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List of works by Antonio Gambardella

3-T magnetic resonance imaging simultaneous automated multimodal approach improves detection of ambiguous visual hippocampal sclerosis.

scientific article published on 18 January 2015

A Loss-of-Function Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability

scientific article published on 06 August 2018

A Novel Mutation in the Notch3 Gene in an Italian Family With Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy

scientific article (publication date: September 2001)

A clinical spectrum of the myoclonic manifestations associated with typical absences in childhood absence epilepsy. A video-polygraphic study

scientific article published on 01 June 2001

A familial t(4;8) translocation segregates with epilepsy and migraine with aura

scientific article published on 21 April 2020

A functional genetic variation of the 5-HTR2A receptor affects age at onset in patients with temporal lobe epilepsy.

scientific article published in July 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 hypofibrinolytic state in overweight patients with cerebral venous thrombosis and isolated intracranial hypertension

scientific article published on 01 November 1999

A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3

article

A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1.

scientific article published in November 2000

A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1.

scientific article

A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability

scientific article published on 21 June 2018

A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit.

scientific article published in March 2004

A possible case of natalizumab-dependent suicide attempt: A brief review about drugs and suicide.

scientific article published on December 2013

A puzzling case without solution: isolated late-onset epileptic seizure

scientific article published on 23 August 2015

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy

scientific article

APOE and risk of cognitive impairment in multiple sclerosis

scientific article published on 01 November 1999

Action palatal tremor in a patient with primary intestinal lymphoma.

scientific article published in September 1997

Advanced MRI morphologic study shows no atrophy in healthy individuals with hippocampal hyperintensity.

scientific article published on 28 February 2013

Advanced morphological neuroimaging study in lateral temporal lobe epilepsy: A multicentric study

scientific article

Advances in genetic testing and optimization of clinical management in children and adults with epilepsy

scientific article published on 27 January 2020

Age at onset predicts good seizure outcome in sporadic non-lesional and mesial temporal sclerosis based temporal lobe epilepsy

scientific article published on 22 October 2010

Alteration of the in vivo nicotinic receptor density in ADNFLE patients: a PET study

scientific article published on 30 June 2006

Amyotrophic lateral sclerosis: a new missense mutation in the SOD1 gene

scientific article

An Italian multicentre study of perampanel in progressive myoclonus epilepsies

scientific article published on 16 August 2019

An SNP site in pri-miR-124, a brain expressed miRNA gene, no contribution to mesial temporal lobe epilepsy in an Italian sample.

scientific article published on 17 May 2016

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

scientific article

Anti-GM1 ganglioside antibodies in Parkinson's disease

scientific article published on 01 July 2002

ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsy

scientific article published in January 2005

Apolipoprotein E polymorphisms and the risk of nonlesional temporal lobe epilepsy

scientific article published on 01 December 1999

Association between the M129V variant allele of PRNP gene and mild temporal lobe epilepsy in women.

scientific article published on 7 November 2006

Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson’s disease in Southern Italy

article

Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis

scientific article published on 28 November 2012

Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene

scientific article published on 18 November 2013

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 recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B)

scientific article published on 01 September 1999

Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family.

scientific article

Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy

scientific article

Benign mesial temporal lobe epilepsy

scientific article published on 25 January 2011

Benign partial epilepsies of adolescence: a report of 37 new cases

scientific article published on 01 December 2001

Benign temporal lobe epilepsy

scientific article published in February 2010

Blocking out the real diagnosis

scientific article published on 01 February 2011

Body weight influences pharmacokinetics of levodopa in Parkinson's disease.

scientific article published in March 2002

Brachial amyotrophic diplegia associated with a novel SOD1 mutation (L106P)

scientific article published on 01 April 2005

Brainstem Posterior Reversible Encephalopathy Syndrome in an Asymptomatic Patient

scientific article published on 01 March 2020

Brand-to-generic levetiracetam switching: a 4-year prospective observational real-life study

scientific article published on 11 January 2018

C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation

scientific article published on 23 April 2015

CAG repeat length and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocity.

scientific article published in October 1998

CAV3 T78M mutation as polymorphic variant in South Italy

scientific article published on 16 May 2012

CNS findings in three cases of septo-optic dysplasia, including one with semilobar holoprosencephaly

scientific article published on 01 August 2005

CONVENTIONAL MRI AND NOTCH3 GENE SCREENING IN SPORADIC CADASIL

article

Cardiac parasympathetic index identifies subjects with adult obstructive sleep apnea: A simultaneous polysomnographic-heart rate variability study.

