Michele Iester

Prof. Michele Iester

1. Clinica Oculistica, DiNOGMI, University of Genoa, 16132 Genoa, Italy
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orcid

Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 August 2014 in PLOS ONE
Verified
Journal Article
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PFPaolo Frezzotti
Paolo Frezzotti
AGAntonio Giorgio
Antonio Giorgio
IMIlaria Motolese
Ilaria Motolese
ALAlessandro De Leucio
Alessandro De Leucio
MIMichele Iester
Michele Iester
NSNicola De Stefano
Nicola De Stefano
In order to test the hypothesis that in primary open angle glaucoma (POAG), an important cause of irreversible blindness, a spreading of neurodegeneration occurs through the brain, we performed multimodal MRI and subsequent whole-brain explorative voxelwise analyses in 13 advanced POAG patients and 12 age-matched normal controls (NC). Altered integrity (decreased fractional anisotropy or increased diffusivities) of white matter (WM) tracts was found not only along the visual pathway of POAG but also in nonvisual WM tracts (superior longitudinal fascicle, anterior thalamic radiation, corticospinal tract, middle cerebellar peduncle). POAG patients also showed brain atrophy in both visual cortex and other distant grey matter (GM) regions (frontoparietal cortex, hippocampi and cerebellar cortex), decreased functional connectivity (FC) in visual, working memory and dorsal attention networks and increased FC in visual and executive networks. In POAG, abnormalities in structure and FC within and outside visual system correlated with visual field parameters in the poorer performing eyes, thus emphasizing their clinical relevance. Altogether, this represents evidence that a vision disorder such as POAG can be considered a widespread neurodegenerative condition.

1 April 2010 in Ophthalmology
Verified
Journal Article
Closed access
NRNicolaas J. Reus
Nicolaas J. Reus
HLHans G. Lemij
Hans G. Lemij
DGDavid Garway-Heath
David Garway-Heath
PAP. Juhani Airaksinen
P. Juhani Airaksinen
AAAlfonso Anton
Alfonso Anton
TZThierry G. Zeyen
Thierry G. Zeyen

1 March 1997 in Ophthalmology
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Journal Article
Closed access
MIMichele Iester
Michele Iester
FMFrederick S. Mikelberg
Frederick S. Mikelberg
SDStephen M. Drance
Stephen M. Drance

16 November 2014 in Graefe's Archive for Clinical and Experimental Ophthalmology
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Journal Article
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AMAngelo Macri
Angelo Macri
CSChiara Scanarotti
Chiara Scanarotti
ABAnna Maria Bassi
Anna Maria Bassi
SGSebastiano Giuffrida
Sebastiano Giuffrida
GSGiorgio Sangalli
Giorgio Sangalli
MIMichele Iester
Michele Iester

1 July 1998 in Cornea
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Journal Article
Closed access
MRMaurizio Rolando
Maurizio Rolando
MIMichele Iester
Michele Iester
AMAngelo Macrí
Angelo Macrí
GCGiovanni Calabria
Giovanni Calabria
Blurred vision in keratoconjunctivitis sicca eyes could be the result of the loss of the glossy surface of the tear film because of changes in composition or thickness irregularities. Spatial-contrast sensitivity in keratoconjunctivitis sicca and normal control eyes was tested before and after a tear substitute. Three different groups of subjects were enrolled: one group of dry eyes with nonsignificant signs of epithelial disease (n = 12), the second group of dry eye positive with 1% Bengal rose staining of the cornea and of the conjunctiva (n = 18), and a third of normal eyes as control group (n = 15). In all the 45 eyes, spatial-contrast sensitivity was tested under the best correction by means of the Vistech Multivision Contrast Tester 8000 (Vistech Consultants, Dayton, OH, U.S.A.) before and 15 min after the instillation of a 0.4% Na-hyaluronate tear substitute without preservatives. A significant decrease of spatial-contrast sensitivity ranging from 35 to 70% was present in keratoconjunctivitis sicca eyes compared with a third group of age-matched normal eyes used as control. The spatial-contrast sensitivity was significantly lower also in the presence of preserved corneal surface. The addition of a tear substitute improved spatial contrast—sensitivity thresholds in all groups. Tear-film disease can affect the transfer function of modulation of the ocular surface.

1 January 2001 in Eye
Verified
Journal Article
Closed access
MIMichele Iester
Michele Iester
AMAndre Mermoud
Andre Mermoud
FAFarid Achache
Farid Achache
SRSylvain Roy
Sylvain Roy