Corneal Subbasal Nerve Plexus Evaluation by in Vivo Confocal Microscopy in Multiple Sclerosis: A Potential New Biomarker
Purpose/Aim: Our study aims to evaluate corneal subbasal nerve plexus morphology by in vivo corneal confocal microscopy (CCM) in Multiple Sclerosis (MS) patients and to explore its potential ability to distinguish between MS patients and healthy subjects. Materials and methods: Cross-sectional study...
Saved in:
Published in | Current eye research Vol. 46; no. 10; pp. 1452 - 1459 |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Taylor & Francis
03.10.2021
|
Subjects | |
Online Access | Get full text |
ISSN | 0271-3683 1460-2202 1460-2202 |
DOI | 10.1080/02713683.2021.1904509 |
Cover
Abstract | Purpose/Aim: Our study aims to evaluate corneal subbasal nerve plexus morphology by in vivo corneal confocal microscopy (CCM) in Multiple Sclerosis (MS) patients and to explore its potential ability to distinguish between MS patients and healthy subjects.
Materials and methods: Cross-sectional study, including 60 MS patients and 22 healthy subjects. Expanded Disability Status Scale (EDSS) was used to assess neurological disability. All participants underwent full ophthalmology evaluation, CCM and optical coherence tomography (OCT). Corneal nerve fibre density (CNFD), branch density (CNBD), fibre length (CNFL) and fibre tortuosity (CNFT) were analysed. Generalized additive regression models were used to analyse the data.
Results: Compared to controls, MS patients had lower CNFD, CNBD and CNFL (p < .001) and higher CNFT (p = .002). The area under the ROC curve to distinguish MS patients from healthy controls with CNFD and CNBD was 0.84 (95%CI: 0.75 to 0.93; 95%CI: 0.75 to 0.92, respectively). A nonlinear association between EDSS and CNFD was found, with an initial density increase followed by a significant decrease until more severe disability status. EDSS was associated with CNFL and CNBD, with values being significantly lower for patients with an EDSS > 2.5 (−2.06 mm/mm2; 95%CI: −3.84 to −0.28; p = .027 and −8.70 branches/mm2; 95%CI: −14.69 to −2.71; p = .006, respectively). An optic neuritis (ON) history did not influence CCM parameters.
Conclusions: Our results confirm CCM parameters' potential to differentiate MS patients from healthy subjects, not being influenced by a previous ON history. A significant relationship between patient's disability and corneal nerve morphology was also found. |
---|---|
AbstractList | Purpose/Aim: Our study aims to evaluate corneal subbasal nerve plexus morphology by in vivo corneal confocal microscopy (CCM) in Multiple Sclerosis (MS) patients and to explore its potential ability to distinguish between MS patients and healthy subjects.
Materials and methods: Cross-sectional study, including 60 MS patients and 22 healthy subjects. Expanded Disability Status Scale (EDSS) was used to assess neurological disability. All participants underwent full ophthalmology evaluation, CCM and optical coherence tomography (OCT). Corneal nerve fibre density (CNFD), branch density (CNBD), fibre length (CNFL) and fibre tortuosity (CNFT) were analysed. Generalized additive regression models were used to analyse the data.
Results: Compared to controls, MS patients had lower CNFD, CNBD and CNFL (p < .001) and higher CNFT (p = .002). The area under the ROC curve to distinguish MS patients from healthy controls with CNFD and CNBD was 0.84 (95%CI: 0.75 to 0.93; 95%CI: 0.75 to 0.92, respectively). A nonlinear association between EDSS and CNFD was found, with an initial density increase followed by a significant decrease until more severe disability status. EDSS was associated with CNFL and CNBD, with values being significantly lower for patients with an EDSS > 2.5 (−2.06 mm/mm2; 95%CI: −3.84 to −0.28; p = .027 and −8.70 branches/mm2; 95%CI: −14.69 to −2.71; p = .006, respectively). An optic neuritis (ON) history did not influence CCM parameters.
