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		<title>BioMedical Engineering OnLine - Most viewed articles</title>
		<link>http://www.biomedical-engineering-online.commostviewed/</link>
		<description>Most viewed articles in last 30 days 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/7/1/19"/>			    
            
				    <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/2/1/6"/>			    
            
				    <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/1/1/1"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/2/1/7"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/6/1/17"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedical-engineering-online.com/content/7/1/10"/>			    
            
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		<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.
Conclusion:
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:subject>Number of accesses: 862</dc:subject>
			<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/7/1/21">
            
            <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&#8211;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&#8211;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.
Conclusion:
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 da Silva Pinheiro and Adson Ferreira da Rocha</dc:creator>
			<dc:source>BioMedical Engineering OnLine 2008, 7:21</dc:source>
			<dc:subject>Number of accesses: 548</dc:subject>
			<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 &#8211; 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 non-invasive measurement conditions.
Conclusion:
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, Hainer Ruhschulte, Cristina Solomon, Siegfried Piepenbrock and Michael Winterhalter</dc:creator>
			<dc:source>BioMedical Engineering OnLine 2008, 7:20</dc:source>
			<dc:subject>Number of accesses: 485</dc:subject>
			<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/2/1/6">
            
            <title>Can ultrasound be used to stimulate nerve tissue?</title>
			<description>Background:
The stimulation of nerve or cortical tissue by magnetic induction is a relatively new tool for the non-invasive study of the brain and nervous system. Transcranial magnetic stimulation (TMS), for example, has been used for the functional mapping of the motor cortex and may have potential for treating a variety of brain disorders.Methods and ResultsA new method of stimulating active tissue is proposed by propagating ultrasound in the presence of a magnetic field. Since tissue is conductive, particle motion created by an ultrasonic wave will induce an electric current density generated by Lorentz forces. An analytical derivation is given for the electric field distribution induced by a collimated ultrasonic beam. An example shows that peak electric fields of up to 8 V/m appear to be achievable at the upper range of diagnostic intensities. This field strength is about an order of magnitude lower than fields typically associated with TMS; however, the electric field gradients induced by ultrasound can be quite high (about 60 kV/m2 at 4 MHz), which theoretically play a more important role in activation than the field magnitude. The latter value is comparable to TMS-induced gradients.
Conclusion:
The proposed method could be used to locally stimulate active tissue by inducing an electric field in regions where the ultrasound is focused. Potential advantages of this method compared to TMS is that stimulation of cortical tissue could be highly localized as well as achieved at greater depths in the brain than is currently possible with TMS.</description>
			<link>http://www.biomedical-engineering-online.com/content/2/1/6</link>		
			<dc:creator>Stephen J Norton</dc:creator>
			<dc:source>BioMedical Engineering OnLine 2003, 2:6</dc:source>
			<dc:subject>Number of accesses: 472</dc:subject>
			<dc:date>2003-03-04</dc:date>
			<dc:identifier>doi:10.1186/1475-925X-2-6</dc:identifier>
			
			
							
					<prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
					
			
							
					<prism:issn>1475-925X</prism:issn>
					
			
							
					<prism:volume>2</prism:volume>
					
			
							
					<prism:startingPage>6</prism:startingPage>
					
			
							
					<prism:publicationDate>2003-03-04</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:subject>Number of accesses: 459</dc:subject>
			<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:subject>Number of accesses: 392</dc:subject>
			<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/1/1/1">
            
