Maurizio Elia
Maurizio Elia
Oasi Research Institute - IRCCS, Troina, Italy
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A genetic variant that disrupts MET transcription is associated with autism
DB Campbell, JS Sutcliffe, PJ Ebert, R Militerni, C Bravaccio, S Trillo, ...
Proceedings of the National Academy of Sciences 103 (45), 16834-16839, 2006
Summary of recommendations for the management of infantile seizures: Task f orce r eport for the ilae c ommission of p ediatrics
JM Wilmshurst, WD Gaillard, KP Vinayan, TN Tsuchida, P Plouin, ...
Epilepsia 56 (8), 1185-1197, 2015
Mutations in NHLRC1 cause progressive myoclonus epilepsy
EM Chan, EJ Young, L Ianzano, I Munteanu, X Zhao, CC Christopoulos, ...
Nature genetics 35 (2), 125-127, 2003
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy
R Nabbout, E Gennaro, B Dalla Bernardina, O Dulac, F Madia, E Bertini, ...
Neurology 60 (12), 1961-1967, 2003
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome
BWM Van Bon, HC Mefford, B Menten, DA Koolen, AJ Sharp, ...
Journal of medical genetics 46 (8), 511-523, 2009
Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome
SA Musumeci, P Bosco, G Calabrese, C Bakker, GB De Sarro, M Elia, ...
Epilepsia 41 (1), 19-23, 2000
Epilepsy and EEG findings in males with fragile X syndrome
SA Musumeci, RJ Hagerman, R Ferri, P Bosco, BD Bernardina, ...
Epilepsia 40 (8), 1092-1099, 1999
Special education versus inclusive education: the role of the TEACCH program
S Panerai, M Zingale, G Trubia, M Finocchiaro, R Zuccarello, R Ferri, ...
Journal of autism and developmental disorders 39, 874-882, 2009
The mismatch negativity and the P3a components of the auditory event-related potentials in autistic low-functioning subjects
R Ferri, M Elia, N Agarwal, B Lanuzza, SA Musumeci, G Pennisi
Clinical neurophysiology 114 (9), 1671-1680, 2003
Sleep in subjects with autistic disorder: a neurophysiological and psychological study
M Elia, R Ferri, SA Musumeci, S Del Gracco, M Bottitta, C Scuderi, ...
Brain and Development 22 (2), 88-92, 2000
Sulphation deficit in “low-functioning” autistic children: a pilot study
A Alberti, P Pirrone, M Elia, RH Waring, C Romano
Biological psychiatry 46 (3), 420-424, 1999
Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1
L Palmieri, V Papaleo, V Porcelli, P Scarcia, L Gaita, R Sacco, J Hager, ...
Molecular psychiatry 15 (1), 38-52, 2010
Sleep in children with autistic spectrum disorder: a questionnaire and polysomnographic study
S Miano, O Bruni, M Elia, A Trovato, A Smerieri, E Verrillo, M Roccella, ...
Sleep medicine 9 (1), 64-70, 2007
No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age
Atherosclerosis, Thrombosis, and Vascular Biology Italian Study Group
Circulation 107 (8), 1117-1122, 2003
Methodology of photic stimulation revisited: updated European algorithm for visual stimulation in the EEG laboratory
D Kasteleijn‐Nolst Trenité, G Rubboli, E Hirsch, A Martins da Silva, S Seri, ...
Epilepsia 53 (1), 16-24, 2012
Association of a Functional Deficit of the BK Ca Channel, a Synaptic Regulator of Neuronal Excitability, With Autism and Mental Retardation
F Laumonnier, S Roger, P Guérin, F Molinari, R M’rad, D Cahard, ...
American Journal of Psychiatry 163 (9), 1622-1629, 2006
SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis
C Marini, IE Scheffer, R Nabbout, D Mei, K Cox, LM Dibbens, ...
Epilepsia 50 (7), 1670-1678, 2009
Clinical, morphological, and biochemical correlates of head circumference in autism
R Sacco, R Militerni, A Frolli, C Bravaccio, A Gritti, M Elia, P Curatolo, ...
Biological psychiatry 62 (9), 1038-1047, 2007
Epilepsy in cerebrovascular diseases: review of experimental and clinical data with meta‐analysis of risk factors
E Ferlazzo, S Gasparini, E Beghi, C Sueri, E Russo, A Leo, A Labate, ...
Epilepsia 57 (8), 1205-1214, 2016
Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene–environment interactions
M D'amelio, I Ricci, R Sacco, X Liu, L D'agruma, LA Muscarella, ...
Molecular psychiatry 10 (11), 1006-1016, 2005
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