Now showing items 1-20 of 24

    • Anomalias oculares e características genéticas na síndrome de Marfan 

      Sallum, Juliana Maria Ferraz [UNIFESP]; Chen, Jane [UNIFESP]; Perez, Ana Beatriz Alvarez [UNIFESP] (Conselho Brasileiro de Oftalmologia, 2002-12-01)
      Purpose: To identify the ocular abnormalities in Marfan´s syndrome patients. Methods: Prospective study of 46 Marfan patients with complete ophthalmologic evaluation. Seventeen patients also underwent a clinical ...
    • Anomalias oculares em pacientes portadores de deficiência auditiva genética 

      Chen, Jane [UNIFESP]; Sallum, Juliana Maria Ferraz [UNIFESP]; Longhitano, Silvia Bragagnolo [UNIFESP]; Brunoni, Decio [UNIFESP] (Conselho Brasileiro de Oftalmologia, 2000-12-01)
      Purpose: In order to verify the prevalence of ocular abnormalities in patients who are deaf due to genetic causes, this paper presents the visual assessment of 97 deaf patients. Methods: 97 patients with definite or suspected ...
    • Aspectos da tomografia de coerência óptica na doença de Stargardt: relato de caso 

      Gouveia, Enéias Bezerra [UNIFESP]; Morales, Maira Saad De Ávila [UNIFESP]; Allemann, Norma [UNIFESP]; Matte, Guilherme [UNIFESP]; Berezovsky, Adriana [UNIFESP]; Sallum, Juliana Maria Ferraz [UNIFESP] (Conselho Brasileiro de Oftalmologia, 2006-08-01)
      The term fundus flavimaculatus (Stargardt disease) describes a group of inherited macular dystrophies characterized by multiple yellow to yellow-white flecks at the level of the retinal pigment epithelium. The authors ...
    • Avaliação da autofluorescência do fundo de olho nas distrofias de retina com o aparelho Heidelberg Retina Angiograph2 

      Côco, Monique [UNIFESP]; Baba, Natalia Tamie [UNIFESP]; Sallum, Juliana Maria Ferraz [UNIFESP] (Conselho Brasileiro de Oftalmologia, 2007-10-01)
      PURPOSE: To define characteristics of the fundus autofluorescence examination, verifying usefulness in the diagnosis and care of hereditary retinal diseases. METHODS: 28 patients, adults, divided equally into four groups ...
    • Avaliação da tomografia de coerência óptica em pacientes portadores de degeneração macular relacionada à idade tratada com terapia fotodinâmica com verteporfina 

      Bordon, Arnaldo Furman [UNIFESP]; Oshima, Akioshi [UNIFESP]; Guia, Tércio Alves [UNIFESP]; Calucci, Daniela [UNIFESP]; Sallum, Juliana Maria Ferraz [UNIFESP]; Farah, Michel Eid [UNIFESP] (Conselho Brasileiro de Oftalmologia, 2008-12-01)
      PURPOSE: To identify the optical coherence tomography (OCT) findings in patients with age-related macular degeneration (ARMD) treated with photodynamic therapy (PDT). STUDY DESIGN: Open, non-randomized, interventional case ...
    • Classificação diagnóstica dos portadores de doenças degenerativas de retina, integrantes dos grupos Retina São Paulo e Retina Vale do Paraíba 

      Unonius, Nichard [UNIFESP]; Farah, Michel Eid [UNIFESP]; Sallum, Juliana Maria Ferraz [UNIFESP] (Conselho Brasileiro de Oftalmologia, 2003-08-01)
      PURPOSE: To organize a regional data bank of all individuals that have retinal degenerative diseases, with the aim to classify each patient according to the type of distrophy and pattern of inheritance. METHODS: During the ...
    • Comparação da densidade óptica de pigmento macular em pacientes diabéticos e indivíduos normais: Avaliação dos principais métodos e associação com a idade 