            <title>Effect of Contour Shape of Nervous System Electromagnetic Stimulation Coils on the Induced Electrical Field Distribution</title>
			<description>Background:
Electromagnetic stimulation of the nervous system has the advantage of reduced discomfort in activating nerves. For brain structures stimulation, it has become a clinically accepted modality. Coil designs usually consider factors such as optimization of induced power, focussing, field shape etc. In this study we are attempting to find the effect of the coil contour shape on the electrical field distribution for magnetic stimulation.Method and resultsWe use the maximum of the induced electric field stimulation in the region of interest as the optimization criterion. This choice required the application of the calculus of variation, with the contour perimeter taken as a pre-set condition. Four types of coils are studied and compared: circular, square, triangular and an 'optimally' shaped contour. The latter yields higher values of the induced electrical field in depths up to about 30 mm, but for depths around 100 mm, the circular shape has a slight advantage. The validity of the model results was checked by experimental measurements in a tank with saline solution, where differences of about 12% were found. In view the accuracy limitations of the computational and measurement methods used, such differences are considered acceptable.
Conclusion:
We applied an optimization approach, using the calculus of variation, which allows to obtain a coil contour shape corresponding to a selected criterion. In this case, the optimal contour showed higher intensities for a longer line along the depth-axis. The method allows modifying the induced field structure and focussing the field to a selected zone or line.</description>
			<link>http://www.biomedical-engineering-online.com/content/1/1/1</link>		
			<dc:creator>Sava P Papazov and Ivan K Daskalov</dc:creator>
			<dc:source>BioMedical Engineering OnLine 2002, 1:1</dc:source>
			<dc:subject>Number of accesses: 351</dc:subject>
			<dc:date>2002-05-14</dc:date>
			<dc:identifier>doi:10.1186/1475-925X-1-1</dc:identifier>
			
			
							
					<prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
					
			
							
					<prism:issn>1475-925X</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>1</prism:startingPage>
					
			
							
					<prism:publicationDate>2002-05-14</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<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'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's home while the base unit remains at the physician'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 "move" to the patient'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>E Kyriacou, S Pavlopoulos, A Berler, M Neophytou, A Bourka, A Georgoulas, A Anagnostaki, D Karayiannis, C Schizas, C Pattichis, A Andreou and D Koutsouris</dc:creator>
			<dc:source>BioMedical Engineering OnLine 2003, 2:7</dc:source>
			<dc:subject>Number of accesses: 334</dc:subject>
			<dc:date>2003-03-24</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>2003-03-24</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedical-engineering-online.com/content/6/1/17">
            
            <title>A model of blood flow in the mesenteric arterial system</title>
			<description>Background:
There are some early clinical indicators of cardiac ischemia, most notably a change in a person's electrocardiogram. Less well understood, but potentially just as dangerous, is ischemia that develops in the gastrointestinal system. Such ischemia is difficult to diagnose without angiography (an invasive and time-consuming procedure) mainly due to the highly unspecific nature of the disease.Understanding how perfusion is affected during ischemic conditions can be a useful clinical tool which can help clinicians during the diagnosis process. As a first step towards this final goal, a computational model of the gastrointestinal system has been developed and used to simulate realistic blood flow during normal conditions.
Methods:
An anatomically and biophysically based model of the major mesenteric arteries has been developed to be used to simulate normal blood flows. The computational mesh used for the simulations has been generated using data from the Visible Human project. The 3D Navier-Stokes equations that govern flow within this mesh have been simplified to an efficient 1D scheme. This scheme, together with a constitutive pressure-radius relationship, has been solved numerically for pressure, vessel radius and velocity for the entire mesenteric arterial network.
Results:
The computational model developed shows close agreement with physiologically realistic geometries other researchers have recorded in vivo. Using this model as a framework, results were analyzed for the four distinct phases of the cardiac cycle &#8211; diastole, isovolumic contraction, ejection and isovolumic relaxation. Profiles showing the temporally varying pressure and velocity for a periodic input varying between 10.2 kPa (77 mmHg) and 14.6 kPa (110 mmHg) at the abdominal aorta are presented. An analytical solution has been developed to model blood flow in tapering vessels and when compared with the numerical solution, showed excellent agreement.
Conclusion:
An anatomically and physiologically realistic computational model of the major mesenteric arteries has been developed for the gastrointestinal system. Using this model, blood flow has been simulated which show physiologically realistic flow profiles.</description>
			<link>http://www.biomedical-engineering-online.com/content/6/1/17</link>		
			<dc:creator>Thusitha DS Mabotuwana, Leo K Cheng and Andrew J Pullan</dc:creator>
			<dc:source>BioMedical Engineering OnLine 2007, 6:17</dc:source>
			<dc:subject>Number of accesses: 290</dc:subject>
			<dc:date>2007-05-08</dc:date>
			<dc:identifier>doi:10.1186/1475-925X-6-17</dc:identifier>
			
