@inproceedings{EibenKunzPietrzyketal., author = {Eiben, Bj{\"o}rn and Kunz, Dietmar and Pietrzyk, Uwe and Palm, Christoph}, title = {Level-Set-Segmentierung von Rattenhirn MRTs}, series = {Bildverarbeitung f{\"u}r die Medizin 2009; Algorithmen - Systeme - Anwendungen ; Proceedings des Workshops vom 22. bis 25. M{\"a}rz 2009 in Heidelberg}, booktitle = {Bildverarbeitung f{\"u}r die Medizin 2009; Algorithmen - Systeme - Anwendungen ; Proceedings des Workshops vom 22. bis 25. M{\"a}rz 2009 in Heidelberg}, publisher = {Springer}, address = {Berlin}, pages = {167 -- 171}, abstract = {In dieser Arbeit wird die Segmentierung von Gehirngewebe aus Kopfaufnahmen von Ratten mittels Level-Set-Methoden vorgeschlagen. Dazu wird ein zweidimensionaler, kontrastbasierter Ansatz zu einem dreidimensionalen, lokal an die Bildintensit{\"a}t adaptierten Segmentierer erweitert. Es wird gezeigt, dass mit diesem echten 3D-Ansatz die lokalen Bildstrukturen besser ber{\"u}cksichtigt werden k{\"o}nnen. Insbesondere Magnet-Resonanz-Tomographien (MRTs) mit globalen Helligkeitsgradienten, beispielsweise bedingt durch Oberfl{\"a}chenspulen, k{\"o}nnen auf diese Weise zuverl{\"a}ssiger und ohne weitere Vorverarbeitungsschritte segmentiert werden. Die Leistungsf{\"a}higkeit des Algorithmus wird experimentell an Hand dreier Rattenhirn-MRTs demonstriert.}, subject = {Dreidimensionale Bildverarbeitung}, language = {de} } @misc{BauerStoffelsPauleitetal., author = {Bauer, Dagmar and Stoffels, Gabriele and Pauleit, Dirk and Palm, Christoph and Hamacher, Kurt and Coenen, Heinz H. and Langen, Karl}, title = {Uptake of F-18-fluoroethyl-L-tyrosine and H-3-L-methionine in focal cortical ischemia}, series = {The Journal of Nuclear Medicine}, volume = {47}, journal = {The Journal of Nuclear Medicine}, number = {Suppl. 1}, pages = {284P}, abstract = {Objectives: C-11-methionine (MET) is particularly useful in brain tumor diagnosis but unspecific uptake e.g. in cerebral ischemia has been reported (1). The F-18-labeled amino acid O-(2-[F-18]fluoroethyl)-L-tyrosine (FET) shows a similar clinical potential as MET in brain tumor diagnosis but is applicable on a wider clinical scale. The aim of this study was to evaluate the uptake of FET and H-3-MET in focal cortical ischemia in rats by dual tracer autoradiography. Methods: Focal cortical ischemia was induced in 12 Fisher CDF rats using the photothrombosis model (PT). One day (n=3) , two days (n=5) and 7 days (n=4) after induction of the lesion FET and H-3-MET were injected intravenously. One hour after tracer injection animals were killed, the brains were removed immediately and frozen in 2-methylbutane at -50°C. Brains were cut in coronal sections (thickness: 20 µm) and exposed first to H-3 insensitive photoimager plates to measure FET distribution. After decay of F-18 the distribution of H-3-MET was determined. The autoradiograms were evaluated by regions of interest (ROIs) placed on areas with increased tracer uptake in the PT and the contralateral brain. Lesion to brain ratios (L/B) were calculated by dividing the mean uptake in the lesion and the brain. Based on previous studies in gliomas a L/B ratio > 1.6 was considered as pathological for FET. Results: Variable increased uptake of both tracers was observed in the PT and its demarcation zone at all stages after PT. The cut-off level of 1.6 for FET was exceeded in 9/12 animals. One day after PT the L/B ratios were 2.0 ± 0.6 for FET vs. 2.1 ± 1.0 for MET (mean ± SD); two days after lesion 2.2 ± 0.7 for FET vs. 2.7 ± 1.0 for MET and 7 days after lesion 2.4 ± 0.4 for FET vs. 2.4 ± 0.1 for MET. In single cases discrepancies in the uptake pattern of FET and MET were observed. Conclusions: FET like MET may exhibit significant uptake in infarcted areas or the immediate vincinity which has to be considered in the differential diagnosis of unkown brain lesions. The discrepancies in the uptake pattern of FET and MET in some cases indicates either differences in the transport mechanisms of both amino acids or a different affinity for certain cellular components.}, language = {en} } @article{MatuschDepboyluPalmetal., author = {Matusch, Andreas and Depboylu, Candan and Palm, Christoph and Wu, Bei and H{\"o}glinger, G{\"u}nter U. and Sch{\"a}fer, Martin K.