Comparison of proliferation, apoptosis and expression of syndecan-1 and α-SMA in edentulous ridge oral mucosa of successful and early failed submerged dental implants--An immunohistochemical study.
Identifieur interne : 006492 ( Ncbi/Merge ); précédent : 006491; suivant : 006493Comparison of proliferation, apoptosis and expression of syndecan-1 and α-SMA in edentulous ridge oral mucosa of successful and early failed submerged dental implants--An immunohistochemical study.
Auteurs : Mladen Cubela [Bosnie-Herzégovine] ; Violeta Soljic [Bosnie-Herzégovine] ; Darko Kero [Croatie] ; Katarina Vukojevic [Croatie] ; Danijela Kalibovic Govorko [Croatie] ; Mirna Saraga-Babic [Croatie]Source :
- Archives of oral biology [ 1879-1506 ] ; 2016.
Descripteurs français
- KwdFr :
- Actines (biosynthèse), Actines (physiologie), Adulte d'âge moyen, Antigènes CD (métabolisme), Antigènes de différenciation des myélomonocytes (métabolisme), Apoptose (physiologie), Bouche édentée (anatomopathologie), Bouche édentée (métabolisme), Caspase-3 (métabolisme), Facteur de croissance transformant bêta (analyse), Facteur de croissance transformant bêta (biosynthèse), Facteur de croissance transformant bêta (physiologie), Femelle, Humains, Implants dentaires (effets indésirables), Macrophages (métabolisme), Muqueuse de la bouche (), Muqueuse de la bouche (anatomopathologie), Muqueuse de la bouche (métabolisme), Mâle, Ostéo-intégration, Pose d'implant dentaire endo-osseux, Prolifération cellulaire (physiologie), Sujet âgé, Syndécane-1 (biosynthèse), Syndécane-1 (physiologie), Échec de restauration dentaire.
- MESH :
- analyse : Facteur de croissance transformant bêta.
- anatomopathologie : Bouche édentée, Muqueuse de la bouche.
- biosynthèse : Actines, Facteur de croissance transformant bêta, Syndécane-1.
- effets indésirables : Implants dentaires.
- métabolisme : Antigènes CD, Antigènes de différenciation des myélomonocytes, Bouche édentée, Caspase-3, Macrophages, Muqueuse de la bouche.
- physiologie : Actines, Apoptose, Facteur de croissance transformant bêta, Prolifération cellulaire, Syndécane-1.
- Adulte d'âge moyen, Femelle, Humains, Muqueuse de la bouche, Mâle, Ostéo-intégration, Pose d'implant dentaire endo-osseux, Sujet âgé, Échec de restauration dentaire.
English descriptors
- KwdEn :
- Actins (biosynthesis), Actins (physiology), Aged, Antigens, CD (metabolism), Antigens, Differentiation, Myelomonocytic (metabolism), Apoptosis (physiology), Caspase 3 (metabolism), Cell Proliferation (physiology), Dental Implantation, Endosseous, Dental Implants (adverse effects), Dental Restoration Failure, Female, Humans, Macrophages (metabolism), Male, Middle Aged, Mouth Mucosa (blood supply), Mouth Mucosa (metabolism), Mouth Mucosa (pathology), Mouth, Edentulous (metabolism), Mouth, Edentulous (pathology), Osseointegration, Syndecan-1 (biosynthesis), Syndecan-1 (physiology), Transforming Growth Factor beta (analysis), Transforming Growth Factor beta (biosynthesis), Transforming Growth Factor beta (physiology).
- MESH :
- chemical , adverse effects : Dental Implants.
- chemical , analysis : Transforming Growth Factor beta.
- chemical , biosynthesis : Actins, Syndecan-1, Transforming Growth Factor beta.
- chemical , metabolism : Antigens, CD, Antigens, Differentiation, Myelomonocytic, Caspase 3.
- chemical , physiology : Actins, Syndecan-1, Transforming Growth Factor beta.
- blood supply : Mouth Mucosa.
- metabolism : Macrophages, Mouth Mucosa, Mouth, Edentulous.
- pathology : Mouth Mucosa, Mouth, Edentulous.
- physiology : Apoptosis, Cell Proliferation.
- Aged, Dental Implantation, Endosseous, Dental Restoration Failure, Female, Humans, Male, Middle Aged, Osseointegration.
Abstract
Pathogenic mechanisms involved in early submerged implant failure are poorly understood. In this study we immunohistochemically analyse differences in proliferation, apoptosis and inflammation in edentulous ridge oral mucosa (ERM) of successful and early failed submerged implants.