scientific article

Cardiac sympathetic index identifies patients with Parkinson's disease and REM behavior disorder

scientific article

Cerebral venous thrombosis and isolated intracranial hypertension without papilledema in CDH

scientific article published on 01 July 2001

Characteristics of a large population of patients with refractory epilepsy attending tertiary referral centers in Italy

scientific article published on 03 February 2010

Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2.

scientific article

Chlorpromazine versus sleep deprivation in activation of EEG in adult-onset partial epilepsy.

scientific article published in October 1994

Chronic neuroborreliosis by B. garinii: an unusual case presenting with epilepsy and multifocal brain MRI lesions.

scientific article published in July 2014

Clinical and Genetic Findings in 26 Italian Patients with Lafora Disease

scientific article published in March 2006

Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy

scientific article published on 01 January 2001

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

scientific article published on 2 November 2011

Clinical spectrum of SCN1A mutations.

scientific article

Combined Neurophysiological Studies in Creutzfeldt-Jakob Disease: A Case Report

scientific article published on 01 April 1989

Combined use of cardiac m-i123-iodobenzylguanidine scintigraphy and ¹²³I-fp-cit single photon emission computed tomography in older adults with rapid eye movement sleep behavior disorder

scientific article

Comment on Brázdil (2012) "unveiling the mystery of dèjà-vù: the structural anatomy of dèjà-vù".

scientific article published on 3 September 2012

Comparison between Electrocardiographic and Earlobe Pulse Photoplethysmographic Detection for Evaluating Heart Rate Variability in Healthy Subjects in Short- and Long-Term Recordings.

scientific article published on 13 March 2018

Consensus on diagnosis and management of JME: From founder's observations to current trends.

scientific article

Correction to: The landscape of epilepsy-related GATOR1 variants

scientific article published on 01 July 2019

Correction: The landscape of epilepsy-related GATOR1 variants

scientific article published on 01 August 2019

Corrigendum to "Advanced morphological neuroimaging study in lateral temporal lobe epilepsy: A multicentric study" [Epilepsy Behav 74 (2017) Pages 69-72].

scientific article published in December 2017

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

article

DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy

scientific article published on 9 May 2014

De novo epileptic confusional status in a patient with cobalamin deficiency

scientific article published on 01 September 1995

Deep Learning Representation from Electroencephalography of Early-Stage Creutzfeldt-Jakob Disease and Features for Differentiation from Rapidly Progressive Dementia.

scientific article published on 3 May 2016

Definition and diagnostic criteria of sleep-related hypermotor epilepsy

scientific article

Dentatorubral-pallidoluysian atrophy: Haplotype of Asian origin in 2 Italian families

article

Detection of hippocampal atrophy in patients with temporal lobe epilepsy: A 3-Tesla MRI shape

scientific article published on 25 July 2013

Diagnostic Biomarkers of Epilepsy

scientific article published on 01 January 2018

Diffusivity of cerebellar hemispheres enables discrimination of cerebellar or parkinsonian multiple system atrophy from progressive supranuclear palsy-Richardson syndrome and Parkinson disease.

scientific article published on 17 January 2013

Disappearance of periodic sharp wave complexes in Creutzfeldt-Jakob disease

scientific article published on 01 September 1997

Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraine ⬇️

scientific article published on 08 February 2013

Dopamine D2 receptor gene polymorphism and the risk of levodopa-induced dyskinesias in PD

scientific article

Early involvement of sympathetic cardiac nerve endings in a patient with rem sleep behaviour disorders.

scientific article published on 19 May 2010

Effects of levetiracetam on EEG abnormalities in juvenile myoclonic epilepsy.

scientific article

Electroclinical features of a family with simple febrile seizures and temporal lobe epilepsy associated with SCN1A loss-of-function mutation.

scientific article published on 12 June 2007

Emotion-induced myoclonic absence-like seizures in a patient with inv-dup(15) syndrome: a clinical, EEG, and molecular genetic study.

scientific article published on September 1999

Epilepsy and sleep disorders improve in adolescents and adults with Angelman syndrome: A multicenter study on 46 patients

scientific article

Epilepsy associated with Leukoaraiosis mainly affects temporal lobe: a casual or causal relationship?