-H. and Becker, Johanna Sabine}, title = {Cerebral bio-imaging of Cu, Fe, Zn and Mn in the MPTP mouse model of Parkinsons disease using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS)}, series = {Journal of the American Society for Mass Spectrometry}, volume = {21}, journal = {Journal of the American Society for Mass Spectrometry}, number = {1}, doi = {10.1016/j.jasms.2009.09.022}, pages = {161 -- 171}, abstract = {Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) has been established as a powerful technique for the determination of metal and nonmetal distributions within biological systems with high sensitivity. An imaging LA-ICP-MS technique for Fe, Cu, Zn, and Mn was developed to produce large series of quantitative element maps in native brain sections of mice subchronically intoxicated with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridin (MPTP) as a model of Parkinson's disease. Images were calibrated using matrix-matched laboratory standards. A software solution allowing a precise delineation of anatomical structures was implemented. Coronal brain sections were analyzed crossing the striatum and the substantia nigra, respectively. Animals sacrificed 2 h, 7 d, or 28 d after the last MPTP injection and controls were investigated. We observed significant decreases of Cu concentrations in the periventricular zone and the fascia dentata at 2 h and 7d and a recovery or overcompensation at 28 d, most pronounced in the rostral periventricular zone (+40\%). In the cortex Cu decreased slightly to -10\%. Fe increased in the interpeduncular nucleus (+40\%) but not in the substantia nigra. This pattern is in line with a differential regulation of periventricular and parenchymal Cu, and with the histochemical localization of Fe, and congruent to regions of preferential MPTP binding described in the rodent brain. The LA-ICP-MS technique yielded valid and statistically robust results in the present study on 39 slices from 19 animals. Our findings underline the value of routine micro-local analytical techniques in the life sciences and affirm a role of Cu availability in Parkinson's disease.}, subject = {ICP-Massenspektrometrie}, language = {en} } @article{BeckerMatuschBeckeretal., author = {Becker, Johanna Sabine and Matusch, Andreas and Becker, Julia Susanne and Wu, Bei and Palm, Christoph and Becker, Albert Johann and Salber, Dagmar}, title = {Mass spectrometric imaging (MSI) of metals using advanced BrainMet techniques for biomedical research}, series = {International Journal of Mass Spectrometry}, volume = {307}, journal = {International Journal of Mass Spectrometry}, number = {1-3}, publisher = {eLSEVIER}, address = {Elsevier}, doi = {10.1016/j.ijms.2011.01.015}, pages = {3 -- 15}, abstract = {Mass spectrometric imaging (MSI) is a young innovative analytical technique and combines different fields of advanced mass spectrometry and biomedical research with the aim to provide maps of elements and molecules, complexes or fragments. Especially essential metals such as zinc, copper, iron and manganese play a functional role in signaling, metabolism and homeostasis of the cell. Due to the high degree of spatial organization of metals in biological systems their distribution analysis is of key interest in life sciences. We have developed analytical techniques termed BrainMet using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) imaging to measure the distribution of trace metals in biological tissues for biomedical research and feasibility studies—including bioaccumulation and bioavailability studies, ecological risk assessment and toxicity studies in humans and other organisms. The analytical BrainMet techniques provide quantitative images of metal distributions in brain tissue slices which can be combined with other imaging modalities such as photomicrography of native or processed tissue (histochemistry, immunostaining) and autoradiography or with in vivo techniques such as positron emission tomography or magnetic resonance tomography. Prospective and instrumental developments will be discussed concerning the development of the metalloprotein microscopy using a laser microdissection (LMD) apparatus for specific sample introduction into an inductively coupled plasma mass spectrometer (LMD-ICP-MS) or an application of the near field effect in LA-ICP-MS (NF-LA-ICP-MS). These nano-scale mass spectrometric techniques provide improved spatial resolution down to the single cell level.