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Características clínicas y epidemiológicas de niños diagnosticados con glaucoma pediátrico en la fundación oftalmológica nacional
(Universidad del RosarioEspecialización en OftalmologíaFacultad de Medicina, 2017)
PURPOSE To describe clinical and epidemiological characteristics of children with glaucoma at Fundación Oftalmológica Nacional (FON), Bogotá - Colombia. METHODS This retrospective descriptive study enrolled patients between ...
Avaliação dos tipos de glaucoma no serviço de oftalmologia da UNICAMPEvaluation of glaucoma types at the sector of ophthalmology - UNICAMP
(Conselho Brasileiro de Oftalmologia, 2003)
CYP1B1 Gene Analysis in Primary Congenital Glaucoma Brazilian Patients Novel Mutations and Association With Poor Prognosis
(Lippincott Williams & WilkinsPhiladelphiaEUA, 2010)
GENETIC-HETEROGENEITY IN PRIMARY CONGENITAL GLAUCOMA
(Soc Brasil GeneticaRibeirao PretBrasil, 1988)
Results of the susanna implant in patients with refractory primary congenital glaucoma
(Mosby, Inc, 2004-12-01)
Purpose: To evaluate the results of the Susanna implant in children with primary congenital glaucoma. Patients and methods: the authors report a retrospective noncomparative interventional case series of data from 24 eyes ...
Avaliação do gene CYP1B1 e da ancestralidade genômica no glaucoma congênito primário
(Universidade Federal de Minas GeraisUFMG, 2013-11-20)
INTRODUCTION: The primary congenital glaucoma is an isolated trabeculodysgenesis causing obstruction of aqueous humor outflow and subsequent increase in intraocular pressure, being a major cause of blindness in children. ...
Molecular genetics of primary congenital glaucoma in Brazil
(Assoc Research Vision Ophthalmology IncBethesdaEUA, 2002)
Glaucoma in Costa Rica: Initial approaches
(Universidad de Costa Rica, 2004)
Primary Congenital Glaucoma: A Novel Single-Nucleotide Deletion and Varying Phenotypic Expression for the 1546-1555dup Mutation in the GLC3A (CYP1B1) Gene in 2 Families of Different Ethnic Origin
(Journal Glaucoma: 12 p. 27-30, 2003-02)
Purpose: To present new molecular genetic data on primary congenital glaucoma from 2 families, 1 isolated case and 3 familial cases due to mutations in the cytochrome P-450 1B1 (CYP1B1) gene.
Methods: All diagnoses were ...