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		<title>BioMedical Engineering OnLine - Latest articles</title>
		<link>http://www.biomedical-engineering-online.com</link>
		<description>The latest articles from BioMedical Engineering OnLine (ISSN 1475-925X) published by 
				
				BioMed Central
		</description>
        <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
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				    <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/7/1/21"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/7/1/20"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/7/1/19"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/7/1/18"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/7/1/17"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/7/1/16"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/7/1/15"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/7/1/14"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/7/1/13"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/7/1/12"/>			    
            
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		<item rdf:about="http://www.biomedical-engineering-online.com/content/7/1/21">
            
            <title>Effect of variable heat transfer coefficient on tissue temperature next to a large vessel during radiofrequency tumor ablation</title>
			<description>Background:
One of the current shortcomings of radiofrequency(RF) tumor ablation is its limited performance in regions close to large blood vessels, resulting in high recurrence rates at these locations. Computer models have been used to determine tissue temperatures during tumor ablation procedures. To simulate large vessels, either constant wall temperature or constant convective heat transfer coefficient (h) have been assumed at the vessel surface to simulate convection. However, the actual distribution of the temperature on the vessel wall is non-uniform and time-varying, and this feature makes the convective coefficient variable.
Methods:
This paper presents a realistic time-varying model in which h is a function of the temperature distribution at the vessel wall. The Finite-element method (FEM) was employed in order to model RF hepatic ablation. Two geometrical configurations were investigated. The RF electrode was placed at distances of 1 and 5 mm from a large vessel (10 mm diameter).
Results:
When the ablation procedure takes longer than 1-2 min, the attained coagulation zone obtained with both time-varying h and constant h does not differ significantly. However, for short duration ablation (5-10 s) and when the electrode is 1 mm away from the vessel, the use of constant h can lead to errors as high as 20% in the estimation of the coagulation zone.
Conclusions:
For tumor ablation procedures typically lasting at least 5 min, this study shows that modeling the heat sink effect of large vessels by applying constant h as a boundary condition will yield precise results while reducing computational complexity. However, for other thermal therapies with shorter treatment using a time-varying h may be necessary.</description>
			<link>http://www.biomedical-engineering-online.com/content/7/1/21</link>
			
			 	<dc:creator>Icaro dos Santos, Dieter Haemmerich, Cleber S Pinheiro and Adson F da Rocha</dc:creator>
			
			<dc:source>BioMedical Engineering OnLine 2008, 7:21</dc:source>
			<dc:date>2008-07-11</dc:date>
			<dc:identifier>doi:10.1186/1475-925X-7-21</dc:identifier>
			
			
							
					<prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
					
			
							
					<prism:issn>1475-925X</prism:issn>
					
			
							
					<prism:volume>7</prism:volume>
					
			
							
					<prism:startingPage>21</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-11</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedical-engineering-online.com/content/7/1/20">
            
            <title>Complex Myograph allows the examination of complex muscle contractions for the assessment of muscle force, shortening, velocity, and work in vivo</title>
			<description>Background:
The devices used for in vivo examination of muscle contractions assess only pure force contractions and the so-called isokinetic contractions. In isokinetic experiments, the extremity and its muscle are artificially moved with constant velocity by the measuring device, while a tetanic contraction is induced in the muscle, either by electrical stimulation or by maximal voluntary activation. With these systems, experiments cannot be performed at pre-defined, constant muscle length, single contractions cannot be evaluated individually and the separate examination of the isometric and the isotonic components of single contractions is not possible.
Methods:
The myograph presented in our study has two newly developed technical units, i.e. a). a counterforce unit which can load the muscle with an adjustable, but constant force and b). a length-adjusting unit which allows for both the stretching and the contraction length to be infinitely adjustable independently of one another. The two units support the examination of complex types of contraction and store the counterforce and length-adjusting settings, so that these conditions may be accurately reapplied in later sessions.
Results:
The measurement examples presented show that the muscle can be brought to every possible pre-stretching length and that single isotonic or complex isometric-isotonic contractions may be performed at every length. The applied forces act during different phases of contraction, resulting into different pre- and after-loads that can be kept constant - uninfluenced by the contraction. Maximal values for force, shortening, velocity and work may be obtained for individual muscles. This offers the possibility to obtain information on the muscle status and to monitor its changes under noninvasive measurement conditions.
Conclusions:
With the Complex Myograph, the whole spectrum of a muscle's mechanical characteristics may be assessed.</description>
			<link>http://www.biomedical-engineering-online.com/content/7/1/20</link>
			