}, subject = {Massenspektrometrie}, language = {en} } @article{BeckerMatuschPalmetal., author = {Becker, Johanna Sabine and Matusch, Andreas and Palm, Christoph and Salber, Dagmar and Morton, Kathryn A. and Becker, Julia Susanne}, title = {Bioimaging of metals in brain tissue by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) and metallomics}, series = {Metallomics}, journal = {Metallomics}, number = {2}, publisher = {Oxford Academic Press}, doi = {10.1039/b916722f}, pages = {104 -- 111}, abstract = {Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) has been developed and established as an emerging technique in the generation of quantitative images of metal distributions in thin tissue sections of brain samples (such as human, rat and mouse brain), with applications in research related to neurodegenerative disorders. A new analytical protocol is described which includes sample preparation by cryo-cutting of thin tissue sections and matrix-matched laboratory standards, mass spectrometric measurements, data acquisition, and quantitative analysis. Specific examples of the bioimaging of metal distributions in normal rodent brains are provided. Differences to the normal were assessed in a Parkinson's disease and a stroke brain model. Furthermore, changes during normal aging were studied. Powerful analytical techniques are also required for the determination and characterization of metal-containing proteins within a large pool of proteins, e.g., after denaturing or non-denaturing electrophoretic separation of proteins in one-dimensional and two-dimensional gels. LA-ICP-MS can be employed to detect metalloproteins in protein bands or spots separated after gel electrophoresis. MALDI-MS can then be used to identify specific metal-containing proteins in these bands or spots. The combination of these techniques is described in the second section.}, subject = {ICP-Massenspektrometrie}, language = {en} } @article{OsterholtSalberMatuschetal., author = {Osterholt, Tobias and Salber, Dagmar and Matusch, Andreas and Becker, Johanna Sabine and Palm, Christoph}, title = {IMAGENA: Image Generation and Analysis}, series = {International Journal of Mass Spectrometry}, volume = {307}, journal = {International Journal of Mass Spectrometry}, number = {1-3}, doi = {10.1016/j.ijms.2011.03.010}, pages = {232 -- 239}, abstract = {Metals are involved in many processes of life. They are needed for enzymatic reactions, are involved in healthy processes but also yield diseases if the metal homeostasis is disordered. Therefore, the interest to assess the spatial distribution of metals is rising in biomedical science. Imaging metal (and non-metal) isotopes by laser ablation mass spectrometry with inductively coupled plasma (LA-ICP-MS) requires a special software solution to process raw data obtained by scanning a sample line-by-line. As no software ready to use was available we developed an interactive software tool for Image Generation and Analysis (IMAGENA). Unless optimised for LA-ICP-MS, IMAGENA can handle other raw data as well. The general purpose was to reconstruct images from a continuous list of raw data points, to visualise these images, and to convert them into a commonly readable image file format that can be further analysed by standard image analysis software. The generation of the image starts with loading a text file that holds a data column of every measured isotope. Specifying general spatial domain settings like the data offset and the image dimensions is done by the user getting a direct feedback by means of a preview image. IMAGENA provides tools for calibration and to correct for a signal drift in the y-direction. Images are visualised in greyscale as well a pseudo-colours with possibilities for contrast enhancement. Image analysis is performed in terms of smoothed line plots in row and column direction.