			
							
					<prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
					
			
							
					<prism:issn>1475-925X</prism:issn>
					
			
							
					<prism:volume>6</prism:volume>
					
			
							
					<prism:startingPage>17</prism:startingPage>
					
			
							
					<prism:publicationDate>2007-05-08</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedical-engineering-online.com/content/7/1/10">
            
            <title>Mathematical modeling of laser lipolysis</title>
			<description>Background and ObjectivesLiposuction continues to be one of the most popular procedures performed in cosmetic surgery. As the public's demand for body contouring continues, laser lipolysis has been proposed to improve results, minimize risk, optimize patient comfort, and reduce the recovery period. Mathematical modeling of laser lipolysis could provide a better understanding of the laser lipolysis process and could determine the optimal dosage as a function of fat volume to be removed.Study design/Materials and MethodsAn Optical-Thermal-Damage Model was formulated using finite-element modeling software (Femlab 3.1, Comsol Inc). The general model simulated light distribution using the diffusion approximation of the transport theory, temperature rise using the bioheat equation and laser-induced injury using the Arrhenius damage model. Biological tissue was represented by two homogenous regions (dermis and fat layer) with a nonlinear air-tissue boundary condition including free convection.Video recordings were used to gain a better understanding of the back and forth movement of the cannula during laser lipolysis in order to consider them in our mathematical model. Infrared video recordings were also performed in order to compare the actual surface temperatures to our calculations. The reduction in fat volume was determined as a function of the total applied energy and subsequently compared to clinical data reported in the literature.
Results:
In patients, when using cooled tumescent anesthesia, 1064 nm Nd:YAG laser or 980 nm diode laser: (6 W, back and forth motion: 100 mm/s) give similar skin surface temperature (max: 41&#176;C). These measurements are in accordance with those obtained by mathematical modeling performed with a 1 mm cannula inserted inside the hypodermis layer at 0.8 cm below the surface. Similarly, the fat volume reduction observed in patients at 6-month follow up can be determined by mathematical modeling. This fat reduction depends on the applied energy, typically 5 cm3 for 3000 J. At last, skin retraction was observed in patients at 6-month follow up. This observation can be easily explained by mathematical modeling showing that the temperature increase inside the lower dermis is sufficient (48&#8211;50&#176;C) to induce skin tighteningDiscussion and ConclusionLaser lipolysis can be described by a theoretical model. Fat volume reduction observed in patients is in accordance with model calculations. Due to heat diffusion, temperature elevation is also produced inside the lower reticular dermis. This interesting observation can explain remodeling of the collagenous tissue, with clinically evident skin tightening.In conclusion, while the heat generated by interstitial laser irradiation provides stimulate lipolysis of the fat cells, the collagen and elastin are also stimulated resulting in a tightening in the skin. This mathematical model should serve as a useful tool to simulate and better understand the mechanism of action of the laser lipolysis</description>
			<link>http://www.biomedical-engineering-online.com/content/7/1/10</link>		
			<dc:creator>Serge R Mordon, Benjamin Wassmer, Jean Pascal Reynaud and Jaouad Zemmouri</dc:creator>
			<dc:source>BioMedical Engineering OnLine 2008, 7:10</dc:source>
			<dc:subject>Number of accesses: 286</dc:subject>
			<dc:date>2008-02-29</dc:date>
			<dc:identifier>doi:10.1186/1475-925X-7-10</dc:identifier>
			
			
							
					<prism:publicationName>BioMedical Engineering OnLine</prism:publicationName>
					
			
							
					<prism:issn>1475-925X</prism:issn>
					
			
							
					<prism:volume>7</prism:volume>
					
			
							
					<prism:startingPage>10</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-02-29</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
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         <cc:permits rdf:resource="http://creativecommons.org/ns#Reproduction"/>
         <cc:permits rdf:resource="http://creativecommons.org/ns#Distribution"/>
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</rdf:RDF>
