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Dive into the research topics where Raffaele Ferri is active.

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Featured researches published by Raffaele Ferri.


Sleep Medicine | 2014

Restless legs syndrome/Willis-Ekbom disease diagnostic criteria: Updated International Restless Legs Syndrome Study Group (IRLSSG) consensus criteria - history, rationale, description, and significance

Richard P. Allen; Daniel L. Picchietti; Diego Garcia-Borreguero; William G. Ondo; Arthur S. Walters; John W. Winkelman; Marco Zucconi; Raffaele Ferri; Claudia Trenkwalder; Hochang B. Lee

BACKGROUND In 2003, following a workshop at the National Institutes of Health, the International Restless Legs Syndrome Study Group (IRLSSG) developed updated diagnostic criteria for restless legs syndrome/Willis-Ekbom disease (RLS/WED). These criteria were integral to major advances in research, notably in epidemiology, biology, and treatment of RLS/WED. However, extensive review of accumulating literature based on the 2003 NIH/IRLSSG criteria led to efforts to improve the diagnostic criteria further. METHODS The clinical standards workshop, sponsored by the WED Foundation and IRLSSG in 2008, started a four-year process for updating the diagnostic criteria. That process included a rigorous review of research advances and input from clinical experts across multiple disciplines. After broad consensus was attained, the criteria were formally approved by the IRLSSG executive committee and membership. RESULTS Major changes are: (i) addition of a fifth essential criterion, differential diagnosis, to improve specificity by requiring that RLS/WED symptoms not be confused with similar symptoms from other conditions; (ii) addition of a specifier to delineate clinically significant RLS/WED; (iii) addition of course specifiers to classify RLS/WED as chronic-persistent or intermittent; and (iv) merging of the pediatric with the adult diagnostic criteria. Also discussed are supportive features and clinical aspects that are important in the diagnostic evaluation. CONCLUSIONS The IRLSSG consensus criteria for RLS/WED represent an international, interdisciplinary, and collaborative effort intended to improve clinical practice and promote further research.


Molecular Psychiatry | 2011

APOE and Alzheimer disease: a major gene with semi-dominant inheritance

Genin E; Didier Hannequin; David Wallon; Kristel Sleegers; Mikko Hiltunen; Onofre Combarros; María J. Bullido; Sebastiaan Engelborghs; De Deyn P; Claudine Berr; Florence Pasquier; Dubois B; Gloria Tognoni; Nathalie Fievet; Nathalie Brouwers; Karolien Bettens; Beatrice Arosio; Eliecer Coto; Del Zompo M; Ignacio Mateo; Jacques Epelbaum; Ana Frank-García; Seppo Helisalmi; Elisa Porcellini; Alberto Pilotto; Paola Forti; Raffaele Ferri; Elio Scarpini; Gabriele Siciliano; Solfrizzi

Apolipoprotein E (APOE) dependent lifetime risks (LTRs) for Alzheimer Disease (AD) are currently not accurately known and odds ratios alone are insufficient to assess these risks. We calculated AD LTR in 7351 cases and 10 132 controls from Caucasian ancestry using Rochester (USA) incidence data. At the age of 85 the LTR of AD without reference to APOE genotype was 11% in males and 14% in females. At the same age, this risk ranged from 51% for APOE44 male carriers to 60% for APOE44 female carriers, and from 23% for APOE34 male carriers to 30% for APOE34 female carriers, consistent with semi-dominant inheritance of a moderately penetrant gene. Using PAQUID (France) incidence data, estimates were globally similar except that at age 85 the LTRs reached 68 and 35% for APOE 44 and APOE 34 female carriers, respectively. These risks are more similar to those of major genes in Mendelian diseases, such as BRCA1 in breast cancer, than those of low-risk common alleles identified by recent GWAS in complex diseases. In addition, stratification of our data by age groups clearly demonstrates that APOE4 is a risk factor not only for late-onset but for early-onset AD as well. Together, these results urge a reappraisal of the impact of APOE in Alzheimer disease.