}, subject = {ICP-Massenspektrometrie}, language = {en} } @inproceedings{PalmPietrzyk, author = {Palm, Christoph and Pietrzyk, Uwe}, title = {Time-Dependent Joint Probability Speed Function for Level-Set Segmentation of Rat-Brain Slices}, series = {Proceedings of the SPIE Medical Imaging 6914: Image Processing 69143U}, booktitle = {Proceedings of the SPIE Medical Imaging 6914: Image Processing 69143U}, number = {6914}, doi = {10.1117/12.770673}, pages = {69143U-1 -- 69143U-8}, abstract = {The segmentation of rat brain slices suffers from illumination inhomogeneities and staining effects. State-of-the-art level-set methods model slice and background with intensity mixture densities defining the speed function as difference between the respective probabilites. Nevertheless, the overlap of these distributions causes an inaccurate stopping at the slice border. In this work, we propose the characterisation of the border area with intensity pairs for inside and outside estimating joint intensity probabilities. Method - In contrast to global object and background models, we focus on the object border characterised by a joint mixture density. This specifies the probability of the occurance of an inside and an outside value in direct adjacency. These values are not known beforehand, because inside and outside depend on the level-set evolution and change during time. Therefore, the speed function is computed time-dependently at the position of the current zero level-set. Along this zero level-set curve, the inside and outside values are derived as mean along the curvature normal directing inside and outside the object. Advantage of the joint probability distribution is to resolve the distribution overlaps, because these are assumed to be not located at the same border position. Results - The novel time-dependent joint probability based speed function is compared expermimentally with single probability based speed functions. Two rat brains with about 40 slices are segmented and the results analysed using manual segmentations and the Tanimoto overlap measure. Improved results are recognised for both data sets.}, subject = {Kernspintomografie}, language = {en} } @article{DammersAxerGraesseletal., author = {Dammers, J{\"u}rgen and Axer, Markus and Gr{\"a}ßel, David and Palm, Christoph and Zilles, Karl and Amunts, Katrin and Pietrzyk, Uwe}, title = {Signal enhancement in polarized light imaging by means of independent component analysis}, series = {NeuroImage}, volume = {49}, journal = {NeuroImage}, number = {2}, publisher = {Elsevier}, doi = {10.1016/j.neuroimage.2009.08.059}, pages = {1241 -- 1248}, abstract = {Polarized light imaging (PLI) enables the evaluation of fiber orientations in histological sections of human postmortem brains, with ultra-high spatial resolution. PLI is based on the birefringent properties of the myelin sheath of nerve fibers. As a result, the polarization state of light propagating through a rotating polarimeter is changed in such a way that the detected signal at each measurement unit of a charged-coupled device (CCD) camera describes a sinusoidal signal. Vectors of the fiber orientation defined by inclination and direction angles can then directly be derived from the optical signals employing PLI analysis. However, noise, light scatter and filter inhomogeneities interfere with the original sinusoidal PLI signals. We here introduce a novel method using independent component analysis (ICA) to decompose the PLI images into statistically independent component maps. After decomposition, gray and white matter structures can clearly be distinguished from noise and other artifacts. The signal enhancement after artifact rejection is quantitatively evaluated in 134 histological whole brain sections. Thus, the primary sinusoidal signals from polarized light imaging can be effectively restored after noise and artifact rejection utilizing ICA. Our method therefore contributes to the analysis of nerve fiber orientation in the human brain within a micrometer scale.