			 	<dc:creator>Niels Rahe-Meyer, Matthias Pawlak, Christian Weilbach, Wilhelm Alexander Osthaus, Heiner Ruschulte, Cristina Solomon, Siegfried Piepenbrock and Michael Winterhalter</dc:creator>
			
			<dc:source>BioMedical Engineering OnLine 2008, 7:20</dc:source>
			<dc:date>2008-07-10</dc:date>
			<dc:identifier>doi:10.1186/1475-925X-7-20</dc:identifier>
			
			
							
					<prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
					
			
							
					<prism:issn>1475-925X</prism:issn>
					
			
							
					<prism:volume>7</prism:volume>
					
			
							
					<prism:startingPage>20</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-10</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedical-engineering-online.com/content/7/1/19">
            
            <title>An in vitro assay of collagen fiber alignment by acupuncture needle rotation</title>
			<description>Background:
During traditional acupuncture therapy, soft tissues attach to and wind around the acupuncture needle. To study this phenomenon in a controlled and quantitative setting, we performed acupuncture needling in vitro. Methods: Acupuncture was simulated in vitro in three-dimensional, type I collagen gels prepared at 1.5 mg/ml, 2.0 mg/ml, and 2.5 mg/ml collagen, and either crosslinked with formalin or left untreated. Acupuncture needles were inserted into the gels and rotated via a computer-controlled motor at 0.3 rev/sec for up to 10 revolutions while capturing the evolution of birefringence under cross-polarization. Results: Simulated acupuncture produced circumferential alignment of collagen fibers close to the needle that evolved into radial alignment as the distance from the needle increased, which generally matched observations from published tissue explant studies. All gels failed prior to 10 revolutions, and the location of failure was near the transition between circumferential and radial alignment. Crosslinked collagen failed at a significantly lower number of revolutions than untreated collagen, whereas collagen concentration had no effect on gel failure. The strength of the alignment field increased with increasing collagen concentration and decreased with crosslinking. Separate studies were performed in which the gel thickness and depth of needle insertion were varied.  As gel thickness increased, gels failed at fewer needle revolutions. For the same depth of insertion, alignment was greater in thinner gels. Alignment increased as the depth of insertion increased. Conclusions: These results indicate that the mechanostructural properties of soft connective tissues may affect their response to acupuncture therapy. The in vitro model provides a platform to study mechanotransduction during acupuncture in a highly controlled and quantitative setting.</description>
			<link>http://www.biomedical-engineering-online.com/content/7/1/19</link>
			
			 	<dc:creator>Margaret Julias, Lowell T Edgar, Helen M Buettner and David I Shreiber</dc:creator>
			
			<dc:source>BioMedical Engineering OnLine 2008, 7:19</dc:source>
			<dc:date>2008-07-07</dc:date>
			<dc:identifier>doi:10.1186/1475-925X-7-19</dc:identifier>
			
			
							
					<prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
					
			
							
					<prism:issn>1475-925X</prism:issn>
					
			
							
					<prism:volume>7</prism:volume>
					
			
							
					<prism:startingPage>19</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-07</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedical-engineering-online.com/content/7/1/18">
            
            <title>Medical information systems: A foundation for healthcare technologies in developing countries</title>
			<description>No Abstract Requested</description>
			<link>http://www.biomedical-engineering-online.com/content/7/1/18</link>
			
			 	<dc:creator>Gari D Clifford, Joaquin A Blaya, Rachel Hall-Clifford and Hamish SF Fraser</dc:creator>
			
			<dc:source>BioMedical Engineering OnLine 2008, 7:18</dc:source>
			<dc:date>2008-06-11</dc:date>
			<dc:identifier>doi:10.1186/1475-925X-7-18</dc:identifier>
			
			
							
					<prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
					
			
							
					<prism:issn>1475-925X</prism:issn>
					
			
							
					<prism:volume>7</prism:volume>
					
			
							
					<prism:startingPage>18</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-06-11</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedical-engineering-online.com/content/7/1/17">
            
