti-Stokes Raman scattering (SECARS) and tip-enhanced coherent anti-Stokes Raman scattering (TECARS) and the corresponding surface-enhanced FAST CARS techniques. Laser pulse shaping of near-field excitations plays an important role in achieving these goals and increasing the signal enhancement.
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Pazin, Wallance M., Leonardo N. Furini, Vita Solovyeva, Tibebe Lemma, Rafael J. G. Rubira, Bjarke Jørgensen, Carlos J. L. Constantino, and Jonathan R. Brewer. "Vibrational Spectroscopic Characterization and Coherent Anti-Stokes Raman Spectroscopy (CARS) Imaging of Artepillin C." Applied Spectroscopy 74, no. 7 (April 30, 2020): 751–57. http://dx.doi.org/10.1177/0003702820904456.

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In the following work, the vibrational spectroscopic characteristics of artepillin C are reported by means of Fourier transform infrared (FT-IR) and Raman spectroscopies, surface-enhanced Raman scattering (SERS), and coherent anti-Stokes Raman scattering (CARS) microscopy. Artepillin C is an interesting compound due to its pharmacological properties, including antitumor activity. It is found as the major component of Brazilian green propolis, a resinous mixture produced by bees to protect their hives against intruders. Vibrational spectroscopic techniques have shown a strong peak at 1599 cm−1, assigned to C=C stretching vibrations from the aromatic ring of artepillin C. From these data, direct visualization of artepillin C could be assessed by means of CARS microscopy, showing differences in the film hydration obtained for its neutral and deprotonated states. Raman-based methods show potential to visualize the uptake and action of artepillin C in biological systems, triggering its interaction with biological systems that are needed to understand its mechanism of action.
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Simon, G. T. "Electron Spectroscopic Imaging." Ultrastructural Pathology 11, no. 5-6 (January 1987): 705–10. http://dx.doi.org/10.3109/01913128709048457.

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Meininger, M., P. M. Jakob, M. von Kienlin, D. Koppler, G. Bringmann, and A. Haase. "Radial Spectroscopic Imaging." Journal of Magnetic Resonance 125, no. 2 (April 1997): 325–31. http://dx.doi.org/10.1006/jmre.1997.1124.

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Jansen, J., and B. Blümich. "Stochastic spectroscopic imaging." Journal of Magnetic Resonance (1969) 99, no. 3 (October 1992): 525–32. http://dx.doi.org/10.1016/0022-2364(92)90207-n.

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Czank, Michael, Joachim Mayer, and Ulrich Klein. "Electron Spectroscopic Imaging (ESI): A new method to reveal the existence of nm-scale exsolution lamellae." European Journal of Mineralogy 9, no. 6 (December 2, 1997): 1199–206. http://dx.doi.org/10.1127/ejm/9/6/1199.

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Dissertations / Theses on the topic "Spectroscoping imaging"

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Ross, Amy Psychiatry Faculty of Medicine UNSW. "Longitudinal study of cognitive and functional brain changes in ageing and cerebrovascular disease, using proton magnetic resonance spectroscopy." Awarded by:University of New South Wales. School of Psychiatry, 2005. http://handle.unsw.edu.au/1959.4/27329.