Conclusions: Our results confirm CCM parameters' potential to differentiate MS patients from healthy subjects, not being influenced by a previous ON history. A significant relationship between patient's disability and corneal nerve morphology was also found. : Our study aims to evaluate corneal subbasal nerve plexus morphology by corneal confocal microscopy (CCM) in Multiple Sclerosis (MS) patients and to explore its potential ability to distinguish between MS patients and healthy subjects. : Cross-sectional study, including 60 MS patients and 22 healthy subjects. Expanded Disability Status Scale (EDSS) was used to assess neurological disability. All participants underwent full ophthalmology evaluation, CCM and optical coherence tomography (OCT). Corneal nerve fibre density (CNFD), branch density (CNBD), fibre length (CNFL) and fibre tortuosity (CNFT) were analysed. Generalized additive regression models were used to analyse the data. : Compared to controls, MS patients had lower CNFD, CNBD and CNFL ( < .001) and higher CNFT ( = .002). The area under the ROC curve to distinguish MS patients from healthy controls with CNFD and CNBD was 0.84 (95%CI: 0.75 to 0.93; 95%CI: 0.75 to 0.92, respectively). A nonlinear association between EDSS and CNFD was found, with an initial density increase followed by a significant decrease until more severe disability status. EDSS was associated with CNFL and CNBD, with values being significantly lower for patients with an EDSS > 2.5 (-2.06 mm/mm2; 95%CI: -3.84 to -0.28; = .027 and -8.70 branches/mm2; 95%CI: -14.69 to -2.71; = .006, respectively). An optic neuritis (ON) history did not influence CCM parameters. : Our results confirm CCM parameters' potential to differentiate MS patients from healthy subjects, not being influenced by a previous ON history. A significant relationship between patient's disability and corneal nerve morphology was also found. Purpose/Aim: Our study aims to evaluate corneal subbasal nerve plexus morphology by in vivo corneal confocal microscopy (CCM) in Multiple Sclerosis (MS) patients and to explore its potential ability to distinguish between MS patients and healthy subjects.Materials and methods: Cross-sectional study, including 60 MS patients and 22 healthy subjects. Expanded Disability Status Scale (EDSS) was used to assess neurological disability. All participants underwent full ophthalmology evaluation, CCM and optical coherence tomography (OCT). Corneal nerve fibre density (CNFD), branch density (CNBD), fibre length (CNFL) and fibre tortuosity (CNFT) were analysed. Generalized additive regression models were used to analyse the data.Results: Compared to controls, MS patients had lower CNFD, CNBD and CNFL (p < .001) and higher CNFT (p = .002). The area under the ROC curve to distinguish MS patients from healthy controls with CNFD and CNBD was 0.84 (95%CI: 0.75 to 0.93; 95%CI: 0.75 to 0.92, respectively). A nonlinear association between EDSS and CNFD was found, with an initial density increase followed by a significant decrease until more severe disability status. EDSS was associated with CNFL and CNBD, with values being significantly lower for patients with an EDSS > 2.5 (-2.06 mm/mm2; 95%CI: -3.84 to -0.28; p = .027 and -8.70 branches/mm2; 95%CI: -14.69 to -2.71; p = .006, respectively). An optic neuritis (ON) history did not influence CCM parameters.Conclusions: Our results confirm CCM parameters' potential to differentiate MS patients from healthy subjects, not being