DOI: 10.1016/j.archoralbio.2016.02.017
PubMed: 26954096
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Electronic address: msb@mefst.hr.</nlm:affiliation><country xml:lang="fr">Croatie</country><wicri:regionArea>Department of Anatomy, Histology and Embryology, School of Medicine, University of Split, Soltanska 2, 21000 Split</wicri:regionArea><wicri:noRegion>21000 Split</wicri:noRegion></affiliation></author></analytic><series><title level="j">Archives of oral biology</title><idno type="eISSN">1879-1506</idno><imprint><date when="2016" type="published">2016</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Actins (biosynthesis)</term><term>Actins (physiology)</term><term>Aged</term><term>Antigens, CD (metabolism)</term><term>Antigens, Differentiation, Myelomonocytic (metabolism)</term><term>Apoptosis (physiology)</term><term>Caspase 3 (metabolism)</term><term>Cell Proliferation (physiology)</term><term>Dental Implantation, Endosseous</term><term>Dental Implants (adverse effects)</term><term>Dental Restoration Failure</term><term>Female</term><term>Humans</term><term>Macrophages (metabolism)</term><term>Male</term><term>Middle Aged</term><term>Mouth Mucosa (blood supply)</term><term>Mouth Mucosa (metabolism)</term><term>Mouth Mucosa (pathology)</term><term>Mouth, Edentulous (metabolism)</term><term>Mouth, Edentulous (pathology)</term><term>Osseointegration</term><term>Syndecan-1 (biosynthesis)</term><term>Syndecan-1 (physiology)</term><term>Transforming Growth Factor beta (analysis)</term><term>Transforming Growth Factor beta (biosynthesis)</term><term>Transforming Growth Factor beta (physiology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Actines (biosynthèse)</term><term>Actines (physiologie)</term><term>Adulte d'âge moyen</term><term>Antigènes CD (métabolisme)</term><term>Antigènes de différenciation des myélomonocytes (métabolisme)</term><term>Apoptose (physiologie)</term><term>Bouche édentée (anatomopathologie)</term><term>Bouche édentée (métabolisme)</term><term>Caspase-3 (métabolisme)</term><term>Facteur de croissance transformant bêta (analyse)</term><term>Facteur de croissance transformant bêta (biosynthèse)</term><term>Facteur de croissance transformant bêta (physiologie)</term><term>Femelle</term><term>Humains</term><term>Implants dentaires (effets indésirables)</term><term>Macrophages (métabolisme)</term><term>Muqueuse de la bouche ()</term><term>Muqueuse de la bouche (anatomopathologie)</term><term>Muqueuse de la bouche (métabolisme)</term><term>Mâle</term><term>Ostéo-intégration</term><term>Pose d'implant dentaire endo-osseux</term><term>Prolifération cellulaire (physiologie)</term><term>Sujet âgé</term><term>Syndécane-1 (biosynthèse)</term><term>Syndécane-1 (physiologie)</term><term>Échec de restauration dentaire</term></keywords><keywords scheme="MESH" type="chemical" qualifier="adverse effects" xml:lang="en"><term>Dental Implants</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Transforming Growth Factor beta</term></keywords><keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>Actins</term><term>Syndecan-1</term><term>Transforming Growth Factor beta</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Antigens, CD</term><term>Antigens, Differentiation, Myelomonocytic</term><term>Caspase 3</term></keywords><keywords scheme="MESH" type="chemical" qualifier="physiology" xml:lang="en"><term>Actins</term><term>Syndecan-1</term><term>Transforming Growth Factor beta</term></keywords><keywords scheme="MESH" qualifier="analyse" xml:lang="fr"><term>Facteur de croissance transformant bêta</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Bouche édentée</term><term>Muqueuse de la bouche</term></keywords><keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr"><term>Actines</term><term>Facteur de croissance transformant bêta</term><term>Syndécane-1</term></keywords><keywords scheme="MESH" qualifier="blood supply" xml:lang="en"><term>Mouth Mucosa</term></keywords><keywords scheme="MESH" qualifier="effets indésirables" xml:lang="fr"><term>Implants dentaires</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Macrophages</term><term>Mouth Mucosa</term><term>Mouth, Edentulous</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Antigènes CD</term><term>Antigènes de différenciation des myélomonocytes</term><term>Bouche édentée</term><term>Caspase-3</term><term>Macrophages</term><term>Muqueuse de la bouche</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Mouth Mucosa</term><term>Mouth, Edentulous</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Actines</term><term>Apoptose</term><term>Facteur de croissance transformant bêta</term><term>Prolifération cellulaire</term><term>Syndécane-1</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Apoptosis</term><term>Cell Proliferation</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Dental Implantation, Endosseous</term><term>Dental Restoration Failure</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Osseointegration</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adulte d'âge moyen</term><term>Femelle</term><term>Humains</term><term>Muqueuse de la bouche</term><term>Mâle</term><term>Ostéo-intégration</term><term>Pose d'implant dentaire endo-osseux</term><term>Sujet âgé</term><term>Échec de restauration dentaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Pathogenic mechanisms involved in early submerged implant failure are poorly understood. In this study we immunohistochemically analyse differences in proliferation, apoptosis and inflammation in edentulous ridge oral mucosa (ERM) of successful and early failed submerged implants.