Retinal Contrast Gain Control and Temporal Modulation Sensitivity Across the Visual Field in Glaucoma at Photopic and Mesopic Light Conditions

Glaucoma affects many aspects of visual performance, including adaptation, and this may depend on ambient luminance. We determine the influence of glaucoma and luminance on temporal aspects of adaptation, specifically on contrast gain control and temporal modulation sensitivity (TMS). This case-cont...

Full description

Saved in:
Bibliographic Details
Published inInvestigative ophthalmology & visual science Vol. 60; no. 13; p. 4270
Main Authors João, Catarina A. R., Scanferla, Lorenzo, Jansonius, Nomdo M.
Format Journal Article
LanguageEnglish
Published United States 01.10.2019
Subjects
Online AccessGet full text
ISSN1552-5783
1552-5783
DOI10.1167/iovs.19-27123

Cover

Abstract Glaucoma affects many aspects of visual performance, including adaptation, and this may depend on ambient luminance. We determine the influence of glaucoma and luminance on temporal aspects of adaptation, specifically on contrast gain control and temporal modulation sensitivity (TMS). This case-control study included 12 glaucoma patients and 25 age-similar controls (50-70 years). Threshold perimetry was performed with a minimized testing grid (fovea and four peripheral locations). Stimuli (Goldmann size III 50 ms increment/decrement) were presented on a time-varying background with sinusoidally-modulated luminance (amplitude 60%; frequency 0-30 Hz; mean background luminance, 1 and 100 cd/m2). TMS (2.5-30 Hz) was measured in the same locations with a sinusoidally-modulated stimulus (Goldmann size IV, 334 ms) on a steady background (1 and 100 cd/m2). In healthy subjects, contrast sensitivity decreased with increasing background modulation frequency and increased again at very high frequencies, indicating contrast gain control. Minimum sensitivity was located between 2.5 and 20 Hz, depending on luminance and eccentricity. In glaucoma patients, the same frequency dependency was found (P = 0.12) but with an overall reduced sensitivity (P = 1 × 10-5), independent of luminance (P = 0.20). Decrements differentiated better between glaucoma and healthy subjects than increments (P = 0.004). TMS was reduced in glaucoma (P = 5 × 10-6) across all frequencies and luminance levels, with complete loss for high frequencies at 1 cd/m2. Contrast gain control is largely unaffected in glaucoma, suggesting intact amacrine cell function. Perimetry with decrements or a high-frequency stimulus on a low-luminance background seems best to differentiate between glaucoma and healthy subjects.
AbstractList Glaucoma affects many aspects of visual performance, including adaptation, and this may depend on ambient luminance. We determine the influence of glaucoma and luminance on temporal aspects of adaptation, specifically on contrast gain control and temporal modulation sensitivity (TMS).PurposeGlaucoma affects many aspects of visual performance, including adaptation, and this may depend on ambient luminance. We determine the influence of glaucoma and luminance on temporal aspects of adaptation, specifically on contrast gain control and temporal modulation sensitivity (TMS).This case-control study included 12 glaucoma patients and 25 age-similar controls (50-70 years). Threshold perimetry was performed with a minimized testing grid (fovea and four peripheral locations). Stimuli (Goldmann size III 50 ms increment/decrement) were presented on a time-varying background with sinusoidally-modulated luminance (amplitude 60%; frequency 0-30 Hz; mean background luminance, 1 and 100 cd/m2). TMS (2.5-30 Hz) was measured in the same locations with a sinusoidally-modulated stimulus (Goldmann size IV, 334 ms) on a steady background (1 and 100 cd/m2).MethodsThis case-control study included 12 glaucoma patients and 25 age-similar controls (50-70 years). Threshold perimetry was performed with a minimized testing grid (fovea and four peripheral locations). Stimuli (Goldmann size III 50 ms increment/decrement) were