Gotowe bibliografie tematyczne / Small animal imaging

Gotowa bibliografia na temat „Small animal imaging”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 13 lutego 2022

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Artykuły w czasopismach na temat "Small animal imaging"

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Lewis, Jason S., S. Achilefu, J. R. Garbow, R. Laforest i M. J. Welch. "Small animal imaging". European Journal of Cancer 38, nr 16 (listopad 2002): 2173–88. http://dx.doi.org/10.1016/s0959-8049(02)00394-5.

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Ntziachristos, Vasilis, Joseph P. Culver, Bradley W. Rice i Special Section Guest Editors. "Small-Animal Optical Imaging". Journal of Biomedical Optics 13, nr 1 (2008): 011001. http://dx.doi.org/10.1117/1.2890838.

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Hutchins, G. D., M. A. Miller, V. C. Soon i T. Receveur. "Small Animal PET Imaging". ILAR Journal 49, nr 1 (1.01.2008): 54–65. http://dx.doi.org/10.1093/ilar.49.1.54.

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de Kemp, R. A., F. H. Epstein, C. Catana, B. M. W. Tsui i E. L. Ritman. "Small-Animal Molecular Imaging Methods". Journal of Nuclear Medicine 51, Supplement_1 (1.05.2010): 18S—32S. http://dx.doi.org/10.2967/jnumed.109.068148.

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Fine, Eugene J., Lawrence Herbst, Linda A. Jelicks, Wade Koba i Daniel Theele. "Small-Animal Research Imaging Devices". Seminars in Nuclear Medicine 44, nr 1 (styczeń 2014): 57–65. http://dx.doi.org/10.1053/j.semnuclmed.2013.08.006.

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Bartling, Soenke, Wolfram Stiller, Wolfhard Semmler i Fabian Kiessling. "Small Animal Computed Tomography Imaging". Current Medical Imaging Reviews 3, nr 1 (1.02.2007): 45–59. http://dx.doi.org/10.2174/157340507779940327.

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PECK, GRAHAM. "Manual of Small Animal Diagnostic Imaging." Journal of Small Animal Practice 36, nr 12 (grudzień 1995): 546. http://dx.doi.org/10.1111/j.1748-5827.1995.tb02808.x.

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Tennant, Bryn. "Small Animal Review". Companion Animal 24, nr 6 (2.06.2019): 286. http://dx.doi.org/10.12968/coan.2019.24.6.286.

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Introduction: Cats showing seizure activity at under 12 months of age are more likely to have primary (structural) epilepsy than idiopathic epilepsy or reactive seizures. Advanced diagnostic imaging is recommended for cats with juvenile-onset seizures once metabolic and toxic causes have been excluded.
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Pomper, M., i J. Lee. "Small Animal Imaging in Drug Development". Current Pharmaceutical Design 11, nr 25 (1.10.2005): 3247–72. http://dx.doi.org/10.2174/138161205774424681.

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FUJII, Hirofumi, Izumi O. UMEDA i Yoshiki KOJIMA. "VIII. Small Animal Imaging Using SPECT". RADIOISOTOPES 57, nr 3 (2008): 219–32. http://dx.doi.org/10.3769/radioisotopes.57.219.

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Rozprawy doktorskie na temat "Small animal imaging"

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Evans, Eleanor. "Improved quantification in small animal PET/MR". Thesis, University of Cambridge, 2015. https://www.repository.cam.ac.uk/handle/1810/252640.

