Intellectual Deficiency
Mostrando 13-21 de 21 artigos, teses e dissertações.
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13. Uma classe de aceleração: seus alunos e sua realidade, uma abordagem qualitativa
The purpose of this dissertation was to analyze the teaching-learning process of the students with a history of school failure in a II level Acceleration Class (3rd and 4th grades of High School), the study of the Acceleration Class of Learning level II is meant to students with a deficiency in grade/age and didnt adapt to the essential concepts of many area
Publicado em: 2006
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14. Phonoaudiological aspects of Saethre-Chotzen syndrome / Aspectos fonoaudiologicos da sindrome de Saethre-Chotzen
Saethre-Chotzen Syndrome (SCS) is characterized by craniosynostosis and several important facial alterations such as: low hair implantation at the front, asymmetry, maxillary hypoplasia, mandibular prognathism, in addition to small, dysmorphic and low-set ears. Among the ocular alterations are: blepharoptosis, strabismus, epicanthus, lachrymal duct stenosis
Publicado em: 2006
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15. Indústria farmacêutica no Brasil, 1990-2000: a oportunidade da inovação tecnológica na interação universidade-empresa
This work evaluates the possibilities that the national pharmaceutical industry has to undertake actions of technological innovation from its relationship with the University and research institutes. During the decade of 1990 the pharmaceutical sector was affected by several changes, between them, the recognition of patents, the occurrence of a period of fre
Publicado em: 2004
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16. Os "contos de fada pessoais" como recurso auxiliar na psicoterapia de orientação junguiana : estudo de caso realizado no Centro de Saude Costa e Silva com pacientes do sexo feminino (Campinas-SP)
This present study was designed to verify the possibility of the "personal faiIy tales" to be used as one auxiliary resource in Jung oriented psychotherapy. In order to verify it, we studied "personal faily tales" and their relations to personal and collective unconscious emergent contents and their relations to the process of individuation. This technique b
Publicado em: 1995
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17. Intellectual ability of adults after lifelong intestinal malabsorption due to coeliac disease
The intellectual impact of lifelong intestinal malabsorption was examined in a consecutive series of 19 adults (mean age, 48 ± 11 years) with untreated coeliac disease. Using a comprehensive test battery no consistent signs of cognitive impairment were found and in the light of recent observations on coeliacs, aspects of nutritional deficiency may prove mor
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18. Neurological involvement in hereditary transcobalamin II deficiency.
A case of hereditary transcobalamin II deficiency with neurological involvement is described. The patient presented in early infancy with megaloblastic anaemia and was treated with folinic acid from 6 weeks of age. The diagnosis of transcobalamin II deficiency was not made until he was 2 years old when he showed severely retarded intellectual development, at
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19. Confusion, dementia and anticholinergics in Parkinson's disease.
Among a population of 75 hospitalised Parkinsonian subjects, confusional states were observed in 46% of demented patients not receiving anticholinergic drugs and in 93% of demented patients under anticholinergic therapy. The sensitivity of demented Parkinsonians to anticholinergic drugs can be attributed to a cholinergic deficiency which has been detected in
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20. Morbidity and mortality in medium chain acyl coenzyme A dehydrogenase deficiency.
Medium chain acyl coenzyme A dehydrogenase (MCAD) deficiency presents with episodic fasting, hypoketotic hypoglycaemia, and coma. It is known to be potentially lethal, but the outlook for survivors is thought to be good. We reassessed all patients with MCAD deficiency diagnosed in New South Wales (population six million) to explore long term morbidity and mo
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21. Presentation, acute illness, and learning difficulties in salt wasting 21-hydroxylase deficiency.
The presentation, pattern of acute illness, and incidence of learning difficulties are described in 63 (33 boys, 30 girls) children with salt wasting 21-hydroxylase deficiency, drawn from a cohort study of congenital adrenal hyperplasia in the South West Region of England between 1968 and 1988. Thirty boys presented with a salt losing crisis from birth where