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Dive into the research topics where Eduardo Motolese is active.

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Featured researches published by Eduardo Motolese.


Acta Ophthalmologica | 2015

Circadian intraocular pressure patterns in healthy subjects, primary open angle and normal tension glaucoma patients with a contact lens sensor

Luca Agnifili; Rodolfo Mastropasqua; Paolo Frezzotti; Vincenzo Fasanella; Ilaria Motolese; Emilio Pedrotti; Angelo Di Iorio; Peter A. Mattei; Eduardo Motolese; Leonardo Mastropasqua

To examine the circadian intraocular pressure (IOP) patterns in healthy subjects, in primary open angle and normal tension glaucoma (POAG; NTG) using a contact lens sensor (CLS; Sensimed Triggerfish, Lausanne, Switzerland).


PLOS ONE | 2014

Structural and Functional Brain Changes beyond Visual System in Patients with Advanced Glaucoma

Paolo Frezzotti; Antonio Giorgio; Ilaria Motolese; Alessandro De Leucio; Michele Iester; Eduardo Motolese; Antonio Federico; 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.


Clinical and Experimental Ophthalmology | 2017

Hydrus microstent compared to selective laser trabeculoplasty in primary open angle glaucoma: One year results

Antonio Maria Fea; Iqbal Ike K. Ahmed; Carlo Lavia; Pietro Mittica; Giulia Consolandi; Ilaria Motolese; Giulia Pignata; Eduardo Motolese; Teresa Rolle; Paolo Frezzotti

To compare the reduction of intraocular pressure (IOP) and glaucoma medications following selective laser trabeculoplasty (SLT) versus stand‐alone placement of the Hydrus microstent, a microinvasive glaucoma surgery device.


Acta Ophthalmologica | 2014

In vivo confocal microscopy of conjunctiva in preservative‐free timolol 0.1% gel formulation therapy for glaucoma

Paolo Frezzotti; Paolo Fogagnolo; Gentiana Haka; Ilaria Motolese; Michele Iester; Simone Alex Bagaglia; Pietro Mittica; Cristina Menicacci; Luca Rossetti; Eduardo Motolese

To evaluate the effects at 1 year of preservative‐free timolol gel and preserved timolol eye drops on conjunctiva and tear parameters.


British Journal of Ophthalmology | 2011

Association between primary open-angle glaucoma (POAG) and WDR36 sequence variance in Italian families affected by POAG

Paolo Frezzotti; Chiara Pescucci; Filomena Tiziana Papa; Michele Iester; V. Mittica; Ilaria Motolese; Sabrina Peruzzi; Rosangela Artuso; Ilaria Longo; Maria Antonietta Mencarelli; Pietro Mittica; Eduardo Motolese; Alessandra Renieri

Background/aims To assess the involvement of WDR36 sequence variance in primary open-angle glaucoma (POAG) in Italian patients. Methods A cohort of 34 Italian families affected by POAG was analysed by denaturing high-performance liquid chromatography for mutation in the WDR36 gene. Among the 34 families enrolled, 25 were affected by high-tension glaucoma (HTG), four by juvenile open-angle glaucoma and one by normal tension glaucoma. In addition, four families presented both juvenile open-angle glaucoma and HTG-POAG patients within the same pedigree. Results Four previously identified intronic polymorphisms (IVS5+30C→T; IVS12+90 G→T; IVS13+89G→A; IVS16-30A→G) and a novel one (IVS21-75G→A) have been identified. In addition, one proband was found to carry the p.D658G mutation reported as the more recurrent disease-causing allele. Conclusions The findings suggest that WDR36 sequence variance is only a rare cause of glaucoma in Italian families. Clearly, investigation of additional families with extensive studies is needed to clarify the role of WDR36 in the pathophysiology of glaucoma.


Ophthalmologica | 1998

Standardized echography, pattern electroretinography and visual-evoked potential and automated perimetry in the early diagnosis of Graves' neuropathy

Luisa Pierro; Eugenio Conforto; Antonio Giordano Resti; Rosangela Lattanzio; F. Genovesi-Ebert; S. Rizzo; S. Chiellini; G. Gabbriellini; F. Laddaga; M. Nardi; A. Romani; M.S. Sartini; Lelio Sabetti; Andrea Toscano; Giuseppe Specchia; Emilio Balestrazzi; Teresio Avitabile; F. Marano; F. Castiglione; Alfredo Reibaldi; V. Russo; M.G. Uva; A. Marino; Elisabetta Zaganelli; Alessandra Tavola; Mario Muraglia; A. Polizzi; M. Schenone; C. Ciurlo; R. Bertagno

Twenty-four patients (47 eyes) affected by Graves’ disease were enrolled to evaluate the role of standardized echography, pattern electroretinogram (P-ERG), visual evoked potentials (P-VEPs) and automated perimetry in the early diagnosis of the compressive optic neuropathy (CON). The P-ERG amplitude reduction was the most sensitive parameter to demonstrate an early impairment of the optic nerve (ON) function. We found a significant negative correlation between the ON diameter and the P-ERG amplitude. VEPs responses were also altered, but their ability in detecting an early ON damage was less sensitive and specific than P-ERG. The visual field damage was often aspecific and delayed with respect to electrophysiological alterations.