scientific article published on 28 October 2014

Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta-analysis of risk factors.

scientific article

Epileptic phenotypes in autoimmune encephalitis: from acute symptomatic seizures to autoimmune-associated epilepsy

scientific article published in 2022

FUS mutations in sporadic amyotrophic lateral sclerosis: Clinical and genetic analysis

scientific article published on 04 November 2011

Failure to confirm association of a polymorphism in KCNMB4 gene with mesial temporal lobe epilepsy.

scientific article

Familial mesial temporal lobe epilepsies: clinical and genetic features.

scientific article published on May 2009

Familial temporal lobe epilepsy autosomal dominant inheritance in a large pedigree from southern Italy

scientific article

Family history and frontal lobe seizures predict long-term remission in newly diagnosed cryptogenic focal epilepsy

scientific article published on 5 August 2013

Focal neuromyotonia associated with a C9ORF72 expansion mutation

scientific article published on 23 June 2020

Functional activity changes in memory and emotional systems of healthy subjects with déjà vu

scientific article published on 07 June 2019

Functional integrity of benzodiazepine receptors of the geniculo-striate visual pathways in Creutzfeldt-Jakob disease. A pharmacological evoked potential study.

scientific article published in January 1993

Functional preservation of benzodiazepine receptors of the primary somatosensory cortex in Creutzfeldt-Jakob disease: a pharmacologic-evoked potential study

scientific article published in February 1996

Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy

scientific article

GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy

scientific article published in February 2003

Gene conversion events in adult-onset spinal muscular atrophy

article

Generalised epilepsy with febrile seizures plus (GEFS(+)): molecular analysis in a restricted area

scientific article published on 20 October 2011

Generalized versus partial reflex seizures: a review.

scientific article

Genetic association of alpha2-macroglobulin polymorphisms with AD in southern Italy

scientific article published on 01 September 2002

Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B) ⬇️

scientific article published on March 1, 1998

Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern.

scientific article published in February 2006

Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22.

scientific article

Genetics of reflex seizures and epilepsies in humans and animals.

scientific article

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

scientific article

Gerstmann-Straussler-Scheinker disease with PRNP P102L heterozygous mutation presenting as progressive myoclonus epilepsy

scientific article published in December 2017

HCN ion channels and accessory proteins in epilepsy: genetic analysis of a large cohort of patients and review of the literature

scientific article published on 08 April 2019

Hepatonecrosis and cholangitis related to long-term phenobarbital therapy: An autopsy report of two patients

scientific article published on 18 June 2007

Hereditary demyelinating neuropathy of infancy: a genetically complex syndrome

scientific article

Hippocampal and thalamic atrophy in mild temporal lobe epilepsy: a VBM study

scientific article published in September 2008

Hippocampal sclerosis worsens autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) phenotype related to CHRNB2 mutation

scientific article published on 17 August 2012

Homozygous STXBP1 variant causes encephalopathy and gain-of-function in synaptic transmission

scientific article published on 01 February 2020

Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences

scientific article published on 5 November 2012

Human iPSC Modeling of Genetic Febrile Seizure Reveals Aberrant Molecular and Physiological Features Underlying an Impaired Neuronal Activity

scientific article published on 05 May 2022

Hyperekplexia in a patient with a brainstem vascular anomaly.

scientific article published in April 1999

Hyperkinetic psychogenic movement disorders remain a diagnosis at first sight.

scientific article published on 2 December 2016

Hypertension, seizures, and epilepsy: a review on pathophysiology and management

scientific article published on 04 May 2019

Ictal 18F-FDG PET/MRI in a Patient With Cortical Heterotopia and Focal Epilepsy

scientific article published on 01 October 2017

Ictal impending danger--"sixth sense seizures"--in patients with benign focal epileptic seizures of adolescence

scientific article published on 03 March 2008

Identification of a new polymorphism (c134G>A) in the exon 2 of the myelin protein zero gene

scientific article published in March 2000

Idiopathic generalized epilepsies with versive or circling seizures

scientific article

Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms

scientific article published in March 2004

Insight into epileptic and physiological déjà vu: from a multicentric cohort study

scientific article published on 26 October 2018

Integrity of the corpus callosum in patients with benign temporal lobe epilepsy

scientific article

Interhemispheric threshold differences in idiopathic generalized epilepsies with versive or circling seizures determined with focal magnetic transcranial stimulation

scientific article published on 01 June 2000

Intrinsic epileptogenicity of human dysplastic cortex as suggested by corticography and surgical results

scientific article published on 01 April 1995

Juvenile Huntington's disease presenting as progressive myoclonic epilepsy.

