PubRank

Roberto Michelucci

Author PubWeight™ 35.00‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy. Hum Mol Genet 2002 2.65
2 LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy. Hum Mutat 2009 1.58
3 Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families. J Neurol 2007 1.54
4 Progressive myoclonic epilepsies: definitive and still undetermined causes. Neurology 2014 1.52
5 Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities. Epilepsia 2007 1.21
6 Transcranial magnetic stimulation and epilepsy. Clin Neurophysiol 2003 1.07
7 Autosomal dominant lateral temporal epilepsy: absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins. Epilepsy Res 2008 1.04
8 Withdrawal of antiepileptic drugs: guidelines of the Italian League Against Epilepsy. Epilepsia 2013 1.01
9 Recommendations of the Italian League against Epilepsy working group on generic products of antiepileptic drugs. Epilepsia 2006 0.95
10 Lateralizing value of the auditory aura in partial seizures. Epilepsia 2006 0.93
11 Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy. Epilepsia 2007 0.91
12 Seizure outcome of epilepsy surgery in focal epilepsies associated with temporomesial glioneuronal tumors: lesionectomy compared with tailored resection. J Neurosurg 2009 0.90
13 A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy. Arch Neurol 2008 0.90
14 A de novo LGI1 mutation in sporadic partial epilepsy with auditory features. Ann Neurol 2004 0.88
15 Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutations. Epilepsia 2011 0.85
16 Low penetrance and effect on protein secretion of LGI1 mutations causing autosomal dominant lateral temporal epilepsy. Epilepsia 2011 0.84
17 The LGI1/epitempin gene encodes two protein isoforms differentially expressed in human brain. J Neurochem 2006 0.84
18 A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy. Epilepsia 2011 0.83
19 Partial monosomy Xq(Xq23 --> qter) and trisomy 4p(4p15.33 --> pter) in a woman with intractable focal epilepsy, borderline intellectual functioning, and dysmorphic features. Brain Dev 2007 0.83
20 Seizure outcome of surgical treatment of focal epilepsy associated with low-grade tumors in children. J Neurosurg Pediatr 2012 0.83
21 Adult-onset Rasmussen's encephalitis: anatomical-electrographic-clinical features of 7 Italian cases. Epilepsia 2006 0.82
22 ILAE Commission of European Affairs Subcommission on European Guidelines 1998-2001: The provision of epilepsy care across Europe. Epilepsia 2003 0.81
23 Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations. Epilepsia 2012 0.81
24 Seizure outcome in surgically treated drug-resistant mesial temporal lobe epilepsy based on the recent histopathological classifications. J Neurosurg 2013 0.81
25 Impact of treatment on the short-term prognosis of status epilepticus in two population-based cohorts. J Neurol 2008 0.79
26 ADAM23, a Gene Related to LGI1, Is Not Linked to Autosomal Dominant Lateral Temporal Epilepsy. Epilepsy Res Treat 2010 0.79
27 Association of intronic variants of the KCNAB1 gene with lateral temporal epilepsy. Epilepsy Res 2011 0.79
28 A PTG variant contributes to a milder phenotype in Lafora disease. PLoS One 2011 0.78
29 Effects of levetiracetam on EEG abnormalities in juvenile myoclonic epilepsy. Epilepsia 2008 0.78
30 Autosomal dominant essential tremor: a novel family with anticipation. Neurol Sci 2012 0.78
31 Copy number variations and susceptibility to lateral temporal epilepsy: a study of 21 pedigrees. Epilepsia 2014 0.78
32 p-ANCA pachymeningitis presenting with isolated "optic neuropathy". Neurol Sci 2010 0.78
33 Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy. Neurosci Lett 2008 0.77
34 Clinical course and variability of non-Rasmussen, nonstroke motor and sensory epilepsia partialis continua: a European survey and analysis of 65 cases. Epilepsia 2011 0.77
35 Open label, long-term, pragmatic study on levetiracetam in the treatment of juvenile myoclonic epilepsy. Epilepsy Res 2006 0.77
36 Biting behavior, aggression, and seizures. Epilepsia 2005 0.76
37 Mild Lafora disease: clinical, neurophysiologic, and genetic findings. Epilepsia 2014 0.76
38 Charles Bonnet syndrome in hemianopia, following antero-mesial temporal lobectomy for drug-resistant epilepsy. Epileptic Disord 2007 0.76
39 Rud syndrome with focal cortical dysplasia: a case report. Brain Dev 2010 0.75
40 Oligodendroglial hamartoma: a potential source of misdiagnosis for oligodendroglioma. J Neurooncol 2010 0.75
41 An overlooked cause of acute symptomatic seizures: psychogenic polydipsia. Am J Med 2013 0.75
42 No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy. Epilepsia 2015 0.75
43 Acute rhabdomyolysis induced by tonic-clonic epileptic seizures in a patient with glucose-6-phosphate dehydrogenase deficiency. J Neurol 2013 0.75