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Journal articles on the topic 'Transport imaging'

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

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1

Bron, W. E., A. Guerra, and C. Suárez. "Imaging through quasi-particle transport." Optics Letters 21, no. 13 (July 1, 1996): 997. http://dx.doi.org/10.1364/ol.21.000997.

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2

Engquist, Bjorn, and Yunan Yang. "Seismic imaging and optimal transport." Communications in Information and Systems 19, no. 2 (2019): 95–145. http://dx.doi.org/10.4310/cis.2019.v19.n2.a1.

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3

Engquist, Bjorn, and Yunan Yang. "Seismic Imaging and Optimal Transport." Notices of the International Congress of Chinese Mathematicians 8, no. 1 (2020): 27–49. http://dx.doi.org/10.4310/iccm.2020.v8.n1.a3.

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4

Osváth, Szabolcs, Levente Herényi, Gergely Agócs, Katalin Kis Petik, and Miklós S. Z. Kellermayer. "Transport Imaging of Living Cells." Biophysical Journal 110, no. 3 (February 2016): 597a. http://dx.doi.org/10.1016/j.bpj.2015.11.3190.

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5

Komuro, Koshi, Yuya Yamazaki, and Takanori Nomura. "Transport-of-intensity computational ghost imaging." Applied Optics 57, no. 16 (May 23, 2018): 4451. http://dx.doi.org/10.1364/ao.57.004451.

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6

Bal, Guillaume, and Kui Ren. "Transport-Based Imaging in Random Media." SIAM Journal on Applied Mathematics 68, no. 6 (January 2008): 1738–62. http://dx.doi.org/10.1137/070690122.

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7

Chung, Francis J., and John C. Schotland. "Inverse Transport and Acousto-Optic Imaging." SIAM Journal on Mathematical Analysis 49, no. 6 (January 2017): 4704–21. http://dx.doi.org/10.1137/16m1104767.

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8

Haegel, N. M., J. D. Fabbri, and M. P. Coleman. "Direct transport imaging in planar structures." Applied Physics Letters 84, no. 8 (February 23, 2004): 1329–31. http://dx.doi.org/10.1063/1.1650544.

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9

Li, Su, Peichi C. Hu, and Noah Malmstadt. "Imaging Molecular Transport across Lipid Bilayers." Biophysical Journal 101, no. 3 (August 2011): 700–708. http://dx.doi.org/10.1016/j.bpj.2011.06.044.

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10

Wolfe, J. P. "Imaging of excitonic transport in semiconductors." Journal of Luminescence 53, no. 1-6 (July 1992): 327–34. http://dx.doi.org/10.1016/0022-2313(92)90166-7.

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11

MURALIDHAR, K. "Imaging unsteady three-dimensional transport phenomena." Pramana 82, no. 1 (January 2014): 3–14. http://dx.doi.org/10.1007/s12043-013-0638-9.

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12

Li, Su, Peichi Hu, and Noah Malmstadt. "Imaging Molecular Transport Across Lipid Bilayers." Biophysical Journal 102, no. 3 (January 2012): 713a. http://dx.doi.org/10.1016/j.bpj.2011.11.3867.

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13

Sleigh, James N., Alessio Vagnoni, Alison E. Twelvetrees, and Giampietro Schiavo. "Methodological advances in imaging intravital axonal transport." F1000Research 6 (March 1, 2017): 200. http://dx.doi.org/10.12688/f1000research.10433.1.