}, subject = {Bildgebendes Verfahren}, language = {en} } @article{PalmAxerGraesseletal., author = {Palm, Christoph and Axer, Markus and Gr{\"a}ßel, David and Dammers, J{\"u}rgen and Lindemeyer, Johannes and Zilles, Karl and Pietrzyk, Uwe and Amunts, Katrin}, title = {Towards ultra-high resolution fibre tract mapping of the human brain}, series = {Frontiers in Human Neuroscience}, volume = {4}, journal = {Frontiers in Human Neuroscience}, doi = {10.3389/neuro.09.009.2010}, pages = {9}, abstract = {Polarised light imaging (PLI) utilises the birefringence of the myelin sheaths in order to visualise the orientation of nerve fibres in microtome sections of adult human post-mortem brains at ultra-high spatial resolution. The preparation of post-mortem brains for PLI involves fixation, freezing and cutting into 100-μm-thick sections. Hence, geometrical distortions of histological sections are inevitable and have to be removed for 3D reconstruction and subsequent fibre tracking. We here present a processing pipeline for 3D reconstruction of these sections using PLI derived multimodal images of post-mortem brains. Blockface images of the brains were obtained during cutting; they serve as reference data for alignment and elimination of distortion artefacts. In addition to the spatial image transformation, fibre orientation vectors were reoriented using the transformation fields, which consider both affine and subsequent non-linear registration. The application of this registration and reorientation approach results in a smooth fibre vector field, which reflects brain morphology. PLI combined with 3D reconstruction and fibre tracking is a powerful tool for human brain mapping. It can also serve as an independent method for evaluating in vivo fibre tractography.}, subject = {Bildgebendes Verfahren}, language = {en} } @inproceedings{SchubertPietrzykReisseletal., author = {Schubert, Nicole and Pietrzyk, Uwe and Reißel, Martin and Palm, Christoph}, title = {Reduktion von Rissartefakten durch nicht-lineare Registrierung in histologischen Schnittbildern}, series = {Bildverarbeitung f{\"u}r die Medizin 2009; Algorithmen - Systeme - Anwendungen; Proceedings des Workshops vom 22. bis 25. M{\"a}rz 2009 in Heidelberg}, booktitle = {Bildverarbeitung f{\"u}r die Medizin 2009; Algorithmen - Systeme - Anwendungen; Proceedings des Workshops vom 22. bis 25. M{\"a}rz 2009 in Heidelberg}, publisher = {Springer}, address = {Berlin}, pages = {410 -- 414}, abstract = {In dieser Arbeit wird ein Verfahren vorgestellt, das Rissartefakte, die in histologischen Rattenhirnschnitten vorkommen k{\"o}nnen, durch nicht-lineare Registrierung reduziert. Um die Optimierung in der Rissregion zu leiten, wird der Curvature Registrierungsansatz um eine Metrik basierend auf der Segmentierung der Bilder erweitert. Dabei erzielten Registrierungen mit der ausschließlichen Segmentierung des Risses bessere Ergebnisse als Registrierungen mit einer Segmentierung des gesamten Hirnschnitts. Insgesamt zeigt sich eine deutliche Verbesserung in der Rissregion, wobei der verbleibende reduzierte Riss auf die Glattheitsbedingungen des Regularisierers zur{\"u}ckzuf{\"u}hren ist.}, subject = {Registrierung }, language = {de} } @article{BeckerZoriyMatuschetal., author = {Becker, Johanna Sabine and Zoriy, Miroslav and Matusch, Andreas and Wu, Bei and Salber, Dagmar and Palm, Christoph and Becker, Julia Susanne}, title = {Bioimaging of Metals by Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS)}, series = {Mass Spectrometry Reviews}, volume = {29}, journal = {Mass Spectrometry Reviews}, doi = {10.1002/mas.20239}, pages = {156 -- 175}, abstract = {The distribution analysis of (essential, beneficial, or toxic) metals (e.g., Cu, Fe, Zn, Pb, and others), metalloids, and non-metals in biological tissues is of key interest in life science. Over the past few years, the development and application of several imaging mass spectrometric techniques has been rapidly growing in biology and medicine. Especially, in brain research metalloproteins are in the focus of targeted therapy approaches of neurodegenerative diseases such as Alzheimer's and Parkinson's disease, or stroke, or tumor growth. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) using double-focusing sector field (LA-ICP-SFMS) or quadrupole-based mass spectrometers (LA-ICP-QMS) has been successfully applied as a powerful imaging (mapping) technique to produce quantitative images of detailed regionally specific element distributions in thin tissue sections of human or rodent brain. Imaging LA-ICP-QMS was also applied to investigate metal distributions in plant and animal sections to study, for example, the uptake and transport of nutrient and toxic elements or environmental contamination. The combination of imaging LA-ICP-MS of metals with proteomic studies using biomolecular mass spectrometry identifies metal-containing proteins and also phosphoproteins. Metal-containing proteins were imaged in a two-dimensional gel after electrophoretic separation of proteins (SDS or Blue Native PAGE). Recent progress in LA-ICP-MS imaging as a stand-alone technique and in combination with MALDI/ESI-MS for selected life science applications is summarized.