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        <title>BioMedical Engineering OnLine - Most accessed articles</title>
        <link>http://www.biomedical-engineering-online.com</link>
        <description>The most accessed research articles published by BioMedical Engineering OnLine</description>
        <dc:date>2010-02-28T00:00:00Z</dc:date>
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                                <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/9/1/14" />
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                                <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/9/1/6" />
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        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/14">
        <title>A novel method for blood vessel detection from retinal images</title>
        <description>Background:
The morphological changes of the retinal blood vessels in retinal images are important indicators for diseases like diabetes, hypertension and glaucoma. Thus the accurate segmentation of blood vessel is of diagnostic value.
Methods:
In this paper, we present a novel method to segment retinal blood vessels to overcome the variations in contrast of large and thin vessels. This method uses adaptive local thresholding to produce a binary image then extract large connected components as large vessels. The residual fragments in the binary image including some thin vessel segments (or pixels), are classified by Support Vector Machine (SVM). The tracking growth is applied to the thin vessel segments to form the whole vascular network.
Results:
The proposed algorithm is tested on DRIVE database, and the average sensitivity is over 77% while the average accuracy reaches 93.2%.
Conclusions:
In this paper, we distinguish large vessels by adaptive local thresholding for their good contrast. Then identify some thin vessel segments with bad contrast by SVM, which can be lengthened by tracking. This proposed method can avoid heavy computation and manual intervention.</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/14</link>
                <dc:creator>Lili Xu</dc:creator>
                <dc:creator>Shuqian Luo</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:14</dc:source>
        <dc:date>2010-02-28T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-14</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>14</prism:startingPage>
        <prism:publicationDate>2010-02-28T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>PDF</prism:versionidentifier>
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        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/9">
        <title>Influence of nanofibers on growth and gene expression of human tendon derived fibroblasts</title>
        <description>Background:
Rotator cuff tears are a common and frequent lesion especially in older patients. The mechanisms of tendon repair are not fully understood. Common therapy options for tendon repair include mini-open or arthroscopic surgery. The use of growth factors in experimental studies is mentioned in the literature. Nanofiber scaffolds, which provide several criteria for the healing process, might be a suitable therapy option for operative treatment. The aim of this study was to explore the effects of nanofiber scaffolds on human tendon derived fibroblasts (TDF&apos;s), as well as the gene expression and matrix deposition of these fibroblasts.
Methods:
Nanofibers composed of PLLA and PLLA/Col-I were seeded with human tendon derived fibroblasts and cultivated over a period of 22 days under growth-inductive conditions, and analyzed during the course of culture, with respect to gene expression of different extra cellular matrix components such as collagens, bigylcan and decorin. Furthermore, we measured cell densities and proliferation by using fluorescene microscopy.
Results:
PLLA nanofibers possessed a growth inhibitory effect on TDF&apos;s. Furthermore, no meaningful influence on the gene expression of collagen I, collagen III and decorin could be observed, while the expression of collagen X increased during the course of cultivation. On the other hand, PLLA/Col-I blend nanofibers had no negative influence on the growth of TDF&apos;s. Furthermore, blending PLLA nanofibers with collagen had a positive effect on the gene expression of collagen I, III, X and decorin. Here, gene expression indicated that focal adherence kinases might be involved.
