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List of works by Roberto Michelucci

A PTG variant contributes to a milder phenotype in Lafora disease

scientific article

A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures.

scientific article

A de novo LGI1 mutation in sporadic partial epilepsy with auditory features

scientific article

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 novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy

scientific article

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy

scientific article

Acute rhabdomyolysis induced by tonic-clonic epileptic seizures in a patient with glucose-6-phosphate dehydrogenase deficiency

scientific article published on 20 September 2013

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

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

scientific article published on 9 February 2014

An overlooked cause of acute symptomatic seizures: psychogenic polydipsia

scientific article published on 12 March 2013

Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy.

scientific article

Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy

scientific article published in March 2011

Autosomal dominant essential tremor: a novel family with anticipation

scientific article published on 13 October 2012

Autosomal dominant lateral temporal epilepsy: Absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins

scientific article published in July 2008

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

scientific article

BRAF V600E mutation in neocortical posterior temporal epileptogenic gangliogliomas.

scientific article published on 27 April 2015

Biting behavior, aggression, and seizures

scientific article published in May 2005

Charles Bonnet syndrome in hemianopia, following antero-mesial temporal lobectomy for drug-resistant epilepsy

scientific article published on 20 September 2007

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

scientific article published on 2 November 2011

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

Copy number variations and susceptibility to lateral temporal epilepsy: a study of 21 pedigrees.

scientific article published on 19 September 2014

DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy

article

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

scientific article published on 01 September 1987

Early ictal speech and motor inhibition in fronto-mesial epileptic seizures: a polygraphic study in one patient.

scientific article published in January 2003

Effects of levetiracetam on EEG abnormalities in juvenile myoclonic epilepsy.

scientific article

Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations.

scientific article published in December 2012

Epilepsy associated tumors: Review article

scientific article

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

Extreme somatosensory evoked potentials (ESEPs) elicited by tapping of hands or feet in children: a somatosensory cerebral evoked potentials study

scientific article published on 01 April 1988

FDG-PET assessment and metabolic patterns in Lafora disease

scientific article published on 19 December 2019

Familial epilepsy and developmental dysphasia: description of an Italian pedigree with autosomal dominant inheritance and screening of candidate loci.

scientific article

Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families

scientific article published on 21 November 2007

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

scientific article published in March 2011

Focal cortical dysplasias in temporal lobe epilepsy surgery: Challenge in defining unusual variants according to the last ILAE classification

scientific article published in April 2015

Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy

article

Genetics of epilepsy and relevance to current practice

scientific article published on August 2012

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

Identical genetic locus for Baltic and Mediterranean myoclonus

scientific article published on 01 May 1992

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

scientific article

Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.

scientific article

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

scientific article

Impact of treatment on the short-term prognosis of status epilepticus in two population-based cohorts

scientific article

In response: DEPDC5 mutations in epilepsy with auditory features

scientific article published on 01 February 2016

Increased expression of LGI1 gene triggers growth inhibition and apoptosis of neuroblastoma cells.

scientific article published on June 2006

Intraoperative monitoring of somatosensory (SSEPs) and transcranial electric motor-evoked potentials (tce-MEPs) during surgical correction of neuromuscular scoliosis in patients with central or peripheral nervous system diseases

scientific article published on 19 October 2015

LGI1 microdeletion in autosomal dominant lateral temporal epilepsy.

scientific article

LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy.

scientific article published on April 2009

Lateral temporal lobe epilepsies: clinical and genetic features

scientific article published on May 2009

Lateralizing value of the auditory aura in partial seizures.

scientific article

Locked-in syndrome in multiple sclerosis with sparing of the ventral portion of the pons

scientific article published in October 1982

Low penetrance and effect on protein secretion of LGI1 mutations causing autosomal dominant lateral temporal epilepsy

scientific article published on 19 April 2011

Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.

scientific article published on 26 April 2013

MicroRNA profiles in hippocampal granule cells and plasma of rats with pilocarpine-induced epilepsy--comparison with human epileptic samples.

scientific article

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

scientific article published on 30 September 2014

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

scientific article

Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel properties

scientific article published on 5 April 2017

Neuropathy in multiple myeloma treated with thalidomide: a prospective study

scientific article published on 01 August 2007

No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy

scientific article published on 06 March 2015

Oligodendroglial hamartoma: a potential source of misdiagnosis for oligodendroglioma

scientific article

Open label, long-term, pragmatic study on levetiracetam in the treatment of juvenile myoclonic epilepsy

scientific article published on 30 June 2006

PME of Unverricht-Lundborg type in the Mediterranean region: linkage and linkage disequilibrium confirm the assignment to the EPM1 locus

scientific article published on 01 June 1994

Partial monosomy Xq(Xq23 --> qter) and trisomy 4p(4p15.33 --> pter) in a woman with intractable focal epilepsy, borderline intellectual functioning, and dysmorphic features

scientific article published on 31 December 2007

Pathology-Based Approach to Seizure Outcome After Surgery for Pharmacoresistant Medial Temporal Lobe Epilepsy

scientific article published on 8 March 2016

Postictal hyperfamiliarity for unknown faces

scientific article published on 15 September 2010

Preface

Progressive myoclonic epilepsies: definitive and still undetermined causes.

scientific article published on 02 January 2014

Rud syndrome with focal cortical dysplasia: a case report

scientific article published on 12 November 2010

SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure.

scientific article

STRUCTURAL ANOMALY OF LEFT LATERAL TEMPORAL LOBE IN EPILEPSY DUE TO MUTATED LGI1

scientific article published on 17 September 2007

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

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

Seizure outcome of surgical treatment of focal epilepsy associated with low-grade tumors in children.

scientific article published on 7 December 2012

Slowly progressive familial dementia with recurrent strokes and white matter hypodensities on CT scan

scientific article

Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1.

scientific article published on 3 April 2015

Sudden falls due to seizure-induced cardiac asystole in drug-resistant focal epilepsy

scientific article published on 6 February 2008

Teaching NeuroImages: Diffusion tensor tractography of cortico-ponto-cerebellar pathways in Rasmussen encephalitis

scientific article published in July 2015

Telephone-induced seizures: a new type of reflex epilepsy

scientific article published in March 2004

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

scientific article published on 19 June 2006

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

scientific article

Transcranial magnetic stimulation and epilepsy

scientific article published on 01 May 2003

Transthyretin-related TTR hereditary amyloidosis of the vitreous body. Clinical and molecular characterization in two Italian families

scientific article published on 01 March 1993

Treatment with metformin in twelve patients with Lafora disease

scientific article published on 21 June 2019

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

scientific article

Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1

scientific article

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

scientific article

p-ANCA pachymeningitis presenting with isolated "optic neuropathy"

article

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