Antonio Gambardella

Antonio Gambardella's AcademicInfluence.com Rankings

Antonio Gambardella

Computer Science

#10271

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#10773

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Machine Learning

#4696

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#4748

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Artificial Intelligence

#5061

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#5126

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Database

#7219

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#7468

Historical Rank

computer-science Degrees

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Computer Science

Antonio Gambardella's Degrees

PhD Computer Science University of Milan
Masters Computer Science University of Milan
Bachelors Computer Science University of Milan

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Antonio Gambardella's Published Works

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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Intrinsic epileptogenicity of human dysplastic cortex as suggested by corticography and surgical results (1995) (699)
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2 (2000) (450)
The nicotinic receptor β2 subunit is mutant in nocturnal frontal lobe epilepsy (2000) (388)
Seizure control and treatment in pregnancy (2006) (276)
Comparative risk of major congenital malformations with eight different antiepileptic drugs: a prospective cohort study of the EURAP registry (2018) (267)
Benign familial neonatal‐infantile seizures: Characterization of a new sodium channelopathy (2004) (256)
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study (2018) (256)
Daily magnesium supplements improve glucose handling in elderly subjects. (1992) (217)
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy (2014) (214)
Advancing age and insulin resistance: role of plasma tumor necrosis factor-alpha. (1998) (201)
Operative Strategies for Patients with Cortical Dysplastic Lesions and Intractable Epilepsy (1994) (199)
Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures. (2005) (198)
Definition and diagnostic criteria of sleep-related hypermotor epilepsy (2016) (195)
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72. (2012) (191)
Opposite effects of short- and long-term fatty acid infusion on insulin secretion in healthy subjects (1995) (189)
Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study. (2005) (187)
Usefulness of focal rhythmic discharges on scalp EEG of patients with focal cortical dysplasia and intractable epilepsy. (1996) (184)
The nicotinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsy. (2000) (182)
Relationship between atrophy of the amygdala and ictal fear in temporal lobe epilepsy. (1994) (181)
Serum levels of insulin-like growth factor-I (IGF-I) and IGF-binding protein-3 in healthy centenarians: relationship with plasma leptin and lipid concentrations, insulin action, and cognitive function. (1997) (179)
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals (2019) (176)
Total-body and myocardial substrate oxidation in congestive heart failure. (1994) (171)
Metabolic benefits deriving from chronic vitamin C supplementation in aged non-insulin dependent diabetics. (1995) (163)
Alteration of the in vivo nicotinic receptor density in ADNFLE patients: a PET study. (2006) (156)
Neuroanatomic correlates of psychogenic nonepileptic seizures: A cortical thickness and VBM study (2012) (147)
Glucose tolerance and insulin action in healthy centenarians. (1996) (146)
ACE inhibition improves insulin-sensitivity in aged insulin-resistant hypertensive patients. (1992) (142)
Consensus on diagnosis and management of JME: From founder's observations to current trends (2013) (136)
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. (2012) (134)
GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy (2003) (130)
Oxidative Stress and Advancing Age: Results in Healthy Centenarians (1998) (125)
Randomized trial comparing two different high doses of methylprednisolone in MS A clinical and MRI study (1998) (122)
Does free fatty acid infusion impair insulin action also through an increase in oxidative stress? (1996) (119)
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy (2014) (115)
Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing. (1996) (114)
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family. (1996) (112)
Modulatory Proteins Can Rescue a Trafficking Defective Epileptogenic Nav1.1 Na+ Channel Mutant (2007) (111)
The landscape of epilepsy-related GATOR1 variants (2018) (110)
Plasma leptin concentrations and cardiac autonomic nervous system in healthy subjects with different body weights. (2000) (105)
Focal Intermittent Delta Activity in Patients with Mesiotemporal Atrophy: A Reliable Marker of the Epileptogenic Focus (1995) (105)
Dopamine D2 receptor gene polymorphism and the risk of levodopa-induced dyskinesias in PD. (1999) (104)
Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta‐analysis of risk factors (2016) (104)
Hippocampal and thalamic atrophy in mild temporal lobe epilepsy (2008) (98)
Deep Learning Representation from Electroencephalography of Early-Stage Creutzfeldt-Jakob Disease and Features for Differentiation from Rapidly Progressive Dementia (2017) (97)
MRI evidence of mesial temporal sclerosis in sporadic “benign” temporal lobe epilepsy (2006) (94)
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population (2012) (94)
Capecitabine plus oxaliplatin for the first‐line treatment of elderly patients with metastatic colorectal carcinoma (2005) (93)
Role of free fatty acids on cardiac autonomic nervous system in noninsulin-dependent diabetic patients: effects of metabolic control. (2001) (92)
Lowering fatty acids potentiates acute insulin response in first degree relatives of people with Type II diabetes (1998) (91)
Epilepsy in tuberous sclerosis complex: Findings from the TOSCA Study (2018) (91)
SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure (2009) (90)
Suppressive Efficacy by a Commercially Available Blue Lens on PPR in 610 Photosensitive Epilepsy Patients (2006) (88)
Clinical spectrum of SCN1A mutations (2009) (88)
Chronic vitamin E administration improves brachial reactivity and increases intracellular magnesium concentration in type II diabetic patients. (2000) (87)
TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study (2018) (85)
Prognostic importance of insulin-mediated glucose uptake in aged patients with congestive heart failure secondary to mitral and/or aortic valve disease. (1999) (84)
PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity (2018) (83)
A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1 (2000) (81)
Progressive myoclonic epilepsies (2014) (77)
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences (2012) (77)
Body Weight Influences Pharmacokinetics of Levodopa in Parkinson's Disease (2002) (77)
Body composition, body fat distribution, and resting metabolic rate in healthy centenarians. (1995) (77)
Benign mesial temporal lobe epilepsy (2011) (74)
White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA Epilepsy study (2019) (74)
Silent Celiac Disease in Patients with Childhood Localization‐Related Epilepsies (2001) (73)
Levetiracetam in patients with generalised epilepsy and myoclonic seizures: An open label study (2006) (73)
Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity. (2001) (71)
Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis (2012) (70)
Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy (2004) (68)
Long‐duration response to levodopa influences the pharmacodynamics of short‐duration response in Parkinson's disease (1997) (67)
Losartan mediated improvement in insulin action is mainly due to an increase in non-oxidative glucose metabolism and blood flow in insulin-resistant hypertensive patients (1997) (67)
Loss of long-duration response to levodopa over time in PD (1999) (65)
Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraine (2013) (65)
Clinical and Genetic Findings in 26 Italian Patients with Lafora Disease (2006) (65)
Generalized versus partial reflex seizures: A review (2014) (64)
Juvenile Huntington’s disease presenting as progressive myoclonic epilepsy (2001) (64)
Open label, long-term, pragmatic study on levetiracetam in the treatment of juvenile myoclonic epilepsy (2006) (63)
Familial temporal lobe epilepsy Autosomal dominant inheritance in a large pedigree from Southern Italy (2000) (62)
Two Novel SCN1A Missense Mutations in Generalized Epilepsy with Febrile Seizures Plus (2003) (62)
Comparison between Electrocardiographic and Earlobe Pulse Photoplethysmographic Detection for Evaluating Heart Rate Variability in Healthy Subjects in Short- and Long-Term Recordings (2018) (61)
Permutation entropy of scalp EEG: A tool to investigate epilepsies Suggestions from absence epilepsies (2014) (61)
Management of psychogenic non‐epileptic seizures: a multidisciplinary approach (2018) (60)
Metabolic and cardiovascular benefits deriving from β-adrenergic blockade in chronic congestive heart failure (1992) (60)
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study (2018) (60)
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study (2020) (60)
Effects of levetiracetam on EEG abnormalities in juvenile myoclonic epilepsy (2008) (59)
The dopamine D2 receptor gene is a susceptibility locus for Parkinson's disease (2000) (58)
Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutations (2011) (57)
APOE and risk of cognitive impairment in multiple sclerosis (1999) (57)
Anti‐GM1 ganglioside antibodies in Parkinson's disease (2002) (56)
Glucose ingestion affects cardiac ANS in healthy subjects with different amounts of body fat. (1997) (56)
Advancing age and insulin resistance: role of plasma tumor necrosis factor-α. (1998) (56)
Prognostic factors in patients with mesial temporal lobe epilepsy (2009) (56)
Genetics of reflex seizures and epilepsies in humans and animals (2016) (55)
Polymorphism of the multidrug resistance 1 gene MDR1/ABCB1 C3435T and response to antiepileptic drug treatment in temporal lobe epilepsy (2015) (55)
Efficacy of the combination of cisplatin with either gemcitabine and vinorelbine or gemcitabine and paclitaxel in the treatment of locally advanced or metastatic non-small-cell lung cancer: a phase III randomised trial of the Southern Italy Cooperative Oncology Group (SICOG 0101). (2006) (54)
Neocortical thinning in “benign” mesial temporal lobe epilepsy (2011) (54)
Effects of insulin on the cardiac autonomic nervous system in insulin-resistant states. (2000) (52)
Mild Non-lesional Temporal Lobe Epilepsy: A Common, Unrecognized Disorder with Onset in Adulthood (1998) (52)
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy (2011) (52)
Association of fasting plasma free fatty acid concentration and frequency of ventricular premature complexes in nonischemic non-insulin-dependent diabetic patients. (1997) (51)
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms. (2004) (51)
Significance of mesial temporal atrophy in relation to intracranial ictal and interictal stereo EEG abnormalities. (1996) (50)
Monotherapy for partial epilepsy: focus on levetiracetam (2008) (49)
Usefulness of a morning routine EEG recording in patients with juvenile myoclonic epilepsy (2007) (49)
Mutational Analysis of EFHC1 Gene in Italian Families with Juvenile Myoclonic Epilepsy (2007) (49)
Guillain-Barré syndrome following BNT162b2 COVID-19 vaccine (2021) (49)
Myoclonic Absence‐Like Seizures and Chromosome Abnormality Syndromes (1998) (48)
Reduced thalamic volume in Parkinson disease with REM sleep behavior disorder: volumetric study. (2014) (48)
Chronic intake of pharmacological doses of vitamin E might be useful in the therapy of elderly patients with coronary heart disease. (1995) (48)
ApoE Epsilon4 Allele and Disease Duration Affect Verbal Learning in Mild Temporal Lobe Epilepsy (2005) (47)
Electroclinical Features of a Family with Simple Febrile Seizures and Temporal Lobe Epilepsy Associated with SCN1A Loss‐of‐Function Mutation (2007) (46)
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 (1998) (44)
Hypertension, seizures, and epilepsy: a review on pathophysiology and management (2019) (44)
Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B) (1998) (43)
Voxel‐based morphometry of sporadic epileptic patients with mesiotemporal sclerosis (2010) (43)
White matter abnormalities differentiate severe from benign temporal lobe epilepsy (2015) (42)
Late‐onset drop attacks in temporal lobe epilepsy (1994) (42)
Vitamin E deficiency due to chylomicron retention disease in Marinesco‐Sjögren syndrome (2000) (41)
The significance of electrocorticographic findings in focal cortical dysplasia: a review of their clinical, electrophysiological and neurochemical characteristics. (1998) (41)
