9 research outputs found

    CONFLICT, DECENTRALISATION AND LOCAL GOVERNANCE IN COLOMBIA, 1974-2004

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    The objective of this paper is to determine the variables that explain the geographical expansion and armed activity of Colombian irregular groups since the mid seventies, taking into account the role of the political, fiscal and budgetary decentralization and its effects over local governance. This period of Colombian history (1974-2004) has been graved by strong economic, social and institutional changes that have deepened particularly since the decentralization process of the mid eighties. In fact, this paper states that decentralization process transformed the conflict into a dispute over the local power, intensifying the use of violence in order to appropriate part of the public goods and resources, interfere the political process and consolidate the group´s territorial control. The analysis of the illegal group´s early activity (1974-1982) shows that the use of violence is explained by grievances such as poverty or inequality. However, subsequent years reveal deep changes in the illegal group´s strategic procedures in which the decentralization process have given them incentives to control the local governments by using violence (greed). The results demonstrate a strong and significant relationship between the intensification of the armed conflict and the greater political, budgetary and fiscal autonomy of local governments. In fact, the presence of local resources such as royalties and taxes triggers violence against politicians being more intense in the municipalities where the actions of the illegal groups are higher.Armed conflict, Violence, Decentralization, Local governance, Spatial Econometrics

    LAS CONSECUENCIAS ECONÓMICAS DE UN NOMBRE ATÍPICO. EL CASO COLOMBIANO

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    Este artículo examina las consecuencias sobre los ingresos laborales de tener un nombre atípico para el caso colombiano. La primera parte del artículo muestra que los jóvenes, hijos de padres no educados, habitantes de zonas rurales y pertenecientes a minorías étnicas tienen una mayor probabilidad de tener un nombre atípico. La segunda parte muestra que el impacto de un nombre atípico sobre los salarios es sustancial (superior al 10%) y que el mismo es mucho mayor para las personas educadas que para los no educadas. Los resultados sugieren la existencia de mecanismos de transmisión intergeneracional alternativos a los tradicionales (restricciones de crédito, herencias, etc.). En Colombia, al menos, los nombres atípicos son no sólo una consecuencia de las desigualdades sociales, sino también una causa de las mismas.atípicos sin tocayo salarios exclusión social

    Metodologías aplicadas en la evaluación de la competencia transversal “Comprensión e Integración” en los estudios universitarios del Grado de Administración y Dirección de Empresas en la Universitat Politècnica de València

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    [ES] Las metodologías aplicadas en la implementación de la Competencia Transversal “Comprensión e integración” en los estudios de Administración y Dirección de Empresas, son muy diversas predominando el estudio de casos y la resolución de problemas. En el presente trabajo se analiza cómo se aplican y qué ventajas e inconvenientes se observan. Se concluye que al evaluar al alumno desde distintas perspectivas con diferentes metodologías, el resultado global integra los distintos niveles de dominio de la competencia[EN] In this paper we analyze the implementation of the Transversal Competence “Understanding and integration” through the subjects of Business Administration and Management degree. It is kept in mind that the proficiency level of the competence can not be the same for 1st and 2nd years, which would correspond to level 1, that for 3rd and 4th years, to which they correlate a higher level 2 The broad range of methodologies and techniques used in the assessment of this skill, allows us to infer that the overall evaluation is correctMarín Sánchez, MDM.; Crespo Abril, F.; Maroto Álvarez, MC.; Palau Ramírez, F.; Palmer Gato, ME.; Úbeda García, JE. (2019). Metodologías aplicadas en la evaluación de la competencia transversal “Comprensión e Integración” en los estudios universitarios del Grado de Administración y Dirección de Empresas en la Universitat Politècnica de València. En JIDDO. I Jornada de innovación en docencia universitaria para la dirección de organizaciones públicas y privadas. Editorial Universitat Politècnica de València. 8-16. https://doi.org/10.4995/JIDDO2019.2019.10247OCS81

    Multiple Sclerosis Risk Variant HLA-DRB1*1501 Associates with High Expression of DRB1 Gene in Different Human Populations

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    The human leukocyte antigen (HLA) DRB1*1501 has been consistently associated with multiple sclerosis (MS) in nearly all populations tested. This points to a specific antigen presentation as the pathogenic mechanism though this does not fully explain the disease association. The identification of expression quantitative trait loci (eQTL) for genes in the HLA locus poses the question of the role of gene expression in MS susceptibility. We analyzed the eQTLs in the HLA region with respect to MS-associated HLA-variants obtained from genome-wide association studies (GWAS). We found that the Tag of DRB1*1501, rs3135388 A allele, correlated with high expression of DRB1, DRB5 and DQB1 genes in a Caucasian population. In quantitative terms, the MS-risk AA genotype carriers of rs3135388 were associated with 15.7-, 5.2- and 8.3-fold higher expression of DQB1, DRB5 and DRB1, respectively, than the non-risk GG carriers. The haplotype analysis of expression-associated variants in a Spanish MS cohort revealed that high expression of DRB1 and DQB1 alone did not contribute to the disease. However, in Caucasian, Asian and African American populations, the DRB1*1501 allele was always highly expressed. In other immune related diseases such as type 1 diabetes, inflammatory bowel disease, ulcerative colitis, asthma and IgA deficiency, the best GWAS-associated HLA SNPs were also eQTLs for different HLA Class II genes. Our data suggest that the DR/DQ expression levels, together with specific structural properties of alleles, seem to be the causal effect in MS and in other immunopathologies rather than specific antigen presentation alone

    Spatiotemporal Characteristics of the Largest HIV-1 CRF02_AG Outbreak in Spain: Evidence for Onward Transmissions

