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L Garnero

Publications and source records attributed to L Garnero.

21 records · Page 2Linked to original sources

A Bayesian approach to introducing anatomo-functional priors in the EEG/MEG inverse problem.

In this paper, we present a new approach to the recovering of dipole magnitudes in a distributed source model for magnetoencephalographic (MEG) and electroencephalographic (EEG) imaging. This method consists in introducing spatial and temporal a priori information as a cure to this ill-posed inverse problem. A nonlinear spatial regularization scheme allows the preservation of dipole moment discontinuities between some a priori noncorrelated sources, for instance, when considering dipoles located on both sides of a sulcus. Moreover, we introduce temporal smoothness constraints on dipole magnitude evolution, at time scales smaller than those of cognitive processes. These priors are easily integrated into a Bayesian formalism, yielding a maximum a posteriori (MAP) estimator of brain electrical activity. Results from EEG simulations of our method are presented and compared with those of classical quadratic regularization and a now popular generalized minimum-norm technique called low-resolution electromagnetic tomography (LORETA).

Algorithms↗

Anatomical data fusion for quantitative reconstruction in myocardial tomoscintigraphy using a spline model of the thorax organs.

We present the fusion of anatomical data as a method for improving the reconstruction in single photon emission computed tomography (SPECT). Anatomical data is used to deduce a parameterized model of organs in a reconstructed slice using spline curves. This model allows us to define the imaging process, i.e., the direct problem, more adequately, and furthermore to restrict the reconstruction to the emitting zones. Instead of the usual square pixels, we use a new kind of discretization pixel, which fits to the contour in the region of interest. In the reconstruction phase, we estimate the activity in the emitting zones and also the optimum parameters of our model. Concentrating on the left ventricular (LV) wall activity, the simulation and phantom results show an accurate estimation of both the myocardial shape and the radioactive emission.

Computer Simulation↗

Chitin synthase homologs in three ectomycorrhizal truffles.

Degenerate PCR primers were used to amplify a conserved gene portion coding chitin synthase from genomic DNA of six species of ectomycorrhizal truffles. DNA was extracted from both hypogeous fruitbodies and in vitro growing mycelium of Tuber borchii. A single fragment of about 600 bp was amplified for each species. The amplification products from Tuber magnatum, T. borchii and T. ferrugineum were cloned and sequenced, revealing a high degree of identity (91.5%) at the nucleotide level. On the basis of the deduced amino acid sequences these clones were assigned to class II chitin synthase. Southern blot experiments performed on genomic DNA showed that the amplification products derive from a single copy gene. Phylogenetic analysis of the nucleotide sequences of class II chitin synthase genes confirmed the current taxonomic position of the genus Tuber, and suggested a close relationship between T. magnatum and T. uncinatum.

Amino Acid Sequence↗