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In translational medicine, complementary functional and morphological imaging techniques are used extensively to observe physiological processes in vivo and to assess structural changes as a result of disease progression. The combination of magnetic resonance imaging (MRI) and positron emission tomography (PET) provides excellent soft tissue contrast from MRI with exceptional sensitivity and specificity from PET. This thesis explores the use of sequentially acquired PET and MR images to improve the quantification of small animal PET data. The primary focus was to improve image-based estimates of the arterial input function (AIF), which defines the amount of PET tracer within blood plasma over time. The AIF is required to produce physiological parameters quantifying key processes such as metabolism or perfusion from dynamic PET images. The gold standard for AIF measurement, however, requires serial blood sampling over the course of a PET scan, which is invasive in rat studies but prohibitive in mice due to small total blood volumes. To address this issue, the geometric transfer matrix (GTM) and recovery coefficient (RC) techniques were applied using anatomical MR images to enable the extraction of partial volume corrected image based AIFs from mouse PET images. A non-invasive AIF extraction method was also developed for rats, beginning with the optimization of an automated voxel selection algorithm to assist in extracting MR contrast agent signal time courses from dynamic susceptibility contrast (DSC) MRI data. This procedure was then combined with dynamic contrast enhanced (DCE) MRI to track a combined injection of Gadolinium-based contrast agent and PET tracer through the rat brain. By comparison with gold standard tracer blood sample data, it was found that normalized MRI-based AIFs could be successfully converted into PET tracer AIFs in the first pass phase when fitted with gamma variate functions. Finally, a MR image segmentation method used to provide PET attenuation correction in mice was validated using the Cambridge split magnet PET/MR scanner?s transmission scanning capabilities. This work recommends that contributions from MR hardware in the PET field of view must be accounted forto gain accurate estimates of tracer uptake and standard uptake values (SUVs). This thesis concludes that small animal MR data taken in the same imaging session can provide non-invasive methods to improve PET image quantification, giving added value to combined PET/MR studies over those conducted using PET alone.
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Weisenberger, Andrew Gerard. "Gamma-ray imaging detector for small animal research". W&M ScholarWorks, 1998. https://scholarworks.wm.edu/etd/1539623944.

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A novel radiation imaging technology for in vivo molecular imaging in small mammals is described. The goal of this project is to develop a new type of imaging detector system suitable for real-time in vivo probe imaging studies in small animals. This technology takes advantage of the gamma-ray and x-ray emission properties of the radioisotope iodine 125 (125I) which is employed as the label for molecular probes. The radioisotope 125I is a gamma-ray emitting radioisotope that can be commercially obtained already attached to biomedically interesting molecules to be used as tracers for biomedical and molecular biology research.;The isotope 125I decays via electron capture consequently emitting a 35 keV gamma-ray followed by the near coincident emission of several 27--32 keV Kalpha and Kbeta shell x-rays. Because of these phenomena, a coincidence condition can be set to detect 125I thus enabling the reduction of any background radiation that could contaminate the image. The detector system is based on an array of CsI(Na) crystal scintillators coupled to a 125 mm diameter position sensitive photomultiplier tube. An additional standard 125 mm diameter photomultiplier tube coupled to a NaI(Tl) scintillator acts as the coincident detector. to achieve high resolution images the detector system utilizes a custom-built copper laminate high resolution collimator. The 125I detector system can achieve a spatial resolution of less than 2 mm FWHM for an object at a distance of 1.5 cm from the collimator. The measured total detector sensitivity while using the copper collimator was 68 cpm/muCi.;Results of in vivo mouse imaging studies of the biodistribution of iodine, melatonin, and a neurotransmitter analog (RTI-55) are presented. Many studies in molecular biology deal with following the expression and regulation of a gene at different stages of an organism's development or under different physiological conditions. This detector system makes it possible for laboratories without access to standard nuclear medicine radiopharmaceuticals to perform in vivo imaging research on small a mammals using a whole range of 125I labeled markers that are obtainable from commercial sources.
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Larsson, Daniel. "Small-Animal Imaging with Liquid-Metal-Jet X-Ray Sources". Doctoral thesis, KTH, Biomedicinsk fysik och röntgenfysik, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-163169.

