Family S Histories
Mostrando 13-23 de 23 artigos, teses e dissertações.
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13. Genética do prognatismo mandibular: avaliação de heredogramas, análise complexa de segregação e análise de ligação com loci candidatos em famílias brasileiras averiguadas a partir de probandos afetados
There is a familial tendency to mandibular prognathism. Various genetic models have been described. It is assumed to be a polygenic trait in the vast majority of cases, with a threshold for expression. The purpose of the current study was to examine specific genetic models of the familial transmission of MP in Brazilian families and to search for evidences o
Publicado em: 2006
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14. O lado duro da vida fácil a exploração sexual de meninas adolescentes da periferia de Fortaleza-CE e o resgate da cidadania
The infant-juvenile sexual exploration is a world problem that uses children and adolescents for prostitution and lucrative ends, transforming them in mere goods, suspending the children s dreams and they are forced to turn women preconciously and stealing them the human dignity. This study had as general objective: to understand the meaning of to be adolesc
Publicado em: 2005
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15. EN HABITANT ESPACES EN MOUVEMENT: INDIVIDU, FAMILLIE ET CONTEXTE SOCIO-HISTORIQUE / HABITANDO ESPAÇOS EM MOVIMENTO: INDIVÍDUO, FAMÍLIA E CONTEXTO SÓCIO-HISTÓRICO / INHABITING MOVING SPACES: INDIVIDUAL, FAMILY AND SOCIO-HISTORICAL CONTEXT
It s specially important for Family Therapy to relate the individual, the family and the socio-historical context. Three perspectives concerning the family-individual relationship are identified, emphasizing an interdisciplinary comprehension, and adding some considerations about Brazil. The socio-historical process of the western culture indicates that the
Publicado em: 2004
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16. Historias de viver o serviço social
The present investigation deals with aspects of the lived professional experience of social workers, in order to grasp the reasons behind choosing to become and to remain a social worker and also the framework of professional frustations and pleasures. Thus, a qualitative research tool was chosen, namely life histories, and social workers were interviewed in
Publicado em: 1996
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17. Mitos e segredos: um estudo sobre a estrutura e a dinâmica familiar no psicodiagnóstico infantil
In this dissertation, family myths and secrets were studied and utilized as interpretative instruments in the psycho-diagnosis of children with the objective of broadening the investigation of children s inner dynamics, within a historical framework of three generations. The initial interviews, anamneses and tri-generational interviews held with parents, as
Publicado em: 1990
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18. Congenital anomalies and genetic disorders in families of children with central nervous system tumours.
Medical genetic histories of 165 children with primary central nervous system (CNS) tumours and 4599 relatives of these probands were examined to identify birth defects or genetic disorders that may be associated with the aetiology of CNS tumours. Twelve primary malignancies were found in 329 (4%) of the parents of probands. Two of 99 half sibs but no full s
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19. A family study of hidradenitis suppurativa.
A family study of hidradenitis suppurativa was undertaken based on 26 subjects with the disease. The probands were obtained from Hospital Activity Analysis (HAA) records for a three year period (1980 to 1983) and by direct referral from hospital specialists over a six month period (1983 to 1984). Family pedigree information was collected by home visits or ho
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20. Risk factors for stroke and myocardial infarction in women in the United Kingdom as assessed in general practice: a case-control study.
Data available in the United Kingdom through the Medical Research Council's General Practice Research Framework were recorded in a study of 603 women aged 45-69 with confirmed diagnoses of stroke or myocardial infarction, each matched by age with two controls. Current cigarette smoking and a family history of myocardial infarction were both strongly associat
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21. Iron deficiency in sickle cell anaemia.
Thirty-seven patients with SCD were studied: 24 were diagnosed as homozygous Hb S on the basis of their haematological findings, and alpha:non-alpha globin chain ratios were found to be balanced in all. Thirteen patients were thought to have alpha or beta thalassaemia interaction with Hb S on the basis of low MCV and MCH, family history and/or presence of Hb
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22. Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C.
Although patients with thromboembolic disease frequently have family histories of thrombosis, well-defined defects such as inherited deficiencies of anticoagulant proteins are found only in a minority of cases. Based on the hypothesis that a poor anticoagulant response to activated protein C (APC) would predispose to thrombosis, a set of new coagulation assa
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23. Purification of a human liver cytochrome P-450 immunochemically related to several cytochromes P-450 purified from untreated rats.
Among characterized forms of liver microsomal cytochromes P-450 in rats are four related isozymes (P-450f-i) notable for their lack of inducibility. Immunoblot analyses demonstrated that human livers microsomes contained several proteins related to these rat P-450s. A human liver P-450, termed HLx, was purified and found by immunochemical assays to resemble