presented on a time-varying background with sinusoidally-modulated luminance (amplitude 60%; frequency 0-30 Hz; mean background luminance, 1 and 100 cd/m2). TMS (2.5-30 Hz) was measured in the same locations with a sinusoidally-modulated stimulus (Goldmann size IV, 334 ms) on a steady background (1 and 100 cd/m2).In healthy subjects, contrast sensitivity decreased with increasing background modulation frequency and increased again at very high frequencies, indicating contrast gain control. Minimum sensitivity was located between 2.5 and 20 Hz, depending on luminance and eccentricity. In glaucoma patients, the same frequency dependency was found (P = 0.12) but with an overall reduced sensitivity (P = 1 × 10-5), independent of luminance (P = 0.20). Decrements differentiated better between glaucoma and healthy subjects than increments (P = 0.004). TMS was reduced in glaucoma (P = 5 × 10-6) across all frequencies and luminance levels, with complete loss for high frequencies at 1 cd/m2.ResultsIn healthy subjects, contrast sensitivity decreased with increasing background modulation frequency and increased again at very high frequencies, indicating contrast gain control. Minimum sensitivity was located between 2.5 and 20 Hz, depending on luminance and eccentricity. In glaucoma patients, the same frequency dependency was found (P = 0.12) but with an overall reduced sensitivity (P = 1 × 10-5), independent of luminance (P = 0.20). Decrements differentiated better between glaucoma and healthy subjects than increments (P = 0.004). TMS was reduced in glaucoma (P = 5 × 10-6) across all frequencies and luminance levels, with complete loss for high frequencies at 1 cd/m2.Contrast gain control is largely unaffected in glaucoma, suggesting intact amacrine cell function. Perimetry with decrements or a high-frequency stimulus on a low-luminance background seems best to differentiate between glaucoma and healthy subjects.ConclusionsContrast gain control is largely unaffected in glaucoma, suggesting intact amacrine cell function. Perimetry with decrements or a high-frequency stimulus on a low-luminance background seems best to differentiate between glaucoma and healthy subjects.
Glaucoma affects many aspects of visual performance, including adaptation, and this may depend on ambient luminance. We determine the influence of glaucoma and luminance on temporal aspects of adaptation, specifically on contrast gain control and temporal modulation sensitivity (TMS). This case-control study included 12 glaucoma patients and 25 age-similar controls (50-70 years). Threshold perimetry was performed with a minimized testing grid (fovea and four peripheral locations). Stimuli (Goldmann size III 50 ms increment/decrement) were presented on a time-varying background with sinusoidally-modulated luminance (amplitude 60%; frequency 0-30 Hz; mean background luminance, 1 and 100 cd/m2). TMS (2.5-30 Hz) was measured in the same locations with a sinusoidally-modulated stimulus (Goldmann size IV, 334 ms) on a steady background (1 and 100 cd/m2). In healthy subjects, contrast sensitivity decreased with increasing background modulation frequency and increased again at very high frequencies, indicating contrast gain control. Minimum sensitivity was located between 2.5 and 20 Hz, depending on luminance and eccentricity. In glaucoma patients, the same frequency dependency was found (P = 0.12) but with an overall reduced sensitivity (P = 1 × 10-5), independent of luminance (P = 0.20). Decrements differentiated better between glaucoma and healthy subjects than increments (P = 0.004). TMS was reduced in glaucoma (P = 5 × 10-6) across all frequencies and luminance levels, with complete loss for high frequencies at 1 cd/m2. Contrast gain control is largely unaffected in glaucoma, suggesting intact amacrine cell function. Perimetry with decrements or a high-frequency stimulus on a low-luminance background seems best to differentiate between glaucoma and healthy subjects.
Author Scanferla, Lorenzo
Jansonius, Nomdo M.
João, Catarina A. R.