influenced by a previous ON history. A significant relationship between patient's disability and corneal nerve morphology was also found.Purpose/Aim: Our study aims to evaluate corneal subbasal nerve plexus morphology by in vivo corneal confocal microscopy (CCM) in Multiple Sclerosis (MS) patients and to explore its potential ability to distinguish between MS patients and healthy subjects.Materials and methods: Cross-sectional study, including 60 MS patients and 22 healthy subjects. Expanded Disability Status Scale (EDSS) was used to assess neurological disability. All participants underwent full ophthalmology evaluation, CCM and optical coherence tomography (OCT). Corneal nerve fibre density (CNFD), branch density (CNBD), fibre length (CNFL) and fibre tortuosity (CNFT) were analysed. Generalized additive regression models were used to analyse the data.Results: Compared to controls, MS patients had lower CNFD, CNBD and CNFL (p < .001) and higher CNFT (p = .002). The area under the ROC curve to distinguish MS patients from healthy controls with CNFD and CNBD was 0.84 (95%CI: 0.75 to 0.93; 95%CI: 0.75 to 0.92, respectively). A nonlinear association between EDSS and CNFD was found, with an initial density increase followed by a significant decrease until more severe disability status. EDSS was associated with CNFL and CNBD, with values being significantly lower for patients with an EDSS > 2.5 (-2.06 mm/mm2; 95%CI: -3.84 to -0.28; p = .027 and -8.70 branches/mm2; 95%CI: -14.69 to -2.71; p = .006, respectively). An optic neuritis (ON) history did not influence CCM parameters.Conclusions: Our results confirm CCM parameters' potential to differentiate MS patients from healthy subjects, not being influenced by a previous ON history. A significant relationship between patient's disability and corneal nerve morphology was also found. |
Author | Alves, Marta Xavier, Catarina Ferreira, Joana Tavares Papoila, Ana Luísa Fernandes, Diogo Cunha, João Paulo Luís, Maria Cardigos, Joana |
Author_xml | – sequence: 1 givenname: Diogo orcidid: 0000-0002-5972-4068 surname: Fernandes fullname: Fernandes, Diogo email: cdiogo777@gmail.com organization: Centro Hospitalar Universitário de Lisboa Central – sequence: 2 givenname: Maria surname: Luís fullname: Luís, Maria organization: Centro Hospitalar Universitário de Lisboa Central – sequence: 3 givenname: Joana surname: Cardigos fullname: Cardigos, Joana organization: Centro Hospitalar Universitário de Lisboa Central – sequence: 4 givenname: Catarina surname: Xavier fullname: Xavier, Catarina organization: Centro Hospitalar Universitário de Lisboa Central – sequence: 5 givenname: Marta surname: Alves fullname: Alves, Marta organization: Centro de Estatística e Aplicações da Universidade de Lisboa – sequence: 6 givenname: Ana Luísa surname: Papoila fullname: Papoila, Ana Luísa organization: Centro de Estatística e Aplicações da Universidade de Lisboa – sequence: 7 givenname: João Paulo surname: Cunha fullname: Cunha, João Paulo organization: Escola Superior de Tecnologia da Saúde de Lisboa – sequence: 8 givenname: Joana Tavares surname: Ferreira fullname: Ferreira, Joana Tavares organization: Centro Hospitalar Universitário de Lisboa Norte |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33734930$$D View this record in MEDLINE/PubMed |