            <title>High-tech biomedical research: lessons from Iran's experience</title>
			<description>Iran has recently made a significant progress in the field of biomedical science and launched an appreciable number of new high-tech biomedical research projects. Review of Iran's experience in advancing its biomedical research and the pitfalls the country encountered during the years of its progress could be of interest to other countries with similar technological conditions. As needs assessment and human resources have pivotal roles in any research infrastructure, here, we have delineated these factors and explored ways by which optimum advantage could be gained from them.</description>
			<link>http://www.biomedical-engineering-online.com/content/7/1/17</link>
			
			 	<dc:creator>Ali Samadikuchaksaraei and Kazem Mousavizadeh</dc:creator>
			
			<dc:source>BioMedical Engineering OnLine 2008, 7:17</dc:source>
			<dc:date>2008-05-23</dc:date>
			<dc:identifier>doi:10.1186/1475-925X-7-17</dc:identifier>
			
			
							
					<prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
					
			
							
					<prism:issn>1475-925X</prism:issn>
					
			
							
					<prism:volume>7</prism:volume>
					
			
							
					<prism:startingPage>17</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-05-23</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedical-engineering-online.com/content/7/1/16">
            
            <title>A new adhesive technique for internal fixation in midfacial surgery</title>
			<description>Background:
The current surgical therapy of midfacial fractures involves internal fixation in which bone fragments are fixed in their anatomical positions with osteosynthesis plates and corresponding screws until bone healing is complete. This often causes new fractures to fragile bones while drilling pilot holes or trying to insert screws. The adhesive fixation of osteosynthesis plates using PMMA bone cement could offer a viable alternative for fixing the plates without screws. In order to achieve the adhesive bonding of bone cement to cortical bone in the viscerocranium, an amphiphilic bone bonding agent was created, analogous to the dentin bonding agents currently on the market.
Methods:
The adhesive bonding strengths were measured using tension tests. For this, metal plates with 2.0 mm diameter screw holes were cemented with PMMA bone cement to cortical bovine bone samples from the femur diaphysis. The bone was conditioned with an amphiphilic bone bonding agent prior to cementing. The samples were stored for 1 to 42 days at 37 degrees C, either moist or completely submerged in an isotonic NaCl-solution, and then subjected to the tension tests.
Results:
Without the bone bonding agent, the bonding strength was close to zero (0.2 MPa). Primary stability with bone bonding agent is considered to be at ca. 8 MPa. Moist storage over 42 days resulted in decreased adhesion forces of ca. 6 MPa. Wet storage resulted in relatively constant bonding strengths of ca. 8 MPa.
Conclusion:
A new amphiphilic bone bonding agent was developed, which builds an optimizied interlayer between the hydrophilic bone surface and the hydrophobic PMMA bone cement and thus leads to adhesive bonding between them. Our in vitro investigations demonstrated the adhesive bonding of PMMA bone cement to cortical bone, which was also stable against hydrolysis. The newly developed adhesive fixing technique could be applied clinically when the fixation of osteosynthesis plates with screws is impossible. With the detected adhesion forces of ca. 6 to 8 MPa, it is assumed that the adhesive fixation system is able to secure bone fragments from the non-load bearing midfacial regions in their orthotopic positions until fracture consolidation is complete.</description>
			<link>http://www.biomedical-engineering-online.com/content/7/1/16</link>
			
			 	<dc:creator>Kira Endres, Rudolf Marx, Joachim Tinschert, Dieter Christian Wirtz, Christian Stoll, Dieter Riediger and Ralf Smeets</dc:creator>
			
			<dc:source>BioMedical Engineering OnLine 2008, 7:16</dc:source>
			<dc:date>2008-05-19</dc:date>
			<dc:identifier>doi:10.1186/1475-925X-7-16</dc:identifier>
			
			
							
					<prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
					
			
							
					<prism:issn>1475-925X</prism:issn>
					
			
							
					<prism:volume>7</prism:volume>
					
			
							
					<prism:startingPage>16</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-05-19</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedical-engineering-online.com/content/7/1/15">
            