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Axonal transport is the active process whereby neurons transport cargoes such as organelles and proteins anterogradely from the cell body to the axon terminal and retrogradely in the opposite direction. Bi-directional transport in axons is absolutely essential for the functioning and survival of neurons and appears to be negatively impacted by both aging and diseases of the nervous system, such as Alzheimer’s disease and amyotrophic lateral sclerosis. The movement of individual cargoes along axons has been studied in vitro in live neurons and tissue explants for a number of years; however, it is currently unclear as to whether these systems faithfully and consistently replicate the in vivo situation. A number of intravital techniques originally developed for studying diverse biological events have recently been adapted to monitor axonal transport in real-time in a range of live organisms and are providing novel insight into this dynamic process. Here, we highlight these methodological advances in intravital imaging of axonal transport, outlining key strengths and limitations while discussing findings, possible improvements, and outstanding questions.
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14

Hu, F., Y. Luan, M. E. Scott, J. Yan, D. G. Mandrus, X. Xu, and Z. Fei. "Imaging exciton–polariton transport in MoSe2 waveguides." Nature Photonics 11, no. 6 (May 8, 2017): 356–60. http://dx.doi.org/10.1038/nphoton.2017.65.

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15

Fricker, M. "Imaging techniques in plant transport: meeting review." Journal of Experimental Botany 50, no. 90001 (June 1, 1999): 1089–100. http://dx.doi.org/10.1093/jexbot/50.suppl_1.1089.

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16

West, L. J., D. I. Stewart, A. M. Binley, and B. Shaw. "Resistivity imaging of soil during electrokinetic transport." Engineering Geology 53, no. 2 (June 1999): 205–15. http://dx.doi.org/10.1016/s0013-7952(99)00034-4.

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17

Scott, Erik R., J. Bradley Phipps, and Henry S. White. "Direct Imaging of Molecular Transport Through Skin." Journal of Investigative Dermatology 104, no. 1 (January 1995): 142–45. http://dx.doi.org/10.1111/1523-1747.ep12613661.

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18

Petrasso, R. D., and K. W. Wenzel. "X‐ray imaging of impurity transport (abstract)." Review of Scientific Instruments 61, no. 10 (October 1990): 3144. http://dx.doi.org/10.1063/1.1141710.

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19

Shin, J., V. Meunier, A. P. Baddorf, and S. V. Kalinin. "Nonlinear transport imaging by scanning impedance microscopy." Applied Physics Letters 85, no. 18 (November 2004): 4240–42. http://dx.doi.org/10.1063/1.1812372.

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20

Misgeld, Thomas, Martin Kerschensteiner, Florence M. Bareyre, Robert W. Burgess, and Jeff W. Lichtman. "Imaging axonal transport of mitochondria in vivo." Nature Methods 4, no. 7 (June 10, 2007): 559–61. http://dx.doi.org/10.1038/nmeth1055.

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21

Kim, Arnold D., and Miguel Moscoso. "Radiative transport theory for optical molecular imaging." Inverse Problems 22, no. 1 (December 9, 2005): 23–42. http://dx.doi.org/10.1088/0266-5611/22/1/002.

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22

Smallwood, R. H., Y. F. Mangnall, and A. D. Leathard. "Transport of gastric contents (electric impedance imaging)." Physiological Measurement 15, no. 2A (May 1, 1994): A175—A188. http://dx.doi.org/10.1088/0967-3334/15/2a/023.

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23

Sölder, Elisabeth, Irena Rohr, Christian Kremser, Peter Hutzler, and Paul L. Debbage. "Imaging of placental transport mechanisms: A review." European Journal of Obstetrics & Gynecology and Reproductive Biology 144 (May 2009): S114—S120. http://dx.doi.org/10.1016/j.ejogrb.2009.02.035.

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24

Chhatriwalla, Adnan K., and Daniel J. Rader. "Intracoronary Imaging, Reverse Cholesterol Transport, and Transcriptomics." Journal of the American College of Cardiology 69, no. 6 (February 2017): 641–43. http://dx.doi.org/10.1016/j.jacc.2016.12.003.

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25

Lee, John, Nicholas P. Bertrand, and Christopher J. Rozell. "Unbalanced Optimal Transport Regularization for Imaging Problems." IEEE Transactions on Computational Imaging 6 (2020): 1219–32. http://dx.doi.org/10.1109/tci.2020.3012954.

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26

White, Henry S. "Electrochemical Imaging of Molecular Transport in Skin." Electrochemical Society Interface 12, no. 3 (September 1, 2003): 30–34. http://dx.doi.org/10.1149/2.f07033if.