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Small-animal x-ray imaging is an important tool for medical research. The penetration power of x-rays makes it possible to investigate the 3D structure of small animals and other thick biological samples by computed tomography (CT). However, small-animal x-ray imaging often requires high resolution due to the small structures involved, and short exposure times due to sample movement. This constitutes a challenge, since these two properties require compact x-ray sources with parameters that are not widely available. In this Thesis we present the first application of liquid-metal-jet sources for small-animal imaging. This source concept was invented at KTH just over ten years ago. The use of a high-speed metal jet as electron-beam target, instead of a solid anode, enables higher x-ray flux while maintaining a small x-ray spot for high-resolution imaging. In the present work, a liquid-metal jet source with a higher-energy spectrum has been developed. It has stronger 24 keV radiation compared to previous sources, which makes it more suitable for imaging of small animals and other few-cm-thick objects, which require the higher penetration of 20-35 keV x-rays. We have applied the liquid-metal-jet x-ray sources for whole-body imaging of sacrificed mice and zebrafish. With high-resolution absorption-contrast CT we have visualized fine bone details of mice. We have also used phase contrast, a new method that can considerably improve imaging of, e.g., soft tissue, for demarcation of mm-sized tumors inside a full mouse and for mouse cartilage imaging. In zebrafish imaging, we have exploited the greatly enhanced contrast of phase-imaging to resolve single muscle fibers (and possibly even myofibrils) in whole zebrafish in a laboratory setting for the first time. The muscle structures have diameters in the 5-7 μm range and extremely low contrast, which makes them difficult to observe. With phase contrast, we have demonstrated low-dose and high-resolution angiography of mouse and rat organs and tissues ex vivo. We show detection of blood vessels with diameters below 10 μm with radiation doses compatible with living small animals, which is not possible with absorption contrast and iodinated contrast agents. In addition, we have investigated the vascular network of tumors in mouse ears and visualized the chaotic arrangement of newly-formed blood vessels. Finally, we present the first results from a new high-power liquid-metal-jet x-ray source prototype, operating at 10× the power of our previous sources, with the same x-ray spot size. This source constitutes an important step towards future in-vivo small-animal laboratory imaging with high resolution.
Röntgenavbildning av små försöksdjur är en viktig metod inom medicinsk forskning. Röntgenstrålar penetrerar material, vilket gör det möjligt att undersöka 3D-strukturen hos försöksdjur och andra tjocka biologiska prov med hjälp av datortomografi (CT). Tyvärr kräver smådjursavbildning ofta dels hög upplösning, eftersom de relevanta strukturerna är små, dels korta exponeringstider, eftersom objektet tenderar att röra sig. Detta är en utmaning, då båda egenskaperna kräver kompakta röntgenkällor med speciella egenskaper som inte är brett tillgängliga. I denna avhandling visar vi den första användningen av metallstråleröntgenkällor för avbildning av hela smådjur. Den här typen av röntgenkälla uppfanns vid KTH för drygt tio år sedan. Genom att låta elektronerna träffa en stråle av flytande metall, istället för en solid metallanod, kan vi generera mer röntgenstrålning men samtidigt behålla en liten källpunkt, vilket behövs för avbildning med hög upplösning. En ny metallstrålekälla utvecklades som en del av denna avhandling. Den ger ett röntgenspektrum med högre energier, vilket gör källan mer lämpad än tidigare källor för avbildning av små försöksdjur och andra centimetertjocka biologiska objekt. Vi har använt metallstrålekällor för att avbilda intakta, avlivade möss och zebrafiskar. Med högupplöst absorptions-CT har vi detekterat små bendetaljer inuti möss. Vi har även använt faskontrastavbildning, en ny metod som avsevärt kan förbättra avbildning av mjukvävnad, till att demarkera millimeterstora tumörer inuti en hel mus, samt för avbildning av brosk i leder hos möss. Faskontrast ger en kraftig förstärkning av kontrasten i bilden, vilket även har använts för att för första gången detektera individuella muskelfibrer (och eventuellt även myofibriller) inuti zebrafiskar med en kompakt röntgenkälla. Muskelstrukturerna har diametrar på 5-7 μm och låg kontrast, vilket gör dem svåra att observera. Med hjälp av faskontrast har vi utvecklat en metod för att avbilda blodkärl med diametrar under 10 μm inuti organ och vävnader från möss och råttor ex vivo, med stråldoser som är kompatibla med studier av levande smådjur. Detta är inte möjligt med konventionell absorptionskontrast och jod-baserade kontrastmedel. Vi har dessutom avbildat nyformade blodkärl kring tumörer i musöron och observerat kärlens kaotiska struktur. Slutligen presenterar vi de första resultaten från en prototyp av en ny högeffektskälla. Källan har tio gånger högre effekt än tidigare metallstrålekällor, men bibehåller samma storlek på källpunkten. Den här högeffektskällan är ett viktigt steg mot framtida laboratoriebaserad avbildning av levande små försöksdjur med hög upplösning.