BookMark | eNqFkctvVCEYxYmpsdPaP0HD0s0ded0HurFO6iPpK6l1S4CBBGVgBO6089_LnZm6cKEryMfvnHyccwKOQgwGgFcYzTEa0FtEeky7gc4JIniOOWIt4s_ADLMONaQOj8BsYpoJOgYnOf9AaBqwF-CY0p4yTtEMPC5iCkZ6eDcqJXO9XJu0MfDWm8cxw4uN9KMsLgaottAF-N1tIlzEYKOu7JXTKWYd17u3q9EXt_YG3mlv6tzld_Ac3sZiQnE75wf40cWVTD9NegmeW-mzOTucp-D-08W3xZfm8ubz18X5ZaMZI6VZ2kFJRi2ztGNtx3suieq0QbxXRHLFBtvzgSwVGSixsueMtLLHE1k1WNJT8Gbvu07x12hyESuXtfFeBhPHLEiLKGOMD6yirw_oqFZmKdbJ1V234imtCrR7YPp1Tsb-QTASUyviqRUxtSIOrVTd-7902pVdqiVJ5_-r_rBXu5p6WsmHmPxSFLn1Mdkkg3ZZ0H9b_AaN2KTx |
CitedBy_id | crossref_primary_10_1080_02713683_2023_2297347 crossref_primary_10_1167_tvst_13_12_22 crossref_primary_10_3390_jcm11206199 crossref_primary_10_1007_s10792_022_02448_6 crossref_primary_10_1177_17562864231204974 crossref_primary_10_1080_09273948_2023_2168698 crossref_primary_10_1016_j_jns_2025_123422 crossref_primary_10_1038_s41433_022_02018_1 crossref_primary_10_1038_s41598_021_01226_1 crossref_primary_10_1016_j_msard_2025_106397 crossref_primary_10_4103_1673_5374_375308 crossref_primary_10_1177_17562864221118731 |
Cites_doi | 10.1016/j.parkreldis.2016.04.033 10.1212/01.WNL.0000156155.19270.F8 10.1016/j.ophtha.2013.09.035 10.1371/journal.pone.0180175 10.1097/OPX.0b013e31824ee8c9 10.1007/s00415-010-5589-1 10.1002/acn3.746 10.1016/j.msard.2018.03.007 10.3109/02713683.2015.1119283 10.1186/s12929-017-0323-2 10.1148/radiol.2243011260 10.1001/jamaophthalmol.2017.1703 10.1371/journal.pone.0183040 10.1016/j.media.2011.05.016 10.1016/j.msard.2019.01.008 10.1097/ICO.0000000000001182 10.1001/jamaophthalmol.2017.1590 10.1186/s40478-014-0097-7 10.1212/WNL.0b013e31827deb39 10.1191/1352458505ms1186oa 10.1016/S1474-4422(12)70059-5 10.1097/ICO.0b013e3182749419 10.1111/opo.12365 10.4103/1673-5374.247421 10.2337/db12-0574 10.1177/1352458508090221 10.2337/dc14-1698 10.1016/j.neuron.2006.09.011 10.1016/j.ensci.2015.09.004 10.1016/j.jns.2015.11.017 10.1093/brain/awg038 10.1177/1352458516677590 10.1016/j.jtos.2016.09.004 10.1016/S1474-4422(17)30470-2 10.1111/cxo.12850 10.1177/1352458517708125 10.1167/iovs.17-22050 10.1186/s12974-016-0612-9 10.2337/dc14-2422 10.1167/iovs.13-13787 10.1001/jamaneurol.2018.2160 10.1136/bjo.2009.164780 |
ContentType | Journal Article |
Copyright | 2021 Taylor & Francis Group, LLC 2021 |
Copyright_xml | – notice: 2021 Taylor & Francis Group, LLC 2021 |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 |
DOI | 10.1080/02713683.2021.1904509 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | MEDLINE MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine Anatomy & Physiology |
EISSN | 1460-2202 |
EndPage | 1459 |
ExternalDocumentID | 33734930 10_1080_02713683_2021_1904509 1904509 |
Genre | Research Article Journal Article |
GroupedDBID | --- 00X 03L 0BK 0R~ 29F 36B 4.4 5GY 5RE AALUX AAMIU AAPUL AAQRR ABBKH ABDBF ABEIZ ABJNI ABLIJ ABLJU ABLKL ABUPF ABXYU ACENM ACGEJ ACGFS ACIEZ ACNCT ACUHS ADCVX ADRBQ ADXPE AECIN AENEX AEOZL AFKVX AGDLA AGFJD AGRBW AGYJP AIJEM AIRBT AJWEG AKBVH ALMA_UNASSIGNED_HOLDINGS ALQZU ALYBC AMDAE BABNJ BLEHA BOHLJ CCCUG CS3 DKSSO DU5 EAP EBC EBD EBS EMB EMK EMOBN EPL ESX F5P H13 HZ~ KRBQP KSSTO KWAYT KYCEM LJTGL M4Z O9- P2P PQQKQ RNANH RVRKI SV3 TBQAZ TDBHL TERGH TFDNU TFL TFW TUROJ TUS UEQFS V1S ~1N AAGDL AAYXX ABWVI ADYSH AFRVT AMPGV CITATION .55 .GJ 34G 39C 53G 5VS AALIY AAORF AAPXX ABWCV ABZEW ACKZS ADFOM ADFZZ AEIIZ AFFNX AFLEI AJVHN AWYRJ BRMBE CAG CGR COF CUY CVF CYYVM CZDIS DRXRE DWTOO ECM EIF EJD JENTW M44 NPM NUSFT QQXMO RIG X7M ZGI ZXP 7X8 TASJS |
ID | FETCH-LOGICAL-c442t-df8ba43f4f36456979a2b6ce097b2a9b48f7982db2832fa79425a715697f4f1a3 |
ISSN | 0271-3683 1460-2202 |