      Lima, Veronica Franco de Castro [UNIFESP] (Universidade Federal de São Paulo (UNIFESP), 2014)
      Objetivos: Comparar os valores de densidade optica de pigmento macular (MPOD) obtidos atraves dos metodos de fotometria de flicker heterocromatico (HFP) e autofluorescencia (AF) em um grupo de pacientes normais; comparar ...
    • Comparação do efeito antiangiogênico do ranibizumab e do bevacizumab in vitro 

      Souto, Alexandre Cupello [UNIFESP]; Maricato, Juliana Terzi [UNIFESP]; Denapoli, Priscila Martins Andrade [UNIFESP]; Sallum, Juliana Maria Ferraz [UNIFESP]; Han, Sang Won [UNIFESP] (Conselho Brasileiro de Oftalmologia, 2011-10-01)
      Purpose: To evaluate the comparative in-vitro antiangiogenic effect of Bevacizumab and Ranibizumab. Methods: Endothelial venous umbilical cells culture (ECV304) cultivated in F12 media with addition of 10% Fetal Bovine ...
    • Correlação Entre Fenótipo E Genótipo De Pacientes Com Doença De Stargardt 

      Salles, Mariana Vallim [UNIFESP] (Universidade Federal de São Paulo (UNIFESP), 2018-08-30)
      Purpose: To Identify Genetic Variants In Brazilian Patients With Clinical Diagnosis Of Stargardt Disease And To Correlate With Its Phenotypic Manifestation And Hereditary Characteristics. Methods: Patients With Clinical ...
    • Córnea plana congênita: relato de caso e revisão de literatura 

      Mascaro, Vera L. D. M. [UNIFESP]; Alvarenga, Lênio S. [UNIFESP]; Sallum, Juliana Maria Ferraz [UNIFESP]; Freitas, Denise de [UNIFESP] (Conselho Brasileiro de Oftalmologia, 2000-04-01)
      Purpose: To report two cases of bilateral cornea plana with high hypermetropia. Case report: Two members of the same family showed se-vere corneal flattening, limbal scleralization. The sha-lowness of the anterior chamber, ...
    • Estudo da etiologia genética do ceratocone 

      Sallum, Juliana Maria Ferraz [UNIFESP] (Universidade Federal de São Paulo (UNIFESP), 1995)
    • Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis 

      Chiang, Pei-Wen; Wang, Juan; Chen, Yang; Fu, Quan; Zhong, Jing; Chen, Yanhua; Yi, Xin; Wu, Renhua; Gan, Haixue; Shi, Yong; Chen, Yanling; Barnett, Christopher; Wheaton, Dianna; Day, Megan; Sutherland, Joanne; Heon, Elise; Weleber, Richard G.; Rassi Gabriel, Luis Alexandre; Cong, Peikuan; Chuang, KuangHsiang; Ye, Sheng; Sallum, Juliana Maria Ferraz [UNIFESP]; Qi, Ming (Nature Publishing Group, 2012-09-01)
      Leber congenital amaurosis (LCA) is an autosomal recessive retinal dystrophy that manifests with genetic heterogeneity. We sequenced the exome of an individual with LCA and identified nonsense (c.507G > A, p.Trp169*) and ...
    • Genética molecular em atrofia óptica autossômica dominante, tipo Kjer 

      Sallum, Juliana Maria Ferraz [UNIFESP] (Universidade Federal de São Paulo (UNIFESP), 1999)
      A atrofia optica autossomica dominante, tipo Kjer ou juvenil, (MCKUSICK 1994; OMIM #l65500, OPAL) e uma neuropatia optica hereditaria que causa perda de acuidade visual, anormalidades da visao de cores e defeitos do campo ...
    • Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil 