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Qian, Jianguo. "A versatile imaging system for in vivo small animal research". W&M ScholarWorks, 2008. https://scholarworks.wm.edu/etd/1539623532.

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In vivo small animal imaging has become an essential technique for molecular biology studies. However, requirements of spatial resolution, sensitivity and image quality are quite challenging for the development of small-animal imaging systems. The capabilities of the system are also significant for carrying out small animal imaging in a wide range of biological studies. The goal of this dissertation is to develop a high-performance imaging system that can readily meet a wide range of requirements for a variety of small animal imaging applications. Several achievements have been made in order to fulfill this goal.;To supplement our system for parallel-hole single photon emission computed tomography (SPECT) based upon a 110 mm diameter circular detector, we have developed novel compact gamma cameras suitable for imaging an entire mouse. These gamma cameras facilitate multi-head (>2) parallel-hole SPECT with the mouse in close proximity to the detector face in order to preserve spatial resolution. Each compact gamma cameras incorporates pixellated Nal(Tl) scintillators and a pair of Hamamatsu H8500 position sensitive photomultiplier tubes (PSPMTs). Two types of copper-beryllium parallel-hole collimators have been designed. These provide high-sensitivity imaging of I-125 or excellent spatial resolution over a range of object-detector distances. Both phantom and animal studies have demonstrated that these gamma cameras perform well for planar scintigraphy and parallel-hole SPECT of mice.;To further address the resolution limitations in parallel-hole SPECT and the sensitivity and limited field of view of single-pinhole SPECT, we have developed novel multipinhole helical SPECT based upon a 110 mm diameter circular detector equipped with a pixellated Nal(Tl) scintillator array. A brass collimator has been designed and produced containing five 1 mm diameter pinholes. Results obtained in SPECT studies of various phantoms show an enlarged field of view, very good resolution and improved sensitivity using this new imaging technique.;These studies in small-animal imaging have been applied to in vivo biological studies related to human health issues including studies of the thyroid and breast cancer. A re-evaluation study of potassium iodide blocking efficiency in radioiodine uptake in mice suggests that the FDA-recommended human dose of stable potassium iodide may not be sufficient to effectively protect the thyroid from radioiodine contamination. Another recent study has demonstrated that multipinhole helical SPECT can resolve the fine structure of the mouse thyroid using a relatively low dose (200 muCi). Another preclinical study has focused on breast tumor imaging using a compact gamma camera and an endogenous reporter gene. In that ongoing study, mammary tumors are imaged at different stages. Preliminary results indicate different functional patterns in the uptake of radiotracers and their potential relationship with other tumor parameters such as tumor size.;In summary, we have developed a versatile imaging system suitable for in vivo small animal research as evidenced by a variety of applications. The modular construction of this system will allow expansion and further development as new needs and new opportunities arise.
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Terrin, Massimo. "Micro-CT for small animal imaging : Optimization of the tube voltage for low-contrast imaging". Thesis, KTH, Skolan för teknik och hälsa (STH), 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-176482.