Epilepsia | 2000

Audiogenic Seizures Susceptibility in Transgenic Mice with Fragile X Syndrome

Sebastiano A. Musumeci; Paolo Bosco; Giuseppe Calabrese; Cathy E. Bakker; Giovanni B. De Sarro; Maurizio Elia; Raffaele Ferri; Ben A. Oostra

Summary: Purpose: To evaluate their susceptibility to audiogenie seizures, five groups of knockout mice with various forms of fragile X genetic involvement [hemizygous males (n = 46), and homozygous (n = 38) and heterozygous females (n = 45), and their normal male (n = 45) and female (n = 52) littermates] were studied.


NeuroImage | 2004

Mapping distributed sources of cortical rhythms in mild Alzheimer's disease. A multicentric EEG study

Claudio Babiloni; Giuliano Binetti; Emanuele Cassetta; Daniele Cerboneschi; Gloria Dal Forno; Claudio Del Percio; Florinda Ferreri; Raffaele Ferri; Bartolo Lanuzza; Carlo Miniussi; Davide Vito Moretti; Flavio Nobili; Roberto D. Pascual-Marqui; Guido Rodriguez; Gian Luca Romani; Serenella Salinari; Franca Tecchio; Paolo Vitali; Orazio Zanetti; Filippo Zappasodi; Paolo Maria Rossini

The study aimed at mapping (i) the distributed electroencephalographic (EEG) sources specific for mild Alzheimers disease (AD) compared to vascular dementia (VaD) or normal elderly people (Nold) and (ii) the distributed EEG sources sensitive to the mild AD at different stages of severity. Resting EEG (10-20 electrode montage) was recorded from 48 mild AD, 20 VaD, and 38 Nold subjects. Both AD and VaD patients had 24-17 of mini mental state examination (MMSE). EEG rhythms were delta (2-4 Hz), theta (4-8 Hz), alpha 1 (8-10.5 Hz), alpha 2 (10.5-13 Hz), beta 1 (13-20 Hz), and beta 2 (20-30 Hz). Cortical EEG sources were modeled by low resolution brain electromagnetic tomography (LORETA). Regarding issue i, there was a decline of central, parietal, temporal, and limbic alpha 1 (low alpha) sources specific for mild AD group with respect to Nold and VaD groups. Furthermore, occipital alpha 1 sources showed a strong decline in mild AD compared to VaD group. Finally, distributed theta sources were largely abnormal in VaD but not in mild AD group. Regarding issue ii, there was a lower power of occipital alpha 1 sources in mild AD subgroup having more severe disease. Compared to previous field studies, this was the first investigation that illustrated the power spectrum profiles at the level of cortical (macroregions) EEG sources in mild AD patients having different severity of the disease with respect to VaD and normal subjects. Future studies should evaluate the clinical usefulness of this approach in early differential diagnosis, disease staging, and therapy monitoring.


Epilepsia | 1999

Epilepsy and EEG findings in males with fragile X syndrome

Sebastiano A. Musumeci; Randi J. Hagerman; Raffaele Ferri; Paolo Bosco; B. Dalla Bernardina; C. A. Tassinari; G.B. De Sarro; Maurizio Elia

Summary: Purpose and Methods: One hundred and ninety‐two fragile X male patients were investigated for seizures and EEG findings, 168 in a retrospective and 24 in another prospective study, to characterize the natural history of seizures, epilepsy, and EEG abnormalities in males with this syndrome.


Journal of Sleep Research | 2007

Sleep habits and circadian preference in Italian children and adolescents

Paolo Maria Russo; Oliviero Bruni; Fabio Lucidi; Raffaele Ferri; Cristiano Violani

Sleep habits and circadian preference (morningness/eveningness, M/E) have been extensively analyzed in adolescents and young adults, while few studies were conducted on children and early adolescents. Aim of the present study was to investigate the developmental changes of circadian preference and to analyze its relationship with sleep habits, sleep problems and circadian preference in a large sample by means of a school‐based survey. One thousand seventy‐three participants (50.8% boys and 49.2% girls; mean age = 10.6; range = 8–14 years), recruited from four schools randomly extracted within the district of Rome, completed a modified version of School Sleep Habits Survey developed by Carskadon et al. The questionnaire included items about sleep habits during schooldays and weekends; a Sleepiness Scale; a Sleep–Wake Problems Behaviour Scale; a Morningness/Eveningness scale. The results show a consistent age‐related change in sleep habits, particularly in the weekends. The difference in sleep duration between schooldays and weekends increases linearly with age. No gender difference was observed in morningness/eveningness, while a significant linear increase in evening preference was found with increasing ages. M/E total scores correlated significantly with both self‐reported sleep/wake problems and daytime sleepiness indicating a higher prevalence of sleep complaints in evening‐type subjects. Overall, the present results support the existence of consistent age‐related changes in sleep habits and M/E dimension in the 8‐ to 14‐year age range.