      Melo, Monica Barbosa de; Mandal, Anil K.; Tavares, Ivan Maynart [UNIFESP]; Ali, Mohammed Hasnat; Kabra, Meha; Cabral de Vasconcellos, Jose Paulo; Senthil, Sirisha; Sallum, Juliana Maria Ferraz [UNIFESP]; Kaur, Inderjeet; Betinjane, Alberto J.; Moura, Christiane Rolim de [UNIFESP]; Paula, Jayter S.; Costa, Karita A. [UNIFESP]; Sarfarazi, Mansoor; Della Paolera, Mauricio; Finzi, Simone; Ferraz, Victor E. F.; Costa, Vital P.; Belfort, Rubens Junior [UNIFESP]; Chakrabarti, Subhabrata (Public Library Science, 2015-05-15)
      BackgroundPrimary congenital glaucoma (PCG), occurs due to the developmental defects in the trabecular meshwork and anterior chamber angle in children. PCG exhibits genetic heterogeneity and the CYP1B1 gene has been widely ...
    • Giant annular posttraumatic choroidal rupture 

      Unonius, Nichard [UNIFESP]; Araujo, J.; Farah, Michel Eid [UNIFESP]; Sallum, Juliana Maria Ferraz [UNIFESP]; Calucci, Daniela [UNIFESP]. (Canadian Ophthal Soc, 2004-08-01)
    • Hemorragia subaracnóidea e síndrome de Terson: estudo prospectivo 

      Sung, Eun Song [UNIFESP]; Bordon, Arnaldo Furman [UNIFESP]; Sallum, Juliana Maria Ferraz [UNIFESP]; Farah, Michel Eid [UNIFESP] (Conselho Brasileiro de Oftalmologia, 2003-10-01)
      PURPOSE: To analyze the incidence, clinical course, ophthalmic findings, and prognosis of the patients with intracranial bleeding and Terson's syndrome. METHODS: A prospective consecutive study of patients admitted to the ...
    • Heterogeneidade genética em atrofia óptica autossômica dominante 

      Sallum, Juliana Maria Ferraz [UNIFESP]; Farah, Michel Eid [UNIFESP]; Maumenee, Irene Hussels (Conselho Brasileiro de Oftalmologia, 2002-08-01)
      Purpose: Autosomal dominant optic atrophy is a hereditary optic neuropathy characterized by progressive visual loss in childhood, color vision anomalies, visual field defects and temporal pallor of the optic disc. This ...
    • Outer retina analysis by optical coherence tomography in cone-rod dystrophy patients 

      Lima, Luiz Henrique Soares Goncalves de [UNIFESP]; Sallum, Juliana Maria Ferraz [UNIFESP]; Spaide, Richard F. (Lippincott Williams & Wilkins, 2013-10-01)
      Purpose: To analyze the outer retinal layers using spectral domain optical coherence tomography (SD-OCT) in patients with cone-rod dystrophy.Methods: The diagnosis of cone-rod dystrophy was determined by primary cone ...
    • PROM1 gene variations in Brazilian patients with macular dystrophy 

      Salles, Mariana Vallim [UNIFESP]; Motta, Fabiana Louise Teixeira [UNIFESP]; Silva, Elton Dias da [UNIFESP]; Teixeira, Patricia Varela Lima [UNIFESP]; Costa, Karita Antunes [UNIFESP]; Silva, Rafael Filippelli da [UNIFESP]; Martin, Renan Paulo [UNIFESP]; Pesquero, João Bosco [UNIFESP]; Sallum, Juliana Maria Ferraz [UNIFESP] (Taylor & Francis Inc, 2017)
      Background: Although the pathogenicity of the prominin-1 (PROM1) gene has already been described as associated with autosomal dominant Stargardt disease, little is known about sequence variations in this gene. Purpose: The ...
    • Retinal function in patients treated with tamoxifen 

      Song Watanabe, Sung Eun [UNIFESP]; Berezovsky, Adriana [UNIFESP]; Motono, Marcia [UNIFESP]; Sacai, Paula Yuri [UNIFESP]; Pereira, Josenilson Martins [UNIFESP]; Sallum, Juliana Maria Ferraz [UNIFESP]; Gebrim, Luiz Henrique [UNIFESP]; Salomão, Solange Rios [UNIFESP] (Springer, 2010-04-01)
      Tamoxifen, an effective treatment of breast cancer, has been shown to cause ocular toxic effects. the purpose of this study was to determine retinal toxicity by full-field and focal electroretinograms (ERGs) in patients ...