}, subject = {Bildgebendes Verfahren}, language = {en} } @article{IlgnerPalmSchuetzetal., author = {Ilgner, Justus F. R. and Palm, Christoph and Sch{\"u}tz, Andreas G. and Spitzer, Klaus and Westhofen, Martin and Lehmann, Thomas M.}, title = {Colour Texture Analysis for Quantitative Laryngoscopy}, series = {Acta Otolaryngologica}, volume = {123}, journal = {Acta Otolaryngologica}, doi = {10.1080/00016480310000412}, pages = {730 -- 734}, abstract = {Whilst considerable progress has been made in enhancing the quality of indirect laryngoscopy and image processing, the evaluation of clinical findings is still based on the clinician's judgement. The aim of this paper was to examine the feasibility of an objective computer-based method for evaluating laryngeal disease. Digitally recorded images obtained by 90 degree- and 70 degree-angled indirect rod laryngoscopy using standardized white balance values were made of 16 patients and 19 healthy subjects. The digital images were evaluated manually by the clinician based on a standardized questionnaire, and suspect lesions were marked and classified on the image. Following colour separation, normal vocal cord areas as well as suspect lesions were analyzed automatically using co-occurrence matrices, which compare colour differences between neighbouring pixels over a predefined distance. Whilst colour histograms did not provide sufficient information for distinguishing between healthy and diseased tissues, consideration of the blue content of neighbouring pixels enabled a correct classification in 81.4\% of cases. If all colour channels (red, green and blue) were regarded simultaneously, the best classification correctness obtained was 77.1\%. Although only a very basic classification differentiating between healthy and diseased tissue was attempted, the results showed progress compared to grey-scale histograms, which have been evaluated before. The results document a first step towards an objective, machine-based classification of laryngeal images, which could provide the basis for further development of an expert system for use in indirect laryngoscopy.}, language = {en} } @article{PalmVietenSalberetal., author = {Palm, Christoph and Vieten, Andrea and Salber, Dagmar and Pietrzyk, Uwe}, title = {Evaluation of Registration Strategies for Multi-modality Images of Rat Brain Slices}, series = {Physics in Medicine and Biology}, volume = {54}, journal = {Physics in Medicine and Biology}, number = {10}, doi = {10.1088/0031-9155/54/10/021}, pages = {3269 -- 3289}, abstract = {In neuroscience, small-animal studies frequently involve dealing with series of images from multiple modalities such as histology and autoradiography. The consistent and bias-free restacking of multi-modality image series is obligatory as a starting point for subsequent non-rigid registration procedures and for quantitative comparisons with positron emission tomography (PET) and other in vivo data. Up to now, consistency between 2D slices without cross validation using an inherent 3D modality is frequently presumed to be close to the true morphology due to the smooth appearance of the contours of anatomical structures. However, in multi-modality stacks consistency is difficult to assess. In this work, consistency is defined in terms of smoothness of neighboring slices within a single modality and between different modalities. Registration bias denotes the distortion of the registered stack in comparison to the true 3D morphology and shape. Based on these metrics, different restacking strategies of multi-modality rat brain slices are experimentally evaluated. Experiments based on MRI-simulated and real dual-tracer autoradiograms reveal a clear bias of the restacked volume despite quantitatively high consistency and qualitatively smooth brain structures. However, different registration strategies yield different inter-consistency metrics. If no genuine 3D modality is available, the use of the so-called SOP (slice-order preferred) or MOSOP (modality-and-slice-order preferred) strategy is recommended.