Sleep Medicine Reviews | 2012

Cyclic alternating pattern (CAP): The marker of sleep instability

Liborio Parrino; Raffaele Ferri; Oliviero Bruni; Mario Giovanni Terzano

Cyclic alternating pattern CAP is the EEG marker of unstable sleep, a concept which is poorly appreciated among the metrics of sleep physiology. Besides, duration, depth and continuity, sleep restorative properties depend on the capacity of the brain to create periods of sustained stable sleep. This issue is not confined only to the EEG activities but reverberates upon the ongoing autonomic activity and behavioral functions, which are mutually entrained in a synchronized oscillation. CAP can be identified both in adult and children sleep and therefore represents a sensitive tool for the investigation of sleep disorders across the lifespan. The present review illustrates the story of CAP in the last 25 years, the standardized scoring criteria, the basic physiological properties and how the dimension of sleep instability has provided new insight into pathophysiolology and management of sleep disorders.


Human Brain Mapping | 2006

Sources of Cortical Rhythms in Adults During Physiological Aging: A Multicentric EEG Study

Claudio Babiloni; Giuliano Binetti; Andrea Cassarino; Gloria Dal Forno; Claudio Del Percio; Florinda Ferreri; Raffaele Ferri; Giovanni B. Frisoni; Silvana Galderisi; Koichi Hirata; Bartolo Lanuzza; Carlo Miniussi; A. Mucci; Flavio Nobili; Guido Rodriguez; Gian Luca Romani; Paolo Maria Rossini

This electroencephalographic (EEG) study tested whether cortical EEG rhythms (especially delta and alpha) show a progressive increasing or decreasing trend across physiological aging. To this aim, we analyzed the type of correlation (linear and nonlinear) between cortical EEG rhythms and age. Resting eyes‐closed EEG data were recorded in 108 young (Nyoung; age range: 18–50 years, mean age 27.3 ± 7.3 SD) and 107 elderly (Nold; age range: 51–85 years, mean age 67.3 ± 9.2 SD) subjects. The EEG rhythms of interest were delta (2–4 Hz), theta (4–8 Hz), alpha 1 (8–10.5 Hz), alpha 2 (10.5–13 Hz), beta 1 (13–20 Hz), and beta 2 (20–30 Hz). EEG cortical sources were estimated by low‐resolution brain electromagnetic tomography (LORETA). Statistical results showed that delta sources in the occipital area had significantly less magnitude in Nold compared to Nyoung subjects. Similarly, alpha 1 and alpha 2 sources in the parietal, occipital, temporal, and limbic areas had significantly less magnitude in Nold compared to Nyoung subjects. These nine EEG sources were given as input for evaluating the type (linear, exponential, logarithmic, and power) of correlation with age. When subjects were considered as a single group there was a significant linear correlation of age with the magnitude of delta sources in the occipital area and of alpha 1 sources in occipital and limbic areas. The same was true for alpha 2 sources in the parietal, occipital, temporal, and limbic areas. In general, the EEG sources showing significant linear correlation with age also supported a nonlinear correlation with age. These results suggest that the occipital delta and posterior cortical alpha rhythms decrease in magnitude during physiological aging with both linear and nonlinear trends. In conclusion, this new methodological approach holds promise for the prediction of dementia in mild cognitive impairment by regional source rather than surface EEG data and by both linear and nonlinear predictors. Hum Brain Mapp, 2005.