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This master thesis evaluated the optimal tube voltage for low-contrast imaging of a micro-CT system (intended for small animal imaging) built at the School of Technology and Health (STH) of the Royal Institute of Technology (KTH). The main goal of this work was to calibrate the above-mentioned device (composed moreover by a Hamamatsu microfocus L10951-01 X-ray tube, a CMOS flat panel Hamamatsu C7942CA-22 and using a Cone-Beam CT reconstruction algorithm) for obtaining the best imaging of low-contrast structures. In order to do this, an analytical model, re-adapted from the previous state-of-the-art Micro-CT studies, was evaluated for finding a sub-optimal tube voltage from which to start the experiments, done on a reference Low-Contrast phantom specifically intended for the calibration of Micro-CT devices.  Finally, by looking to the results from the experiments, a good tube setting for the optimization of the CT for low-contrast imaging was found. The optimal tube voltage for low-contrast imaging, from the experiments on the QRM phantom, was found to be between 48 and 50 kV. This tube voltage values gave the best CNR and contrast profiles results.  Ultimately, we found that the usage of a 1mm Al filtration reduced the absorbed dose without affecting the image quality.
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Manivannan, Niranchana. "Use of Multiple Imaging Views for Improving Image Quality in Small Animal MR Imaging Studies". The Ohio State University, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=osu1436753010.

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Daibes, Figueroa Said. "Discrete NaI(TI) crystal detector optimization for small animal SPECT molecular imaging". Diss., Columbia, Mo. : University of Missouri-Columbia, 2005. http://hdl.handle.net/10355/5821.

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Thesis (Ph.D.)--University of Missouri-Columbia, 2005.
The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical general description, or public abstract, appears in the public.pdf file. Title from title screen of research.pdf file viewed on (November 15, 2006) Vita. Includes bibliographical references.
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Kujala, Naresh Gandhi Yu Ping. "Frequency domain fluorescent molecular tomography and molecular probes for small animal imaging". Diss., Columbia, Mo. : University of Missouri--Columbia, 2009. http://hdl.handle.net/10355/7021.

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Title from PDF of title page (University of Missouri--Columbia, viewed on Feb 26, 2010). The entire thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file; a non-technical public abstract appears in the public.pdf file. Dissertation advisor: Dr. Ping Yu. Vita. Includes bibliographical references.
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Cooper, Reynold James. "Performance of the SmartPET Positron Emission Tomography System for Small Animal Imaging". Thesis, University of Liverpool, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.491374.

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The experimental results presented in this study demonstrate the performance of a prototype Positron Emission Tomography system utilising planar HPGe detector technology. The experimental measurements undertaken provide evidence of the feasibility of such a system for small animal imaging. It has been shown how the use of digital Pulse Shape Analysis techniques may be employed in order to improve the achievable image quality. By performing high precision scans of one the SmartPET HPGe detectors with finely collimated gamma-ray beams at a range of energies the performance and response of the detector as a function of gamma-ray interaction position has been quantified. This analysis has facilitated the development of parametric Pulse Shape Analysis techniques and algorithms for the correction of imperfections in detector response. These algorithms have then been applied to data from PET imaging measurements using both SmartPET detectors in conjunction with the specially designed rotating gantry. A number of point sources have been imaged and it has been shown how, when using simple PSA approaches, the nature of an event has direct implications for the quality of the resulting image. Over 60% of coincident events from 511keV gamma rays have been processed in imaging these point sources, increasing the imaging sensitivity by a factor of three in comparison to previous work. The absolute detection sensitivity of the SmartPET system has been found to be 0.99%. The SmartPET system has been used to image distributed sources for the first time. A 22Na line source was imaged in a number of different orientations and reconstructed with a spatial resolution approaching the fundamental limitations imposed by gamma-ray non-colinearity and positron range blurring. Increasingly complex source distributions have been imaged, demonstrating the ability of the system to resolve multiple features with fine spatial resolution. These measurements then allowed the current limitations of the system to be identified. Supplied by The British Library - 'The world's knowledge'
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Valastyán, Iván. "Software Solutions for Nuclear Imaging Systems in Cardiology, Small Animal Research and Education". Doctoral thesis, KTH, Medicinsk teknik, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-12069.