Author_xml – sequence: 1
  givenname: Catarina A. R.
  surname: João
  fullname: João, Catarina A. R.
  organization: Department of Ophthalmology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands, Graduate School of Medical Sciences (Research School of Behavioural and Cognitive Neurosciences), University of Groningen, Groningen, The Netherlands
– sequence: 2
  givenname: Lorenzo
  surname: Scanferla
  fullname: Scanferla, Lorenzo
  organization: Department of Ophthalmology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands, Graduate School of Medical Sciences (Research School of Behavioural and Cognitive Neurosciences), University of Groningen, Groningen, The Netherlands
– sequence: 3
  givenname: Nomdo M.
  surname: Jansonius
  fullname: Jansonius, Nomdo M.
  organization: Department of Ophthalmology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands, Graduate School of Medical Sciences (Research School of Behavioural and Cognitive Neurosciences), University of Groningen, Groningen, The Netherlands
BackLink https://www.ncbi.nlm.nih.gov/pubmed/31618763$$D View this record in MEDLINE/PubMed
BookMark eNptkc1KJDEURsOgjD8zS7eSpZvSSlJJJUtp7J6BFmWU2YZbqbQdSSVtJSX4Ej6z1dUKIq5yA-eeC993hPZCDBahE1KeEyLqCxef0zlRBa0JZT_QIeGcFryWbO_TfICOUnosS0oILX-iA0YEkbVgh-j1n80ugMezGHIPKeMFuLD7RY8htPjedpvYj8h1bAcP2cWA72xILrtnl1_wpeljSjivLf7v0jCCc2d9i0fNwsNgYgcYMr5dxxw3zkzOa5umeeke1nl7rXVbb_qF9lfgk_39_h6ju_nV_exPsbxZ_J1dLgvDGM2FairBhVmBpEAraduWm4a3AEbIUvFGqJWtgJjKci4FASAlUVIKqYRqanaMznbWTR-fBpuy7lwy1nsINg5JU1aKSnGmqhE9fUeHprOt3vSug_5FfyQ4AmwHTCn0dqWNy1NIY5zOa1LqbU9625MmSk89jVvFl60P8ff8GziZlys
CitedBy_id crossref_primary_10_3233_JPD_223481
crossref_primary_10_1016_j_visres_2023_108188
crossref_primary_10_1167_iovs_63_11_16
crossref_primary_10_1016_j_preteyeres_2022_101160
crossref_primary_10_1167_tvst_10_12_16
Cites_doi 10.1371/journal.pone.0193663
10.1111/j.1475-1313.2004.00223.x
10.1113/jphysiol.1978.sp012571
10.1085/jgp.19.2.321
10.1364/JOSAA.10.001792
10.1167/iovs.15-16753
10.1016/S0161-6420(00)00624-2
10.1167/iovs.05-0321
10.1111/j.1755-3768.2010.01988.x
10.1111/aos.13695
10.1038/s41598-018-20480-4
10.1073/pnas.1310442111
10.1364/JOSA.36.000624
10.1038/scientificamerican0173-70
10.3109/02713689409047005
10.1523/JNEUROSCI.0504-11.2011
10.1186/1471-2202-14-S1-P7
10.1016/S0042-6989(96)00228-3
10.1163/156856897X00357
10.1111/j.1600-0420.2005.00423.x
10.1002/cne.24074
10.1017/S0952523800173110
10.1167/iovs.15-16481
10.1163/156856897X00366
10.1097/MAJ.0000000000000319
10.1167/16.15.18
10.1167/iovs.12-11300
10.1085/jgp.34.5.657
10.1136/bjo.83.5.546
10.1016/j.neuron.2014.02.020
10.1111/j.1442-9071.2010.02488.x
10.1167/17.14.5
10.1167/iovs.17-22497
10.1017/S0952523800008865
ContentType Journal Article