scientific article

Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features

scientific article published on 01 January 2019

Kufs' disease presenting as late-onset epilepsia partialis continua

scientific article published on 01 October 1998

Lacosamide in patients with temporal lobe epilepsy: An observational multicentric open-label study.

scientific article published on 8 April 2016

Lacosamide monotherapy in clinical practice: A retrospective chart review

scientific article published on 14 March 2018

Late drug-resistance in mild MTLE: Can it be influenced by preexisting white matter alterations?

scientific article published on 20 April 2020

Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man.

scientific article published in June 2011

Letter: Beyond and within CA1 subfield in magnetic resonance imaging negative temporal lobe epilepsy

scientific article published in September 2015

Levetiracetam in patients with generalised epilepsy and myoclonic seizures: an open label study.

scientific article published on 18 January 2006

Limited chronic focal encephalitis: another variant of Rasmussen syndrome?

scientific article

Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families

scientific article published in June 2006

Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing

article

Long-term outcome of mild mesial temporal lobe epilepsy: A prospective longitudinal cohort study.

scientific article

Looking for indicative magnetic resonance imaging signs of hippocampal developmental abnormalities in patients with mesial temporal lobe epilepsy and healthy controls

scientific article published on 22 July 2020

Loss of long-duration response to levodopa over time in PD: implications for wearing-off

scientific article published on 01 March 1999

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

scientific article published on 26 April 2013

MRI evidence of mesial temporal sclerosis in sporadic "benign" temporal lobe epilepsy.

scientific article published in February 2006

MRI of skeletal muscles in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths

scientific article published on 01 January 1998

Management of psychogenic nonepileptic seizures (PNES): a multidisciplinary approach

scientific article published on 29 November 2018

Migraine attack triggering a generalised seizure: is this a case of migralepsy or ictal epileptic headache?

scientific article published on 08 November 2011

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

scientific article published on 30 September 2014

Mild non-lesional temporal lobe epilepsy. A common, unrecognized disorder with onset in adulthood.

scientific article published in November 1998

Modulation of GABAergic dysfunction due to SCN1A mutation linked to Hippocampal Sclerosis

scientific article published on 05 August 2020

Modulatory proteins can rescue a trafficking defective epileptogenic Nav1.1 Na+ channel mutant

scientific article published on 01 October 2007

Monotherapy for partial epilepsy: focus on levetiracetam

scientific article

Movement time and aging: a normative study in healthy subjects with the "Movement Time Analyzer".

scientific article published in June 2005

Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism.

scientific article published on 17 September 2011

Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia.

scientific article

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

scientific article

Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP

scientific article published on 23 January 2013

Mutations of the orexin system, a regulator of sleep arousal, are not a common cause of ADNFLE.

scientific article

Myoclonic absence-like seizures and chromosome abnormality syndromes

scientific article

NOS2A as a candidate gene in Relapsing-Remitting Multiple Sclerosis: a haplotype study using selected subsets of single nucleotide polymorphisms

scientific article published on 3 March 2011

Negative Myoclonic Status Due to Antiepileptic Drug Tapering: Report of Three Cases ⬇️

scientific article published on July 1, 1997

Negative myoclonus during valproate-related stupor. Neurophysiological evidence of a cortical non-epileptic origin.

scientific article published on February 1995

Neocortical thinning in “benign” mesial temporal lobe epilepsy

scientific article published on 31 March 2011

Neuro-anatomical differences among epileptic and non-epileptic déjà-vu

scientific article published on 7 October 2014

Neuroanatomic correlates of psychogenic nonepileptic seizures: a cortical thickness and VBM study.

scientific article

Neuropsychological profile of mild temporal lobe epilepsy

scientific article published on 02 July 2018

No evidence for a role of the coding variant of the Toll-like receptor 4 gene in temporal lobe epilepsy.