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The sensitivity for observing physiological processes makes nuclear imaging an important tool in medical diagnostics. Different types of nuclear imaging modalities, with emphasis on the software components and image reconstructions, are presented in this thesis:  the Cardiotom for myocardial heart studies at the Karolinska University Hospital, the small animal Positron Emission Tomograph (PET) scanners for research and the SPECT, PET, spiral CT and Cardiotom demonstrators for the Royal Institute of Technology medical imaging laboratory. A modular and unified software platform has been developed for data representation, acquisition, visualization, reconstruction and presentation of the programs of the imaging devices mentioned above. The high performance 3D ML-EM and OS-EM iterative image reconstruction methods are implemented both on Cardiotom and miniPET scanners. As a result, the in-slice resolution of the first two prototypes of the Cardiotom today is the same as the formerly used filtered back-projection, however the in-depth resolution is considerably increased. Another improvement due to the new software is the shorter time that is required for data acquisition and image reconstruction. The new electronics with the newly developed software ensure images for medical diagnosis within 10 minutes from the start ofthe examination. The first system from the standardized production of the Cardiotom cameras is in the test phase. The performance parameters (sensitivity, spatial and energy resolution, coincidence time resolution) of the full ring mini PET camera are comparable to other small animal PETsystems.
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Książki na temat "Small animal imaging"

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Kiessling, Fabian, Bernd J. Pichler i Peter Hauff, red. Small Animal Imaging. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-42202-2.

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Kiessling, Fabian, i Bernd J. Pichler, red. Small Animal Imaging. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-12945-2.

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Kupinski, Matthew A., i Harrison H. Barrett, red. Small-Animal Spect Imaging. Boston, MA: Springer US, 2005. http://dx.doi.org/10.1007/b107067.

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Kagadis, George C., Nancy L. Ford, Dimitrios N. Karnabatidis i George K. Loudos, red. Handbook of Small Animal Imaging. Boca Raton: Taylor & Francis, 2016. | Series: Imaging in medical diagnosis and therapy: CRC Press, 2018. http://dx.doi.org/10.1201/9781315373591.

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Gavin, Patrick R. Practical small animal MRI. Ames, Iowa: Wiley-Blackwell, 2009.

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Elliott, Ian. Handbook of small animal MRI. Chichester, West Sussex, U.K: Wiley-Blackwell, 2010.

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Elliott, Ian. Handbook of small animal MRI. Chichester, West Sussex, U.K: Wiley-Blackwell, 2010.

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Ayers, Mary H. Small animal radiographic techniques and positioning. Chichester, West Sussex, UK: Wiley-Blackwell, 2012.

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Lackas, Christian. Advanced methods in multiplexing multi-pinhole imaging: Design and implementation of a high-resolution and high-sensitivity small-animal SPECT imaging system. Jülich: Forschungszentrum Jülich, Zentralbibliothek, 2006.

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Zaidi, Habib, red. Molecular Imaging of Small Animals. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-0894-3.

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Części książek na temat "Small animal imaging"

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Schulz, Ralf B., i Vasilis Ntziachristos. "Optical Imaging". W Small Animal Imaging, 267–79. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-12945-2_20.

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Alves, Frauke, Julia Bode, Peter Cimalla, Ingrid Hilger, Martin Hofmann, Volker Jaedicke, Edmund Koch i in. "Optical Imaging". W Small Animal Imaging, 403–90. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-42202-2_16.

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Waerzeggers, Yannic, Bastian Zinnhardt, Alexandra Winkeler, Parisa Monfared, Sonja Schelhaas, Thomas Viel i Andreas H. Jacobs. "Imaging in Neurooncology". W Small Animal Imaging, 689–725. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-42202-2_28.

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Schiffer, Wynne K. "Imaging in Neurology Research III: Focus on Neurotransmitter Imaging". W Small Animal Imaging, 515–41. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-12945-2_34.

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Hein, Marc, Anna B. Roehl i René H. Tolba. "Animal Anesthesia and Monitoring". W Small Animal Imaging, 83–91. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-12945-2_7.

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Henriksen, Gjermund, i Alexander Drzezga. "Imaging in Neurology Research II: PET Imaging of CNS Disorders". W Small Animal Imaging, 499–513. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-12945-2_33.