Conclusion:
This study indicates that the use of nanofibers influence expression of genes associated with the extra cellular matrix formation. The composition of the nanofibers plays a critical role. While PLLA/Col-I blend nanofibers enhance the collagen I and III formation, their expression on PLLA nanofibers was more comparable to controls. However, irrespective of the chemical composition of the fibres, the collagen deposition was altered, an effect which might be associated with a decreased expression of biglycanes.</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/9</link>
                <dc:creator>Christina Theisen</dc:creator>
                <dc:creator>Susanne Fuchs-Winkelmann</dc:creator>
                <dc:creator>Karola Knappstein</dc:creator>
                <dc:creator>Turgay Efe</dc:creator>
                <dc:creator>Jan Schmitt</dc:creator>
                <dc:creator>Juergen Paletta</dc:creator>
                <dc:creator>Markus Schofer</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:9</dc:source>
        <dc:date>2010-02-17T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-9</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>9</prism:startingPage>
        <prism:publicationDate>2010-02-17T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/8">
        <title>Non-rigid registration of breast surfaces using the laplace and diffusion equations</title>
        <description>A semi-automated, non-rigid breast surface registration method is presented that involves solving the Laplace or diffusion equations over undeformed and deformed breast surfaces. The resulting potential energy fields and isocontours are used to establish surface correspondence. This novel surface-based method, which does not require intensity images, anatomical landmarks, or fiducials, is compared to a gold standard of thin-plate spline (TPS) interpolation. Realistic finite element simulations of breast compression and further testing against a tissue-mimicking phantom demonstrate that this method is capable of registering surfaces experiencing 6 - 36 mm compression to within a mean error of 0.5 - 5.7 mm.</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/8</link>
                <dc:creator>Rowena Ong</dc:creator>
                <dc:creator>Jao Ou</dc:creator>
                <dc:creator>Michael Miga</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:8</dc:source>
        <dc:date>2010-02-12T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-8</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>8</prism:startingPage>
        <prism:publicationDate>2010-02-12T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/10">
        <title>Towards treatment planning and treatment of deep-seated solid tumors by electrochemotherapy</title>
        <description>Background:
Electrochemotherapy treats tumors by combining specific chemotherapeutic drugs with an intracellular target and electric pulses, which increases drug uptake into the tumor cells. Electrochemotherapy has been successfully used for treatment of easily accessible superficial tumor nodules. In this paper, we present the first case of deep-seated tumor electrochemotherapy based on numerical treatment planning.
Methods:
The aim of our study was to treat a melanoma metastasis in the thigh of a patient. Treatment planning for electrode positioning and electrical pulse parameters was performed for two different electrode configurations: one with four and another with five long needle electrodes. During the procedure, the four electrode treatment plan was adopted and the patient was treated accordingly by electrochemotherapy with bleomycin. The response to treatment was clinically and radiographically evaluated. Due to a partial response of the treated tumor, the metastasis was surgically removed after 2 months and pathological analysis was performed.
Results:
A partial response of the tumor to electrochemotherapy was obtained. Histologically, the metastasis showed partial necrosis due to electrochemotherapy, estimated to represent 40-50% of the tumor. Based on the data obtained, we re-evaluated the electrical treatment parameters in order to correlate the treatment plan with the clinical response. Electrode positions in the numerical model were updated according to the actual positions during treatment. We compared the maximum value of the measured electric current with the current predicted by the model and good agreement was obtained. Finally, tumor coverage with an electric field above the reversible threshold was recalculated and determined to be approximately 94%. Therefore, according to the calculations, a small volume of tumor cells remained viable after electrochemotherapy, and these were sufficient for tumor regrowth.
Conclusions:
In this, the first reported clinical case, deep-seated melanoma metastasis in the thigh of the patient was treated by electrochemotherapy, according to a treatment plan obtained by numerical modeling and optimization. Although only a partial response was obtained, the presented work demonstrates that treatment of deep-seated tumor nodules by electrochemotherapy is feasible and sets the ground for numerical treatment planning-based electrochemotherapy.Trial registration: EudraCT:2008-008290-54</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/10</link>
                <dc:creator>Damijan Miklavcic</dc:creator>
                <dc:creator>Marko Snoj</dc:creator>
                <dc:creator>Anze Zupanic</dc:creator>
                <dc:creator>Bor Kos</dc:creator>
                <dc:creator>Maja Cemazar</dc:creator>
                <dc:creator>Mateja Kropivnik</dc:creator>
                <dc:creator>Matej Bracko</dc:creator>
                <dc:creator>Tjasa Pecnik</dc:creator>
                <dc:creator>Eldar Gadzijev</dc:creator>
                <dc:creator>Gregor Sersa</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:10</dc:source>
        <dc:date>2010-02-23T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-10</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>10</prism:startingPage>
        <prism:publicationDate>2010-02-23T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>PDF</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/13">
        <title>A statistical model for multidimensional irreversible electroporation cell death in tissue</title>
        <description>Background:
Irreversible electroporation (IRE) is a minimally invasive tissue ablation technique which utilizes electric pulses delivered by electrodes to a targeted area of tissue to produce high high amplitude electric fields, thus inducing irreversible damage to the cell membrane lipid bilayer.  An important application of this technique is for cancer tissue ablation. Mathematical modelling is considered important in IRE treatment planning. In the past, IRE mathematical modelling used a deterministic single value for the amplitude of the electric field required for causing cell death.  However, tissue, particularly cancerous tissue, is comprised of a population of different cells of different sizes and orientations, which in conventional IRE are exposed to complex electric fields; therefore, using a deterministic single value is overly simplistic.
