Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 15 de 15
Filtrar
1.
PLoS One ; 10(9): e0137077, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26335684

RESUMO

Global climate change and increases in sea levels will affect coastal marine communities. The conservation of these ecologically important areas will be a challenge because of their wide geographic distribution, ecological diversity and species richness. To address this problem, we need to better understand how the genetic variation of the species in these communities is distributed within local populations, among populations and between distant regions. In this study we apply genotyping by sequencing (GBS) and examine 955 SNPs to determine Sailfin molly (Poecilia latipinna) genetic diversity among three geographically close mangrove salt marsh flats in the Florida Keys compared to populations in southern and northern Florida. The questions we are asking are whether there is sufficient genetic variation among isolated estuarine fish within populations and whether there are significant divergences among populations. Additionally, we want to know if GBS approaches agree with previous studies using more traditional molecular approaches. We are able to identify large genetic diversity within each saltmarsh community (π ≈ 36%). Additionally, among the Florida Key populations and the mainland or between southern and northern Florida regions, there are significant differences in allele frequencies seen in population structure and evolutionary relationships among individuals. Surprisingly, even though the cumulative FST value using all 955 SNPs within the three Florida Key populations is small, there are 29 loci with significant FST values, and 11 of these were outliers suggestive of adaptive divergence. These data suggest that among the salt marsh flats surveyed here, there is significant genetic diversity within each population and small but significant differences among populations. Much of the genetic variation within and among populations found here with GBS is very similar to previous studies using allozymes and microsatellites. However, the meaningful difference between GBS and these previous measures of genetic diversity is the number of loci examined, which allows more precise delineations of population structure as well as facilitates identifying loci with excessive FST values that could indicate adaptive divergence.


Assuntos
Variação Genética , Poecilia/genética , Animais , Mudança Climática , Ecossistema , Florida , Frequência do Gene , Genótipo , Isoenzimas/genética , Metagenômica , Repetições de Microssatélites/genética
2.
Percept Mot Skills ; 119(3): 925-48, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-25375826

RESUMO

Reading is a multi-sensory and multi-cognitive task, and its difficulties (e.g., dyslexia) are not a unitary disorder. There are probably a variety of manifestations that relate to the actual site of impairment. A randomized, pre-test/post-test nonequivalent-groups design was conducted over 4 months with three groups aged between 6 and 8 years. One group comprised 76 participants (34 boys, 42 girls) with reading difficulties and altered sensory fusion (RD+ASF), a second group was made up of 123 students (59 boys, 64 girls) with reading difficulties but without altered sensory fusion (RD), and a third group comprised 81 participants (39 boys, 42 girls) who were young readers (RL) without reading delay, paired with the RD group on reading level. The experimental groups received intervention in the skills of control, stimulus recognition, and phonological awareness during a 4-month period. Both pre-test and post-test measures of errors in reading mechanics and reading routes (word and pseudo-word) were obtained. Poorer results in mechanics and reading routes of the RD+ASF group suggest that the effectiveness of the intervention depended on the characteristics of the groups and on the presence of sensory fusion deficits in the RD students.


Assuntos
Dislexia/fisiopatologia , Dislexia/terapia , Leitura , Percepção Visual/fisiologia , Análise de Variância , Conscientização/fisiologia , Criança , Feminino , Seguimentos , Humanos , Testes de Linguagem/estatística & dados numéricos , Masculino , Fonética , Reconhecimento Psicológico/fisiologia , Estudantes/psicologia , Resultado do Tratamento
3.
Univ. psychol ; 13(2): 781-797, abr.-jun. 2014. tab
Artigo em Inglês | LILACS | ID: lil-735230

RESUMO

El concepto de autorregulación del aprendizaje ha asumido una importancia creciente en la literatura, ya que la investigación ha sugerido que los alumnos participan activamente en su proceso de aprendizaje, monitorizando y regulando su proceso de estudio con el fin de alcanzar determinados objetivos. La información recogida en revistas indexadas en la base Scielo, en cuanto a la autorregulación, todavía no ha sido sistematizada convenientemente. Por ello, se ha realizado una revisión sistemática de la literatura, con base en datos SciELO.org, en el período comprendido entre el año 2001 y el año 2011, para analizar las evidencias recogidas en diferentes investigaciones sobre: a) la naturaleza del aprendizaje autorregulado, b) su evaluación, c) la promoción de habilidades para la autorregulación y su utilidad en el contexto educativo y d) la posibilidad de implicación de los profesores en la promoción de dicho aprendizaje.


