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Istituto Universitario Di Studi Superiori Di Pavia
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14 Projects, page 1 of 3
  • Funder: European Commission Project Code: 101207792
    Funder Contribution: 209,483 EUR

    The project aims to advance theoretical and practical knowledge in psycholinguistics and developmental neuroscience, focusing on symptoms of Developmental Language Disorder (DLD). Specifically, I will investigate underlying cognitive factors of syntactic difficulties manifested by children with DLD. I will test the project's hypotheses regarding the inflexibility of statistical learning of syntactic structures in DLD. To this end, I will examine the production and comprehension of relative clauses (RCs) in Italian- and Polish-speaking children with DLD. The RC is a subordinate clause that exhibits different syntactic structures in Italian and Polish. Therefore, the cross-linguistic study will provide a quantitative analysis of local linguistic elements that signify thematic role assignments in RCs and distinguish between Italian (IT) and Polish (PL). Additionally, I will analyze the global RC sentence structure, including length, complexity, and the distance related to syntactic movement. This linguistic analysis will further allow testing of the hypothesis that basic cognitive components and their interactions contribute to the errors typical for children with DLD. Specifically, based on linguistic analysis, I will test neuropsychological hypotheses that the following cognitive elements contribute to DLD deficits: i) executive control, triggered by the probabilistic properties of word/morpheme flow within the sentence; ii) performance in encoding rare linguistic elements, as reflected in inflectional suffixes; iii) working memory load, related to sentence length and syntactic movement. The achievement of the project's aims will impact the international research community by providing new insights into the cognitive aspects of language skills, particularly the development of specific grammatical-syntactic constructions. Finally, the results of the project will be relevant to clinicians in designing targeted, more effective therapeutic programs for children with DLD.

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  • Funder: European Commission Project Code: 101045733
    Overall Budget: 1,854,190 EURFunder Contribution: 1,854,190 EUR

    As the master figure of speech, metaphor is a powerful communicative tool that might nevertheless come with costs for our processing system. Research in different fields has highlighted that a full-fledged metaphor comprehension capacity is a late achievement in development, it may decay as a consequence of several pathological conditions, and it evokes distinctive electrical activity in our brain compared to literal equivalents. However, we still miss a comprehensive framework able to account for all these empirical findings in a unitary fashion, and this despite a vast number of linguistic and cognitive accounts of metaphor. This project will ground on theoretical insights from the pragmatics of language to sketch a novel and comprehensive model of metaphor understanding able to account for neural, developmental, and clinical findings. The leading hypothesis is that metaphor comprehension is an inferential process that involves first adjusting the lexical concepts, and then deriving the implicated -non-literal- meaning. The model also takes into account the multiplicity of metaphor types, which might in turn engage visual images and sensory-motor processes, in line with recent multimodal accounts of lexical and semantic processing. The model will be tested and refined through a series of behavioral and electrophysiological studies employing innovative experimental paradigms and involving neurotypical adults, children, and individuals with psychiatric and neurodegenerative diseases. This multidisciplinary approach will lead to a significant breakthrough in our understanding of metaphor as the pinnacle of human verbal creativity, in addition to disclosing important aspects for research on language processing, development and decay.

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  • Funder: European Commission Project Code: 295122
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  • Funder: UK Research and Innovation Project Code: MR/N025881/1
    Funder Contribution: 914,762 GBP

    Dementia is a complex and multifaceted clinical state, which shows marked variations in the biological mechanisms and molecular structure of brain pathology, and in the effects that these pathologies have on brain function. Importantly, not all people with dementia are suffering from Alzheimer's disease (though this remains the commonest underlying pathology), and not all experience forgetfulness as the first sign of mental difficulty. One type of dementia presentation that has been extensively studied over recent years is one that begins with selective difficulty understanding and/or producing speech and language - a pattern known as primary progressive aphasia (PPA). Because language is such a complex mental ability, and relies on a number of widely distributed brain areas, PPA can take a variety of forms. Currently, three distinct patterns are recognised. Some patients experience a reduced ability to appreciate the meaning of words or objects ('semantic dementia'), while in others the problems lie in the production of words and sentences ('progressive nonfluent aphasia'). A third group displays milder problems, along with a striking inability to repeat spoken sentences ('logopenic progressive aphasia'). At the level of pathology these three dementia syndromes are far from distinct, making their biological basis difficult to determine during life. Improved understanding should lead to the development of disease specific treatments, but because of their relative rarity (less than 5% of cases of dementia begin with PPA), clinical trials will necessitate large scale, international collaborations, and these will inevitably include patients who speak languages other than English. Such a diversity of language communities will obviously present problems in the context of a condition that primarily affects language itself. The principal aim of this project, therefore, is to lay the foundations of a common descriptive currency, in which the three types of PPA can be described, and patients' abilities quantified on the same scale, regardless of the language in which they are assessed. To achieve this, we will develop a brief language assessment instrument, which will allow the three PPA syndromes to be distinguished from one another on a common set of criteria and monitored over time using equivalent levels of severity. In view of the worldwide impact and importance of the Mini Mental State Examination (MMSE) in defining and quantifying dementia more generally, this brief language test will be given the title of the Mini Linguistic State Examination (or 'MLSE'). The instrument is intended to be comprehensive yet brief, and capable of being administered by clinicians without special expertise in language assessment. It would be unrealistic to try to develop versions of the MLSE for all the world's major languages at once, so we will concentrate on two European languages: English and Italian, the native languages of around 360 million and 60 million people, respectively. We will ensure that the same classifications emerge from the MLSE as are currently recognized by expert clinicians by validating the test against expert clinical opinion, and against the patterns of aphasia suffered by patients following a stroke. We will also look for validation in the MR imaging appearances that are known to be associated with each variant. When English and Italian versions of the instrument have been fully developed and validated, we will gather additional data from populations of patients with movement related neurodegenerative disorders (such as Parkinson's disease) in order to gain deeper insights into the effects of these groups of disorders on the brain, and to identify ways in which sufferers' quality of life can be improved through rehabilitation.

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  • Funder: European Commission Project Code: 607452
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