<?xml version="1.0" encoding="UTF-8"?>
<article article-type="research-article" dtd-version="1.3" xml:lang="en">
  <front>
    <journal-meta>
      <journal-title-group>
        <journal-title>Czech and Slovak Ophthalmology</journal-title>
      </journal-title-group>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id">470</article-id>
      <article-categories>
        <subj-group>
          <subject>Original article</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Retinopathy of Prematurity Part I</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Prepiaková</surname>
            <given-names>Zuzana</given-names>
          </name>
          <contrib-id contrib-id-type="orcid">https://orcid.org/0009-0004-4596-2657</contrib-id>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Tomčíková</surname>
            <given-names>Dana</given-names>
          </name>
          <contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9285-7066</contrib-id>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Kostolná</surname>
            <given-names>Barbora</given-names>
          </name>
          <contrib-id contrib-id-type="orcid">https://orcid.org/0009-0003-6780-0539</contrib-id>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Gerinec</surname>
            <given-names>Anton</given-names>
          </name>
        </contrib>
      </contrib-group>
      <pub-date date-type="pub" publication-format="electronic">
        <day>22</day>
        <month>4</month>
        <year>2014</year>
      </pub-date>
      <issue>2</issue>
      <elocation-id>1</elocation-id>
      <abstract>
        <p>Retinopathy of prematurity (ROP) is a disease that affects immature vasculature in the eyes of premature babies that potentially leads to blindness. Authors describe incidence,risk factors, pathophysiology and international classification of retinopathy of prematurity (ICROP).</p>
      </abstract>
      <kwd-group>
        <kwd>retinopathy of prematurity</kwd>
        <kwd>incidence</kwd>
        <kwd>pathophysiology</kwd>
        <kwd>international classification</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <back>
    <ref-list>
      <title>References</title>
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      </ref>
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      </ref>
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      </ref>
      <ref id="R10853">
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      </ref>
      <ref id="R10854">
        <mixed-citation>The STOP-ROP Multicenter Study Group: Supplemental therapeutic oxygen for prethreshold retinopathy of prematurity (STOP-ROP): a randomized, controlled trial I: primary outcomes. Pediatrics, 105; 2000: 295–310. the disease, AP-ROP, in retinopathies beginning in the nasal part of the retina an above all in very premature infants with the presence of risk factors, the probability of spontaneous regression is negligible. In general it applies that the later the beginning of ROP, and thus the better developed the vascular system of the retina and the more peripheral the localisation of manifestations of ROP, the better the prognosis of the disease. Regression of ROP The active phase of ROP may leave regressive changes on the retina (termed cicatricose in the past). These involutionary changes on the retina are classified according to the International Commission for ROP: A. Vascular and retinal changes in the periphery of the retina. B. Vascular and retinal changes on the posterior pole of </mixed-citation>
      </ref>
    </ref-list>
  </back>
</article>