The concept of self-regulation in learning has been assuming a rising importance in the literature once the research has suggested that students participate actively in their learning process, monitoring and regulating their study process to achieve self-set goals. Nevertheless, the information about self-regulation has not been yet systematized on the journals indexed in Scielo. Therefore, the current study performed a systematic review of the literature on Scielo.org, between the period 2001 and 2011 to analyze the existence evidence regarding: a) the nature of self-regulated learning, b) it's assessment, c) the promotion of self-regulated skills and their usefulness in the context of education, and d) the potential implication of teachers on the promotion of lifelong learning.


Assuntos
Educação , Autocontrole , Aprendizagem
5.
Neuroimage ; 25(4): 1197-204, 2005 May 01.
Artigo em Inglês | MEDLINE | ID: mdl-15850737

RESUMO

Allelic variants in the promoter region of the serotonin transporter (5-HTT) gene have been implicated in several psychiatric disorders and personality traits. In particular, two common alleles in a variable repeat sequence of the promoter region (SLC6A4) have been differentially associated with a display of abnormal levels of anxiety and affective illness in individuals carrying the "s" allele. The aim of this study was to compare the basal cerebral metabolic activity of non-psychiatric subjects in fronto-limbic structures to determine whether differences exist in basal metabolic activity within this functional polymorphism. PET scans with fluorine-18 fluorodeoxyglucose as radiotracer were performed in 71 non-psychiatric subjects previously screened for psychopathology and subsequently genotyped for SLC6A4; PET images were compared with SPM2 according to s/s (n = 27), s/l (n = 25), and l/l (n = 19) groups considering a significance threshold in a priori selected areas of P < 0.001 and an extent threshold > or =5 voxels. The analysis showed an effect of interest among the three genotype groups in right anterior cingulate gyrus (ACC), left middle frontal gyrus, and left posterior cingulate gyrus (PCC). Comparison between l/l vs. s/s showed increased metabolism for l/l in left middle frontal gyrus and an increase for s/s in right ACC and left PCC. Comparison between s/s vs. s/l showed an increase for s/s in left PCC and right ACC. Increased basal metabolism in fronto-limbic structures for the s/s group may be conceived as an "overactive metabolic state" of these structures, possibly related to an increased susceptibility for developing an anxiety-depression spectrum disorder.


Assuntos
Lobo Frontal/metabolismo , Sistema Límbico/metabolismo , Glicoproteínas de Membrana/genética , Proteínas de Membrana Transportadoras/genética , Proteínas do Tecido Nervoso/genética , Polimorfismo Genético/genética , Adulto , Alelos , Mapeamento Encefálico , Feminino , Lobo Frontal/diagnóstico por imagem , Genótipo , Humanos , Processamento de Imagem Assistida por Computador , Sistema Límbico/diagnóstico por imagem , Masculino , Pessoa de Meia-Idade , Tomografia por Emissão de Pósitrons , Proteínas da Membrana Plasmática de Transporte de Serotonina
6.
Blood Press ; 11(3): 144-50, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12126260

RESUMO

In a sample comprising 51 normotensive subjects and 51 subjects with in-clinic arterial hypertension [blood pressures (BPs) > or = 140/90 mmHg), we investigated the prevalence of target organ damage [left ventricular hypertrophy (LVH) and retinal vasculopathy] in white coat hypertension (WCH) groups defined using: (a) the "optimal ambulatory BP" criterion of the Seventh International Consensus Conference (in-clinic BPs >140/90 mmHg, daytime mean BPs < 130/80 mmHg) and (b) the "normal ambulatory BP" criterion proposed in 1997 by Verdecchia and co-workers (in-clinic BPs >140/ 90 mmHg, daytime mean BPs < 135/85 mmHg), and we compared the results with those obtained for the normotensive group and for a WCH group defined as in a 1996 study of the same data. We found that the newer criteria did not alter the conclusions reached in 1996: namely, that WCH constitutes a state of risk intermediate between normotension and sustained hypertension, which demands in-depth evaluation and active monitoring, if not immediate therapy. We also found that when the WCH group was defined as those patients with in-clinic BPs > or = 140/90 mmHg and 24-h mean BPs < 121/78 mmHg, the prevalence of target organ damage was similar to that found in the control group. We conclude that if WCH status is to imply absence of elevated risk of target organ damage, then the ambulatory BP threshold defining WCH should be lower than the upper limit of ambulatory BPs among subjects who are normotensive in the clinic. The desirability of predicting target organ damage in both hypertensive and normotensive subjects using criteria combining in-clinic BPs, daytime mean ambulatory BPs and night-time mean ambulatory BPs is suggested.