Clinical Neurophysiology | 2003

The mismatch negativity and the P3a components of the auditory event-related potentials in autistic low-functioning subjects

Raffaele Ferri; Maurizio Elia; Nivedita Agarwal; Bartolo Lanuzza; Sebastiano A. Musumeci; Giovanni Pennisi

OBJECTIVE In order to understand better the psychophysiological basis of auditory processing abnormalities in autism, we decided to study two automatic components of the auditory event-related potentials (ERPs): the mismatch negativity (MMN)--a component of the ERP which is recorded when, during repetitive auditory stimulation, rare changes are introduced--and the novelty-related P3a which is recorded as a response to unexpected novel events occurring in a sequence of repetitive stimuli. METHODS Ten male subjects, mean age 12.3 years (SD 4.95), affected by autism and mental retardation were admitted to this study. All patients were also mentally retarded. Ten normal male subjects, mean age 12.2 years (SD 3.94), were used as controls. Auditory evoked potentials were recorded from 19 scalp electrodes (10-20 system), and stimuli were presented in sequences consisting of 2000 tones (70 dB, ISI=800 ms). Three types of stimuli were presented: (1) standard stimuli (1000 Hz tones, 80% of total stimuli), (2) deviant stimuli (1300 Hz tones, 10% of total stimuli), and (3) novel stimuli (complex and non-monotonal, 10% of total stimuli). To quantify the MMN, the evoked response to the standard tones was subtracted from the corresponding deviant stimulus response and its amplitude and latency at peak were measured over Fz, Cz and Pz; similarly, the P3a component of the ERP was obtained by subtracting the response to the standard tone from that to the novel stimuli and its amplitude and latency at peak were measured over Fz, Cz and Pz. Also, the amplitude and latency at peak for the N1 component of the auditory evoked potential obtained with the standard stimuli were measured over Fz, Cz and Pz. The correlation between age and MMN and P3a amplitude was also analyzed. RESULTS N1 showed significantly shorter latencies in the autistic groups. MMN elicited by deviant stimuli, but not that elicited by novel stimuli, was found to be significantly larger in autistic children than in normal controls. P3a showed higher amplitude in autistic subjects than in normal controls during childhood; the opposite was observed during young adulthood. DISCUSSION Our findings indicate that significant changes in ERPs can also be seen in non-cooperative individuals with autism and mental retardation, which might be different from the changes already reported for high-functioning autistic subjects and deserve further insight. These changes show developmental modifications that should be taken into consideration when analyzing data from autistic subjects.


Journal of Sleep Research | 2005

Odds, prevalence and predictors of sleep problems in school-age normal children.

Karen Spruyt; Louise O'Brien; Raymond Cluydts; Gino Verleye; Raffaele Ferri

The objectives of the study were to describe the prevalence, odds, and predictors of 36 paediatric sleep behaviours and describe their coexistence in a school‐age normal population. The design was community‐based questionnaire survey of sleep–wake patterns, sleep environment, and 36 sleep behaviours indicative of six sleep disorder‐subscales using the Health‐Behaviour Questionnaire. A caregivers’ report of 3045 children aged 6–13 years in Belgium constituted the participants. Prevalence of each sleep behaviour was calculated. Log‐linear modelling within and between the sleep disorder‐subscales was used to screen for coexistence. The effect size of selected night‐time parameters to the likelihood of sleep behaviours and disorder‐subscale was expressed as odds ratios via logit regression analysis. Significant differences in sleep–wake patterns were found between weekday and weekend. Ranking by odds showed that: (1) sleep problems such as ‘tired when waking up’, ’repetitive limb movements’, ‘going to bed reluctantly’, and ‘sleep paralysis’ and; (2) the disorder‐subscale ‘excessive somnolence’ are common in children. Coexistences within and between disorder‐subscales of sleep problems are evident in a school‐age, normal population. These results suggest that disorders of excessive somnolence (DES) are highly prevalent in a non‐clinical sample of school‐age children. Furthermore, sleep‐onset latency and a noisy, not well‐darkened room are predictive towards the odds for exhibiting sleep problems and disorders. It is advocated that more information on the importance of good sleep–wake hygiene should reach parents and children.

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Oliviero Bruni

Sapienza University of Rome

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Marco Zucconi

Vita-Salute San Raffaele University

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Luigi Ferini-Strambi

Vita-Salute San Raffaele University

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Claudio Babiloni

Sapienza University of Rome

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