729 resultados para Keating, Jenny
Resumo:
El treball pretén aportar un coneixement de caràcter psicosocial sobre els contextos on els professionals del sistema jurídic-penal ofereixen atenció a les víctimes de violència de gènere, concretament, les unitats i oficines habilitades per recollir la denúncia o atestat dins de les comissaries dels Mossos d’esquadra i els jutjats d´instrucció de la dona. L´àmbit territorial va ser Barcelona i Girona. Es va obtenir informació sobre judicis realitzats a l´Audiència provincial, així com documents legals en relació al tema. S’ha analitzat les necessitats i dificultats juntament amb la identificació dels recursos psicosocials que aporten tant aquests professionals com les dones que han patit o estan patit un procés de maltractament per part de la parella. La pretensió es oferir una mirada particular per suggerir transformacions que facilitin el procés d´atenció en aquests contextos, sovint difícil i, que comporta conseqüències emocionals per part de les víctimes i dels mateixos agents que les atenen. S’ha partit de les narracions de les víctimes i dels agents jurídics, com pràctiques socials a partir de les quals podem detectar valors, posicions, normes, emocions i efectes de gènere que permetrà dirigir la intervenció. Com a eines d´anàlisi s’ha fet ús els repertoris interpretatius els quals han permès analitzar les construccions socials i els seus efectes al voltant del maltracte, de les identitats de les víctimes i els victimaris.
Resumo:
OBJECTIVES: The objective of this study is to describe the prenatal sonographic features and the results of DNA analysis on three fetuses with dyssegmental dysplasia, Silverman-Handmaker type (DD-SH). METHODS: A retrospective review of three fetuses with confirmed DD-SH was conducted. The fetal ultrasound findings, the radiological characteristics, and the results of the mutation analysis of the heparan sulphate perlecan gene 2 (HSPG2) were reviewed. RESULTS: There were three cases in two families with DD-SH diagnosed prenatally. The main prenatal ultrasound and the radiological features of DD-SH were severe limb shortening and vertebral segmentation and fusion defects (anisospondyly). The DNA analysis of the HSPG2 gene showed that the two affected fetuses in a nonconsanguineous family had a compound heterozygote for the c.646G > T transversion in exon 7 and a c.5788C > T transition in exon 46. The fetus born to the consanguineous couple had a homozygous mutation c.1356-27_1507 + 59del. CONCLUSION: DD-SH can be diagnosed prenatally using fetal ultrasound as early as 13 weeks. Xrays and DNA analysis of the HSPG2 gene are important for the confirmation of the diagnosis and for the preimplantation and prenatal diagnosis in pregnancies at risk. © 2013 John Wiley & Sons, Ltd.
Resumo:
Between June 1988 and September 1994, 100 girls and 32 boys 2 months to 15.5 years old (average 4.9 years) with 204 refluxing ureteral units were treated by endoscopic subureteral collagen injection. The collagen injected was of bovine origin and cross-linked with glutaraldehyde (Zyplast*). Followup ranged from 3 to 75 months (mean 33). Reflux was absent in 62.7% of cases 3 months after 1 endoscopic subureteral injection. Improvement to reflux grades I and II, generally not requiring further treatment, occurred in a further 15.2% of cases. A total of 66 ureters was injected twice. The overall cure rate after 1 or 2 injections was 79.4% 3 months after injection. There was no correlation between the risk of recurrent reflux and initial degree of reflux. Late recurrence of reflux following a reflux-free period occurred in 11.3% of the 204 units during the observation period, which varied from 3 months to 6 1/4 years. Reflux was absent after 1 or 2 injections, including late recurrence, in 70.6% of cases and in an additional 13.2% recurrent reflux was grade I or II, not necessitating any further treatment. Considering these results, subureteral collagen injection remains an adequate method of treatment for vesicoureteral reflux in children.