Assuntos
Hipertensão/complicações , Hipertensão/diagnóstico , Hipertrofia Ventricular Esquerda/etiologia , Oclusão da Veia Retiniana/etiologia , Pressão Sanguínea , Monitorização Ambulatorial da Pressão Arterial , Estudos de Casos e Controles , Feminino , Humanos , Hipertensão/psicologia , Hipertrofia Ventricular Esquerda/diagnóstico , Masculino , Visita a Consultório Médico , Prevalência , Prognóstico , Valores de Referência , Oclusão da Veia Retiniana/diagnóstico
7.
An Otorrinolaringol Ibero Am ; 22(1): 57-66, 1995.
Artigo em Espanhol | MEDLINE | ID: mdl-7710012

RESUMO

The most common manifestation of mycobacterial infection encountered in E.N.T. practice is cervical lymphadenitis. Mycobacterial cervical lymphadenitis, the so-called scrofula, remains a diagnostic challenge, because it mimics other resembling processes. We present 13 cases of cervical granulomatous lymphadenitis treated from 1967 until 1990.


Assuntos
Mycobacterium/isolamento & purificação , Tuberculose dos Linfonodos/microbiologia , Adolescente , Adulto , Idoso , Criança , Humanos , Masculino , Pessoa de Meia-Idade , Pescoço , Estudos Retrospectivos , Tuberculose dos Linfonodos/complicações , Tuberculose dos Linfonodos/cirurgia
8.
An Otorrinolaringol Ibero Am ; 22(1): 67-73, 1995.
Artigo em Espanhol | MEDLINE | ID: mdl-7710013

RESUMO

Kikuchi-Fujimoto disease (KFD) is a rare entity of uncertain cause which commonly presents as a lymphoadenopathy unresponsive to antibiotic therapy. Although usually it follows a benign self-limited course KFD has been repeatedly misdiagnosed as lymphoma. With this new case data about the etiology and clinical trend of KFD are added. Review of the literature.


Assuntos
Linfadenite/diagnóstico , Otolaringologia , Criança , Diagnóstico Diferencial , Feminino , Humanos
9.
Pediatr Infect Dis J ; 11(10): 836-40, 1992 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-1408482

RESUMO

From January to April, 1990, 695 measles cases were reported to the Puerto Rico Health Department; there were 12 measles-associated deaths (case fatality ratio, 17/1000), more than in any year since 1967. We conducted a case-control study of risk factors for severe measles. We identified 16 children (ages 5 to 34 months) with severe measles and selected children with nonsevere measles as controls (39 hospitalized and 38 nonhospitalized). Controls were frequency matched to severe measles cases by region of residence. One case and two controls had been vaccinated. An underlying illness was present in 50% of cases and 16% of nonhospitalized controls (Mantel-Haenszel weighted odds ratio 5.3; 95% confidence interval 1.4, 20.2). In a multivariate analysis cases were significantly more likely than hospitalized controls to be from families with an annual income of < $5000 (odds ratio (OR), 26.9), to have a mother without a high school degree (OR 11.1), to be anemic (hemoglobin < 10 g/dl) (OR 15.9) and have an underlying illness (OR 18.3). During measles outbreaks preventing severe illness requires aggressive control measures and strategies to increase vaccine coverage of children with underlying illnesses and of low socioeconomic status.


Assuntos
Sarampo/epidemiologia , Pré-Escolar , Feminino , Hospitalização , Humanos , Lactente , Masculino , Porto Rico/epidemiologia , Estudos Retrospectivos , Fatores de Risco
15.
Bull. W.H.O. (Print) ; 31(4): 565-567, 1964.
Artigo em Inglês | WHO IRIS | ID: who-267035
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA