scispace - formally typeset
J

J.M. Peters

Researcher at University of Liège

Publications -  21
Citations -  1666

J.M. Peters is an academic researcher from University of Liège. The author has contributed to research in topics: Neuroscience of sleep & Fission products. The author has an hindex of 7, co-authored 21 publications receiving 1611 citations.

Papers
More filters
Journal ArticleDOI

Functional neuroanatomy of human rapid-eye-movement sleep and dreaming.

TL;DR: A group study of seven subjects who maintained steady REM sleep during brain scanning and recalled dreams upon awakening shows that regional cerebral blood flow is positively correlated with REM sleep in pontine tegmentum, left thalamus, both amygdaloid complexes, anterior cingulate cortex and right parietal operculum.
Journal ArticleDOI

Functional neuroanatomy of human slow wave sleep.

TL;DR: The results show that rCBF is decreased more in some cortical areas (especially in orbitofrontal cortex) than in the rest of the cortex, and it is hypothesize that cellular processes taking place during SWS might be modulated differently in these regions.
Journal ArticleDOI

A Positron Emission Tomography Study of Voluntarily and Electrically Contracted Human Quadriceps

TL;DR: This research focused on the role of muscular blood flow in the development of positron emission tomography and its role in the determination of nuclear magnetic resonance.
Journal ArticleDOI

Production of oxygen-15, nitrogen-13 and carbon-11 and of their low molecular weight derivatives for biomedical applications

TL;DR: In this article, the authors describe and discuss the methodological and practical aspects of the routine, high efficiency, production of these gases, with the specifications that result from their medical use.
Journal ArticleDOI

Automated preparation of carbon-11 ethanol and carbon-11 butanol for human studies using positron emission tomography

TL;DR: In this paper, an automated continuous flow process was developed for the synthesis of 11C-ethanol and 11Cbutanol via the same route, which was completely automated to limit radiation exposure to personnel, reduce preparation time, and increase reproducibility.