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">26954096</PMID><DateCompleted><Year>2017</Year><Month>02</Month><Day>08</Day></DateCompleted><DateRevised><Year>2017</Year><Month>02</Month><Day>08</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1879-1506</ISSN><JournalIssue CitedMedium="Internet"><Volume>66</Volume><PubDate><Year>2016</Year><Month>Jun</Month></PubDate></JournalIssue><Title>Archives of oral biology</Title><ISOAbbreviation>Arch. Oral Biol.</ISOAbbreviation></Journal><ArticleTitle>Comparison of proliferation, apoptosis and expression of syndecan-1 and α-SMA in edentulous ridge oral mucosa of successful and early failed submerged dental implants--An immunohistochemical study.</ArticleTitle><Pagination><MedlinePgn>155-64</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1016/j.archoralbio.2016.02.017</ELocationID><ELocationID EIdType="pii" ValidYN="Y">S0003-9969(16)30054-1</ELocationID><Abstract><AbstractText Label="AIMS" NlmCategory="OBJECTIVE">Pathogenic mechanisms involved in early submerged implant failure are poorly understood. In this study we immunohistochemically analyse differences in proliferation, apoptosis and inflammation in edentulous ridge oral mucosa (ERM) of successful and early failed submerged implants.</AbstractText><AbstractText Label="MATERIALS AND METHODS" NlmCategory="METHODS">30 samples of ERM covering successful and early failed submerged implants were obtained at the end of osseointegration period along with control samples of healthy ERM. Sections were stained with Ki-67 (proliferation), caspase-3 (apoptosis) and syndecan-1 (epithelial marker). Percentage of positive cells was analysed by Kruskal-Wallis test and Dunn's post hoc test. Co-localization of Ki-67 and caspase-3 with α-SMA, CD68 and TGF-β was done by double immunofluorescence.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">There was no significant difference in number of Ki-67 positive cells within surface epithelium (SE) in all groups. Proliferation was significantly higher in underlying connective tissue (UCT) of ERM of early failed submerged implants (26%) compared to ERM of successful submerged implants (3%) and controls (4%). More apoptotic cells appeared in UCT of early failed submerged implants (8%) compared to UCT of successful submerged implants (4%) and UCT of control ERM (3%). Co-localization of Ki-67 and α-SMA in ERM of early failed submerged implants disclosed proliferating fibroblasts and pericytes of blood vessels. Macrophages and cells expressing TGF-β appeared in UCT of failed implants. Expression of syndecan-1 was significantly weaker in SE of early failed submerged implants.</AbstractText><AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Imbalance between proliferation and apoptosis, changes in syndecan-1 expression and inflammation are histopathological features of ERM of early failed submerged implants.</AbstractText><CopyrightInformation>Copyright © 2016 Elsevier Ltd. All rights reserved.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Cubela</LastName><ForeName>Mladen</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Dental Clinic Cubela, KMV Humskog bb, Mostar, Bosnia and Herzegovina.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Soljic</LastName><ForeName>Violeta</ForeName><Initials>V</Initials><AffiliationInfo><Affiliation>Department of Anatomy, School of Medicine, University of Mostar, Mostar, Bosnia and Herzegovina.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Kero</LastName><ForeName>Darko</ForeName><Initials>D</Initials><AffiliationInfo><Affiliation>Study Programme of Dental Medicine, School of Medicine, University of Split, Soltanska 2, 21000 Split, Croatia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Vukojevic</LastName><ForeName>Katarina</ForeName><Initials>K</Initials><AffiliationInfo><Affiliation>Department of Anatomy, Histology and Embryology, School of Medicine, University of Split, Soltanska 2, 21000 Split, Croatia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Govorko</LastName><ForeName>Danijela Kalibovic</ForeName><Initials>DK</Initials><AffiliationInfo><Affiliation>Study Programme of Dental Medicine, School of Medicine, University of Split, Soltanska 2, 21000 Split, Croatia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Saraga-Babic</LastName><ForeName>Mirna</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Department of Anatomy, Histology and Embryology, School of Medicine, University of Split, Soltanska 2, 21000 Split, Croatia. Electronic address: msb@mefst.hr.