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The neurophysiological basis of cognition changes with age is relatively unexplained, with most studies reporting weak relationships between cognition and measures of brain function, such as event related potentials, brain size and cerebral blood flow. Proton magnetic resonance spectroscopy (1H-MRS) is an in vivo method used to detect metabolites within the brain that are relevant to certain brain processes. Recent studies have shown that these metabolites, in particular N-acetyl aspartate (NAA), which is associated with neuronal viability, correlate with performance on neuropsychological tests or other measures of cognitive function in patients with a variety of cognitive disorders associated with ageing and in normal ageing subjects. We have studied the relationship between metabolites and cognitive function in elderly patients 3 months and 3 years after a stroke or transient ischemic attack (TIA) and in an ageing comparison group. Metabolites were no different between stroke/TIA patients and elderly controls, however, there were significant metabolite differences between stroke/TIA patients with cognitive impairment (Vascular Cognitive Impairment and Vascular Dementia) and those without. Frontal measures of NAA and NAA/Cr predicted cognitive decline over 12 months and 3 years in stroke/TIA patients and elderly controls, and these measures were superior predictors than structural MRI measures. Longitudinal stability of metabolites in ageing over 3 years was associated with stability of cognitive function. The results indicate that 1H-MRS is a useful tool in differentiating stroke/TIA patients with and without cognitive impairment, with possibly superior predictive ability than structural MRI for assessing future cognitive decline. The changes in 1H-MRS that occur with ageing and cognitive decline have implications for the neurophysiological mechanisms and processes that are occurring in the brain, as well as application to clinical diagnosis, the early detection of pathology and the examination of longitudinal change.
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Davidson, David William. "Imaging and spectroscopic radiation detectors." Thesis, University of Glasgow, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.404443.

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Bao, Sumi. "Clinically relevant magnetic resonance imaging and spectroscopic imaging development." Thesis, Massachusetts Institute of Technology, 1999. http://hdl.handle.net/1721.1/9133.

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Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Nuclear Engineering, 1999.
Includes bibliographical references (p. 129-137).
As one result of this thesis, a single slab 3D fast spin echo imaging (3DFSE) method has been implemented and optimized. This involved sequence design and implementation, SAR considerations, parameter adjustments and clinical testing. The method can deliver 3D Tl or T2 weighted brain image with isotropic Imm3 voxel resolution in approximately 10 minutes. The ability to obtain high spatial resolution in reasonable time periods has wide clinical applications such as improvement of treatment planning protocols for brain tumor patients, precise radiotherapy planning, and tissue segmentation for following the progression of diseases like multiple sclerosis. The other part of this thesis is devoted to developing and implementing spectroscopic imaging methods, which include 20 chemical shift imaging(2DCSI) methods, 20 line scan spectroscopic imaging(2D LSSI) methods, spin echo planar spectroscopic imaging(SEPSI) methods and ~ingle shot line scan spin echo planar spectroscopic imaging(SSLSEPSI) method. The former two methods are applied to oil phantoms and bone marrow studies. The SEPSI method can provide simultaneous spectroscopic measurements, R2 and R2' images and field distribution images. A time domain spectral analysis method, LP-HSVD was implemented and applied to spectroscopic imaging studies. The SEPSI method was applied to get lipid characterization of bone marrow as well as to get the R2 and R2' brain images. The SSLSEPSI method can provide instant line spectroscopic imaging which might be useful to image moving objects and can provide high temporal resolution for dynamic studies. With further development, both SEPSI and SSLSEPSI methods may prove useful for trabecular bone studies as well as functional magnetic resonance imaging( tMRI) studies.
by Sumi Bao.
Ph.D.
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Paul, Provakar. "Multipoint spectroscopic analyzing & imaging method." Thesis, Högskolan i Gävle, Avdelningen för elektronik, matematik och naturvetenskap, 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-15274.

