Missing Person
Mostrando 1-9 de 9 artigos, teses e dissertações.
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1. Avaliação da implantação da atenção à pessoa com fissura labiopalatina em um centro de reabilitação brasileiro
Resumo Introdução A fissura labiopalatina é a anomalia craniofacial mais prevalente na população. Apesar das iniciativas de tratamento e reabilitação pelo SUS existirem desde 1993, há poucos estudos sobre a realidade dos centros brasileiros. Objetivo Avaliar a implantação da atenção à pessoa com fissura labiopalatina em um centro de reabilit
Cad. saúde colet.. Publicado em: 2019-03
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2. Investigator Argus X-12 study on the population of northern Croatia
Abstract X chromosome STR typing has emerged recently as a powerful tool, complementary to autosomal STR typing, in solving complex forensic and missing person cases. Investigator® Argus X-12 is a commercial product that allows co-amplification of 12 X chromosomal markers belonging to four linkage groups (LGs). In this study, we analyzed by capillary electr
Genet. Mol. Biol.. Publicado em: 20/10/2016
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3. GeraÃÃo de prole virtual por reproduÃÃo simulada aplicada ao problema de pessoas desaparecidas / Generation of offspring by reproduction simulated virtual applied to the problem of missing persons
A realidade virtual tem aplicaÃÃes em diferentes Ãreas do conhecimento como Engenharia, CiÃncias, Artes, Entretenimento e EducaÃÃo. Neste trabalho, a realidade virtual à usada como apoio no problema de busca de pessoas desaparecidas. A metodologia proposta utiliza a geraÃÃo de personagens virtuais simulando o processo de reproduÃÃo de seres diplÃ
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 25/02/2011
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4. Orfandade e estigma: vivências de jovens órfãos em decorrência da aids / Orphans and stigma: young orphans living with aids
The aids epidemic affects the life of children and youngs, not only because of the presence of HIV/Aids, but also because of the sickness, death of parents, stigma, discrimination, and others. This research had the main intention of understanding the meaning of being an orphan to young people that have lost one or both parents in result of aids and the stigm
Publicado em: 2009
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5. Investigando a reestruturação de famílias após o desaparecimento de um filho
The disappearance of a child is a complex phenomenon that affects the family system in various ways, but the sense of loss permeates all of them because, generally, the confirmation of the fact is watered the mystery and lack of family members, since no tend to have the possibility of losing a person in such manner. Thus, the issues involving the loss within
Publicado em: 2009
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6. Vivência de perdas: relação entre eventos significativos, luto e depressão, em pacientes internados com doença arterial coronariana / Experience of losses: relation between significatives events, mourning and depression, in hospitalized patients with coronary artery disease
Since the attendance of hospitalized cardiac patients was created the category experience of losses caused by significative(s) event(s) that implicated in the mourning process. According to Freud (1916), mourning is a psychic process that requires time for the loss elaboration and changing of the psychic reality, shaped by the lost object missing. Mourning i
Publicado em: 2008
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7. GENE LOSS IN HUMAN TERATOMAS*
If benign cystic teratomas (dermoid cysts) of the ovary arise from a germ cell that has undergone meiosis, they should be missing genes which are present in the person. Three independently segregating allelic isozymes in 11 benign cystic teratomas of the human female ovary were compared with normal tissue of the same case. Dermoid cysts from persons heterozy
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8. Studying Parents and Grandparents to Assess Genetic Contributions to Early-Onset Disease
Suppose DNA is available from affected individuals, their parents, and their grandparents. Particularly for early-onset diseases, maternally mediated genetic effects can play a role, because the mother determines the prenatal environment. The proposed maximum-likelihood approach for the detection of apparent transmission distortion treats the triad consistin
The American Society of Human Genetics.
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9. Presence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome).
Peroxisomes have not been detected in liver and kidney of patients with Zellweger syndrome. Some peroxisome proteins are missing; others are present in normal amounts but are located in the cytosol. We have prepared an antiserum against the 22-kDa integral membrane protein characteristic of rat liver peroxisomes. The antiserum crossreacts with the human live