scientific article published on 27 June 2013

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

scientific article published on 06 March 2015

Nonmetabolic causes of triphasic waves: a reappraisal

scientific article published in July 1990

Novel spastin (SPG4) mutations in Italian patients with hereditary spastic paraplegia

article

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

scientific article published on 30 June 2006

PCDH19 mutations in female patients from Southern Italy

scientific article published on 30 August 2014

PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy

scientific article

PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity

scientific article published on 15 March 2018

Perampanel as first add-on choice on the treatment of mesial temporal lobe epilepsy: an observational real-life study

scientific article published on 09 August 2020

Pharmacological modulation in mesial temporal lobe epilepsy: Current status and future perspectives.

scientific article published on 19 September 2016

Photic-Induced Epileptic Negative Myoclonus: A Case Report

scientific article published on 01 May 1996

Photosensitive benign myoclonic epilepsy in infancy

scientific article published in January 2007

Polymorphism of the multidrug resistance 1 gene MDR1/ABCB1 C3435T and response to antiepileptic drug treatment in temporal lobe epilepsy

article

Positivity to p-ANCA in patients with status epilepticus

scientific article

Potential Role of miRNAs as Theranostic Biomarkers of Epilepsy

scientific article published on 13 September 2018

Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease.

scientific article

Presenilin enhancer-2 gene: identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease

scientific article published in November 2011

Presenilin-2 gene mutation presenting as Lewy Body dementia?

article

Prodynorphin Gene Promoter Polymorphism and Temporal Lobe Epilepsy

article

Professional Acquisition of M. bovis in Calabria Region (Southern Italy): A Challenging Case of Osteomyelitis in a Migrant Patient from Bulgaria

scientific article published on 14 July 2015

Profile of brivaracetam and its potential in the treatment of epilepsy

scientific article

Prognostic factors in patients with mesial temporal lobe epilepsy

article

Progressive myoclonic epilepsies: definitive and still undetermined causes.

scientific article published on 02 January 2014

Proteomic profiling of cerebrospinal fluid in Creutzfeldt-Jakob disease.

scientific article published on December 2010

Psychiatric Assessment in Patients with Mild Temporal Lobe Epilepsy

scientific article published on 14 January 2019

Psychopathological constellation in patients with PNES: A new hypothesis

scientific article

Purulent meningitis due to spontaneous anterior sacral meningocele perforation. Case report

scientific article published on 01 April 1989

Randomized trial comparing two different high doses of methylprednisolone in MS: a clinical and MRI study

scientific article published in June 1998

Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

article

Rating scale for psychogenic nonepileptic seizures: scale development and clinimetric testing.

scientific article published on 4 May 2011

Reduced thalamic volume in Parkinson disease with REM sleep behavior disorder: volumetric study

scientific article

Reflex periodic spasms induced by eating

scientific article published on 18 January 2006

Relationship between atrophy of the amygdala and ictal fear in temporal lobe epilepsy

scientific article published in August 1994

Relationship between genetic variant in pre-microRNA-146a and genetic predisposition to temporal lobe epilepsy: A case–control study

scientific article published on 20 December 2012

Relationship between severity of migraine and vitamin D deficiency: a case-control study

scientific article published on 01 June 2018

Relevance of clinical context in the diagnostic-therapeutic approach to status epilepticus.

scientific article

Reversible symmetrical external capsule hyperintensity as an early finding of autoimmune encephalitis

scientific article published on 01 July 2014

Role of pharmacogenomics in antiepileptic drug therapy: current status and future perspectives.

scientific article published on 10 September 2017

Rosacea-like facial rash related to metformin administration in a young woman.

scientific article

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

scientific article

Sacsin-Related Spastic Ataxia Caused by a Novel Missense Mutation p.Arg272His in a Patient from Sicily, Southern Italy

article

Screening of depressive symptoms in young-old hemodialysis patients: relationship between Beck Depression Inventory and 15-item Geriatric Depression Scale

scientific article published on 26 June 2007

Sensory evoked potentials in herpes simplex encephalitis

scientific article published in October 1991

Septo-optic dysplasia plus bilateral perisylvian polymicrogyria: a case report

scientific article published on 04 November 2012

Sequential occurrence of benign partial epilepsy and childhood absence epilepsy in three patients

scientific article published on 01 May 1996

Serotonin transporter gene (5-Htt): Association analysis with temporal lobe epilepsy

article

Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study

scientific article published in April 2005

Significance of mesial temporal atrophy in relation to intracranial ictal and interictal stereo EEG abnormalities

scientific article

Silent celiac disease in patients with childhood localization-related epilepsies

scientific article

Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study

article

Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron gene.