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27

Larsen, Jannik Bruun, Nayere Taebnia, Alireza Dolatshahi-Pirouz, Anne Zebitz Eriksen, Claudia Hjørringgaard, Kasper Kristensen, Nanna Wichmann Larsen, et al. "Imaging therapeutic peptide transport across intestinal barriers." RSC Chemical Biology 2, no. 4 (2021): 1115–43. http://dx.doi.org/10.1039/d1cb00024a.

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Understanding how pharmaceutical peptides transport across the intestinal barrier could increase their bio-availability. To this end, fluorescence imaging offers a unique combination of spatiotemporal resolution and compatibility with living systems.
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28

Schmölzer, Georg M., Megan O’Reilly, and Po-Yin Cheung. "Noninvasive Monitoring during Interhospital Transport of Newborn Infants." Critical Care Research and Practice 2013 (2013): 1–8. http://dx.doi.org/10.1155/2013/632474.

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The main indications for interhospital neonatal transports are radiographic studies (e.g., magnet resonance imaging) and surgical interventions. Specialized neonatal transport teams need to be skilled in patient care, communication, and equipment management and extensively trained in resuscitation, stabilization, and transport of critically ill infants. However, there is increasing evidence that clinical assessment of heart rate, color, or chest wall movements is imprecise and can be misleading even in experienced hands. The aim of the paper was to review the current evidence on clinical monitoring equipment during interhospital neonatal transport.
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29

Tokunaga, M., and N. Imamoto. "Single molecule imaging of nucleocytoplasmic transport of proteins." Seibutsu Butsuri 41, supplement (2001): S95. http://dx.doi.org/10.2142/biophys.41.s95_1.

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30

Cody, George D., and Robert E. Botto. "Proton NMR imaging of pyridine transport in coal." Energy & Fuels 7, no. 4 (July 1993): 561–62. http://dx.doi.org/10.1021/ef00040a018.

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31

Xiao, Chuanxiao, Chun-Sheng Jiang, John Moseley, John Simon, Kevin Schulte, Aaron J. Ptak, Steve Johnston, et al. "Near-field transport imaging applied to photovoltaic materials." Solar Energy 153 (September 2017): 134–41. http://dx.doi.org/10.1016/j.solener.2017.05.056.

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32

Kaech, S., C.-F. Huang, C. Fang, B. Jenkins, and G. Banker. "Imaging Kinesin-mediated Transport in Cultured Hippocampal Neurons." Microscopy and Microanalysis 16, S2 (July 2010): 1000–1001. http://dx.doi.org/10.1017/s1431927610062513.

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33

Crooker, S. A. "Imaging Spin Transport in Lateral Ferromagnet/Semiconductor Structures." Science 309, no. 5744 (September 30, 2005): 2191–95. http://dx.doi.org/10.1126/science.1116865.

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34

STOTLER, D., B. LABOMBARD, J. TERRY, and S. ZWEBEN. "Neutral transport simulations of gas puff imaging experiments." Journal of Nuclear Materials 313-316 (March 2003): 1066–70. http://dx.doi.org/10.1016/s0022-3115(02)01495-2.

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35

BAL, GUILLAUME, and OLIVIER PINAUD. "IMAGING USING TRANSPORT MODELS FOR WAVE–WAVE CORRELATIONS." Mathematical Models and Methods in Applied Sciences 21, no. 05 (May 2011): 1071–93. http://dx.doi.org/10.1142/s0218202511005258.

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We consider the imaging of objects buried in unknown heterogeneous media. The medium is probed by using classical (e.g. acoustic or electromagnetic) waves. When heterogeneities in the medium become too strong, inversion methodologies based on a microscopic description of wave propagation (e.g. a wave equation or Maxwell's equations) become strongly dependent on the unknown details of the heterogeneous medium. In some situations, it is preferable to use a macroscopic model for a quantity that is quadratic in the wave fields. Here, such macroscopic models take the form of radiative transfer equations also referred to as transport equations. They can model either the energy density of the propagating wave fields or more generally the correlation of two wave fields propagating in possibly different media. In particular, we consider the correlation of the two fields propagating in the heterogeneous medium when the inclusion is absent and present, respectively. We present theoretical and numerical results showing that reconstructions based on this correlation are more accurate than reconstructions based on measurements of the energy density.
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36

Mamonov, Alexander V., and Kui Ren. "Quantitative photoacoustic imaging in the radiative transport regime." Communications in Mathematical Sciences 12, no. 2 (2014): 201–34. http://dx.doi.org/10.4310/cms.2014.v12.n2.a1.