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2016</Year><Month>03</Month><Day>02</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Arch Oral Biol</MedlineTA><NlmUniqueID>0116711</NlmUniqueID><ISSNLinking>0003-9969</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C541116">ACTA2 protein, human</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000199">Actins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D015703">Antigens, CD</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D015214">Antigens, Differentiation, Myelomonocytic</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C067980">CD68 antigen, human</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D015921">Dental Implants</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D053668">Syndecan-1</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D016212">Transforming Growth Factor beta</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 3.4.22.-</RegistryNumber><NameOfSubstance UI="D053148">Caspase 3</NameOfSubstance></Chemical></ChemicalList><CitationSubset>D</CitationSubset><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000199" MajorTopicYN="N">Actins</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="Y">biosynthesis</QualifierName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D015703" MajorTopicYN="N">Antigens, CD</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015214" MajorTopicYN="N">Antigens, Differentiation, Myelomonocytic</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017209" MajorTopicYN="N">Apoptosis</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D053148" MajorTopicYN="N">Caspase 3</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D049109" MajorTopicYN="N">Cell Proliferation</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003758" MajorTopicYN="N">Dental Implantation, Endosseous</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D015921" MajorTopicYN="N">Dental Implants</DescriptorName><QualifierName UI="Q000009" MajorTopicYN="Y">adverse effects</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D019232" MajorTopicYN="Y">Dental Restoration Failure</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008264" MajorTopicYN="N">Macrophages</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009061" MajorTopicYN="N">Mouth Mucosa</DescriptorName><QualifierName UI="Q000098" MajorTopicYN="N">blood supply</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D009066" MajorTopicYN="N">Mouth, Edentulous</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D016348" MajorTopicYN="N">Osseointegration</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D053668" MajorTopicYN="N">Syndecan-1</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="Y">biosynthesis</QualifierName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D016212" MajorTopicYN="N">Transforming Growth Factor beta</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName><QualifierName UI="Q000096" MajorTopicYN="N">biosynthesis</QualifierName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading></MeshHeadingList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Apoptosis</Keyword><Keyword MajorTopicYN="N">Early implant failure</Keyword><Keyword MajorTopicYN="N">Inflammation</Keyword><Keyword MajorTopicYN="N">Oral mucosa</Keyword><Keyword MajorTopicYN="N">Proliferation</Keyword><Keyword MajorTopicYN="N">Syndecan-1</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2015</Year><Month>11</Month><Day>03</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2016</Year><Month>02</Month><Day>18</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2016</Year><Month>02</Month><Day>26</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2016</Year><Month>3</Month><Day>9</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2016</Year><Month>3</Month><Day>10</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2017</Year><Month>2</Month><Day>9</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">26954096</ArticleId><ArticleId IdType="pii">S0003-9969(16)30054-1</ArticleId><ArticleId IdType="doi">10.1016/j.archoralbio.2016.02.017</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Bosnie-Herzégovine</li><li>Croatie</li></country></list><tree><country name="Bosnie-Herzégovine"><noRegion><name sortKey="Cubela, Mladen" sort="Cubela, Mladen" uniqKey="Cubela M" first="Mladen" last="Cubela">Mladen Cubela</name></noRegion><name sortKey="Soljic, Violeta" sort="Soljic, Violeta" uniqKey="Soljic V" first="Violeta" last="Soljic">Violeta Soljic</name></country><country name="Croatie"><noRegion><name sortKey="Kero, Darko" sort="Kero, Darko" uniqKey="Kero D" first="Darko" last="Kero">Darko Kero</name></noRegion><name sortKey="Govorko, Danijela Kalibovic" sort="Govorko, Danijela Kalibovic" uniqKey="Govorko D" first="Danijela Kalibovic" last="Govorko">Danijela Kalibovic Govorko</name><name sortKey="Saraga Babic, Mirna" sort="Saraga Babic, Mirna" uniqKey="Saraga Babic M" first="Mirna" last="Saraga-Babic">Mirna Saraga-Babic</name><name sortKey="Vukojevic, Katarina" sort="Vukojevic, Katarina" uniqKey="Vukojevic K" first="Katarina" last="Vukojevic">Katarina Vukojevic</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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