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List of works by Roberto Michelucci

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Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1

scientific article
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy

scientific article
LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy.

scientific article published on April 2009
Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.

scientific article
Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families

scientific article
Neuropathy in multiple myeloma treated with thalidomide: a prospective study

scientific article published on 01 August 2007
Transcranial magnetic stimulation and epilepsy

scientific article published on 01 May 2003
MicroRNA profiles in hippocampal granule cells and plasma of rats with pilocarpine-induced epilepsy--comparison with human epileptic samples.

scientific article
Double-blind study of vigabatrin in the treatment of drug-resistant epilepsy

scientific article published on 01 September 1987
SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure

scientific article
Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases.

scientific article
The prevention of neural complications in the surgical treatment of scoliosis: the role of the neurophysiological intraoperative monitoring

scientific article
Withdrawal of antiepileptic drugs: guidelines of the Italian League Against Epilepsy

scientific article
Seizure outcome of epilepsy surgery in focal epilepsies associated with temporomesial glioneuronal tumors: lesionectomy compared with tailored resection

scientific article published in December 2009
Progressive myoclonic epilepsies: definitive and still undetermined causes.

scientific article published on 02 January 2014
Seizure outcome of surgical treatment of focal epilepsy associated with low-grade tumors in children.

scientific article published on 7 December 2012
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy

scientific article published in May 2011
A de novo LGI1 mutation in sporadic partial epilepsy with auditory features

scientific article
Seizure outcome in surgically treated drug-resistant mesial temporal lobe epilepsy based on the recent histopathological classifications

scientific article
Identification of miRNAs differentially expressed in human epilepsy with or without granule cell pathology

scientific article
Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy.

scientific article
Lateralizing value of the auditory aura in partial seizures

scientific article
Lateral temporal lobe epilepsies: clinical and genetic features

scientific article published on May 2009
A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures.

scientific article
Adult-onset Rasmussen's encephalitis: anatomical-electrographic-clinical features of 7 Italian cases

scientific article
An educational campaign about epilepsy among Italian primary school teachers. 2. The results of a focused training program.

scientific article published on 12 December 2014
Slowly progressive familial dementia with recurrent strokes and white matter hypodensities on CT scan

scientific article
Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation.

scientific article published in March 2011
A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy

scientific article
Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutations.

scientific article published on 2 November 2011
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1.

scientific article published on 3 April 2015
Epilepsy associated tumors: Review article

scientific article
An educational campaign toward epilepsy among Italian primary school teachers: 1. Survey on knowledge and attitudes

scientific article published on 9 February 2014
Identical genetic locus for Baltic and Mediterranean myoclonus

scientific article published on 01 May 1992
STRUCTURAL ANOMALY OF LEFT LATERAL TEMPORAL LOBE IN EPILEPSY DUE TO MUTATED LGI1

scientific article published on 17 September 2007
Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families

scientific article published on 21 November 2007
Autosomal dominant lateral temporal epilepsy: Absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins

scientific article published in July 2008
Epilepsy in primary cerebral tumors: the characteristics of epilepsy at the onset (results from the PERNO study--Project of Emilia Romagna Region on Neuro-Oncology).

scientific article published on October 2013
Clinical course and variability of non-Rasmussen, nonstroke motor and sensory epilepsia partialis continua: a European survey and analysis of 65 cases

scientific article published on 14 February 2011
Effects of levetiracetam on EEG abnormalities in juvenile myoclonic epilepsy.

scientific article
A PTG variant contributes to a milder phenotype in Lafora disease

scientific article
Mild Lafora disease: clinical, neurophysiologic, and genetic findings.

scientific article published on 30 September 2014
Increased expression of LGI1 gene triggers growth inhibition and apoptosis of neuroblastoma cells.

scientific article published on June 2006
Biting behavior, aggression, and seizures

scientific article published in May 2005
Open label, long-term, pragmatic study on levetiracetam in the treatment of juvenile myoclonic epilepsy

scientific article published on 30 June 2006
ILAE Commission of European Affairs Subcommission on European Guidelines 1998-2001: The provision of epilepsy care across Europe

scientific article published on 01 May 2003
LGI1 microdeletion in autosomal dominant lateral temporal epilepsy.

scientific article
Tubular proteinuria in mice and humans lacking the intrinsic lysosomal protein SCARB2/Limp-2

scientific article
The LGI1/epitempin gene encodes two protein isoforms differentially expressed in human brain

scientific article published on 19 June 2006
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.

scientific article published on 26 April 2013

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