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37

Ward, Adam S., Michael N. Gooseff, and Kamini Singha. "Imaging hyporheic zone solute transport using electrical resistivity." Hydrological Processes 24, no. 7 (March 30, 2010): 948–53. http://dx.doi.org/10.1002/hyp.7672.

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38

Tokunaga, M., and N. Imamoto. "Single molecule imaging of nucleocytoplasmic transport of proteins." Seibutsu Butsuri 40, supplement (2000): S182. http://dx.doi.org/10.2142/biophys.40.s182_1.

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39

Balasubramanian, Kannan, Yuwei Fan, Marko Burghard, Klaus Kern, Marcel Friedrich, Uli Wannek, and Alf Mews. "Photoelectronic transport imaging of individual semiconducting carbon nanotubes." Applied Physics Letters 84, no. 13 (March 29, 2004): 2400–2402. http://dx.doi.org/10.1063/1.1688451.

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40

Waller, Laura, Lei Tian, and George Barbastathis. "Transport of Intensity imaging with higher order derivatives." Optics Express 18, no. 12 (May 27, 2010): 12552. http://dx.doi.org/10.1364/oe.18.012552.

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41

Shi, Wenqing, and Lane A. Baker. "Imaging heterogeneity and transport of degraded Nafion membranes." RSC Advances 5, no. 120 (2015): 99284–90. http://dx.doi.org/10.1039/c5ra20291d.

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Accelerated aging experiments of Nafion® 212 (N212) membranes were carried out. Characterization of degraded N212 membrane samples was performed by microscopy, spectroscopy and electrochemical methods.
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42

Abbott, Carla J., Tiffany E. Choe, Theresa A. Lusardi, Claude F. Burgoyne, Lin Wang, and Brad Fortune. "Imaging axonal transport in the rat visual pathway." Biomedical Optics Express 4, no. 2 (January 30, 2013): 364. http://dx.doi.org/10.1364/boe.4.000364.

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43

Chakraborty, Tonmoy, and Jonathan C. Petruccelli. "Source diversity for transport of intensity phase imaging." Optics Express 25, no. 8 (April 11, 2017): 9122. http://dx.doi.org/10.1364/oe.25.009122.

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44

Vinegar, Harold, and William Rothwell. "4719423 NMR imaging of materials for transport properties." Magnetic Resonance Imaging 6, no. 5 (September 1988): X. http://dx.doi.org/10.1016/0730-725x(88)90174-9.

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45

Enochs, W. S., B. Schaffer, P. G. Bhide, N. Nossiff, M. Papisov, A. Bogdanov, T. J. Brady, and R. Weissleder. "MR Imaging of Slow Axonal Transport in Vivo." Experimental Neurology 123, no. 2 (October 1993): 235–42. http://dx.doi.org/10.1006/exnr.1993.1156.

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46

Le Roux, Lucia G., Xudong Qiu, Megan C. Jacobsen, Mark D. Pagel, Seth T. Gammon, David Piwnica-Worms, and Dawid Schellingerhout. "Axonal Transport as an In Vivo Biomarker for Retinal Neuropathy." Cells 9, no. 5 (May 22, 2020): 1298. http://dx.doi.org/10.3390/cells9051298.

