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Featured researches published by Wener Cella.


Arquivos Brasileiros De Oftalmologia | 2001

Paracoccidioidomicose primária de pálpebra e conjuntiva

Ezon Vinicius Alves Pinto Ferraz; Wener Cella; Eduardo Melani Rocha; Roberto Caldato

Paracoccidioidomycosis is the most frequent systemic mycosis in Brazil, but ocular involvement is rare and, if present, often secondary to another site. The authors report a case of paracoccidioidomycosis of eyelid and conjunctiva where no extraocular focus was found. A brief review of the literature is made discussing the importance of diagnostic suspecion in a population at risk and early treatment for a good visual prognosis.


SciELO | 2002

Adaptação de questionário de avaliação da qualidade de vida para aplicação em portadores de catarata

Ezon Vinicius Alves Pinto Ferraz; Cláudia Assis Lima; Wener Cella; Carlos Eduardo Leite Arieta

Purpose: Cataract represents a public health problem because patients presenting the disease are unable to adequately perform routine activities, with a negative influence on their quality of life. The purpose of this research is to evaluate the impact of reduced visual acuity on the quality of life of these patients. The authors adjusted a specific questionnaire to the Brazilian social reality and tested its response adequacy and reliability. Methods: 30 cataract patients with surgical indication were interviewed. The questionnaire was applied and the same interview was done twice within a one-hour interval. Results: More than 80% of questions were answered the first time they were asked. Consistence analysis showed that only one patient answered four questions in a different manner during the interviews. Conclusion: The authors concluded that the adjusted questionnaire is applicable to a population with a low level of formal education, being a reliable instrument in the evaluation of quality of life in cataract patients.


Arquivos Brasileiros De Oftalmologia | 2018

Morphological and functional findings in Alström syndrome: a study of two families

Álvaro Buno Botentuit Serra de Castro; Bruno Nobre Lins Coronado; Ráysa Hellen Assunção Costa; Maria Regina Chalita; Wener Cella; Marcos Pereira de Ávila

Alström syndrome is a rare disorder characterized by mutations to the ALMS1 gene and clinical findings of childhood obesity, diabetes mellitus, dilated cardiomyopathy, sensorineural hearing loss, and progressive cone-rod dystrophy, which may result in blindness. Ocular manifestations occur in the first decade of life with nystagmus, blepharospasm, and photophobia leading to progressive and severe reductions in visual acuity. This study describes the retinal structure and functional aspects of four patients (8 eyes) from two different families as determined by optical coherence tomography (OCT), fundus autofluorescence, and full-field electroretinography. There was a correlation between morphological and functional findings, evidenced by typical funduscopic changes of retinal dystrophy in spectral domain-OCT and electrophysiological analyses. Foveal characteristics include a single layer of undifferentiated photoreceptors with retinal disorganization mainly from external segments, in agreement with previous reports in the literature. Fundus autofluorescence showed areas of hyperautofluorescence interspersed by hypoautofluorescence dots suggesting, respectively, involvement and atrophy of retinal pigmented epithelial cells in the macular zone. Electroretinographic analyses showed early dysfunction of the cones followed by rapid rod deterioration.


Arquivos Brasileiros De Oftalmologia | 2011

Axonal electrovisiogram as an electrophysiological test to evaluate optic nerve and inner retina electrical potentials: findings in normal subjects

Wener Cella; Adalmir Morterá Dantas; Alexandre Vasconcelos Lima; Marcos Pereira de Ávila

PURPOSES To standardize and validate the technique of axonal electrovisiogram (AxEvg), defining its normative values and parameters and characterizing its findings in normal individuals. METHODS We enrolled 140 normal individuals (280 eyes) divided into seven groups according to age, each one with 10 males and 10 females. The technique was based on monocular visual stimulation by a 0 dB intensity bright flash on Ganzfeld bowl at a presentation rate of 1.4 Hz. Golden cup electrodes were used and electrical waves were acquired after artifact rejection. For each amplitude and implicit time peak we calculated the mean, median, pattern deviation, minimum and maximum values and 95% confidence interval. RESULTS Monocular visual stimulation with bright flash under mesopic conditions was the standard technical procedure established. The normal AxEvg waveform consists of an initial positive wave (named P1, with mean amplitude of 2.0 mV and mean implicit time peak of 23.1 ms) followed by a negative wave (named N1, with mean amplitude of -3.9 mV and mean implicit time peak of 41.4 ms). No significant differences were observed between males and females or between right and left eyes, but there was an increased P1 and N1 implicit time peaks according to age. Implicit time characteristics suggest that P1 wave represents an optic nerve electrical potential and N1 wave represents an inner retinal layers potential. CONCLUSIONS AxEvg can be considered a pre-chiasmatic visual evoked potential capable to reliably record the electrical activity of optic nerve and inner retina. The findings suggest that AxEvg may be useful as an electrophysiological test in the diagnosis of neuroretinal diseases.


Investigative Ophthalmology & Visual Science | 2006

Structural assessment of PITX2, FOXC1, CYP1B1, and GJA1 genes in patients with Axenfeld-Rieger syndrome with developmental glaucoma.

Wener Cella; José Paulo Cabral de Vasconcellos; Mônica Barbosa de Melo; Bianca Kneipp; Fernando Ferreira Costa; Carlos Alberto Longui; Vital Paulino Costa


Journal of Pediatric Ophthalmology & Strabismus | 2002

Xerophthalmia Secondary to Short Bowel Syndrome

Wener Cella; Andreia Peltier Urbano; Willian Santos Vinhadelli; Maurício Donatti; Eduardo Melani Rocha


Investigative Ophthalmology & Visual Science | 2005

Mutation Screening of FOXC1 and PITX2 Genes in Brazilian Patients With Axenfeld–Rieger Malformations

José Paulo Cabral de Vasconcellos; Mônica Barbosa de Melo; Wener Cella; B. Kneipp; M.N. Rocha; F. Richeti; Carlos Alberto Longui; Vital Paulino Costa


Archive | 2005

Rastreamento de mutações nos genes PITX2, FOXC1 e GJA1 em pacientes com sindrome de Axenfeld-Rieger associada a glaucoma

Wener Cella; José Paulo Cabral de Vasconcellos


Investigative Ophthalmology & Visual Science | 2003

Risk Factors Associated With the Progression to Blindness in POAG Patients

Vital Paulino Costa; Wener Cella; José Paulo Cabral de Vasconcellos

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Vital Paulino Costa

State University of Campinas

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Adalmir Morterá Dantas

Federal University of Rio de Janeiro

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B. Kneipp

State University of Campinas

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Bianca Kneipp

State University of Campinas

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