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Download Neuropsychiatric Dysfunction in Multiple Sclerosis by Dr. Silvia Romano, Prof. Carlo Caltagirone, Dr. Ugo PDF

By Dr. Silvia Romano, Prof. Carlo Caltagirone, Dr. Ugo Nocentini (auth.), Ugo Nocentini, Carlo Caltagirone, Gioacchino Tedeschi (eds.)

This publication offers accomplished and updated details at the neuropsychiatric disturbances that could be skilled by means of sufferers with a number of sclerosis. the 1st part is designed essentially to explain the overall medical features of a number of sclerosis, from epidemiology to overview instruments. The position of neuroimaging and particularly MRI is then defined, and therapy techniques and rehabilitation options are defined. The middle portion of the amount is the second one, within which many of the different types of neuropsychiatric disorder are thought of extensive. specifically, unique cognizance is dedicated to melancholy, however the different major different types of disturbance also are defined and mentioned. the ultimate part addresses cognitive dysfunctions considering they symbolize many of the worst occasions that sufferers with a number of sclerosis can undergo and are in detail on the topic of neuropsychiatric dysfunction.

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It U. Nocentini et al. 1007/978-88-470-2676-6_8, # Springer-Verlag Italia 2012 43 44 G. Tedeschi et al. 1 Clinical Applications To identify focal WM lesions in MS, c-MRI relies on T2/PD (Proton Density) and T1 sequences, the latter usually acquired pre- and post-contrast medium administration (gadolinium-DTPA [Gd] at the standard dosage of 0,1 mmol/Kg). , Cerebro-Spinal Fluid – CSF) signal. Compared with surrounding tissues, focal WM lesions appear hyperintense on T2, DP and T2-FLAIR images and isointense or hypointense on pre-contrast T1 images.

Zamboni and colleagues initially reported 100 % sensitivity, specificity and positive and negative predictive values for detecting CCSVI in MS patients [27] but no study, since this report, has yielded similar results, while a great variability of CCSVI has been found in both MS patients and in control subjects [28–32]. This wide variability is explained by methodological aspects, problems in assessing CCSVI, and differences among clinical series. Moreover, some abnormalities were reported in other neurological conditions such as transient global amnesia and neurodegenerative diseases [33–35].

The recent revision of the McDonald criteria [3] recommends modifications of MRI criteria for dissemination in space (DIS). In the past version of the McDonald criteria, DIS demonstrated by MRI was based on the above-mentioned Barkhof/ Tintore´ criteria [4, 5]. Despite having good sensitivity and specificity, these criteria have been difficult to apply consistently by non-imaging specialists. The MAGNIMS multicenter collaborative research network suggests that DIS can be demonstrated with at least one T2 lesion in at least two of four locations considered characteristic S.

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