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Spectroscopy is a technique as the interaction of different radiation spectrum with matter to analysis of a sample. This thesis work proposed two methods are multiple pointes spectroscopies analyzing then imaging detection methods for solid samples. Developed method one is using Ultraviolet (UV), Visible (Vis) and Infrared (IR) detection. Where detection was assembled with deuterium as well tungsten-halogen lamp source (which were able to generate 175 nm to 3300 nm wavelength), a manual X-Y stepper for scan an inhomogeneous biological sample, optical design beside Indium gallium arsenide (InGaAs) detection unit was used of Lamda 950 by PerkingElmer. Second improved methodology is Vis detection imaging of samples. In Vis detection imaging was constructed with Helium-Neon (HeNe) red laser as a source (able to generate 632.8 nm wavelengths), a silicon pin photodiode detector, lens, multimeter, X-Y positioner stepper motors to scan samples. The work show successfully detected and imaged of water, fresh leaf, brain phantom in addition 3mm horizontal and 1.5 mm vertical cooper line. The thesis works proposed methods has obtained accurate results of all the samples detection specifically has devised imaging of samples. This spectroscopic process is suitable for any type of liquid, solid also gas detecting moreover imaging approach can be applicable in any type of inhomogeneous matter.
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Lau, Condon. "Detecting cervical dysplasia with quantitative spectroscopic imaging." Thesis, Massachusetts Institute of Technology, 2009. http://hdl.handle.net/1721.1/106718.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2009.
Includes bibliographical references.
This thesis extends quantitative spectroscopy, a form of model-based reflectance and fluorescence spectroscopy, from a small area, contact-probe implementation to wide-area quantitative spectroscopic imaging (QSI) for complete coverage of at-risk tissue. QSI uses the scanning virtual probe concept that is critical for model-based spectroscopy and offers spatial resolution advantages over conventional wide-field illumination. We develop a QSI system capable of imaging cervical dysplasia in vivo. Using the QSI system, we conduct a clinical study to train and prospectively evaluate QSI's ability to distinguish high-grade squamous intraepithelial lesions (HSIL) from non-HSILs (less severe conditions) in cervical transformation zone. This is a clinically important distinction because HSIL requires treatment. The results show measuring the per-patient normalized reduced scattering coefficient alone accurately performs the distinction. This is in good agreement with our previous contact-probe study of HSIL. Due to improved accuracy, QSI used as an adjunct to colposcopy can potentially reduce the number of unnecessary biopsies over colposcopy alone. The results also suggest a simplified optical instrument can be used to detect HSIL and this may advance cervical dysplasia detection in developing countries, where cervical cancer mortality is highest.
by Condon Lau.
Ph.D.
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Meng, Jiqun J. "Line scan proton magnetic resonance spectroscopic imaging." Thesis, Massachusetts Institute of Technology, 1995. http://hdl.handle.net/1721.1/36963.

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Forsyth, Robert J. "Spectroscopic and imaging studies of nightglow variations." Thesis, University of Aberdeen, 1989. http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU020230.

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A survey of the literature on the techniques used in and the results obtained from studies of nightglow variability is presented. Three microprocessor controlled instruments (an eight channel tilting filter spectrometer, an earlier six channel version and a CCD based low light level camera) have been constructed with the aim of studying variations in the nightglow, especially of the type associated with the passage of gravity waves through the emitting layers. The final stages of development of the eight channel spectrometer are described, including the design of automatic dark count and reference light systems, a temperature control system for the filters and an interface for transferring the spectrometer data into a computer. Calibration experiments to determine the wavelength, line shape and intensity response of this spectrometer are described. The development of suites of computer programmes for analysing the data from both spectrometers and the camera is then discussed. For the spectrometers, these perform the functions of subtraction of dark count, reduction of the calibration data to a form suitable for use in the analysis of data spectra in terms of a set of line shapes and continuum response functions, and execution of this analysis to produce plots of the emission intensities and OH rotational temperature versus time. For the camera, software was produced to allow separation of stellar images from the airglow emission; stellar image intensities were analysed in an attempt to characterise atmospheric absorption. Software was also written to correct airglow intensities for absorption and the van Rhijn effect and finally to reproject the images in the form of a map of the emitting layer. Observations made with the instruments working separately and in conjunction are described and the results are presented as an example of the performance of the instruments and the software.
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Fernandez, Daniel Celestino. "Fourier-transform infrared spectroscopic imaging of prostate histopathology." [Tampa, Fla.] : University of South Florida, 2003. http://purl.fcla.edu/fcla/etd/SFE0000617.

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Amrania, Hemmel. "Ultrafast Mid-Infrared Spectroscopic Imaging with Biomedical Applications." Thesis, Imperial College London, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.526408.

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Glassford, Stefanie Elizabeth. "Applications of ATR-FTIR spectroscopic imaging to proteins." Thesis, Imperial College London, 2013. http://hdl.handle.net/10044/1/24835.