}, subject = {Histologie}, language = {en} } @article{AxerAmuntsGraesseletal., author = {Axer, Markus and Amunts, Katrin and Gr{\"a}ßel, David and Palm, Christoph and Dammers, J{\"u}rgen and Axer, Hubertus and Pietrzyk, Uwe and Zilles, Karl}, title = {Novel Approach to the Human Connectome}, series = {NeuroImage}, volume = {54}, journal = {NeuroImage}, number = {2}, doi = {10.1016/j.neuroimage.2010.08.075}, pages = {1091 -- 1101}, abstract = {Signal transmission between different brain regions requires connecting fiber tracts, the structural basis of the human connectome. In contrast to animal brains, where a multitude of tract tracing methods can be used, magnetic resonance (MR)-based diffusion imaging is presently the only promising approach to study fiber tracts between specific human brain regions. However, this procedure has various inherent restrictions caused by its relatively low spatial resolution. Here, we introduce 3D-polarized light imaging (3D-PLI) to map the three-dimensional course of fiber tracts in the human brain with a resolution at a submillimeter scale based on a voxel size of 100 μm isotropic or less. 3D-PLI demonstrates nerve fibers by utilizing their intrinsic birefringence of myelin sheaths surrounding axons. This optical method enables the demonstration of 3D fiber orientations in serial microtome sections of entire human brains. Examples for the feasibility of this novel approach are given here. 3D-PLI enables the study of brain regions of intense fiber crossing in unprecedented detail, and provides an independent evaluation of fiber tracts derived from diffusion imaging data.}, subject = {Bildgebendes Verfahren}, language = {en} } @inproceedings{EibenPalmPietrzyketal., author = {Eiben, Bj{\"o}rn and Palm, Christoph and Pietrzyk, Uwe and Davatzikos, Christos and Amunts, Katrin}, title = {Error Correction using Registration for Blockface Volume Reconstruction of Serial Histological Sections of the Human Brain}, series = {Bildverarbeitung f{\"u}r die Medizin 2010; Algorithmen - Systeme - Anwendungen ; Proceedings des Workshops vom 22. bis 25. M{\"a}rz 2009 in Heidelberg}, booktitle = {Bildverarbeitung f{\"u}r die Medizin 2010; Algorithmen - Systeme - Anwendungen ; Proceedings des Workshops vom 22. bis 25. M{\"a}rz 2009 in Heidelberg}, publisher = {Springer}, address = {Berlin}, pages = {301 -- 305}, abstract = {For accurate registration of histological sections blockface images are frequently used as three dimensional reference. However, due to the use of endocentric lenses the images suffer from perspective errors such as scaling and seemingly relative movement of planes which are located in different distances parallel to the imaging sensor. The suggested correction of those errors is based on the estimation of scaling factors derived from image registration of regions characterized by differing distances to the point of view in neighboring sections. The correction allows the generation of a consistent three dimensional blockface volume.}, subject = {Histologie}, language = {en} } @misc{BeyerWeigertPalmetal., author = {Beyer, Thomas and Weigert, Markus and Palm, Christoph and Quick, Harald H. and M{\"u}ller, Stefan P. and Pietrzyk, Uwe and Vogt, Florian and Martinez, M.J. and Bockisch, Andreas}, title = {Towards MR-based attenuation correction for whole-body PET/MR imaging}, series = {The Journal of Nuclear Medicine}, volume = {47}, journal = {The Journal of Nuclear Medicine}, number = {Suppl. 1}, pages = {384P}, subject = {Kernspintomografie}, language = {en} } @misc{GraesselAxerPalmetal., author = {Gr{\"a}ßel, David and Axer, Markus and Palm, Christoph and Dammers, J{\"u}rgen and Amunts, Katrin and Pietrzyk, Uwe and Zilles, Karl}, title = {Visualization of Fiber Tracts in the Postmortem Human Brain by Means of Polarized Light}, series = {NeuroImage}, volume = {47}, journal = {NeuroImage}, number = {Suppl. 1}, doi = {10.1016/S1053-8119(09)71415-6}, pages = {142}, subject = {Gehirn}, language = {en} } @misc{WeigertBeyerQuicketal., author = {Weigert, Markus and Beyer, Thomas and Quick, Harald H. and Pietrzyk, Uwe and Palm, Christoph and M{\"u}ller, Stefan P.