scientific article

Spontaneous obliteration of MRI-silent cerebral angiomatosis revealed by CT angiography in a patient with Sturge–Weber syndrome

scientific article published on 27 August 2007

Spontaneous remission of childhood epilepsy in two patients with focal extraopercular cortical dysplasia.

scientific article published in September 1997

Startle epilepsy complicating aspartylglucosaminuria.

scientific article published in March 2004

Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study.

scientific article published on 22 January 2018

Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephaly

scientific article

TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis

article

Temporal lobe abnormalities on brain MRI in healthy volunteers: A prospective case-control study

scientific article published on 20 January 2010

Thalamotemporal impairment in benign temporal lobe epilepsy: same hypotheses?

scientific article published in June 2014

The ENIGMA-Epilepsy working group: Mapping disease from large data sets

scientific article published on 29 May 2020

The Natural History of Epilepsy in 163 Untreated Patients: Looking for "Oligoepilepsy"

scientific article

The application of artificial intelligence to understand the pathophysiological basis of psychogenic nonepileptic seizures

scientific article published on 28 September 2018

The dopamine D2 receptor gene is a susceptibility locus for Parkinson's disease

scientific article published on 01 January 2000

The fragile X premutation presenting as postprandial hypotension

scientific article published in December 2004

The landscape of epilepsy-related GATOR1 variants

scientific article published on 10 August 2018

The long-duration response to L-dopa in the treatment of early PD.

scientific article

The mystery of unexplained traumatic sudden falls. A clinical case that adds a new feasible cause

scientific article

The p.Arg416Cys mutation in SPG3a gene associated with a pure form of spastic paraplegia

article

The parkin gene is not involved in late-onset Parkinson's disease

scientific article published on 01 July 2001

The relation of spike foci and of clinical seizure characteristics to different patterns of mesial temporal atrophy

scientific article published on 01 March 1995

The role of calcium channel mutations in human epilepsy.

scientific article published on January 2014

Topiramate and temporal lobe epilepsy: an open-label study.

scientific article published on June 2012

Treatment of palatal myoclonus with sumatriptan

scientific article published on 01 January 1998

Tremor pattern differentiates drug-induced resting tremor from Parkinson disease.

scientific article published on 3 February 2016

Triphasic waves and cerebral tumors.

scientific article published in January 1990

Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus

scientific article (publication date: September 2003)

Unilateral basal ganglia atrophy in a patient with tuberous sclerosis complex and hemichorea.

scientific article

Usefulness of a morning routine EEG recording in patients with juvenile myoclonic epilepsy

scientific article published on 11 September 2007

Usefulness of cardiac parasympathetic index in CPAP-treated patients with obstructive sleep apnea: A preliminary study

scientific article published on 31 July 2019

Usefulness of focal rhythmic discharges on scalp EEG of patients with focal cortical dysplasia and intractable epilepsy

scientific article published in April 1996

Usefulness of latero-orbital electrodes in detecting interictal epileptiform activity--a study of 60 patients with complex partial seizures.

scientific article published in August 1998

Usefulness of rectal biopsy for the diagnosis of Kufs disease: a controlled study and review of the literature.

scientific article published on 08 May 2012

Validation Study of Italian Version of Inventory for Déjà Vu Experiences Assessment (I-IDEA): A Screening Tool to Detect Déjà Vu Phenomenon in Italian Healthy Individuals

scientific article published on 07 August 2017

Value of Clinical Features to Differentiate Refractory Epilepsy from Mimics A prospective longitudinal cohort study

scientific article

Variable course of Unverricht-Lundborg disease: Early prognostic factors.

scientific article

Voxel-based morphometry of adulthood patients with temporal lobe epilepsy.

scientific article published on 19 May 2010

Voxel-based morphometry of sporadic epileptic patients with mesiotemporal sclerosis

scientific article published on 22 September 2009

White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study

scientific article published on 20 August 2020

White matter abnormalities differentiate severe from benign temporal lobe epilepsy.

scientific article published on 19 June 2015

Why should we change the term psychogenic nonepileptic seizures?

scientific article published on 01 July 2015

[Generalized epilepsy with febrile seizures plus: clinical and genetic analysis of three Serbian families]

scientific article published on 01 January 2005

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