E. Meyer
McGill University
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Featured researches published by E. Meyer.
NeuroImage | 1992
Alan C. Evans; S. Marrett; Peter Neelin; Louis Collins; Keith J. Worsley; Weiqian Dai; Sylvain Milot; E. Meyer; Daniel Bub
Numerous applications have been reported for the stereotactic mapping of focal changes in cerebral blood flow during sensory and cognitive activation as measured with positron emission tomography (PET) subtraction images. Since these images lack significant anatomical information, analysis of these kinds of data has been restricted to an automated search for peaks in the PET subtraction dataset and localization of the peak coordinates within a standardized stereotactic atlas. This method is designed to identify isolated foci with dimensions smaller than the image resolution. Details of activation patterns that may extend over finite distances, following the underlying anatomical structures, will not be apparent. We describe the combined mapping into stereotactic coordinate space of magnetic resonance imaging (MRI) and PET information from each of a set of subjects such that the major features of the activation pattern, particularly extended tracts of increased blood flow, can be immediately assessed within their true anatomical context as opposed to that presumed using a standard atlas alone. Near areas of high anatomical variability, e.g., central sulcus, or of sharp curvature, e.g., frontal and temporal poles, this information can be essential to the localization of a focus to the correct gyrus or for the rejection of extracerebral peaks. It also allows for the removal from further analysis of data from cognitively-normal subjects with abnormal anatomy such as enlarged ventricles. In patients with neuropathology, e.g., Alzheimers disease, arteriovenous malformation, stroke, or neoplasm, the use of correlated MRI is mandatory for correct localization of functional activation.
Journal of Cognitive Neuroscience | 1996
Robert J. Zatorre; Andrea R. Halpern; David W. Perry; E. Meyer; Alan C. Evans
Neuropsychological studies have suggested that imagery processes may be mediated by neuronal mechanisms similar to those used in perception. To test this hypothesis, and to explore the neural basis for song imagery, 12 normal subjects were scanned using the water bolus method to measure cerebral blood flow (CBF) during the performance of three tasks. In the control condition subjects saw pairs of words on each trial and judged which word was longer. In the perceptual condition subjects also viewed pairs of words, this time drawn from a familiar song; simultaneously they heard the corresponding song, and their task was to judge the change in pitch of the two cued words within the song. In the imagery condition, subjects performed precisely the same judgment as in the perceptual condition, but with no auditory input. Thus, to perform the imagery task correctly an internal auditory representation must be accessed. Paired-image subtraction of the resulting pattern of CBF, together with matched MRI for anatomical localization, revealed that both perceptual and imagery. tasks produced similar patterns of CBF changes, as compared to the control condition, in keeping with the hypothesis. More specifically, both perceiving and imagining songs are associated with bilateral neuronal activity in the secondary auditory cortices, suggesting that processes within these regions underlie the phenomenological impression of imagined sounds. Other CBF foci elicited in both tasks include areas in the left and right frontal lobes and in the left parietal lobe, as well as the supplementary motor area. This latter region implicates covert vocalization as one component of musical imagery. Direct comparison of imagery and perceptual tasks revealed CBF increases in the inferior frontal polar cortex and right thalamus. We speculate that this network of regions may be specifically associated with retrieval and/or generation of auditory information from memory.
Journal of Cerebral Blood Flow and Metabolism | 1997
David C. Reutens; Michael McHugh; Paule Joanne Toussaint; Alan C. Evans; Albert Gjedde; E. Meyer; Duncan J. Stewart
Nitric oxide is a potent vasodilator. Infusion of its precursor, L-arginine, results in increased cerebral blood flow (CBF) in experimental animals. We examined the effects of L-arginine infusion on CBF in humans using positron emission tomography and the quantitative H215O method. Six subjects received 500 ml of 0.9% NaCl solution, and six subjects received an infusion of L-arginine (16.7 mg/kg/min; 500 mg/kg). Before and after the i.v. infusion, paired CBF measurements were performed at baseline and with vibrotactile stimulation of the right hand. In scans performed without vibrotactile stimulation, mean whole-brain CBF increased from 34.9 ± 3.7 ml 100 g–1 min–1 to 38.2 ± 4.4 ml 100 g–1 min–1 (9.5%; p < 0.005) after L-arginine infusion. The temporal pattern of CBF changes differed from that of plasma growth hormone and insulin levels and of arterial pH. In contrast, in the saline group, mean whole-brain CBF did not change significantly (35.8 ± 5.9 ml 100 g–1 min–1 to 35.9 ± 6.4 ml 100 g–1 min–1; 0.3%). Vibrotactile stimulation produced significant focal increases in CBF, which were unaffected by L-arginine infusion. L-arginine infusion was associated with an increase in plasma L-citrulline, a byproduct of nitric oxide synthesis.
Archive | 1988
Albert Gjedde; Curt Beil; E. Meyer; Alan C. Evans; Antoine M. Hakim
The regional density of capillaries varies in the brain, some regions having more capillaries per unit weight, other regions having fewer. This arrangement is anatomical and does not reflect a functional coupling of flow, capillary permeability, or cerebral metabolic rate. The total number of capillaries in anyone region is a reflection of the normal average energy requirement of the region and of the fact that individual capillaries have similar properties (radius, length, permeability) in different regions. This observation does not address the question of how many capillaries actually are perfused at anyone time and how this number varies with the changing energy requirements of individual regions.
Science | 1992
Robert J. Zatorre; Alan C. Evans; E. Meyer; Albert Gjedde
Annals of Neurology | 1991
E. Meyer; S. S. G. Ferguson; Robert J. Zatorre; Bessie Alivisatos; S. Marrett; Alan C. Evans; A. M. Hakim
JSAI Workshops | 1999
Manoucher Vafaee; E. Meyer; Sean Marrett; Tomáš Paus; Alan C. Evans; Albert Gjedde
American Journal of Physiology-endocrinology and Metabolism | 1989
C. Redies; L. J. Hoffer; C. Beil; Errol B. Marliss; Alan C. Evans; F. Lariviere; S. Marrett; E. Meyer; Mirko Diksic; Albert Gjedde
Annals of Nuclear Medicine | 1993
L. Ribeiro; Hiroto Kuwabara; E. Meyer; H. Fujita; S. Marrett; Alan C. Evans; Albert Gjedde
Archive | 1993
Tomáš Paus; Michael Petrides; Alan C. Evans; E. Meyer