Results 61 to 70 of about 45,874 (216)
Resumo Objetivo: Determinar a frequência da microftalmia associada à catarata congênita e sua frequência etiológica. Comparar o resultado visual após a cirurgia da catarata congênita em olhos microftálmicos, com o resultado visual obtido em olhos não ...
Silvia Prado Smit Kitadai, Mauro Nishi
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Obra ressenyada: Agata IGNACIUK, Teresa ORTIZ GÓMEZ, Anticoncepción, mujeres y género. La "píldora" en España y Polonia (1960-1980).
Ballester, Rosa
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Profile of patient with aphakic/pseudopfakic bullous keratopaty attended at public hospital [PDF]
Objetivo: Identificar e analisar criticamente o perfil dos pacientes com ceratopatia bolhosa atendidos em um hospital municipal. Métodos: Foi realizada análise retrospectiva de 35 olhos de 35 pacientes em acompanhamento no setor de córnea e doenças ...
BERTINO, Pedro Moreira +7 more
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Síndrome hereditária hiperferritinemia-catarata: caso clínico
Hereditary hyperferritinemia-cataract syndrome is an autosomal dominant genetic disorder that is characterized by high serum ferritin levels without iron overload and early-onset cataracts. The authors describe the case of a 26-year-old woman with hyperferritinemia (1153.3 ng/mL, reference range 11.0 - 306.8 ng/mL), with no other abnormalities in iron ...
Carolina Fernandes +4 more
openaire +3 more sources
Country Reports 30 November 2001 [PDF]
A compilation of country reports on the activities of the various European Clean Clothes Campaigns from June 2001 to November ...
Clean Clothes Campaign
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A retrospective study was conducted to identify the occurrence and types of ocular disorders in 57 Amazon parrots admitted to the Ophthalmology Service, Veterinary Teaching Hospital, School of Veterinary Medicine, University of São Paulo, Brazil from ...
Ana Paula Hvenegaard +4 more
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Catarata congénita y baja visión. Habilitación visual en un grupo de pacientes
La catarata congénita es una las causas más frecuentes de baja visión en Cuba y enel mundo, y se manifiesta desde los primeros momentos de la vida. Se considera laresponsable de 10% de la pérdida visual en el niño y la causa más frecuente deprivación ...
Eduardo Ariel Ramos Gómez +5 more
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Nance-Horan syndrome, congenital cataracts and dental anomalies
Introduction: The presence of atypical dentofacial structures may be the first indicator of other congenital defects related to syndromes of likewise genetic origin.
Ana Maria Rodriguez Diaz +3 more
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A- and B-modes ultrasonographic changes in the thickness of various structures of the eyeball in male and female English Cocker Spaniel dogs with and without nondiabetic cataracts were evaluated.
M.L. Silva +4 more
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The evaluation of lens by ultrasonography, previously to phacoemulsification, can offer relevant information, markedly such as aspects and dimensions, allowing design safer surgical strategies with enhanced outcomes. Within the contents of this research,
B.C. Martins, F.S. Lima, J.L. Laus
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