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Protein aggregation and crystallisation play an important role in the development of biopharmaceuticals and for structural proteomics but both processes are still poorly understood. There is a demand for new methods to screen the extensive range of conditions that promote crystallisation and aggregation as well as provide insight into the behaviour of the proteins. Attenuated Total Reflection (ATR)-Fourier Transform Infrared (FTIR) spectroscopic imaging is a powerful analytical tool which can be applied to study proteins. This technique combines ATR-FTIR spectroscopy with an infrared array detector allowing for both spatial and chemical information to be obtained from the sample. There are a range of imaging fields of view and spatial resolution possible with ATR-FTIR spectroscopic imaging and this presents multiple opportunities for the study of proteins. The purpose of this research was to further develop the application of ATR-FTIR spectroscopic imaging within the field of protein studies. ATR-FTIR imaging has been applied to study the effects of different conditions for microbatch protein crystallisation in a high throughput manner, where many samples can be analysed at the same time on the surface of a Macro ATR crystal by building a wax grid with multiple wells for different samples. Additionally, Micro ATR-FTIR imaging was combined with hanging drop protein crystallisation for high spatial resolution imaging of the growth of protein crystals. The surface properties of Silicon ATR crystals were modified to create a gradient of hydrophobicity allowing the effect of different surface properties on protein adsorption and crystallisation to be studied in situ. The development of these approaches will advance the use of spectroscopic imaging within the field of biopharmaceuticals, where it is has the potential to help the optimisation of both biopharmaceutical drug discovery processes and structural proteomics studies.
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Books on the topic "Spectroscoping imaging"

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Salzer, Reiner, and Heinz W. Siesler, eds. Infrared and Raman Spectroscopic Imaging. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527678136.

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Srinivasan, Gokulakrishnan. Vibrational spectroscopic imaging for biomedical applications. New York: McGraw-Hill, 2010.

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Druy, Mark A., Brown Christopher D, and Richard A. Crocombe. Next-generation spectroscopic technologies III: 5-6 April 2010, Orlando, Florida, United States. Edited by SPIE (Society). Bellingham, Wash: SPIE, 2010.

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Druy, Mark A., Brown Christopher D, and Richard A. Crocombe. Next-generation spectroscopic technologies III: 5-6 April 2010, Orlando, Florida, United States. Edited by SPIE (Society). Bellingham, Wash: SPIE, 2010.

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Md.) Next-Generation Spectroscopic Technologies (Conference) (5th 2013 Baltimore. Next-Generation Spectroscopic Technologies V: 23-24 April 2012, Baltimore, Maryland, United States. Edited by Druy Mark A, Crocombe Richard A, and SPIE (Society). Bellingham, Washington, USA: SPIE, 2012.

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(Society), SPIE, ed. Next-generation spectroscopic technologies II: 13 April 2009, Orlando, Florida, United States. Bellingham, Wash: SPIE, 2009.

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1944-, Denton M. Bonner, and Royal Society of Chemistry (Great Britain), eds. Further developments in scientific optical imaging. Cambridge: Royal Society of Chemistry, 2000.

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Biomedical Topical Meetings (2000 Miami Beach, Fla.). Biomedical Topical Meetings: April 2-5, 2000, Fountainbleau Hilton Resort and Towers, Miami Beach, Florida. Washington, DC: Optical Society of America, 2000.

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Azar, Fred S. Multimodal biomedical imaging III: 19 and 21 January 2008, San Jose, California, USA. Bellingham, Wash: SPIE, 2008.

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Azar, Fred S. Multimodal biomedical imaging V: 23-25 January 2010, San Francisco, California, United States. Edited by SPIE (Society). Bellingham, Wash: SPIE, 2010.

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Book chapters on the topic "Spectroscoping imaging"

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Demuth, J. E., R. J. Hamers, and R. M. Tromp. "Spectroscoping Imaging of Surfaces with Atomic Resolution." In Solvay Conference on Surface Science, 236–43. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-74218-7_22.

