Maurizio Elia

Overview

Best Publications

• Abnormal colonic fermentation in irritable bowel syndrome

  TS King;M Elia;JO Hunter

  627
  Citations

• A genetic variant that disrupts MET transcription is associated with autism

  Daniel B. Campbell;James S. Sutcliffe;Philip J. Ebert;Roberto Militerni

  540
  Citations

• Summary of recommendations for the management of infantile seizures: Task Force Report for the ILAE Commission of Pediatrics.

  Jo M. Wilmshurst;William D. Gaillard;Kollencheri Puthenveettil Vinayan;Tammy N. Tsuchida

  453
  Citations

• Mutations in NHLRC1 cause progressive myoclonus epilepsy

  Elayne M Chan;Edwin J Young;Leonarda Ianzano;Iulia Munteanu

  385
  Citations

• Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy

  Rima Nabbout;E. Gennaro;B. Dalla Bernardina;O. Dulac

  325
  Citations

• Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome.

  Sebastiano A. Musumeci;Paolo Bosco;Giuseppe Calabrese;Cathy Bakker

  315
  Citations

• Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome

  B W M van Bon;H C Mefford;B Menten;D A Koolen

  314
  Citations

• Epilepsy and EEG findings in males with fragile X syndrome

  S. A. Musumeci;Randi J Hagerman;R. Ferri;P. Bosco

  291
  Citations

• 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

  267
  Citations

• Sulphation deficit in "low-functioning" autistic children: a pilot study.

  Antonino Alberti;Patrizia Pirrone;Maurizio Elia;Rosemary H Waring

  253
  Citations

• 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

  252
  Citations

• Special Education Versus Inclusive Education: The Role of the TEACCH Program

  Simonetta Panerai;Marinella Zingale;Grazia Trubia;Maria Finocchiaro

  248
  Citations

• Methodology of photic stimulation revisited: Updated European algorithm for visual stimulation in the EEG laboratory

  Dorothée Kasteleijn-Nolst Trenité;Guido Rubboli;Edouard Hirsch;Antonio Martins da Silva

  244
  Citations

• Sleep in subjects with autistic disorder: a neurophysiological and psychological study

  Maurizio Elia;Raffaele Ferri;Sebastiano A. Musumeci;Stefano Del Gracco

  235
  Citations

• Sleep in children with autistic spectrum disorder: a questionnaire and polysomnographic study.

  Silvia Miano;Oliviero Bruni;Maurizio Elia;Alessia Trovato

  233
  Citations

• Association of a functional deficit of the BKCa channel, a synaptic regulator of neuronal excitability, with autism and mental retardation.

  Frédéric Laumonnier;Sébastien Roger;Pascaline Guérin;Florence Molinari

  204
  Citations

• Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

  Tianyun Wang;Kendra Hoekzema;Davide Vecchio;Huidan Wu

  199
  Citations

• SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis

  Carla Marini;Ingrid E. Scheffer;Ingrid E. Scheffer;Rima Nabbout;Davide Mei

  197
  Citations

• Clinical, Morphological, and Biochemical Correlates of Head Circumference in Autism

  Roberto Sacco;Roberto Militerni;Alessandro Frolli;Carmela Bravaccio

  180
  Citations

• 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

  166
  Citations