Vision Disorders
Mostrando 1-12 de 41 artigos, teses e dissertações.
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1. Management of thyroid disorders during the COVID-19 outbreak: a position statement from the Thyroid Department of the Brazilian Society of Endocrinology and Metabolism (SBEM)
ABSTRACT This position statement was prepared to guide endocrinologists on the best approach to managing thyroid disorders during the coronavirus disease (COVID-19) pandemic. The most frequent thyroid hormonal findings in patients with COVID-19, particularly in individuals with severe disease, are similar to those present in the non-thyroidal illness syndrom
Arch. Endocrinol. Metab.. Publicado em: 2021-06
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2. Thyroid surgery – Does the scar matter?
ABSTRACT This position statement was prepared to guide endocrinologists on the best approach to managing thyroid disorders during the coronavirus disease (COVID-19) pandemic. The most frequent thyroid hormonal findings in patients with COVID-19, particularly in individuals with severe disease, are similar to those present in the non-thyroidal illness syndrom
Arch. Endocrinol. Metab.. Publicado em: 2021-06
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3. Evaluation of the color vision acuity pattern of undergraduates of health courses in a Brazilian university
RESUMO Objetivo: O objetivo do estudo é analisar a acuidade visual média para cores de estudantes da área de saúde e discutir o impacto das doenças que a afetam nessa população. Deficiências cromáticas interferem de forma significativa no dia a dia de profissionais da área da saúde que necessitam de discernir diferentes matizes em diversas situa�
Rev. bras.oftalmol.. Publicado em: 12/08/2019
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4. Validation of the scale to evaluate physical damages related to the Abusive Use of Technology in daily life (PDAUTS).
BACKGROUND INFORMATION: New computer technologies, namely smart cellphones and tablets, among others, interacting along the daily life of individuals may contribute toward the rise of problems: depression, stress and physical damage (undue postures, upper and lower extremity disorders, vision problems, obesity), all of them related to excessive time spent o
MedicalExpress (São Paulo, online). Publicado em: 04/07/2019
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5. X-LINKED ADRENOLEUKODYSTROPHY IN BRAZIL: A CASE SERIES
RESUMO Objetivo: Descrever pacientes com diferentes formas de adrenoleucodistrofia ligada ao X: pré-sintomática, adrenoleucodistrofia inflamatória desmielinizante cerebral, adrenomieloneuropatia e insuficiência adrenal primária. Métodos: Dados específicos relacionados a epidemiologia, fenótipo, diagnóstico e tratamento de 24 pacientes com adreno
Rev. paul. pediatr.. Publicado em: 19/06/2019
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6. Expert Opinions on Managing Fertility and Pregnancy in Patients With Mucopolysaccharidosis
Abstract The mucopolysaccharidosis (MPS) disorders are rare genetic diseases caused by deficiencies in lysosomal enzymes involved in the degradation of glycosaminoglycans, leading to pulmonary, cardiac and neurological dysfunctions, skeletal anomalies, impaired vision, and/or hearing and shortened life spans. Whereas in the past, few individuals with MPS rea
J. inborn errors metab. screen.. Publicado em: 30/05/2019
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7. Use of Idebenone for the Treatment of Leber’s Hereditary Optic Neuropathy
Abstract Leber’s hereditary optic neuropathy (LHON) is one of the most frequent mitochondrial disorders. It is caused by mutations in genes of the mitochondrial DNA coding for subunits of the respiratory chain and leads to severe bilateral vision loss, from which spontaneous recovery is infrequent. Retinal ganglion cells show a selective vulnerability to m
J. inborn errors metab. screen.. Publicado em: 16/05/2019
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8. Outcomes of a Physician Survey on the Type, Progression, Assessment, and Treatment of Neurological Disease in Mucopolysaccharidoses
Abstract The mucopolysaccharidosis (MPS) disorders are a group of rare, inherited lysosomal storage disorders. In each of the 11 MPS (sub)types, deficiency in a specific lysosomal enzyme (1 of 11 identified enzymes) leads to accumulation of glycosaminoglycans, resulting in cell, tissue, and multi-organ dysfunction. There is great heterogeneity in the clinica
J. inborn errors metab. screen.. Publicado em: 28/02/2019
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9. Prevalência de doenças oculares e causas de comprometimento visual em crianças atendidas em um Centro de Referência em Oftalmologia do centro-oeste do Brasil
Objetivo: Identificar os níveis de comprometimento visual e a prevalência de oftalmopatias e ametropias em crianças atendidas em um centro de referência em oftalmologia do centro-oeste brasileiro. Comparar os achados com dados publicados referentes a outras regiões do Brasil. Métodos: Estudo transversal, descritivo e retrospectivo com análise de pr
Rev. bras.oftalmol.. Publicado em: 2014-08
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10. Relação entre funções cognitivas e perdas adquiridas na visão de cores de pacientes com esclerose múltipla tipo remitente recorrente / Relationship between cognitive functions and acquired color vision loss in patients with relapsing-remitting type of multiple sclerosis
Multiple sclerosis (MS) is an autoimmune inflammatory disease characterized by demyelination and central nervous system (CNS) degeneration. It is two times more frequent in women. It can be presented in two subtypes: the relapsing-remitting (RR), most common type, characterized by two or more episodes of focal disorders in different sites of the CNS, and rem
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 12/09/2012
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11. Função visual e motora ocular na esclerose múltipla / Visual and ocular motor function in multiple sclerosis
A esclerose múltipla é uma doença crônica imunomediada do sistema nervoso central, caracterizada por inflamação, desmielinização e lesão axonal na fase inicial, e desmielinização crônica, degeneração progressiva e perda axonal, atrofia cerebral e gliose na fase crônica. O acometimento do sistema visual e motor ocular são manifestações comun
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 26/08/2011
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12. Indicadores precoces de disfunção temporomandibular e identificação de sinais e sintomas em crianças e adolescentes / Early indicators of the temporomandibular dysfunction. Identification of the signs and symptoms in children and adolescents
The objective of this work is to identify and discuss signs and symptoms of temporomandibular disorders present in children and adolescents during the intensive phase of growth and craniofacial development. Adult patients were selected for this work, who did not receive the necessary therapeutic attention and care that certainly defined their present, very d
Publicado em: 2010