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Diem, Max, Melisa J. Romeo, Susie Boydston-White, and Christian Matthäus. "IR Spectroscopic Imaging." In Spectrochemical Analysis Using Infrared Multichannel Detectors, 189–203. Oxford, UK: Blackwell Publishing Ltd, 2007. http://dx.doi.org/10.1002/9780470988541.ch9.

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Hattingen, Elke, and Ulrich Pilatus. "MR Spectroscopic Imaging." In Brain Tumor Imaging, 55–73. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/174_2014_1031.

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Fraser-Miller, Sara J., Jukka Saarinen, and Clare J. Strachan. "Vibrational Spectroscopic Imaging." In Advances in Delivery Science and Technology, 523–89. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-4029-5_17.

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Reimer, Ludwig. "Electron Spectroscopic Imaging." In Springer Series in Optical Sciences, 347–400. Berlin, Heidelberg: Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-540-48995-5_7.

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Eversberg, Thomas, and Klaus Vollmann. "Remarks About Dioptric Imaging Systems." In Spectroscopic Instrumentation, 85–154. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-44535-8_3.

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Engler, P., R. L. Barbour, J. H. Gibson, M. S. Hazle, D. G. Cameron, and R. H. Duff. "Imaging with Spectroscopic Data." In Advances in X-Ray Analysis, 69–75. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-1035-8_7.

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Pelletier, M. J., and C. C. Pelletier. "Spectroscopic Theory for Chemical Imaging." In Raman, Infrared, and Near-Infrared Chemical Imaging, 1–20. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9780470768150.ch1.

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Edkins, Stephen. "Spectroscopic-Imaging STM (SI-STM)." In Visualising the Charge and Cooper-Pair Density Waves in Cuprates, 23–49. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-65975-6_2.

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Lainhart, Janet E., Jason Cooperrider, and June S. Taylor. "Spectroscopic Brain Imaging in Autism." In Imaging the Brain in Autism, 231–88. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-6843-1_9.

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Conference papers on the topic "Spectroscoping imaging"

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Lee, Yeon Ui, Junxiang Zhao, Gary C. H. Mo, Shilong Li, Guangru Li, Qian Ma, Qingqing Yang, Ratnesh Lal, Jin Zhang, and Zhaowei Liu. "Metamaterial assisted cellular imaging using photobleaching kinetics." In Enhanced Spectroscopies and Nanoimaging 2020, edited by Prabhat Verma and Yung Doug Suh. SPIE, 2020. http://dx.doi.org/10.1117/12.2568896.

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Bar, Ilana. "Raman-based point and proximal detection and imaging." In Next-Generation Spectroscopic Technologies XI, edited by Mark A. Druy, Richard A. Crocombe, Steven M. Barnett, Luisa T. Profeta, and Abul K. Azad. SPIE, 2018. http://dx.doi.org/10.1117/12.2304783.

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French, Rebecca, Sylvain Gigan, and Otto L. Muskens. "A speckle-based approach to compressive hyperspectral imaging." In Next-Generation Spectroscopic Technologies XI, edited by Mark A. Druy, Richard A. Crocombe, Steven M. Barnett, Luisa T. Profeta, and Abul K. Azad. SPIE, 2018. http://dx.doi.org/10.1117/12.2303993.

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Wei, Hong. "Photothermal properties of plasmonic nanostructures for modulation and imaging." In Enhanced Spectroscopies and Nanoimaging 2020, edited by Prabhat Verma and Yung Doug Suh. SPIE, 2020. http://dx.doi.org/10.1117/12.2567886.

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Yano, Taka-aki, and Takuo Tanaka. "Multimodal tip-enhanced spectroscopy for nanoscale analysis and imaging." In Enhanced Spectroscopies and Nanoimaging 2020, edited by Prabhat Verma and Yung Doug Suh. SPIE, 2020. http://dx.doi.org/10.1117/12.2569369.