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
DOI 10.1167/iovs.19-27123
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 - Academic
MEDLINE
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
EISSN 1552-5783
ExternalDocumentID 31618763
10_1167_iovs_19_27123
Genre Research Support, Non-U.S. Gov't
Journal Article
GroupedDBID ---
18M
2WC
34G
39C
5GY
5RE
AAYXX
ACGFO
ACNCT
ADBBV
AENEX
ALMA_UNASSIGNED_HOLDINGS
BAWUL
CITATION
CS3
DIK
DU5
E3Z
EBS
EJD
F5P
GROUPED_DOAJ
GX1
N9A
OK1
P2P
RPM
SJN
TR2
TRV
W8F
WH7
WOQ
WOW
AFOSN
CGR
CUY
CVF
ECM
EIF
NPM
7X8
ID FETCH-LOGICAL-c332t-9b4656cfa82a248edd5cb5daac68095b69fe4a1c4e55861aa10198868969b73
ISSN 1552-5783
IngestDate Fri Sep 05 14:12:07 EDT 2025
Thu Apr 03 07:08:49 EDT 2025
Thu Apr 24 23:13:13 EDT 2025
Wed Oct 01 03:10:39 EDT 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 13
Language English
License http://creativecommons.org/licenses/by-nc-nd/4.0
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c332t-9b4656cfa82a248edd5cb5daac68095b69fe4a1c4e55861aa10198868969b73
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://iovs.arvojournals.org/arvo/content_public/journal/iovs/938216/i1552-5783-60-13-4270.pdf
PMID 31618763
PQID 2306495394
PQPubID 23479
ParticipantIDs proquest_miscellaneous_2306495394
pubmed_primary_31618763
crossref_citationtrail_10_1167_iovs_19_27123
crossref_primary_10_1167_iovs_19_27123
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2019-10-01
PublicationDateYYYYMMDD 2019-10-01
PublicationDate_xml – month: 10
  year: 2019
  text: 2019-10-01
  day: 01
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Investigative ophthalmology & visual science
PublicationTitleAlternate Invest Ophthalmol Vis Sci
PublicationYear 2019
References i1552-5783-60-13-4270-b16
i1552-5783-60-13-4270-b38
i1552-5783-60-13-4270-b17
i1552-5783-60-13-4270-b39
i1552-5783-60-13-4270-b14
i1552-5783-60-13-4270-b36
i1552-5783-60-13-4270-b15
i1552-5783-60-13-4270-b37
i1552-5783-60-13-4270-b12
i1552-5783-60-13-4270-b34
i1552-5783-60-13-4270-b13
i1552-5783-60-13-4270-b35
i1552-5783-60-13-4270-b10
i1552-5783-60-13-4270-b32
i1552-5783-60-13-4270-b11
i1552-5783-60-13-4270-b33
i1552-5783-60-13-4270-b18
i1552-5783-60-13-4270-b19
i1552-5783-60-13-4270-b30
i1552-5783-60-13-4270-b31
i1552-5783-60-13-4270-b05
i1552-5783-60-13-4270-b27
i1552-5783-60-13-4270-b06
i1552-5783-60-13-4270-b28
i1552-5783-60-13-4270-b03
i1552-5783-60-13-4270-b25
i1552-5783-60-13-4270-b04
i1552-5783-60-13-4270-b26
i1552-5783-60-13-4270-b01
i1552-5783-60-13-4270-b23
i1552-5783-60-13-4270-b02
i1552-5783-60-13-4270-b24
i1552-5783-60-13-4270-b21
i1552-5783-60-13-4270-b22
i1552-5783-60-13-4270-b09
i1552-5783-60-13-4270-b07
i1552-5783-60-13-4270-b29
i1552-5783-60-13-4270-b08
i1552-5783-60-13-4270-b20
