RESUMEN La crisis de legitimidad de las democracias representativas y del proyecto de globalización económica ha colocado en el centro del debate público la capacidad de ciertos grupos intelectuales, tradicionales o emergentes, para intervenir en la esfera pública y normalizar o alterar el horizonte establecido de posibilidades politicas y económicas. La popularización de conceptos como "posverdad" guarda relación con una transformación del papel que se había atribuido históricamente a los expertos e intelectuales en los sistemas democráticos y la aparición de (...) nuevas figuras capaces de movilizar la sensibilidad colectiva. En este contexto se está produciendo una intensificación de la recepción de la obra de Antonio Gramsci como fuente de utilidades analíticas. Este artículo propone, precisamente, una revisión de la noción de "intelectual orgánico" como una herramienta esclarecedora para las tareas contemporáneas de la filosofía política. ABSTRACT The crisis of legitimacy of representative democracies and the economic globalization project has placed the power of certain intellectual groups, traditional or emerging, to intervene in the public sphere and legitimize or transform the current political and economic paradigm at the center of public debate. The popularization of concepts such as "post-truth" is related to a transformation of the role that had been historically attributed to experts and intellectuals in democratic systems and the appearance of new figures capable of mobilizing collective sensitivity. In this context, an intensification of the reception of the work of Antonio Gramsci is taking place, as a source of analytical utilities. This article proposes a revision of the notion of "organic intellectual" as an illuminating tool for the contemporary tasks of political philosophy. (shrink)

_El exilio como síntoma_ es un libro complejo. Lo es por su tema, lo es por el tratamiento del tema, cuidadoso, lúcido, “desde dentro”, por la mucha literatura, las muchas fuentes con las que —rigurosamente— se va tramando, por su escritura plural, autobiográfica y heterográfica a la vez, de ensayo y testimonio, de comentario y —casi me atrevería a decir— de responso, el responso de un duelo resistente...

La textualidad de conferencias y seminarios pronunciados por Enrique Leff en los últimos años, en una errancia iluminada por el Diálogo de Saberes, se transforma en Discursos Sustentables, en una cartografía vital para navegar por las costas del archipiélago complejo de una época, donde todavía las señales, muchas veces signos evanescentes, apenas si son una velada luz amanecida, transida de misterios, cuyas voces iniciales gorjean los sonidos de “una nueva comprensión del mundo y de los pr..

El libro está constituido por un conjunto de ensayos de carácter multidisciplinario sobre diferentes visiones del concepto de calidad de vida, presentados en una conferencia realizada en Helsinski durante el mes de julio de 1988 organizada por Martha Nussbaum y Amartya Sen. La obra probablemente constituye el resultado de un primer gran esfuerzo de carácter internacional por confrontar ideas entre filósofos, sociólogos, médicos y economistas con el objeto de replantear el concepto de desarrol..

Children, because of age-related reasons, are a vulnerable population, and protecting their health is a social, scientific and emotional priority. The increased susceptibility of children and fetuses to environmental agents has been widely discussed by the scientific community. Children may experience different levels of chemical exposure than adults, and their sensitivity to chemical toxicities may be increased or decreased in comparison with adults. Such considerations also apply to unborn and newborn children. Therefore, research on children is necessary in both clinical (...) and environmental fields, to provide age-specific relevant data regarding the efficacy and safety of medical treatments, and regarding the assessment of risk from unintended environmental exposure. In this context, the stakeholders are many, including children and their parents, physicians and public health researchers, and the society as a whole, with its ethical, regulatory, administrative and political components. The important ethical issues are information of participants and consent to participate. Follow-up and protection of data should be discussed in the context of biobanks, where children obtain individual rights when they become adults. It is important to realise that there are highly variable practices within European countries, which may have, in the past, led to differences in practical aspects of research in children. A number of recommendations are provided for research with children and environmental health. Environmental research with children should be scientifically justified, with sound research questions and valid study protocols of sufficient statistical power, ensuring the autonomy of the child and his/her family at the time of the study and later in life, if data and samples are used for follow-up studies. When children are enrolled, we recommend a consent dyad, including parental informed consent and the child’s assent and/or informed consent from older minors. For evaluation of the studies including children, a paediatrician should always be involved in the research ethics committee. (shrink)

This comment calls attention to the nature of the Aristotelian and classical logics, and the difficulty of representing their judgments and inferences by means of Venn diagrams. The meaning of ‘all’ in the different calculi produces problems. A second problem is that the specification of existence in Venn diagrams for statements and arguments cannot be restricted to a single class, overlooked by Wiebe. This problem is further complicated by his adoption of classical (Renaissance) syllogistic, which is inconsistent. Aristotle’s term logic (...) is consistent. So also is the medieval extension, though the inclusion of singular premisses renders it less perspicuous though more flexible. (shrink)

Background: The factors influencing parents’ willingness to enroll their children in biobanks are poorly understood. This study sought to assess parents’ willingness to enroll their children, and their perceived benefits, concerns, and information needs under different consent and data-sharing scenarios, and to identify factors associated with willingness. Methods: This large, experimental survey of patients at the 11 eMERGE Network sites used a disproportionate stratified sampling scheme to enrich the sample with historically underrepresented groups. Participants were randomized to receive one of (...) three consent and data-sharing scenarios. Results: In total, 90,000 surveys were mailed and 13,000 individuals responded (15.8% response rate). 5737 respondents were parents of minor children. Overall, 55% (95% confidence interval 50–59%) of parents were willing to enroll their youngest minor child in a hypothetical biobank; willingness did not differ between consent and data-sharing scenarios. Lower educational attainment, higher religiosity, lower trust, worries about privacy, and attitudes about benefits, concerns, and information needs were independently associated with less willingness to allow their child to participate. Of parents who were willing to participate themselves, 25% were not willing to allow their child to participate. Being willing to participate but not willing to allow one’s child to participate was independently associated with multiple factors, including race, lower educational attainment, lower annual household income, public health care insurance, and higher religiosity. Conclusions: Fifty-five percent of parents were willing to allow their youngest minor child to participate in a hypothetical biobank. Building trust, protecting privacy, and addressing attitudes may increase enrollment and diversity in pediatric biobanks. (shrink)