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Jariwala, Deep. "Near-field imaging and spectroscopy of layered excitonic heterostructures." In Enhanced Spectroscopies and Nanoimaging 2020, edited by Prabhat Verma and Yung Doug Suh. SPIE, 2020. http://dx.doi.org/10.1117/12.2569061.

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Zhao, Junxiang, Yeon Ui Lee, Qian Ma, Larousse Khosravi Khorashad, Clara Posner, Guangru Li, Zachary Burns, Jin Zhang, and Zhaowei Liu. "Super-resolution imaging enabled by metamaterial-assisted speckle illumination nanoscopy." In Enhanced Spectroscopies and Nanoimaging 2020, edited by Prabhat Verma and Yung Doug Suh. SPIE, 2020. http://dx.doi.org/10.1117/12.2568829.

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Gao, Hongwen, and Chunmin Zhang. "Throughput of a polarization interference imaging spectrometer in remote sensing." In Next-Generation Spectroscopic Technologies IV. SPIE, 2011. http://dx.doi.org/10.1117/12.883795.

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Bartolomeo, Giovanni Luca, Guillaume Goubert, and Renato Zenobi. "Tip-Enhanced Raman Spectroscopy (TERS) for nanoscale imaging of biological membranes." In Enhanced Spectroscopies and Nanoimaging 2020, edited by Prabhat Verma and Yung Doug Suh. SPIE, 2020. http://dx.doi.org/10.1117/12.2568010.

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Schuck, P. James. "Imaging strain-localized exciton states in 2D semiconductors at room temperature." In Enhanced Spectroscopies and Nanoimaging 2020, edited by Prabhat Verma and Yung Doug Suh. SPIE, 2020. http://dx.doi.org/10.1117/12.2568221.

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Reports on the topic "Spectroscoping imaging"

1

Bhargava, Rohit. Infrared Spectroscopic Imaging for Prostate Pathology. Fort Belvoir, VA: Defense Technical Information Center, March 2008. http://dx.doi.org/10.21236/ada510089.

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Bhargava, Rohit. Infrared Spectroscopic Imaging for Prostate Pathology Practice. Fort Belvoir, VA: Defense Technical Information Center, March 2009. http://dx.doi.org/10.21236/ada503971.

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Barker, Peter B. Proton MR Spectroscopic Imaging in NF-1. Fort Belvoir, VA: Defense Technical Information Center, July 2005. http://dx.doi.org/10.21236/ada443758.

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4

Ho, Wilson. Spectroscopic Imaging of Molecular Functions at Surfaces. Office of Scientific and Technical Information (OSTI), December 2018. http://dx.doi.org/10.2172/1485203.

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5

Bhargava, Rohit. Infrared Spectroscopic Imaging for Prostate Pathology Practice. Fort Belvoir, VA: Defense Technical Information Center, March 2010. http://dx.doi.org/10.21236/ada548847.

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6

Bhargava, Rohit. Infrared Spectroscopic Imaging for Prostate Pathology Practice. Fort Belvoir, VA: Defense Technical Information Center, April 2011. http://dx.doi.org/10.21236/ada548863.

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MacDowell, A. A., T. Warwick, S. Anders, G. M. Lamble, M. C. Martin, W. R. McKinney, and H. A. Padmore. Imaging spectroscopic analysis at the Advanced Light Source. Office of Scientific and Technical Information (OSTI), May 1999. http://dx.doi.org/10.2172/751742.

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Weiss, Paul. Local Optical Spectroscopies for Subnanometer Spatial Resolution Chemical Imaging. Office of Scientific and Technical Information (OSTI), January 2014. http://dx.doi.org/10.2172/1115418.

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Thomas, Michael A. Echo-Planar Imaging Based J-Resolved Spectroscopic Imaging for Improved Metabolite Detection in Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, October 2012. http://dx.doi.org/10.21236/ada567967.

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Thomas, Michael A. Echo-Planar Imaging Based J-Resolved Spectroscopic Imaging for Improved Metabolite Detection in Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, October 2013. http://dx.doi.org/10.21236/ada594378.

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