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Brom, M., W. A. Eter, I. van der Kroon, S. M. A. Willekens, A. Eek, M. Boss, M. Buitinga i M. Gotthardt. "Beta Cell Imaging as Part of “Imaging on Metabolic Diseases”". W Small Animal Imaging, 605–25. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-42202-2_24.

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Vandoorne, Katrien, Stav Sapoznik, Tal Raz, Inbal Biton i Michal Neeman. "Imaging in Developmental Biology". W Small Animal Imaging, 417–36. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-12945-2_29.

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Laschke, Matthias W., i Michael D. Menger. "Imaging in Gynecology Research". W Small Animal Imaging, 437–47. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-12945-2_30.

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Schäfers, Michael, Klaus Tiemann, Michael Kuhlmann, Lars Stegger, Klaus Schäfers i Sven Hermann. "Imaging in Cardiovascular Research". W Small Animal Imaging, 449–71. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-12945-2_31.

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Streszczenia konferencji na temat "Small animal imaging"

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MILLER, M. A., N. C. ROUZE i G. D. HUTCHINS. "SMALL ANIMAL PET IMAGING". W Proceedings of the 8th Conference. WORLD SCIENTIFIC, 2004. http://dx.doi.org/10.1142/9789812702708_0057.

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Jian-Hung Liu, Geng-Shi Jeng, Tung-Ke Wu i Pai-Chi Li. "ECG Gated Ultrasonic Small Animal Imaging". W 2005 IEEE Engineering in Medicine and Biology 27th Annual Conference. IEEE, 2005. http://dx.doi.org/10.1109/iembs.2005.1616787.

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Loudos, George K., Carlos Granja, Claude Leroy i Ivan Stekl. "Advances in Small Animal Imaging Systems". W Nuclear Physics Medthods and Accelerators in Biology and Medicine. AIP, 2007. http://dx.doi.org/10.1063/1.2825762.

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Leavesley, Silas, Yanan Jiang, Valery Patsekin, Heidi Hall, Douglas Vizard i J. Paul Robinson. "Hyperspectral small animal fluorescence imaging: spectral selection imaging". W Biomedical Optics (BiOS) 2008, redaktorzy Fred S. Azar i Xavier Intes. SPIE, 2008. http://dx.doi.org/10.1117/12.763935.

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Ford, Nancy L., Michael M. Thornton i David W. Holdsworth. "Noise limitations for small-animal microcomputed tomography". W Medical Imaging 2002, redaktorzy Larry E. Antonuk i Martin J. Yaffe. SPIE, 2002. http://dx.doi.org/10.1117/12.465578.

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Wilson, Emmanuel, Chris Chiodo, Kenneth H. Wong, Stanley Fricke, Mira Jung i Kevin Cleary. "Robotically assisted small animal MRI-guided mouse biopsy". W SPIE Medical Imaging. SPIE, 2010. http://dx.doi.org/10.1117/12.845566.

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Hyman, Alexandra, Lingling Zhao i Xavier Intes. "Multi-modal Imaging Cassette for Small Animal Molecular Imaging". W 2013 39th Annual Northeast Bioengineering Conference (NEBEC). IEEE, 2013. http://dx.doi.org/10.1109/nebec.2013.25.

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Chatziioannou, Arion F., Qinan Bao i N. Karakatsanis. "System sensitivity in preclinical small animal imaging". W 2008 5th IEEE International Symposium on Biomedical Imaging (ISBI 2008). IEEE, 2008. http://dx.doi.org/10.1109/isbi.2008.4541272.

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Bal, Girish, Paul D. Acton, Floris Jansen i Bruce H. Hasegawa. "Revolving multipinhole SPECT for small animal imaging". W 2008 IEEE Nuclear Science Symposium and Medical Imaging conference (2008 NSS/MIC). IEEE, 2008. http://dx.doi.org/10.1109/nssmic.2008.4774511.

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Stolin, Alexander, Donald Pole, Randolph Wojcik i Mark B. Williams. "Dual-modality scanner for small animal imaging". W 2006 IEEE Nuclear Science Symposium Conference Record. IEEE, 2006. http://dx.doi.org/10.1109/nssmic.2006.354397.

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