Abstract
Presently the interest in non-invasive devices for monitoring the cardiovascular system has increased in importance, especially in the diagnosis of some pathologies. The proposed optical device reveals an attractive instrumental solution for local pulse wave velocity (PWV) assessment and other hemodynamic parameters analysis, such as Augmentation Index (AIx), Subendocardial Viability Ratio (SEVR), Maximum Rate of Pressure Change (dP/dtmax) and Ejection Time Index (ETI). These parameters allow a better knowledge on the cardiovascular condition and management of many disease states. Two studies were performed in order to validate this technology. Firstly, a comparative test between the optical system and a gold-standard in PWV assessment was carried out. Afterwards, a large study was performed in 131 young subjects to establish carotid PWV reference values as well as other hemodynamic parameters and to find correlations between these and the population characteristics. The results allowed the use of this new technique as a reliable method to determine these parameters. For the total of subjects values for carotid PWV vary between 3-7.69 m s-1 a clear correlation with age and smoking status was found out. The Aix varies between -6.15% and 11.46% and exhibit a negative correlation with heart, and dP/dtmax parameter shows a significant decrease with age.

Abstract
In this article, an algorithm to identify LPV State Space models is proposed. The LPV State Space system is in the companion reachable canonical form. Both the state matrix and the output vector coefficients are linear combinations of a set of nonlinear basis functions dependent on the scheduling signal. This model structure, although simple, can describe accurately the behaviour of many nonlinear systems by an adequate choice of the scheduling signal. The identification algorithm minimises a quadratic criterion of the output error. Since this error is a linear function of the output vector parameters, a separable nonlinear least squares approach is used to minimise the criterion function by a gradient method. The derivatives required by the algorithm are the states of LPV systems that need to be simulated at every iteration. The effectiveness of the algorithm is assessed by two simulated examples.

Abstract
Cardiovascular diseases (CVDs) are the leading cause of death in the world. The pulse wave analysis provides a new insight in the analysis of these pathologies, while data mining techniques can contribute for an efficient diagnostic method. Amongst the various available techniques, artificial neural networks (ANNs) are well established in biomedical applications and have numerous successful classification applications. Also, clustering procedures have proven to be very useful in assessing different risk groups in terms of cardiovascular function in healthy populations. In this paper, a robust data mining approach was performed for cardiac risk patterns identification. Eight classifiers were tested: C4.5, Random Forest, RIPPER, Naive Bayes, Bayesian Network, Multy-layer perceptron (MLP) (1 and 2-hidden layers) and radial basis function (RBF). As for clustering procedures, k-means clustering (using Euclidean distance) and expectation-maximization (EM) were the chosen algorithms. Two datasets were used as case studies to perform classification and clustering analysis. The accuracy values are good with intervals between 88.05% and 97.15%. The clustering techniques were essential in the analysis of a dataset where little information was available, allowing the identification of different clusters that represent different risk group in terms cardiovascular function. The three cluster analysis has allowed the characterization of distinctive features for each of the clusters. Reflected wave time (T_RP) and systolic wave time (T_SP) were the selected features for clusters visualization. Data mining methodologies have proven their usefulness in screening studies due to its descriptive and predictive power.

Abstract
There is good evidence that naltrexone, an opioid antagonist, has a strong neuroprotective role and may be a potential drug for the treatment of fibromyalgia. In previous work, some of the authors used experimental clinical data to identify input-output linear time invariant models that were used to extract useful information about the effect of this drug on fibromyalgia symptoms. Additional factors such as anxiety, stress, mood, and headache, were considered as additive disturbances. However, it seems reasonable to think that these factors do not affect the drug actuation, but only the way in which a participant perceives how the drug actuates on herself. Under this hypothesis the linear time invariant models can be replaced by State-Space Affine Linear Parameter Varying models where the disturbances are seen as a scheduling signal signal only acting at the parameters of the output equation. In this paper a new algorithm for identifying such a model is proposed. This algorithm minimizes a quadratic criterion of the output error. Since the output error is a linear function of some parameters, the Affine Linear Parameter Varying system identification is formulated as a separable nonlinear least squares problem. Likewise other identification algorithms using gradient optimization methods several parameter derivatives are dynamical systems that must be simulated. In order to increase time efficiency a canonical parametrization that minimizes the number of systems to be simulated is chosen. The effectiveness of the algorithm is assessed in a case study where an Affine Parameter Varying Model is identified from the experimental data used in the previous study and compared with the time-invariant model.

Abstract
An indirect downsampling approach for continuous-time input/output system identification is proposed. This modus operandi was introduced to system identification through a sub-space algorithm, where the input/output data set is partitioned into lower rate m subsets. Then, a state-space discrete-time model is identified by fusing the data subsets into a single one. In the present work the identification of the input/output downsampled model is performed by a least squares and a simplified refined instrumental variables (IV) procedures. In this approach, the inter-sample behaviour is preserved by the addition of fictitious inputs, leading to an increase of excitation requirements of the input signal. This over requirement is removed by directly estimating from the data the parameters of the transfer function numerator. The performance of the method is illustrated using the Rao-Garnier test system.

Abstract
Localized neurodevelopmental defects provide an opportunity to study structure-function correlations in the human nervous system. This unique multimodal case report of epileptogenic dysplasia in the visual cortex allowed exploring visual function across distinct pathways in retinotopic regions and the dorsal stream, in relation to fMRI retinotopic mapping and spike triggered BOLD responses. Pre-surgical EEG/video monitoring, MRI/DTI, EEG/fMRI, PET and SPECT were performed to characterize structure/function correlations in this patient with a very early lesion onset. In addition, we included psychophysical methods (assessing parvo/konio and magnocellular pathways) and retinotopic mapping. We could identify dorsal stream impairment (with extended contrast sensitivity deficits within the input magno system contrasting with more confined parvocellular deficits) with disrupted active visual field input representations in regions neighboring the lesion. Simultaneous EEG/fMRI identified perilesional and retinotopic bilaterally symmetric BOLD deactivation triggered by interictal spikes, which matched the contralateral spread of magnocellular dysfunction revealed in the psychophysical tests. Topographic changes in retinotopic organization further suggested long term functional effects of abnormal electrical discharges during brain development. We conclude that fMRI based visual field cortical mapping shows evidence for retinotopic dissociation between magno and parvocellular function well beyond striate cortex, identifiable in high level dorsal visual representations around visual area V3A which is consistent with the effects of epileptic spike triggered negative BOLD.