}, title = {Generation of a MRI reference data set for the validation of automatic, non-rigid image co-registration algorithms}, series = {Nuklearmedizin}, volume = {46}, journal = {Nuklearmedizin}, number = {2}, pages = {A116}, subject = {Kernspintomografie}, language = {en} } @article{SouzaJrMendelStrasseretal., author = {Souza Jr., Luis Antonio de and Mendel, Robert and Strasser, Sophia and Ebigbo, Alanna and Probst, Andreas and Messmann, Helmut and Papa, Jo{\~a}o Paulo and Palm, Christoph}, title = {Convolutional Neural Networks for the evaluation of cancer in Barrett's esophagus: Explainable AI to lighten up the black-box}, series = {Computers in Biology and Medicine}, volume = {135}, journal = {Computers in Biology and Medicine}, publisher = {Elsevier}, issn = {0010-4825}, doi = {10.1016/j.compbiomed.2021.104578}, url = {http://nbn-resolving.de/urn:nbn:de:bvb:898-opus4-20126}, pages = {1 -- 14}, abstract = {Even though artificial intelligence and machine learning have demonstrated remarkable performances in medical image computing, their level of accountability and transparency must be provided in such evaluations. The reliability related to machine learning predictions must be explained and interpreted, especially if diagnosis support is addressed. For this task, the black-box nature of deep learning techniques must be lightened up to transfer its promising results into clinical practice. Hence, we aim to investigate the use of explainable artificial intelligence techniques to quantitatively highlight discriminative regions during the classification of earlycancerous tissues in Barrett's esophagus-diagnosed patients. Four Convolutional Neural Network models (AlexNet, SqueezeNet, ResNet50, and VGG16) were analyzed using five different interpretation techniques (saliency, guided backpropagation, integrated gradients, input × gradients, and DeepLIFT) to compare their agreement with experts' previous annotations of cancerous tissue. We could show that saliency attributes match best with the manual experts' delineations. Moreover, there is moderate to high correlation between the sensitivity of a model and the human-and-computer agreement. The results also lightened that the higher the model's sensitivity, the stronger the correlation of human and computational segmentation agreement. We observed a relevant relation between computational learning and experts' insights, demonstrating how human knowledge may influence the correct computational learning.}, subject = {Deep Learning}, language = {en} } @inproceedings{PietrzykBauerVietenetal., author = {Pietrzyk, Uwe and Bauer, Dagmar and Vieten, Andrea and Bauer, Andreas and Langen, Karl-Josef and Zilles, Karl and Palm, Christoph}, title = {Creating consistent 3D multi-modality data sets from autoradiographic and histological images of the rat brain}, series = {IEEE Nuclear Science Symposium Conference Record}, volume = {6}, booktitle = {IEEE Nuclear Science Symposium Conference Record}, doi = {10.1109/NSSMIC.2004.1466754}, pages = {4001 -- 4003}, abstract = {Volumetric representations of autoradiographic and histological images gain ever more interest as a base to interpret data obtained with /spl mu/-imaging devices like microPET. Beyond supporting spatial orientation within rat brains especially autoradiographic images may serve as a base to quantitatively evaluate the complex uptake patterns of microPET studies with receptor ligands or tumor tracers. They may also serve for the development of rat brain atlases or data models, which can be explored during further image analysis or simulation studies. In all cases a consistent spatial representation of the rat brain, i.e. its anatomy and the corresponding quantitative uptake pattern, is required. This includes both, a restacking of the individual two-dimensional images and the exact registration of the respective volumes. We propose strategies how these volumes can be created in a consistent way and trying to limit the requirements on the circumstances during data acquisition, i.e. being independent from other sources like video imaging of the block face prior to cutting or high resolution micro-X-ray CT or micro MRI.}, language = {en} }