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1. |
Record Nr. |
UNINA990001437180403321 |
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Autore |
Hofbauer, Josef |
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Titolo |
Evolutionary games and population dynamics / Josef Hofbauer, Karl Sigmund |
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Pubbl/distr/stampa |
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Cambridge : Cambridge University Press, 1998 |
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ISBN |
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Descrizione fisica |
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Disciplina |
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Locazione |
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Collocazione |
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123-C-7 |
123-C-8 |
MXIX-D-68 |
125-A- 10 |
125-A-10-(BIS |
02 68 B 17 |
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Lingua di pubblicazione |
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Formato |
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Livello bibliografico |
Monografia |
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2. |
Record Nr. |
UNINA9910261141703321 |
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Autore |
Yuri Bozzi |
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Titolo |
Autism Spectrum Disorders: Developmental Trajectories, Neurobiological Basis, Treatment Update |
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Pubbl/distr/stampa |
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Descrizione fisica |
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1 online resource (139 p.) |
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Collana |
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Frontiers Research Topics |
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Soggetti |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Sommario/riassunto |
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This Research Topic has the aim to fill the gap of the many unresolved scientific issues on Autism Spectrum Disorders (ASD) that are still in need of investigation, Targeted treatments based on the understanding of the underlying pathogenic mechanisms of disease are still lacking. Further research is awaited and should be obtained through a significant effort on experimental treatment trials and neuroscience research. This Topic is divided in two main sections, one covering clinical issues and another on basic neurosciences of Autism Spectrum Disorders. A more detailed description of the contents of the articles is provided in the editorial at the beginning of the issue. |
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3. |
Record Nr. |
UNINA9910557595503321 |
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Autore |
Merlo Marco |
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Titolo |
Characterization and Clinical Management of Dilated Cardiomyopathy |
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Pubbl/distr/stampa |
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Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021 |
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Descrizione fisica |
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1 online resource (232 p.) |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Sommario/riassunto |
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Dilated cardiomyopathy (DCM) is a particular phenotype of non-ischemic systolic heart failure, frequently recognizing a genetic background and affecting relatively young patients with few comorbidities. Nowadays, long-term survival of DCM patients has been markedly improved due to an early diagnosis and uninterrupted and tailored follow-up under constant optimal medical and non-pharmacological evidence-based treatments. Nevertheless, DCM is still one of the most common causes of heart transplantation in the western world. Clinical management requires an integrated and systematic use of diagnostic tools and a deeper investigation of the basic mechanisms underlying the disease. However, several emerging issues remain debated. Specifically, the genotype-phenotype correlation, the role of advanced imaging techniques and genetic testing, the lack of appropriate risk stratification models, the need for a multiparametric and multidisciplinary approach for device implantation, and a continuous reclassification of the disease during follow-up remain challenging issues in clinical practice. Therefore, the aim of this Special Issue is to shed the light on the most recent advancements in characterization and clinical management of DCM in order to unveil the conundrum of this particular disease. |
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