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            <subfield code="a">10.1155/2014/179070</subfield>
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            <subfield code="0">(orcid)0000-0002-6305-9283</subfield>
            <subfield code="a">Manzano, Sara</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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        <datafield tag="245" ind1=" " ind2=" ">
            <subfield code="a">Cartilage Dysfunction in ALS Patients as Side Effect of Motion Loss: 3D Mechano-Electrochemical Computational Model</subfield>
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        <datafield tag="260" ind1=" " ind2=" ">
            <subfield code="c">2014</subfield>
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            <subfield code="a">Amyotrophic lateral sclerosis (ALS) is a debilitating motor neuron disease characterized by progressive weakness, muscle atrophy, and fasciculation. This fact results in a continuous degeneration and dysfunction of articular soft tissues. Specifically, cartilage is an avascular and nonneural connective tissue that allows smooth motion in diarthrodial joints. Due to the avascular nature of cartilage tissue, cells nutrition and by-product exchange are intermittently occurring during joint motions. Reduced mobility results in a change of proteoglycan density, osmotic pressure, and permeability of the tissue. This work aims to demonstrate the abnormal cartilage deformation in progressive immobilized articular cartilage for ALS patients. For this aim a novel 3D mechano-electrochemical model based on the triphasic theory for charged hydrated soft tissues is developed. ALS patient parameters such as tissue porosity, osmotic coefficient, and fixed anions were incorporated. Considering different mobility reduction of each phase of the disease, results predicted the degree of tissue degeneration and the reduction of its capacity for deformation. The present model can be a useful tool to predict the evolution of joints in ALS patients and the necessity of including specific cartilage protectors, drugs, or maintenance physical activities as part of the symptomatic treatment in amyotrophic lateral sclerosis.</subfield>
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            <subfield code="a">MEDICINE, RESEARCH &amp; EXPERIMENTAL</subfield>
            <subfield code="b">85 / 123 = 0.691</subfield>
            <subfield code="c">2014</subfield>
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            <subfield code="a">BIOTECHNOLOGY &amp; APPLIED MICROBIOLOGY</subfield>
            <subfield code="b">106 / 162 = 0.654</subfield>
            <subfield code="c">2014</subfield>
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        <datafield tag="700" ind1=" " ind2=" ">
            <subfield code="a">Gaffney, Eamonn A.</subfield>
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            <subfield code="0">(orcid)0000-0001-8741-6452</subfield>
            <subfield code="a">Doblaré, Manuel</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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        <datafield tag="700" ind1=" " ind2=" ">
            <subfield code="0">(orcid)0000-0003-0088-7222</subfield>
            <subfield code="a">Hamdy Doweidar, Mohamed</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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        <datafield tag="710" ind1="2" ind2=" ">
            <subfield code="1">5004</subfield>
            <subfield code="2">605</subfield>
            <subfield code="a">Universidad de Zaragoza</subfield>
            <subfield code="b">Departamento de Ingeniería Mecánica</subfield>
            <subfield code="c">Mec. de Medios Contínuos y Teor. de Estructuras</subfield>
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            <subfield code="g">2014 (2014), 179070 [13 pp]</subfield>
            <subfield code="p">BioMed res. int.</subfield>
            <subfield code="t">BioMed Research International</subfield>
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            <subfield code="p">articulos</subfield>
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            <subfield code="a">2016-12-16-14:54:23</subfield>
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