Age at onset predicts good seizure outcome in sporadic non-lesional and mesial temporal sclerosis based temporal lobe epilepsy (2010) (41)
Effects of different insulin infusion rates on heart rate variability in lean and obese subjects. (1999) (40)
Antioxidants In adipose tissue and risk of myocardial Infarction (1994) (40)
Metabolic aspects of the extreme longevity (2008) (40)
Inflammatory Cytokines and SIRT1 Levels in Subcutaneous Abdominal Fat: Relationship With Cardiac Performance in Overweight Pre-diabetics Patients (2018) (39)
Eyelid fluttering, typical EEG pattern, and impaired intellectual function: A homogeneous epileptic condition among the patients presenting with eyelid myoclonia (2009) (39)
FUS mutations in sporadic amyotrophic lateral sclerosis: Clinical and genetic analysis (2012) (39)
Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer’s disease (2013) (38)
Serotonin transporter gene (5-Htt): Association analysis with temporal lobe epilepsy (2007) (38)
The long-duration response to l-dopa in the treatment of early PD (2000) (37)
Epilepsy associated with Leukoaraiosis mainly affects temporal lobe: a casual or causal relationship? (2015) (36)
Apolipoprotein E Polymorphisms and the Risk of Nonlesional Temporal Lobe Epilepsy (1999) (36)
Temporal Lobe Epilepsy as a Unique Manifestation of Multiple Sclerosis (2003) (35)
Characteristics of a large population of patients with refractory epilepsy attending tertiary referral centers in Italy (2010) (35)
Familial mesial temporal lobe epilepsies: Clinical and genetic features (2009) (35)
The parkin gene is not involved in late-onset Parkinson’s disease (2001) (34)
Homozygous STXBP1 variant causes encephalopathy and gain-of-function in synaptic transmission (2019) (34)
Insulin resistance and advancing age: what role for dehydroepiandrosterone sulfate? (1997) (34)
Brivaracetam: review of its pharmacology and potential use as adjunctive therapy in patients with partial onset seizures (2015) (34)
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy (2015) (33)
A clinical spectrum of the myoclonic manifestations associated with typical absences in childhood absence epilepsy. A video-polygraphic study. (2001) (33)
Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families. (2008) (33)
Photosensitive Benign Myoclonic Epilepsy in Infancy (2007) (33)
The ENIGMA‐Epilepsy working group: Mapping disease from large data sets (2020) (32)
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations (2013) (32)
Simvastatin reduces plasma lipid levels and improves insulin action in elderly, non-insulin dependent diabetics (2004) (31)
Pharmacodynamics of the long-duration response to levodopa in PD (1999) (31)
Familial mesial temporal lobe epilepsy (FMTLE) (2007) (31)
Relationship between cerebrospinal fluid β-endorphin and plasma pituitary-gonadal hormone levels in women (1990) (31)
Diffusivity of cerebellar hemispheres enables discrimination of cerebellar or parkinsonian multiple system atrophy from progressive supranuclear palsy-Richardson syndrome and Parkinson disease. (2013) (31)
Potential Role of miRNAs as Theranostic Biomarkers of Epilepsy (2018) (30)
Left ventricular hypertrophy is associated with a stronger impairment of non‐oxidative glucose metabolism in hypertensive patients (1995) (30)
Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects. (2020) (30)
Mild Lafora disease: Clinical, neurophysiologic, and genetic findings (2014) (30)
Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron gene (1998) (30)
A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability (2018) (29)
Advances in genetic testing and optimization of clinical management in children and adults with epilepsy (2020) (29)
Autosomal dominant lateral temporal epilepsy: Absence of mutations in ADAM22 and Kv1 channel genes encoding LGI1-associated proteins (2008) (29)
Baseline heart rate variability in healthy centenarians: differences compared with aged subjects (>75 years old). (1999) (29)
The application of artificial intelligence to understand the pathophysiological basis of psychogenic nonepileptic seizures (2018) (28)
Amyotrophic lateral sclerosis: a new missense mutation in the SOD1 gene (2013) (28)
Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy (2007) (28)