Methods:
We introduce and describe a new methodology for evaluating IRE induced cell death in tissue. Our approach employs a statistical Peleg-Fermi model to correlate probability of cell death in heterogeneous tissue to the parameters of electroporation pulses such as the number of pulses, electric field amplitude and pulse length. For treatment planning, the Peleg-Fermi model is combined with a numerical solution of the multidimensional electric field equation cast in a dimensionless form.  This is the first time in which this concept is used for evaluating IRE cell death in multidimensional situations.
Results:
We illustrate the methodology using data reported in literature for prostate cancer cell death by IRE. We show how to fit this data to a Fermi function in order to calculate the critical statistic parameters. To illustrate the use of the methodology, we simulated 2-D irreversible electroporation protocols and produced 2-D maps of the statistical distribution of cell death in the treated region. These plots were compared to plots produced using a deterministic model of cell death by IRE and the differences were noted.
Conclusions:
In this work we introduce a new methodology for evaluation of tissue ablation by IRE using statistical models of cell death. We believe that the use of a statistical model rather than a deterministic model for IRE cell death will improve the accuracy of treatment planning for cancer treatment with IRE.</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/13</link>
                <dc:creator>Alex Golberg</dc:creator>
                <dc:creator>Boris Rubinsky</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:13</dc:source>
        <dc:date>2010-02-26T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-13</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>13</prism:startingPage>
        <prism:publicationDate>2010-02-26T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>PDF</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedical-engineering-online.com/content/2/1/7">
        <title>Multi-purpose HealthCare Telemedicine Systems with mobile communication link support</title>
        <description>The provision of effective emergency telemedicine and home monitoring solutions are the major fields of interest discussed in this study. Ambulances, Rural Health Centers (RHC) or other remote health location such as Ships navigating in wide seas are common examples of possible emergency sites, while critical care telemetry and telemedicine home follow-ups are important issues of telemonitoring. In order to support the above different growing application fields we created a combined real-time and store and forward facility that consists of a base unit and a telemedicine (mobile) unit. This integrated system: can be used when handling emergency cases in ambulances, RHC or ships by using a mobile telemedicine unit at the emergency site and a base unit at the hospital-expert&apos;s site, enhances intensive health care provision by giving a mobile base unit to the ICU doctor while the telemedicine unit remains at the ICU patient site and enables home telemonitoring, by installing the telemedicine unit at the patient&apos;s home while the base unit remains at the physician&apos;s office or hospital. The system allows the transmission of vital biosignals (3&#8211;12 lead ECG, SPO2, NIBP, IBP, Temp) and still images of the patient. The transmission is performed through GSM mobile telecommunication network, through satellite links (where GSM is not available) or through Plain Old Telephony Systems (POTS) where available. Using this device a specialist doctor can telematically &quot;move&quot; to the patient&apos;s site and instruct unspecialized personnel when handling an emergency or telemonitoring case. Due to the need of storing and archiving of all data interchanged during the telemedicine sessions, we have equipped the consultation site with a multimedia database able to store and manage the data collected by the system. The performance of the system has been technically tested over several telecommunication means; in addition the system has been clinically validated in three different countries using a standardized medical protocol.</description>
        <link>http://www.biomedical-engineering-online.com/content/2/1/7</link>
                <dc:creator>Efthyvoulos Kyriacou</dc:creator>
                <dc:creator>Pavlopoulos Sotiris</dc:creator>
                <dc:creator>Alexander Berler</dc:creator>
                <dc:creator>Marios Neophytou</dc:creator>
                <dc:creator>Athena Bourka</dc:creator>
                <dc:creator>Angelos Georgoulas</dc:creator>
                <dc:creator>Anthoula Anagnostaki</dc:creator>
                <dc:creator>Dimitris Karayiannis</dc:creator>
                <dc:creator>Christos Schizas</dc:creator>
                <dc:creator>Constantinos Pattichis</dc:creator>
                <dc:creator>Andreas Andreou</dc:creator>
                <dc:creator>Dimitris Koutsouris</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2003, 2:7</dc:source>
        <dc:date>2003-03-24T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-2-7</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>2</prism:volume>
        <prism:startingPage>7</prism:startingPage>
        <prism:publicationDate>2003-03-24T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/12">
        <title>Measurement of intrinsic optical backscattering characteristics of cells using fiber-guided near infrared light

</title>
        <description>Background:
Intrinsic optical signals (IOS), which reflect changes in transmittance and scattering light, have been applied to characterize the physiological conditions of target biological tissues. Backscattering approaches allow mounting of the source and detector on the same side of a sample which creates a more compact physical layout of device. This study presents a compact backscattering design using fiber-optic guided near-infrared (NIR) light to measure the amplitude and phase changes of IOS under different osmotic challenges.