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    Background and Aim: The circulating recombinant form 02_AG (CRF02_AG) is the predominant clade among the human immunodeficiency virus type-1 (HIV-1) non-Bs with a prevalence of 5.97% (95% Confidence Interval-CI: 5.41–6.57%) across Spain. Our aim was to estimate the levels of regional clustering for CRF02_AG and the spatiotemporal characteristics of the largest CRF02_AG subepidemic in Spain.Methods: We studied 396 CRF02_AG sequences obtained from HIV-1 diagnosed patients during 2000–2014 from 10 autonomous communities of Spain. Phylogenetic analysis was performed on the 391 CRF02_AG sequences along with all globally sampled CRF02_AG sequences (N = 3,302) as references. Phylodynamic and phylogeographic analysis was performed to the largest CRF02_AG monophyletic cluster by a Bayesian method in BEAST v1.8.0 and by reconstructing ancestral states using the criterion of parsimony in Mesquite v3.4, respectively.Results: The HIV-1 CRF02_AG prevalence differed across Spanish autonomous communities we sampled from (p < 0.001). Phylogenetic analysis revealed that 52.7% of the CRF02_AG sequences formed 56 monophyletic clusters, with a range of 2–79 sequences. The CRF02_AG regional dispersal differed across Spain (p = 0.003), as suggested by monophyletic clustering. For the largest monophyletic cluster (subepidemic) (N = 79), 49.4% of the clustered sequences originated from Madrid, while most sequences (51.9%) had been obtained from men having sex with men (MSM). Molecular clock analysis suggested that the origin (tMRCA) of the CRF02_AG subepidemic was in 2002 (median estimate; 95% Highest Posterior Density-HPD interval: 1999–2004). Additionally, we found significant clustering within the CRF02_AG subepidemic according to the ethnic origin.Conclusion: CRF02_AG has been introduced as a result of multiple introductions in Spain, following regional dispersal in several cases. We showed that CRF02_AG transmissions were mostly due to regional dispersal in Spain. The hot-spot for the largest CRF02_AG regional subepidemic in Spain was in Madrid associated with MSM transmission risk group. The existence of subepidemics suggest that several spillovers occurred from Madrid to other areas. CRF02_AG sequences from Hispanics were clustered in a separate subclade suggesting no linkage between the local and Hispanic subepidemics

    Las consecuencias económicas de un nombre atípico. El caso colombiano

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    Este artículo examina las consecuencias en los ingresos laborales de tener un nombre atípico para el caso colombiano. La primera parte del artículo muestra que los jóvenes, hijos de padres no escolarizados, habitantes de zonas rurales y pertenecientes a minorías étnicas tienen una mayor probabilidad de tener un nombre atípico. La segunda parte muestra que el efecto de un nombre atípico en los salarios es grande (superior a 10%) y que el mismo es mucho mayor para las personas escolarizadas que para los no escolarizadas. Los resultados sugieren la existencia de mecanismos de trasmisión intergeneracional distinto de los tradicionales (restricciones de crédito, mecanismos hereditarios, transferencias de ingresos, etc.)

    Clinical and economic impact of community-onset urinary tract infections caused by ESBL-producing Klebsiella pneumoniae requiring hospitalization in Spain: an observational cohort study

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    Objective: To analyze the clinical and economic impact of community-onset urinary tract infections (UTIs) caused by extended-spectrum beta-lactamase (ESBL)-producing Klebsiella pneumoniae requiring hospitalization. Methods: A retrospective cohort study that included all adults with a UTI caused by K. pneumoniae that were admitted to a tertiary care hospital in Barcelona, Spain, between 2011 and 2015. Demographic, clinical, and economic data were analyzed. Results: One hundred and seventy-three episodes of UTIs caused by K. pneumoniae were studied; 112 were non-ESBL-producing and 61 were ESBL-producing. Multivariate analysis identified ESBL production, acute confusional state associated with UTI, shock, and the time taken to obtain adequate treatment as risk factors for clinical failure during the first seven days. An economic analysis showed differences between ESBL-producing and non-ESBL-producing K. pneumoniae for the total cost of hospitalization per episode (mean EUR 6718 vs EUR 3688, respectively). Multivariate analysis of the higher costs of UTI episodes found statistically significant differences for ESBL production and the time taken to obtain adequate treatment. Conclusion: UTIs caused by ESBL-producing K. pneumoniae requiring hospitalization and the time taken to obtain adequate antimicrobial therapy are associated with worse clinical and economic outcomes

    Distribution and genotype-phenotype correlation of GDAP1 mutations in Spain

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    Mutations in the GDAP1 gene can cause Charcot-Marie-Tooth disease. These mutations are quite rare in most Western countries but not so in certain regions of Spain or other Mediterranean countries. This cross-sectional retrospective multicenter study analyzed the clinical and genetic characteristics of patients with GDAP1 mutations across Spain. 99 patients were identified, which were distributed across most of Spain, but especially in the Northwest and Mediterranean regions. The most common genotypes were p.R120W (in 81% of patients with autosomal dominant inheritance) and p.Q163X (in 73% of autosomal recessive patients). Patients with recessively inherited mutations had a more severe phenotype, and certain clinical features, like dysphonia or respiratory dysfunction, were exclusively detected in this group. Dominantly inherited mutations had prominent clinical variability regarding severity, including 29% of patients who were asymptomatic. There were minor clinical differences between patients harboring specific mutations but not when grouped according to localization or type of mutation. This is the largest clinical series to date of patients with GDAP1 mutations, and it contributes to define the genetic distribution and genotype-phenotype correlation in this rare form of CMT
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