Deaf Blind
Mostrando 1-7 de 7 artigos, teses e dissertações.
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1. A comunicação do aluno surdocego no cotidiano da escola inclusiva.
Os documentos oficiais da atual política educacional brasileira preconizam que o processo de escolarização dos alunos com necessidades educacionais especiais seja desenvolvido no sistema regular de ensino. A presente pesquisa buscou estudar o processo de inclusão escolar de alunos com surdocegueira inseridos no Ensino Básico de escolas regulares da cida
Publicado em: 2010
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2. A legislação brasileira e italiana sobre Educação Especial : da década de 1970 aos dias atuais
The opinions of several countries on how to enforce the education of people with disability promote international discussions aimed at identifying elements, whether from the political, organizational or methodological sphere, that can solve the existing problems in their respective educational contexts. Essentially, there are countries which provide educatio
Publicado em: 2010
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3. A aquisição da linguagem por uma surdocega pré-lingüística numa perspectiva socio-cognitivo-interacionista / Aquisition of language by a pre-linguistic deaf-blind person ina a socio-cognitive interactionist perspective
This paper consists of a study of language acquisition by a pre-linguistic deafblind child in a social-cognitive interactionist perspective. Pre-linguistic deafblindness sets in before the deaf-blind person acquires a language, be it oral or signs. In the context of deaf-blindness, learning becomes a complex endeavor, and we do not have a model to explain al
Publicado em: 2008
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4. The primary ultrastructural defect caused by anophthalmic white (Wh) in the Syrian hamster.
Anophthalmic white (Wh) of the Syrian hamster is a highly pleiotropic dominant spotting color mutation causing homozygotes to be deaf, blind, and white. An ultrastructural analysis of embryonic tissue reveals that Wh causes the retention of cilia by cells of opposing layers of the embryonic retina and by the lens fiber cells. Previous ultrastructural analyse
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5. Cross-modal reorganization of callosal connectivity without altering thalamocortical projections
Mammalian cerebral cortex is composed of a multitude of different areas that are each specialized for a unique purpose. It is unclear whether the activity pattern and modality of sensory inputs to cortex play an important role in the development of cortical regionalization. The modality of sensory inputs to cerebral cortex can be altered experimentally. Neon
The National Academy of Sciences.
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6. Abnormal phagocytosis by retinal pigmented epithelium that lacks myosin VIIa, the Usher syndrome 1B protein
Mutations in the myosin VIIa gene (MYO7A) cause Usher syndrome type 1B (USH1B), a major type of the deaf-blind disorder, Usher syndrome. We have studied mutant phenotypes in the retinas of Myo7a mutant mice (shaker1), with the aim of elucidating the role(s) of myosin VIIa in the retina and what might underlie photoreceptor degeneration in USH1B patients.
National Academy of Sciences.
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7. Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity.
Irreversible hearing loss is a catastrophic complication of treatment with aminoglycoside antibiotics such as streptomycin, gentamycin, and kanamycin. Many kindreds showing a matrilineal pattern of inheritance of this trait have been described in China where the widespread use of aminoglycoside antibiotics accounts for approximately 25% of profound deafness