Methods:
High-frequency intensity-modulated light was guided via optic fiber, which was controlled by micromanipulator to closely aim at a minimum cluster of cortical neurons. Several factors including the probe design, wavelength selection, optimal measuring distance between the fiber-optical probe and cells were considered. Our experimental setup was tested in cultured cells to observe the relationship between the changes in backscattered NIR light and cellular IOS, which is believed mainly caused by cell volume changes in hypo/hyperosmotic solutions (+/-20, +/-40 and +/-60 mOsm).
Results:
The critical parameters of the current setup including the optimal measuring distance from fiber-optical probe to target tissue and the linear relationship between backscattering intensity and cell volume were determined. The backscattering intensity was found to be inversely proportional to osmotic changes. However, the phase shift exhibited a nonlinear feature and reached a plateau at hyperosmotic solution.
Conclusions:
Our study indicated that the backscattering NIR light guided by fiber-optical probe makes it a potential alternative for continuous observation of intrinsic optical properties of cell culture under varied physical or chemical challenges.</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/12</link>
                <dc:creator>Ching-Huang Hsu</dc:creator>
                <dc:creator>Gwo-Ching Chang</dc:creator>
                <dc:creator>En-Ting Li</dc:creator>
                <dc:creator>Yu-Jing Lin</dc:creator>
                <dc:creator>Jia-Jin Chen</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:12</dc:source>
        <dc:date>2010-02-25T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-12</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>12</prism:startingPage>
        <prism:publicationDate>2010-02-25T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>PDF</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.biomedical-engineering-online.com/content/3/1/28">
        <title>Real time electrocardiogram QRS detection using combined adaptive threshold</title>
        <description>Background:
QRS and ventricular beat detection is a basic procedure for electrocardiogram (ECG) processing and analysis. Large variety of methods have been proposed and used, featuring high percentages of correct detection. Nevertheless, the problem remains open especially with respect to higher detection accuracy in noisy ECGs
Methods:
A real-time detection method is proposed, based on comparison between absolute values of summed differentiated electrocardiograms of one of more ECG leads and adaptive threshold. The threshold combines three parameters: an adaptive slew-rate value, a second value which rises when high-frequency noise occurs, and a third one intended to avoid missing of low amplitude beats.Two algorithms were developed: Algorithm 1 detects at the current beat and Algorithm 2 has an RR interval analysis component in addition.The algorithms are self-adjusting to the thresholds and weighting constants, regardless of resolution and sampling frequency used. They operate with any number L of ECG leads, self-synchronize to QRS or beat slopes and adapt to beat-to-beat intervals.
Results:
The algorithms were tested by an independent expert, thus excluding possible author&apos;s influence, using all 48 full-length ECG records of the MIT-BIH arrhythmia database. The results were: sensitivity Se = 99.69 % and specificity Sp = 99.65 % for Algorithm 1 and Se = 99.74 % and Sp = 99.65 % for Algorithm 2.
