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Silvio R. Bareggi

Researcher at University of Milan

Publications -  54
Citations -  1294

Silvio R. Bareggi is an academic researcher from University of Milan. The author has contributed to research in topics: Pharmacokinetics & High-performance liquid chromatography. The author has an hindex of 18, co-authored 54 publications receiving 1204 citations.

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Clinical pharmacokinetics of atypical antipsychotics: a critical review of the relationship between plasma concentrations and clinical response.

TL;DR: This review of the literature concerning the relationships between plasma concentrations of SGAs and clinical responses is divided by dividing the studies on the basis of the length of their observation periods by indicating a relationship between clinical outcomes and plasma concentrations.
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Clioquinol: review of its mechanisms of action and clinical uses in neurodegenerative disorders.

TL;DR: The first methods for determining plasma and tissue clioquinol levels were set up in the 1970s and involved HPLC separation with UV detection, followed by a more sensitive GC method with electron capture detection and a gaschromatographic‐massspectrometric method, which has proved to be as highly sensitive and specific as the GC‐MS.
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Decreased CSF Concentrations of Homovanillic Acid and γ-Aminobutyric Acid in Alzheimer's Disease: Age- or Disease-Related Modifications?

TL;DR: The decrease in HVA level was more pronounced in patients with severe mental deterioration and therefore appeared to be disease related, when compared with the age-matched controls.
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Understanding the pharmacokinetics of anxiolytic drugs

TL;DR: A need for a more balanced assessment of the benefits and risks associated with benzodiazepine use, particularly considering pharmacokinetic profile of the drugs to ensure that patients, who would truly benefit from these agents, are not denied appropriate treatment.
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Predictors of clinical outcome in schizophrenic patients responding to clozapine.

TL;DR: The results seem to suggest the importance of pharmacodynamic, constitutional, and genetic data over strict pharmacokinetics in determining the clinical response to CLZ.