            <title>A model-based time-reversal of left ventricular motion improves cardiac motion analysis using tagged MRI data</title>
			<description>Background:
Myocardial motion is an important observable for the assessment of heart condition. Accurate estimates of ventricular (LV) wall motion are required for quantifying myocardial deformation and assessing local tissue function and viability. Harmonic Phase (HARP) analysis was developed for measuring regional LV motion using tagged magnetic resonance imaging (tMRI) data. With current computer-aided postprocessing tools including HARP analysis, large motions experienced by myocardial tissue are, however, often intractable to measure. This paper addresses this issue and provides a solution to make such measurements possible.
Methods:
To improve the estimation performance of large cardiac motions while analyzing tMRI data sets, we propose a two-step solution. The first step involves constructing a model to describe average systolic motion of the LV wall within a subject group. The second step involves time-reversal of the model applied as a spatial coordinate transformation to digitally relax the contracted LV wall in the experimental data of a single subject to the beginning of systole. Cardiac tMRI scans were performed on four healthy rats and used for developing the forward LV model. Algorithms were implemented for preprocessing the tMRI data, optimizing the model parameters and performing the HARP analysis. Slices from the midventricular level were then analyzed for all systolic phases.
Results:
The time-reversal operation derived from the LV model accounted for the bulk portion of the myocardial motion, which was the average motion experienced within the overall subject population. In analyzing the individual tMRI data sets, removing this average with the time-reversal operation left small magnitude residual motion unique to the case. This remaining residual portion of the motion was estimated robustly using the HARP analysis.
Conclusion:
Utilizing a combination of the forward LV model and its time reversal improves the performance of motion estimation in evaluating the cardiac function.</description>
			<link>http://www.biomedical-engineering-online.com/content/7/1/15</link>
			
			 	<dc:creator>Tareq Alrefae, Irina V Smirnova, Larry T Cook and Mehmet Bilgen</dc:creator>
			
			<dc:source>BioMedical Engineering OnLine 2008, 7:15</dc:source>
			<dc:date>2008-05-19</dc:date>
			<dc:identifier>doi:10.1186/1475-925X-7-15</dc:identifier>
			
			
							
					<prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
					
			
							
					<prism:issn>1475-925X</prism:issn>
					
			
							
					<prism:volume>7</prism:volume>
					
			
							
					<prism:startingPage>15</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-05-19</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedical-engineering-online.com/content/7/1/14">
            
            <title>Assessment of a non-invasive high-throughput classifier for behaviours associated with sleep and wake in mice</title>
			<description>This work presents a non-invasive high-throughput system for automatically detecting characteristic behaviours in mice over extended periods of time, useful for phenotyping experiments. The system classifies time intervals on the order of 2 to 4 seconds as corresponding to motions consistent with either active wake or inactivity associated with sleep. A single Polyvinylidine Difluoride (PVDF) sensor on the cage floor generates signals from motion resulting in pressure. This paper develops a linear classifier based on robust features extracted from normalized power spectra and autocorrelation functions, as well as novel features from the collapsed average (autocorrelation of complex spectrum), which characterize transient and periodic properties of the signal envelope. Performance is analyzed through an experiment comparing results from direct human observation and classification of the different behaviours with an automatic classifier used in conjunction with this system. Experimental results from over 28.5 hours of data from 4 mice indicate a 94% classification rate relative to the human observations. Examples of sequential classifications (2 second increments) over transition regions between sleep and wake behaviour are also presented to demonstrate robust performance to signal variation and explain performance limitations.</description>
			<link>http://www.biomedical-engineering-online.com/content/7/1/14</link>
			
			 	<dc:creator>Kevin D Donohue, Dharshan C Medonza, Eli R Crane and Bruce F O'Hara</dc:creator>
			
			<dc:source>BioMedical Engineering OnLine 2008, 7:14</dc:source>
			<dc:date>2008-04-11</dc:date>
			<dc:identifier>doi:10.1186/1475-925X-7-14</dc:identifier>
			
			
							
					<prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
					
			
							
					<prism:issn>1475-925X</prism:issn>
					
			
							
					<prism:volume>7</prism:volume>
					
			
							
					<prism:startingPage>14</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-04-11</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedical-engineering-online.com/content/7/1/13">
            