Conclusion:
The statistical indices are higher than, or comparable to those, cited in the scientific literature.</description>
        <link>http://www.biomedical-engineering-online.com/content/3/1/28</link>
                <dc:creator>Ivaylo Christov</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2004, 3:28</dc:source>
        <dc:date>2004-08-27T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-3-28</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>3</prism:volume>
        <prism:startingPage>28</prism:startingPage>
        <prism:publicationDate>2004-08-27T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.biomedical-engineering-online.com/content/9/1/6">
        <title>Quantitative Analysis of Sensor for Pressure Waveform Measurement</title>
        <description>Background:
Arterial pressure waveforms contain important diagnostic and physiological information since their contour depends on a healthy cardiovascular system 1. A sensor was placed at the measured artery and some contact pressure was used to measure the pressure waveform. However, where is the location of the sensor just about enough to detect a complete pressure waveform for the diagnosis? How much contact pressure is needed over the pulse point? These two problems still remain unresolved.MethodIn this study, we propose a quantitative analysis to evaluate the pressure waveform for locating the position and applying the appropriate force between the sensor and the radial artery. The two-axis mechanism and the modified sensor have been designed to estimate the radial arterial width and detect the contact pressure. The template matching method was used to analyze the pressure waveform. In the X-axis scan, we found that the arterial diameter changed waveform (ADCW) and the pressure waveform would change from small to large and then back to small again when the sensor was moved across the radial artery. In the Z-axis scan, we also found that the ADCW and the pressure waveform would change from small to large and then back to small again when the applied contact pressure continuously increased.
Results:
In the X-axis scan, the template correlation coefficients of the left and right boundaries of the radial arterial width were 0.987 &#177; 0.016 and 0.978 &#177; 0.028, respectively. In the Z-axis scan, when the excessive contact pressure was more than 100 mm Hg, the template correlation was below 0.983. In applying force, when using the maximum amplitude as the criteria level, the lower contact pressure (r = 0.988 &#177; 0.004) was better than the higher contact pressure (r = 0.976 &#177; 0.012).
Conclusions:
Although, the optimal detective position has to be close to the middle of the radial arterial, the pressure waveform also has a good completeness with a template correlation coefficient of above 0.99 when the position was within &#177; 1 mm of the middle of the radial arterial range. In applying force, using the maximum amplitude as the criteria level, the lower contact pressure was better than the higher contact pressure.</description>
        <link>http://www.biomedical-engineering-online.com/content/9/1/6</link>
                <dc:creator>Shing-Hong Liu</dc:creator>
                <dc:creator>Chu-Chang Tyan</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2010, 9:6</dc:source>
        <dc:date>2010-01-21T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-9-6</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>6</prism:startingPage>
        <prism:publicationDate>2010-01-21T00:00:00Z</prism:publicationDate>
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        <title>Biological effects of exposure to magnetic resonance imaging: an overview</title>
        <description>The literature on biological effects of magnetic and electromagnetic fields commonly utilized in magnetic resonance imaging systems is surveyed here. After an introduction on the basic principles of magnetic resonance imaging and the electric and magnetic properties of biological tissues, the basic phenomena to understand the bio-effects are described in classical terms. Values of field strengths and frequencies commonly utilized in these diagnostic systems are reported in order to allow the integration of the specific literature on the bio-effects produced by magnetic resonance systems with the vast literature concerning the bio-effects produced by electromagnetic fields. This work gives an overview of the findings about the safety concerns of exposure to static magnetic fields, radio-frequency fields, and time varying magnetic field gradients, focusing primarily on the physics of the interactions between these electromagnetic fields and biological matter. The scientific literature is summarized, integrated, and critically analyzed with the help of authoritative reviews by recognized experts, international safety guidelines are also cited.</description>
        <link>http://www.biomedical-engineering-online.com/content/3/1/11</link>
                <dc:creator>Domenico Formica</dc:creator>
                <dc:creator>Sergio Silvestri</dc:creator>
                <dc:source>BioMedical Engineering OnLine 2004, 3:11</dc:source>
        <dc:date>2004-04-22T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1475-925X-3-11</dc:identifier>
        <prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
        <prism:issn>1475-925X</prism:issn>
        <prism:volume>3</prism:volume>
        <prism:startingPage>11</prism:startingPage>
        <prism:publicationDate>2004-04-22T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
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