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Paola Frati

Researcher at Sapienza University of Rome

Publications -  195
Citations -  2921

Paola Frati is an academic researcher from Sapienza University of Rome. The author has contributed to research in topics: Medicine & Health care. The author has an hindex of 23, co-authored 159 publications receiving 1916 citations. Previous affiliations of Paola Frati include American Board of Legal Medicine & University of Sannio.

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The right to be informed and fear of disclosure: sustainability of a full error disclosure policy at an Italian cancer centre/clinic.

TL;DR: The authors found that physicians were in favour of a full policy disclosure at the IRCCS CROB – the Oncology Centre of Basilicata, and the extent to which such a policy could help reduce administration and legal costs was found to be significant.
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MicroRNAs: The New Challenge for Traumatic Brain Injury Diagnosis.

TL;DR: The importance of microRNA research holds promise to find biomarkers able to unearth primary and secondary molecular patterns altered upon TBI, to ultimately identify key points of regulation, as valuable support in forensic pathology and potential therapeutic targets for clinical treatment.
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Mesenchymal stem cells in neurodegenerative diseases: Opinion review on ethical dilemmas

TL;DR: An ethical assessment of tissue regeneration through mesenchymal stem cells in neurodegenerative diseases is provided with the aim to rule out the fundamental issues related to research and clinical translation.
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Death after the Administration of COVID-19 Vaccines Approved by EMA: Has a Causal Relationship Been Demonstrated?

TL;DR: A literature review of COVID-19-vaccine-related deaths has been carried out to understand if there is a causal relationship between vaccination and death and to highlight the real extent of such events.
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Not only a clinical nightmare: amniotic fluid embolism in court.

TL;DR: The Authors reviewed the main national law cases on medical malpractice claims involving both physicians and hospitals to highlight the need to introduce a National register as a useful tool to raise the awareness of this disease among physicians and to improve the quality of care, which can be achieved through a proper identification and reporting of AFE cases.