Resumo:
Une classification simplifiee du genre Colaniella LIKHAREV est proposee: Colaniella ex gr. parva, Colaniella ex gr. lepida, Colaniella ex gr. minima. Elle correspond a la division du taxon en trois groupes morphologiques. La repartition geographique de ce taxon est inventoriée de meme que les environnements sedimentaires et les microfaunes associees. Les nouvelles decouvertes de C. ex gr. parva dans Ie Permien superieur des coupes de Mesagros (ile d'Egine, Grece), d'Emarat (N Elbourz, Iran) et du Wadi Wasil dans les montagnes centrales d'Oman sont decrites en detail. L'importance des Colanielles dans la biostratigraphie du Permien superieur tethysien est analysee et clarifiee au vu des travaux recents et Ie problème des migrations est abordé. A simplified taxonomic classification in 3 groups of the genus Colaniella LIKHAREV is proposed: Colaniella ex gr. parva, Colaniella ex gr. lepida, Colaniella ex gr. minima. The repartition of the eight main Colaniella biofacies is given and the paleogeographic distribution of this genus is presented on a late Permian map configuration. New late Permian localities with Colaniella ex gr. parva have been found: Aegina island (Greece), Emmarat in the northern Alborz (Iran) and Wadi Wasit in the central Oman Mountains. The stratigraphic range of Colaniella ex gr. parva is much longer than previously accepted even by specialists. This range begins in the early Midian (Abadehian) and ends in the late Changhsingian (Dorashamian), very close to the range of the genus. For environmental reasons and slow eastward migration we have apparent shorter ranges in the Eastern part of the Tethyan domain.
Resumo:
Opinnäytetyömme ensimmäisenä tarkoituksena on kuvata imeväisikäisen potilaan hoidossa tarvittavaa osaamista. Toisena tarkoituksena on luoda kirjallisuuskatsauksen avulla arviointiväline eli mittari, jonka avulla arvioidaan perustason sairaankuljettajien osaamista imeväisikäisten kohdalla. Työmme on ensimmäinen osa KUOSCE- hanketta, joka on Keski- Uudenmaan pelastuslaitoksen ja Helsingin ammattikorkeakoulu Stadian monivuotinen yhteistyöhanke. Hankkeen tarkoituksena on luoda osaamisen kehittymisen malli ensihoidon koulutusohjelman ja Keski- Uudenmaan pelastuslaitoksen käyttöön. Olemme kirjallisuuskatsauksessa kuvanneet imeväisikäisen potilaan kehitystä ja hoidossa tarvittavaa osaamista. Hoidon osaamisessa keskityimme siihen, mitä perustason sairaankuljettajan tulee osata hoitaessaan imeväisikäistä potilasta. Kirjallisuuskatsauksessa olemme kuvanneet myös OSCE - menetelmää, sillä arviointivälineemme on kehitetty sen pohjalta. Arviointivälineen kehittämiseksi olemme saaneet ehdotuksia Keski-Uudenmaan pelastuslaitoksen työelämänohjaajilta. Vaikka imeväisikäinen potilas on erittäin harvinainen potilasryhmä, päädyimme silti työelämänohjaajien kanssa siihen lopputulokseen, että kyseisen ryhmän ensihoidon osaamista on tarpeellista testata. Arviointivälineemme on lähetetty työelämän asiantuntijoille, jotta he voisivat arvioida sen osaamisalueiden selkeyttä, yksiselitteisyyttä, arvioitavuutta ja tärkeyttä. Näistä arvioista saimme yhden tarkistettuna takaisin. Arviointivälineen toimivuutta ja käyttökelpoisuutta testasimme viimeisen vuoden ensihoitajaopiskelijoilla (n=15). Esitestauksessa ei ollut tarkoitus arvioida testattavien parien työskentelyä, vaan arviointivälineen luotettavuutta ja käyttökelpoisuutta. Esitestauksen jälkeen jouduimme vielä muokkaamaan arviointivälinettä sillä huomasimme, että siinä eivät kaikki väittämät edenneet loogisesti. Itse arviointivälineen sisältöön emme juurikaan puuttuneet enää esitestauksen jälkeen. Jatkossa aiomme toisessa opinnäyetyössämme testata arviointivälinettä pienellä ryhmällä Keski-Uudenmaan perustason sairaankuljettajia.
Resumo:
In this paper, an extension of the multi-scale finite-volume (MSFV) method is devised, which allows to Simulate flow and transport in reservoirs with complex well configurations. The new framework fits nicely into the data Structure of the original MSFV method,and has the important property that large patches covering the whole well are not required. For each well. an additional degree of freedom is introduced. While the treatment of pressure-constraint wells is trivial (the well-bore reference pressure is explicitly specified), additional equations have to be solved to obtain the unknown well-bore pressure of rate-constraint wells. Numerical Simulations of test cases with multiple complex wells demonstrate the ability of the new algorithm to capture the interference between the various wells and the reservoir accurately. (c) 2008 Elsevier Inc. All rights reserved.