IngestDate | Fri Sep 05 02:42:16 EDT 2025 Wed Feb 19 02:27:11 EST 2025 Tue Jul 01 00:42:48 EDT 2025 Thu Apr 24 23:05:51 EDT 2025 Wed Dec 25 09:05:59 EST 2024 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 10 |
Keywords | expanded disability status scale Corneal subbasal nerve plexus confocal microscopy optical coherence tomography multiple sclerosis |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c442t-df8ba43f4f36456979a2b6ce097b2a9b48f7982db2832fa79425a715697f4f1a3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ORCID | 0000-0002-5972-4068 |
OpenAccessLink | http://hdl.handle.net/10400.21/13623 |
PMID | 33734930 |
PQID | 2503444984 |
PQPubID | 23479 |
PageCount | 8 |
ParticipantIDs | proquest_miscellaneous_2503444984 crossref_primary_10_1080_02713683_2021_1904509 pubmed_primary_33734930 informaworld_taylorfrancis_310_1080_02713683_2021_1904509 crossref_citationtrail_10_1080_02713683_2021_1904509 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 10/3/2021 |
PublicationDateYYYYMMDD | 2021-10-03 |
PublicationDate_xml | – month: 10 year: 2021 text: 10/3/2021 day: 03 |
PublicationDecade | 2020 |
PublicationPlace | England |
PublicationPlace_xml | – name: England |
PublicationTitle | Current eye research |
PublicationTitleAlternate | Curr Eye Res |
PublicationYear | 2021 |
Publisher | Taylor & Francis |
Publisher_xml | – name: Taylor & Francis |
References | cit0011 cit0033 cit0012 cit0034 cit0031 cit0010 cit0032 cit0030 Dabbah MA (cit0021) 2010; 13 cit0019 cit0017 cit0039 cit0018 cit0015 cit0037 cit0016 cit0038 cit0013 cit0035 cit0014 cit0036 cit0022 cit0001 cit0023 Petropoulos IN (cit0028) 2019; 102 cit0020 cit0042 cit0043 cit0040 cit0041 cit0008 cit0009 cit0006 cit0007 cit0029 cit0004 cit0026 cit0005 cit0027 cit0002 cit0024 cit0003 cit0025 |
References_xml | – ident: cit0012 doi: 10.1016/j.parkreldis.2016.04.033 – ident: cit0019 doi: 10.1212/01.WNL.0000156155.19270.F8 – volume: 13 start-page: 300 issue: 1 year: 2010 ident: cit0021 publication-title: Med Image Comput Comput Assist Interv – ident: cit0010 doi: 10.1016/j.ophtha.2013.09.035 – ident: cit0014 doi: 10.1371/journal.pone.0180175 – ident: cit0043 doi: 10.1097/OPX.0b013e31824ee8c9 – ident: cit0006 doi: 10.1007/s00415-010-5589-1 – ident: cit0016 doi: 10.1002/acn3.746 – ident: cit0033 doi: 10.1016/j.msard.2018.03.007 – ident: cit0009 doi: 10.3109/02713683.2015.1119283 – ident: cit0003 doi: 10.1186/s12929-017-0323-2 – ident: cit0004 doi: 10.1148/radiol.2243011260 – ident: cit0013 doi: 10.1001/jamaophthalmol.2017.1703 – ident: cit0042 doi: 10.1371/journal.pone.0183040 – ident: cit0020 doi: 10.1016/j.media.2011.05.016 – ident: cit0030 doi: 10.1016/j.msard.2019.01.008 – ident: cit0038 doi: 10.1097/ICO.0000000000001182 – ident: cit0026 doi: 10.1001/jamaophthalmol.2017.1590 – ident: cit0002 doi: 10.1186/s40478-014-0097-7 – ident: cit0008 doi: 10.1212/WNL.0b013e31827deb39 – ident: cit0017 doi: 10.1191/1352458505ms1186oa – ident: cit0032 doi: 10.1016/S1474-4422(12)70059-5 – ident: cit0023 doi: 10.1097/ICO.0b013e3182749419 – ident: cit0037 doi: 10.1111/opo.12365 – ident: cit0035 doi: 10.4103/1673-5374.247421 – ident: cit0040 doi: 10.2337/db12-0574 – ident: cit0011 doi: 10.1177/1352458508090221 – ident: cit0039 doi: 10.2337/dc14-1698 – ident: cit0027 doi: 10.1016/j.neuron.2006.09.011 – ident: cit0031 doi: 10.1016/j.ensci.2015.09.004 – ident: cit0007 doi: 10.1016/j.jns.2015.11.017 – ident: cit0005 doi: 10.1093/brain/awg038 – ident: cit0025 doi: 10.1177/1352458516677590 – ident: cit0041 doi: 10.1016/j.jtos.2016.09.004 – ident: cit0018 doi: 10.1016/S1474-4422(17)30470-2 – volume: 102 start-page: 1 issue: 1 year: 2019 ident: cit0028 publication-title: Clin Exp Optom doi: 10.1111/cxo.12850 – ident: cit0001 doi: 10.1177/1352458517708125 – ident: cit0024 doi: 10.1167/iovs.17-22050 – ident: cit0036 doi: 10.1186/s12974-016-0612-9 – ident: cit0015 doi: 10.2337/dc14-2422 – ident: cit0022 doi: 10.1167/iovs.13-13787 – ident: cit0029 doi: 10.1001/jamaneurol.2018.2160 – ident: cit0034 doi: 10.1136/bjo.2009.164780 |
SSID | ssj0002714 |
Score | 2.3787968 |
Snippet | Purpose/Aim: Our study aims to evaluate corneal subbasal nerve plexus morphology by in vivo corneal confocal microscopy (CCM) in Multiple Sclerosis (MS)... : Our study aims to evaluate corneal subbasal nerve plexus morphology by corneal confocal microscopy (CCM) in Multiple Sclerosis (MS) patients and to explore... |
SourceID | proquest pubmed crossref informaworld |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 1452 |
SubjectTerms | Adolescent Adult Aged Area Under Curve confocal microscopy Cornea - innervation Corneal Diseases - diagnosis Corneal subbasal nerve plexus Cross-Sectional Studies expanded disability status scale Female Humans Male Microscopy, Confocal Middle Aged multiple sclerosis Multiple Sclerosis - diagnosis Nerve Fibers - pathology optical coherence tomography Retinal Ganglion Cells - pathology ROC Curve Tomography, Optical Coherence Tonometry, Ocular Trigeminal Nerve - pathology Visual Acuity - physiology Young Adult |
Title | Corneal Subbasal Nerve Plexus Evaluation by in Vivo Confocal Microscopy in Multiple Sclerosis: A Potential New Biomarker |
URI | https://www.tandfonline.com/doi/abs/10.1080/02713683.2021.1904509 https://www.ncbi.nlm.nih.gov/pubmed/33734930 https://www.proquest.com/docview/2503444984 |
Volume | 46 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3da9swEBdZCmMvY2v3kX2hwdhLcLAl2Y72ln5RBil9aEfejOSPYmjtkjhrs39t_9zubFlxRrauewmOZclK7mfdWfe7O0I-MSQwxTqB51vEjtAJd5QvMscNw7HOADA6RY_u9DQ4uRBfZ_6s1_vZYS0tKz2Kf2yNK_kfqcI5kCtGyT5AsnZQOAHHIF_4BAnD5z_J-KCcF5gYGJ5-0EZwcIr8xeHZVXq3XAyPbCJvtDHzYvgt_17WIX6ov5Awj5ksy5u6bWqJhXAPOJ8vmpj1s7JCPlE99i1WrrxGPs-8a9O2KZ7SFZZg6eyOdbapG2M9Ly9LywBa1j76w4WJGMrXlCEE7WVpHBSqsA0zhUrcxC1CD9Ni9ixYQ5rjnaWNhZ7Dg6aEzShtll4RuA5j7sbabLYnDQbdzkrriSbzrdHa8FVu1QiGQgk3xPuNcDYjMIKE78q1Cmzd_r9pRstX9NpEqmaYCIeJzDCPyA4LwXDrk53J_uH-sTUE4OI6e1n7Y9sAMkztvm0-G6bRRuLcP7_-1GbQ-TPy1Ly_0EkDxueklxa7ZG9SqKq8XtHPtGYU166aXfJ4aogbe-TOQJW2UKU1VGkDVbqGKtUrmhcUoUpbqNI1VLGthSq1UP1CJ9QCFUa-pRaoL8jF8dH5wYljin44sRCscpJsrJXgmcjQQR7IUCqmgzh1ZaiZklqMs1COWaKxxlamQJ0wX4UeXgl9PMVfkn5RFulrQn2uU6V8MLK1Fiz2taczJUQoEz-RXMkBEe3_HcUmIz4WZrmK_irvARnZbjdNSpj7OsiuMKOq3ovLmsI5Eb-n78dW8hEs_OjNU0VaLhcRvLtwIYQciwF51UDCTofzkAvJ3TcPnepb8mT9vL4j_Wq-TN-D1V3pDwbdvwBltcyu |
linkProvider | EBSCOhost |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Corneal+Subbasal+Nerve+Plexus+Evaluation+by+in+Vivo+Confocal+Microscopy+in+Multiple+Sclerosis%3A+A+Potential+New+Biomarker&rft.jtitle=Current+eye+research&rft.au=Fernandes%2C+Diogo&rft.au=Lu%C3%ADs%2C+Maria&rft.au=Cardigos%2C+Joana&rft.au=Xavier%2C+Catarina&rft.date=2021-10-03&rft.issn=0271-3683&rft.eissn=1460-2202&rft.volume=46&rft.issue=10&rft.spage=1452&rft.epage=1459&rft_id=info:doi/10.1080%2F02713683.2021.1904509&rft.externalDBID=n%2Fa&rft.externalDocID=10_1080_02713683_2021_1904509 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0271-3683&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0271-3683&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0271-3683&client=summon |