            <title>Effective x-ray attenuation coefficient measurements from two full field digital mammography systems for data calibration applications</title>
			<description>Background:
Breast density is a significant breast cancer risk factor. Currently, there is no standard method for measuring this important factor. Work presented here represents an essential component of an ongoing project that seeks to determine the appropriate method for calibrating (standardizing) mammography image data to account for the x-ray image acquisition influences. Longer term goals of this project are to make accurate breast density measurements in support of risk studies.
Methods:
Logarithmic response calibration curves and effective x-ray attenuation coefficients were measured from two full field digital mammography (FFDM) systems with breast tissue equivalent phantom imaging and compared. Normalization methods were studied to assess the possibility of reducing the amount of calibration data collection. The percent glandular calibration map functional form was investigated. Spatial variations in the calibration data were used to assess the uncertainty in the calibration application by applying error propagation analyses.
Results:
Logarithmic response curves are well approximated as linear. Measured effective x-ray attenuation coefficients are characteristic quantities independent of the imaging system and are in agreement with those predicted numerically. Calibration data collection can be reduced by applying a simple normalization technique. The calibration map is well approximated as linear. Intrasystem calibration variation was on the order of four percent, which was approximately half of the intersystem variation.
Conclusion:
FFDM systems provide a quantitative output, and the calibration quantities presented here may be used for data acquired on similar FFDM systems.</description>
			<link>http://www.biomedical-engineering-online.com/content/7/1/13</link>
			
			 	<dc:creator>John J Heine and Jerry A Thomas</dc:creator>
			
			<dc:source>BioMedical Engineering OnLine 2008, 7:13</dc:source>
			<dc:date>2008-03-28</dc:date>
			<dc:identifier>doi:10.1186/1475-925X-7-13</dc:identifier>
			
			
							
					<prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
					
			
							
					<prism:issn>1475-925X</prism:issn>
					
			
							
					<prism:volume>7</prism:volume>
					
			
							
					<prism:startingPage>13</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-03-28</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedical-engineering-online.com/content/7/1/12">
            
            <title>A quantitative method for determining spatial discriminative capacity</title>
			<description>Background:
The traditional two-point discrimination (TPD) test, a widely used tactile spatial acuity measure, has been criticized as being imprecise because it is based on subjective criteria and involves a number of non-spatial cues. The results of a recent study showed that as two stimuli were delivered simultaneously, vibrotactile amplitude discrimination became worse when the two stimuli were positioned relatively close together and was significantly degraded when the probes were within a subject's two-point limen. The impairment of amplitude discrimination with decreasing inter-probe distance suggested that the metric of amplitude discrimination could possibly provide a means of objective and quantitative measurement of spatial discrimination capacity.
Methods:
A two alternative forced-choice (2AFC) tracking procedure was used to assess a subject's ability to discriminate the amplitude difference between two stimuli positioned at near-adjacent skin sites. Two 25 Hz flutter stimuli, identical except for a constant difference in amplitude, were delivered simultaneously to the hand dorsum. The stimuli were initially spaced 30 mm apart, and the inter-stimulus distance was modified on a trial-by-trial basis based on the subject's performance of discriminating the stimulus with higher intensity. The experiment was repeated via sequential, rather than simultaneous, delivery of the same vibrotactile stimuli.
Results:
Results obtained from this study showed that the performance of the amplitude discrimination task was significantly degraded when the stimuli were delivered simultaneously and were near a subject's two-point limen. In contrast, subjects were able to correctly discriminate between the amplitudes of the two stimuli when they were sequentially delivered at all inter-probe distances (including those within the two-point limen), and improved when an adapting stimulus was delivered prior to simultaneously delivered stimuli.
Conclusion:
Subjects' capacity to discriminate the amplitude difference between two vibrotactile stimulations was degraded as the inter-stimulus distance approached the limit of their two-point spatial discriminative capacity. This degradation of spatial discriminative capacity lessened when an adapting stimulus was used. Performance of the task, as well as improvement on the task with adaptation, would most likely be impaired if the cortical information processing capacity of a subject or subject population were systemically altered, and thus, the methods described could be effective measures for use in clinical or clinical research applications.</description>
			<link>http://www.biomedical-engineering-online.com/content/7/1/12</link>
			
			 	<dc:creator>Zheng Zhang, Vinay Tannan, Jameson K Holden, Robert G Dennis and Mark Tommerdahl</dc:creator>
			
			<dc:source>BioMedical Engineering OnLine 2008, 7:12</dc:source>
			<dc:date>2008-03-10</dc:date>
			<dc:identifier>doi:10.1186/1475-925X-7-12</dc:identifier>
			
			
							
					<prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
					
			
							
					<prism:issn>1475-925X</prism:issn>
					
			
							
					<prism:volume>7</prism:volume>
					
			
							
					<prism:startingPage>12</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-03-10</prism:publicationDate>
					

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