Resumo:
Este relatório descreve em grande parte, o processo de estágio nomeadamente, a caracterização dos serviços onde este decorreu. Passa ainda a descrever as respectivas intervenções e actividades realizadas nas enfermarias consoante as demandas de cada uma. Os estudos de casos, e as avaliações psicológicas realizadas dos mesmos estão aqui apresentados com as devidas fundamentações, compreensibilidades, e as respectivas hipóteses diagnósticas.
Resumo:
El desarrollo de la maricultura en la Bahía de Samanco ha ocasionado descarga de restos orgánicos al ecosistema marino; se efectuaron monitoreos en esta Bahía en época de veda y de actividad pesquera industrial del 2005 al 2010; temperatura, salinidad y nutrientes se mantuvieron normales, pudiéndose afirmar que la capacidad de resiliencia del ecosistema no está afectada. Los parámetros fisicoquímicos, aceites y grasa presentaron altas concentraciones del 2007 al 2010, en relación al valor límite de los Estándares de Calidad Ambiental. La pesca artesanal generó 21.416 t de recursos hidrobiológicos, conformado por moluscos 57,78%, peces óseos 38,68%, equinodermos 3,20% y crustáceos, celentéreos y algas. La diversidad correspondió a 114 especies, mayor relevancia íctica dada por pejerrey, lisa, machete, lorna y coco; los invertebrados fueron concha de abanico, navajuela, calamar, marucha, caracol y ancoco. La captura de la pesca industrial de madera y artesanal anchovetera para consumo fue de 7.039 t, se identificaron 15 especies: peces (13) e invertebrados (2), la anchoveta aportó 98,71%. Se registraron 11 especies de fitoplancton potencialmente tóxicos, diatomeas: Pseudonitzschia cf delicatissima y P. pungens; dinoflagelados: Alexandrium sp., Dinophysis acuminata, D. caudata, D. rotundata, D. tripos, Gymnodinium sp., Prorocentrum mínimum, Protoperidinium crassipes y P. depressum.
Resumo:
High blood pressure (BP) is more prevalent and contributes to more severe manifestations of cardiovascular disease (CVD) in African Americans than in any other United States ethnic group. Several small African-ancestry (AA) BP genome-wide association studies (GWASs) have been published, but their findings have failed to replicate to date. We report on a large AA BP GWAS meta-analysis that includes 29,378 individuals from 19 discovery cohorts and subsequent replication in additional samples of AA (n = 10,386), European ancestry (EA) (n = 69,395), and East Asian ancestry (n = 19,601). Five loci (EVX1-HOXA, ULK4, RSPO3, PLEKHG1, and SOX6) reached genome-wide significance (p < 1.0 × 10(-8)) for either systolic or diastolic BP in a transethnic meta-analysis after correction for multiple testing. Three of these BP loci (EVX1-HOXA, RSPO3, and PLEKHG1) lack previous associations with BP. We also identified one independent signal in a known BP locus (SOX6) and provide evidence for fine mapping in four additional validated BP loci. We also demonstrate that validated EA BP GWAS loci, considered jointly, show significant effects in AA samples. Consequently, these findings suggest that BP loci might have universal effects across studied populations, demonstrating that multiethnic samples are an essential component in identifying, fine mapping, and understanding their trait variability.
Resumo:
This paper explores the possibility of using data from social bookmarking services to measure the use of information by academic researchers. Social bookmarking data can be used to augment participative methods (e.g. interviews and surveys) and other, non-participative methods (e.g. citation analysis and transaction logs) to measure the use of scholarly information. We use BibSonomy, a free resource-sharing system, as a case study. Results show that published journal articles are by far the most popular type of source bookmarked, followed by conference proceedings and books. Commercial journal publisher platforms are the most popular type of information resource bookmarked, followed by websites, records in databases and digital repositories. Usage of open access information resources is low in comparison with toll access journals. In the case of open access repositories, there is a marked preference for the use of subject-based repositories over institutional repositories. The results are consistent with those observed in related studies based on surveys and citation analysis, confirming the possible use of bookmarking data in studies of information behaviour in academic settings. The main advantages of using social bookmarking data are that is an unobtrusive approach, it captures the reading habits of researchers who are not necessarily authors, and data are readily available. The main limitation is that a significant amount of human resources is required in cleaning and standardizing the data.
