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            <subfield code="a">10.1080/02713683.2017.1387272</subfield>
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            <subfield code="2">sideral</subfield>
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            <subfield code="a">ART-2017-103914</subfield>
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            <subfield code="a">eng</subfield>
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        <datafield tag="100" ind1=" " ind2=" ">
            <subfield code="0">(orcid)0000-0002-6134-8698</subfield>
            <subfield code="a">Sierra, M.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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        <datafield tag="245" ind1=" " ind2=" ">
            <subfield code="a">Effect of cryopreserved amniotic membrane on the mechanical properties of skeletal muscle after strabismus surgery in rabbits</subfield>
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        <datafield tag="260" ind1=" " ind2=" ">
            <subfield code="c">2017</subfield>
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            <subfield code="a">Access copy available to the general public</subfield>
            <subfield code="f">Unrestricted</subfield>
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            <subfield code="a">Purpose: To study the functional recovery of the superior rectus muscle (SRM) after its partial resection in a rabbit model with and without cryopreserved amniotic membrane (AM).
Material and methods: Resection of the right and left SRMs of 30 rabbits was performed. On the left eyes, a single sheet of equine cryopreserved AM was placed covering the muscle edge sutured. Active and passive mechanical properties of muscles operated with and without AM were monitored over time at 30 (n = 10), 60 (n = 10), and 90 (n = 10) days after surgery. Muscle samples were extracted and electrically stimulated to register the force exerted by the samples, characterizing its active behavior. They were, then, subjected to stretching test to obtain its resistance to deformation, known as passive behavior. Moreover, right and left eyes of a control group (n = 5) were equally subjected to active and passive tests to characterize the physiological behavior of SRM muscles.
Results: On active function examination, statistically significant differences were documented between the following: control vs AM and no AM at 30 days (p = 0.002 and p = 0.04, respectively). All other comparisons were insignificant (p > 0.05). On passive function analysis, significant differences were only found between control vs. no AM at 30 days (p = 0.004) and between AM vs. no AM at 30 days (p = 0.002). Indeed, muscle operated without AM did not recover a normal passive function until 60 days after surgery.
Conclusion: Cryopreserved AM is effective in accelerating recovery of SRM passive function in rabbits. Nevertheless, AM produced no significant effect on recovery of SRM active function.¿</subfield>
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            <subfield code="9">info:eu-repo/grantAgreement/ES/DGA/T88</subfield>
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            <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/DPI2017-84047-R</subfield>
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            <subfield code="9">info:eu-repo/semantics/openAccess</subfield>
            <subfield code="a">All rights reserved</subfield>
            <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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            <subfield code="a">2.12</subfield>
            <subfield code="b">2017</subfield>
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            <subfield code="a">OPHTHALMOLOGY</subfield>
            <subfield code="b">27 / 59 = 0.458</subfield>
            <subfield code="c">2017</subfield>
            <subfield code="d">Q2</subfield>
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        <datafield tag="593" ind1=" " ind2=" ">
            <subfield code="a">Ophthalmology</subfield>
            <subfield code="c">2017</subfield>
            <subfield code="d">Q2</subfield>
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            <subfield code="a">Sensory Systems</subfield>
            <subfield code="c">2017</subfield>
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            <subfield code="a">Cellular and Molecular Neuroscience</subfield>
            <subfield code="c">2017</subfield>
            <subfield code="d">Q3</subfield>
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            <subfield code="0">(orcid)0000-0003-2770-4617</subfield>
            <subfield code="a">Ortillés, A.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="0">(orcid)0000-0001-5981-5448</subfield>
            <subfield code="a">Miana-Mena, F.J.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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        <datafield tag="700" ind1=" " ind2=" ">
            <subfield code="0">(orcid)0000-0002-6870-0594</subfield>
            <subfield code="a">Grasa, J.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="0">(orcid)0000-0001-9713-1813</subfield>
            <subfield code="a">Calvo, B.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="1">1005</subfield>
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            <subfield code="a">Universidad de Zaragoza</subfield>
            <subfield code="b">Dpto. Farmacología y Fisiolog.</subfield>
            <subfield code="c">Área Fisiología</subfield>
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            <subfield code="a">Universidad de Zaragoza</subfield>
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            <subfield code="a">Universidad de Zaragoza</subfield>
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            <subfield code="b">Dpto. Patología Animal</subfield>
            <subfield code="c">Área Medicina y Cirugía Animal</subfield>
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            <subfield code="g">43, 2 (2017), 193-199</subfield>
            <subfield code="p">Curr. eye res.</subfield>
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