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We illuminate a possible explanatory pathophysiologic mechanism for retinal cellular neuropathy by means of a novel diagnostic method using ophthalmoscopic imaging and a molecular imaging agent targeted to fast axonal transport. The retinal neuropathies are a group of diseases with damage to retinal neural elements. Retinopathies lead to blindness but are typically diagnosed late, when substantial neuronal loss and vision loss have already occurred. We devised a fluorescent imaging agent based on the non-toxic C fragment of tetanus toxin (TTc), which is taken up and transported in neurons using the highly conserved fast axonal transport mechanism. TTc serves as an imaging biomarker for normal axonal transport and demonstrates impairment of axonal transport early in the course of an N-methyl-D-aspartic acid (NMDA)-induced excitotoxic retinopathy model in rats. Transport-related imaging findings were dramatically different between normal and retinopathic eyes prior to presumed neuronal cell death. This proof-of-concept study provides justification for future clinical translation.
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47

Chandra, Subhash. "Imaging transported and endogenous calcium independently at a subcellular resolution: ion microscopy imaging of calcium stable isotopes." Proceedings, annual meeting, Electron Microscopy Society of America 50, no. 2 (August 1992): 1604–5. http://dx.doi.org/10.1017/s0424820100132650.

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Ion microscopy, based on secondary ion mass spectrometry (SIMS), is a unique isotopic imaging technique. The use of stable isotopes as tracers and their SIMS localization at a subcellular resolution has introduced a significant new approach for molecular localization and ion transport studies. A molecule of interest may be tagged with stable 2H, 13C, 15N, etc. and imaged with SIMS for its intracellular location. Stable isotopes of physiologically important elements such as calcium and magnesium provide excellent tracers for ion transport imaging studies with SIMS. in a recent study with 44Ca, the brush border region in the small intestine was observed to be the main barrier for calcium transport from the intestinal lumen to the lamina propria region in chickens suffering from Rickets, a vitamin D-deficiency condition.An example of the use of 44Ca stable isotope for imaging calcium-calcium exchange between the intracellular and extracellular calcium with SIMS is shown in figure 1. 3T3 cells were grown on high purity germanium chips to about 80% confluency.
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48

Harris, J. Aaron, Yi Liu, Pinfen Yang, Peter Kner, and Karl F. Lechtreck. "Single-particle imaging reveals intraflagellar transport–independent transport and accumulation of EB1 in Chlamydomonas flagella." Molecular Biology of the Cell 27, no. 2 (January 15, 2016): 295–307. http://dx.doi.org/10.1091/mbc.e15-08-0608.

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The microtubule (MT) plus-end tracking protein EB1 is present at the tips of cilia and flagella; end-binding protein 1 (EB1) remains at the tip during flagellar shortening and in the absence of intraflagellar transport (IFT), the predominant protein transport system in flagella. To investigate how EB1 accumulates at the flagellar tip, we used in vivo imaging of fluorescent protein–tagged EB1 (EB1-FP) in Chlamydomonas reinhardtii. After photobleaching, the EB1 signal at the flagellar tip recovered within minutes, indicating an exchange with unbleached EB1 entering the flagella from the cell body. EB1 moved independent of IFT trains, and EB1-FP recovery did not require the IFT pathway. Single-particle imaging showed that EB1-FP is highly mobile along the flagellar shaft and displays a markedly reduced mobility near the flagellar tip. Individual EB1-FP particles dwelled for several seconds near the flagellar tip, suggesting the presence of stable EB1 binding sites. In simulations, the two distinct phases of EB1 mobility are sufficient to explain its accumulation at the tip. We propose that proteins uniformly distributed throughout the cytoplasm like EB1 accumulate locally by diffusion and capture; IFT, in contrast, might be required to transport proteins against cellular concentration gradients into or out of cilia.
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49

Wüstner, Daniel, and Daniel Sage. "Multicolor bleach-rate imaging enlightens in vivo sterol transport." Communicative & Integrative Biology 3, no. 4 (July 2010): 370–73. http://dx.doi.org/10.4161/cib.3.4.11972.

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50

Filler, A. G., and B. A. Bell. "Axonal transport, imaging, and the diagnosis of nerve compression." British Journal of Neurosurgery 6, no. 4 (January 1992): 293–95. http://dx.doi.org/10.3109/02688699209023786.

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