i1552-5783-60-13-4270-b40
References_xml – ident: i1552-5783-60-13-4270-b07
  doi: 10.1371/journal.pone.0193663
– ident: i1552-5783-60-13-4270-b27
– ident: i1552-5783-60-13-4270-b15
  doi: 10.1111/j.1475-1313.2004.00223.x
– ident: i1552-5783-60-13-4270-b39
  doi: 10.1113/jphysiol.1978.sp012571
– ident: i1552-5783-60-13-4270-b18
  doi: 10.1085/jgp.19.2.321
– ident: i1552-5783-60-13-4270-b26
  doi: 10.1364/JOSAA.10.001792
– ident: i1552-5783-60-13-4270-b37
  doi: 10.1167/iovs.15-16753
– ident: i1552-5783-60-13-4270-b04
  doi: 10.1016/S0161-6420(00)00624-2
– ident: i1552-5783-60-13-4270-b10
  doi: 10.1167/iovs.05-0321
– ident: i1552-5783-60-13-4270-b03
  doi: 10.1111/j.1755-3768.2010.01988.x
– ident: i1552-5783-60-13-4270-b01
  doi: 10.1111/aos.13695
– ident: i1552-5783-60-13-4270-b22
  doi: 10.1038/s41598-018-20480-4
– ident: i1552-5783-60-13-4270-b35
  doi: 10.1073/pnas.1310442111
– ident: i1552-5783-60-13-4270-b31
  doi: 10.1364/JOSA.36.000624
– ident: i1552-5783-60-13-4270-b08
  doi: 10.1038/scientificamerican0173-70
– ident: i1552-5783-60-13-4270-b20
– ident: i1552-5783-60-13-4270-b24
– ident: i1552-5783-60-13-4270-b29
  doi: 10.3109/02713689409047005
– ident: i1552-5783-60-13-4270-b34
  doi: 10.1523/JNEUROSCI.0504-11.2011
– ident: i1552-5783-60-13-4270-b32
  doi: 10.1186/1471-2202-14-S1-P7
– ident: i1552-5783-60-13-4270-b12
  doi: 10.1016/S0042-6989(96)00228-3
– ident: i1552-5783-60-13-4270-b16
  doi: 10.1163/156856897X00357
– ident: i1552-5783-60-13-4270-b14
  doi: 10.1111/j.1600-0420.2005.00423.x
– ident: i1552-5783-60-13-4270-b11
  doi: 10.1002/cne.24074
– ident: i1552-5783-60-13-4270-b13
  doi: 10.1017/S0952523800173110
– ident: i1552-5783-60-13-4270-b30
– ident: i1552-5783-60-13-4270-b28
  doi: 10.1167/iovs.15-16481
– ident: i1552-5783-60-13-4270-b17
  doi: 10.1163/156856897X00366
– ident: i1552-5783-60-13-4270-b02
  doi: 10.1097/MAJ.0000000000000319
– ident: i1552-5783-60-13-4270-b36
  doi: 10.1167/16.15.18
– ident: i1552-5783-60-13-4270-b21
  doi: 10.1167/iovs.12-11300
– ident: i1552-5783-60-13-4270-b19
  doi: 10.1085/jgp.34.5.657
– ident: i1552-5783-60-13-4270-b05
  doi: 10.1136/bjo.83.5.546
– ident: i1552-5783-60-13-4270-b33
  doi: 10.1016/j.neuron.2014.02.020
– ident: i1552-5783-60-13-4270-b09
  doi: 10.1111/j.1442-9071.2010.02488.x
– ident: i1552-5783-60-13-4270-b25
– ident: i1552-5783-60-13-4270-b38
  doi: 10.1167/17.14.5
– ident: i1552-5783-60-13-4270-b06
  doi: 10.1167/iovs.17-22497
– ident: i1552-5783-60-13-4270-b23
– ident: i1552-5783-60-13-4270-b40
  doi: 10.1017/S0952523800008865
SSID ssj0021120
Score 2.333799
Snippet Glaucoma affects many aspects of visual performance, including adaptation, and this may depend on ambient luminance. We determine the influence of glaucoma and...
SourceID proquest
pubmed
crossref
SourceType Aggregation Database
Index Database
Enrichment Source
StartPage 4270
SubjectTerms Aged
Case-Control Studies
Color Vision - physiology
Contrast Sensitivity - physiology
Female
Glaucoma, Open-Angle - physiopathology
Healthy Volunteers
Humans
Light
Male
Mesopic Vision - physiology
Middle Aged
Retina - physiology
Visual Acuity - physiology
Visual Field Tests
Visual Fields - physiology
Title Retinal Contrast Gain Control and Temporal Modulation Sensitivity Across the Visual Field in Glaucoma at Photopic and Mesopic Light Conditions
URI https://www.ncbi.nlm.nih.gov/pubmed/31618763
https://www.proquest.com/docview/2306495394
Volume 60
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVAON
  databaseName: DOAJ Directory of Open Access Journals
  customDbUrl:
  eissn: 1552-5783
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0021120
  issn: 1552-5783
  databaseCode: DOA
  dateStart: 20160101
  isFulltext: true
  titleUrlDefault: https://www.doaj.org/
  providerName: Directory of Open Access Journals
– providerCode: PRVBFR
  databaseName: Free Medical Journals
  customDbUrl:
  eissn: 1552-5783
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0021120
  issn: 1552-5783
  databaseCode: DIK
  dateStart: 19620101
  isFulltext: true
  titleUrlDefault: http://www.freemedicaljournals.com
  providerName: Flying Publisher
– providerCode: PRVFQY
  databaseName: GFMER Free Medical Journals
  customDbUrl:
  eissn: 1552-5783
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0021120
  issn: 1552-5783
  databaseCode: GX1
  dateStart: 0
  isFulltext: true
  titleUrlDefault: http://www.gfmer.ch/Medical_journals/Free_medical.php
  providerName: Geneva Foundation for Medical Education and Research
– providerCode: PRVAQN
  databaseName: PubMed Central
  customDbUrl:
  eissn: 1552-5783
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0021120
  issn: 1552-5783
  databaseCode: RPM
  dateStart: 20070101
  isFulltext: true
  titleUrlDefault: https://www.ncbi.nlm.nih.gov/pmc/
  providerName: National Library of Medicine
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Jb9NAFB6FIlW9IPaGpRokxKW4xJ7x2HOsgLYsQYgW1Js1tidKUGJHtZNDfwR_gj_Ke7M4iSAScLEsLzNR3ue3L4Q8l0xJ7IoC33eRBDwqRKB4HgflAIRfUfIiNw1Mh5_E2Vf-_jK-7PV-rmUtLdr8qLj-Y13J_1AVrgFdsUr2HyjbLQoX4BzoC0egMBz_isZfsF7ZWP_oom3aw1Nli_hM9jm6xC9s56kpzjxzg7qAPVSYqGWGRhwbKWm0z2-TBktJTjClDb0gp1O1gB-tsNzx87hu67lr7TrUjTn_iHY97lZOVl6_7z4zvmvfsdSH9XzcjtV0Zvs9IdiWdjMnf1dpPCZuz2pXmwh2fKWAdXXRqHMAwgg9kMadUF_p6rruXlZYxzZZNDYcNStr5-l1Po1QdtlxIJIcH47BRk7sjBvPqO3gAQ9ItsZ2eWSnj_wuDwRGpCf1sjmCXaIktMXNa9iYzww4GA4O8Lx2swG3v3WD3IwSIXBMxpt3HzqrHhTWgW_eKpJXG3vtkV3_9qbes8WYMUrNxW1yy1kj9NhC6w7p6eou2R26fIt75IdDGPUIo4gw6hBGAQ3UI4yuEEbXEEYtwiggjFqEUYMwCst4hFHVUo8ws6ZDGDUIoyuE3SfnJ28vXp8FboJHUDAWtYHMsR1fMVJppCKe6rKM4eMvlSpECrp9LuRIcxUWXMdxKkKlQEDINBWpFDJP2AOyU9WV3ieUDTTXTMXlQCkeJknKGYjaSMcFyJxBKfvkpf93s8I1t8cZK9PMGLkiyZAuWSgzQ5c-edE9PrddXbY9-MyTKgO-i8E0Vel60WTGdJcxk7xPHloadkt5mj_aeucx2Vvh_gnZaa8W-ilot21-YNB1YHxDvwCRiaq7
linkProvider Flying Publisher
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=Retinal+Contrast+Gain+Control+and+Temporal+Modulation+Sensitivity+Across+the+Visual+Field+in+Glaucoma+at+Photopic+and+Mesopic+Light+Conditions&rft.jtitle=Investigative+ophthalmology+%26+visual+science&rft.au=Jo%C3%A3o%2C+Catarina+A+R&rft.au=Scanferla%2C+Lorenzo&rft.au=Jansonius%2C+Nomdo+M&rft.date=2019-10-01&rft.eissn=1552-5783&rft.volume=60&rft.issue=13&rft.spage=4270&rft_id=info:doi/10.1167%2Fiovs.19-27123&rft_id=info%3Apmid%2F31618763&rft.externalDocID=31618763
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1552-5783&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1552-5783&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1552-5783&client=summon