Ophthalmologica | 1998

Alterations of the Internal Reflectivity of Extra-Ocular Muscles Associated with Several Clinical Stages of Graves’ Ophthalmopathy

Luisa Pierro; Eugenio Conforto; Antonio Giordano Resti; Rosangela Lattanzio; F. Genovesi-Ebert; S. Rizzo; S. Chiellini; G. Gabbriellini; F. Laddaga; M. Nardi; A. Romani; M.S. Sartini; Lelio Sabetti; Andrea Toscano; Giuseppe Specchia; Emilio Balestrazzi; Teresio Avitabile; F. Marano; F. Castiglione; Alfredo Reibaldi; V. Russo; M.G. Uva; A. Marino; Elisabetta Zaganelli; Alessandra Tavola; Mario Muraglia; A. Polizzi; M. Schenone; C. Ciurlo; R. Bertagno

In the period between February 1992 and June 1996, the authors performed extra-ocular muscle echobiometry on 163 patients with Graves’ disease. The aim of this study is the evaluation of changes occurring in several clinical stages. The authors noted an increase in internal muscular reflectivity in the advanced phases and an irregular structure in the early stages. Controversial results in the literature warrant mastery of the method and further research.


European Journal of Ophthalmology | 2007

Ocular manifestations of chronic graft-versus-host disease in patients treated with extracorporeal photochemotherapy

Eduardo Motolese; Rubegni P; Poggiali S; P. A. Motolese; Marotta G; Russo L; D'Ascenzo G; Carcagni Mr; Mario Fruschelli; Ilaria Motolese; Fimiani M

Purpose Eye involvement has long been appreciated in patients with chronic graft versus host disease (cGVHD). In particular, ocular complications are frequent and can be potentially severe in patients with steroid-refractory cGVHD, and therefore necessitate close monitoring. This prospective study was designed to describe eye manifestations of cGVHD in a large series of patients monitoring them before and after 1 year of extracorporeal photochemotherapy (ECP). ECP is a relatively new therapeutic approach based on the biological effects of psoralen 8-methoxypsoralen (8-MOP) and ultraviolet A light (UVA) on mononuclear cells collected by apheresis, and reinfused into the patient. Methods Only patients with steroid-refractory cGVHD under treatment with ECP, who developed cGVHD-related eye symptoms, were selected for the study. Ophthalmologic examination was repeated every 3 months. Only patients with complete recovery of the ocular manifestations and symptoms were considered responsive. Results In our study we observed eye alterations in 24 out of 140 patients (17%) with cGVHD. After 12 months of ECP, 10 out of 21 patients (48%) completely responded to the therapy. In all these cases the contribution of ECP was also essential in all the other organs subject to cGVHD. Conclusions Further studies are necessary to clarify the role of ECP in patients with cGVHD, especially in associated eye manifestations. Although our experience is limited, it suggests that ECP could be a safe and effective therapy for steroid-refractory eye manifestations of cGVHD.


European Journal of Ophthalmology | 2010

Use of amniotic membrane transplantation in isolated conjunctival Bowen disease: a case report.

Ilaria Motolese; Luigi Mazzera; Paolo Frezzotti; P. A. Motolese; Eduardo Motolese

Purpose. To report a case of isolated conjunctival Bowen disease treated with surgical resection and amniotic membrane transplantation. Methods. Interventional case report. Results. A 70-year-old man was admitted to our clinic with a large conjunctival verrucous plaque well-demarcated in the correspondence of the bulbar conjunctiva in the superior quadrant of the left eye with involved limbal and corneal surface. Ophthalmologic examination on slit-lamp examination and color fundus photographs were carried out before surgery and the results were evaluated. Conclusions. Treatment options and treatment studies of Bowen disease are difficult because there are a variety of different protocols and the success of the management depends on several factors (body site, lesion size, number of lesions, and thickness). In the conjunctival localization of the lesion, amniotic membrane transplantation appears to be a useful therapeutic choice after surgical resection of the lesion used to reconstruct ocular and conjunctival surface.


Ophthalmologica | 1998

Power Doppler Ultrasonography in Ocular and Orbital Diseases

Luisa Pierro; Eugenio Conforto; Antonio Giordano Resti; Rosangela Lattanzio; F. Genovesi-Ebert; S. Rizzo; S. Chiellini; G. Gabbriellini; F. Laddaga; M. Nardi; A. Romani; M.S. Sartini; Lelio Sabetti; Andrea Toscano; Giuseppe Specchia; Emilio Balestrazzi; Teresio Avitabile; F. Marano; F. Castiglione; Alfredo Reibaldi; V. Russo; M.G. Uva; A. Marino; Elisabetta Zaganelli; Alessandra Tavola; Mario Muraglia; A. Polizzi; M. Schenone; C. Ciurlo; R. Bertagno

Purpose: The authors present a preliminary report to test the usefulness of a new technique called power Doppler ultrasonography (PD) in the study of orbital vessels. Material and Methods: The ophthalmic artery and vein as well as the central retinal artery and vein have been examined in 10 patients with a General Electric Logiq 5000 that allows the examination with both color Doppler ultrasonography (CD) and PD. Results: PD does not alias, is relatively angle independent and is able to better detect the pathways of these vessels. Conclusions: PD is a new promising technique that may be superior to CD in detecting orbital and ocular vessels.

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