Resumo:
BACKGROUND: Qualitative frameworks, especially those based on the logical discrete formalism, are increasingly used to model regulatory and signalling networks. A major advantage of these frameworks is that they do not require precise quantitative data, and that they are well-suited for studies of large networks. While numerous groups have developed specific computational tools that provide original methods to analyse qualitative models, a standard format to exchange qualitative models has been missing. RESULTS: We present the Systems Biology Markup Language (SBML) Qualitative Models Package ("qual"), an extension of the SBML Level 3 standard designed for computer representation of qualitative models of biological networks. We demonstrate the interoperability of models via SBML qual through the analysis of a specific signalling network by three independent software tools. Furthermore, the collective effort to define the SBML qual format paved the way for the development of LogicalModel, an open-source model library, which will facilitate the adoption of the format as well as the collaborative development of algorithms to analyse qualitative models. CONCLUSIONS: SBML qual allows the exchange of qualitative models among a number of complementary software tools. SBML qual has the potential to promote collaborative work on the development of novel computational approaches, as well as on the specification and the analysis of comprehensive qualitative models of regulatory and signalling networks.
Resumo:
The prevalence of hypertension in African Americans (AAs) is higher than in other US groups; yet, few have performed genome-wide association studies (GWASs) in AA. Among people of European descent, GWASs have identified genetic variants at 13 loci that are associated with blood pressure. It is unknown if these variants confer susceptibility in people of African ancestry. Here, we examined genome-wide and candidate gene associations with systolic blood pressure (SBP) and diastolic blood pressure (DBP) using the Candidate Gene Association Resource (CARe) consortium consisting of 8591 AAs. Genotypes included genome-wide single-nucleotide polymorphism (SNP) data utilizing the Affymetrix 6.0 array with imputation to 2.5 million HapMap SNPs and candidate gene SNP data utilizing a 50K cardiovascular gene-centric array (ITMAT-Broad-CARe [IBC] array). For Affymetrix data, the strongest signal for DBP was rs10474346 (P= 3.6 × 10(-8)) located near GPR98 and ARRDC3. For SBP, the strongest signal was rs2258119 in C21orf91 (P= 4.7 × 10(-8)). The top IBC association for SBP was rs2012318 (P= 6.4 × 10(-6)) near SLC25A42 and for DBP was rs2523586 (P= 1.3 × 10(-6)) near HLA-B. None of the top variants replicated in additional AA (n = 11 882) or European-American (n = 69 899) cohorts. We replicated previously reported European-American blood pressure SNPs in our AA samples (SH2B3, P= 0.009; TBX3-TBX5, P= 0.03; and CSK-ULK3, P= 0.0004). These genetic loci represent the best evidence of genetic influences on SBP and DBP in AAs to date. More broadly, this work supports that notion that blood pressure among AAs is a trait with genetic underpinnings but also with significant complexity.
Resumo:
Oculofaciocardiodental (OFCD) and Lenz microphthalmia syndromes form part of a spectrum of X-linked microphthalmia disorders characterized by ocular, dental, cardiac and skeletal anomalies and mental retardation. The two syndromes are allelic, caused by mutations in the BCL-6 corepressor gene (BCOR). To extend the series of phenotypes associated with pathogenic mutations in BCOR, we sequenced the BCOR gene in patients with (1) OFCD syndrome, (2) putative X-linked ('Lenz') microphthalmia syndrome, (3) isolated ocular defects and (4) laterality phenotypes. We present a new cohort of females with OFCD syndrome and null mutations in BCOR, supporting the hypothesis that BCOR is the sole molecular cause of this syndrome. We identify for the first time mosaic BCOR mutations in two females with OFCD syndrome and one apparently asymptomatic female. We present a female diagnosed with isolated ocular defects and identify minor features of OFCD syndrome, suggesting that OFCD syndrome may be mild and underdiagnosed. We have sequenced a cohort of males diagnosed with putative X-linked microphthalmia and found a mutation, p.P85L, in a single case, suggesting that BCOR mutations are not a major cause of X-linked microphthalmia in males. The absence of BCOR mutations in a panel of patients with non-specific laterality defects suggests that mutations in BCOR are not a major cause of isolated heart and laterality defects. Phenotypic analysis of OFCD and Lenz microphthalmia syndromes shows that in addition to the standard diagnostic criteria of congenital cataract, microphthalmia and radiculomegaly, patients should be examined for skeletal defects, particularly radioulnar synostosis, and cardiac/laterality defects.