Reflex periodic spasms induced by eating (2006) (28)
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP (2013) (28)
Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study (2010) (28)
A hyaluronic acid‐based compound inhibits fibroblast senescence induced by oxidative stress in vitro and prevents oral mucositis in vivo (2015) (27)
Apolipoprotein E polymorphisms and Parkinson's disease (1999) (27)
The relation of spike foci and of clinical seizure characteristics to different patterns of mesial temporal atrophy. (1995) (26)
Screening of Depressive Symptoms in Young–Old Hemodialysis Patients: Relationship between Beck Depression Inventory and 15-Item Geriatric Depression Scale (2007) (26)
Linkage Analysis and Disease Models in Benign Familial Infantile Seizures: A Study of 16 Families (2006) (26)
Idiopathic generalized epilepsies with versive or circling seizures (1999) (26)
Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephaly (2004) (26)
Detection of hippocampal atrophy in patients with temporal lobe epilepsy: A 3-Tesla MRI shape (2013) (26)
A hypofibrinolytic state in overweight patients with cerebral venous thrombosis and isolated intracranial hypertension (1999) (26)
Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia (2010) (25)
COVID-19 risk contagion: Organization and procedures in a South Italy geriatric oncology ward (2020) (25)
Genetic association of &agr;2-macroglobulin polymorphisms with AD in southern Italy (2002) (25)
Negative myoclonus during valproate-related stupor. Neurophysiological evidence of a cortical non-epileptic origin. (1995) (24)
Long-term outcome of mild mesial temporal lobe epilepsy (2016) (24)
Genetic heterogeneity in patients with pantothenate kinase–associated neurodegeneration and classic magnetic resonance imaging eye‐of‐the‐tiger pattern (2006) (24)
Hereditary demyelinating neuropathy of infancy: a genetically complex syndrome. (1997) (24)
Cerebral venous thrombosis and isolated intracranial hypertension without papilledema in CDH (2001) (24)
PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy (2015) (24)
Sleep-related hypermotor epilepsy (SHE): Contribution of known genes in 103 patients (2019) (24)
Abdominal Fat SIRT6 Expression and Its Relationship with Inflammatory and Metabolic Pathways in Pre-Diabetic Overweight Patients (2019) (24)
Interhemispheric threshold differences in idiopathic generalized epilepsies with versive or circling seizures determined with focal magnetic transcranial stimulation (2000) (23)
HCN ion channels and accessory proteins in epilepsy: genetic analysis of a large cohort of patients and review of the literature (2019) (23)
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1 q 43 , 2 p 16 . 1 , 2 q 22 . 3 and 17 q 21 . 32 (2012) (23)
Rating scale for psychogenic nonepileptic seizures: Scale development and clinimetric testing (2011) (23)
Intralipid infusion combined with propranolol administration has favorable metabolic effects in elderly malnourished cancer patients. (1999) (23)
A Novel Exon 1 Mutation in a Patient with Atypical Lafora Progressive Myoclonus Epilepsy Seen as Childhood‐onset Cognitive Deficit (2004) (23)
Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals. (2021) (23)
Sequential occurrence of benign partial epilepsy and childhood absence epilepsy in three patients (1996) (22)
Lisinopril administration improves insulin action in aged patients with hypertension. (1995) (22)
Effects of magnesium and nifedipine infusions on insulin action, substrate oxidation, and blood pressure in aged hypertensive patients. (1993) (22)
Relationship between genetic variant in pre-microRNA-146a and genetic predisposition to temporal lobe epilepsy: a case-control study. (2013) (22)
Nonmetabolic Causes of Triphasic Waves: A Reappraisal (1990) (21)
Cognitive impairment and Type 2 Diabetes Mellitus: Focus of SGLT2 Inhibitors Treatment. (2022) (21)
Sleep-induced masticatory myoclonus: a rare parasomnia associated with insomnia. (1991) (21)
A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability (2018) (21)
Metabolic and cardiovascular benefits deriving from beta-adrenergic blockade in chronic congestive heart failure. (1992) (20)
Facemask headache: a new nosographic entity among healthcare providers in COVID-19 era (2021) (20)
Mean arterial blood pressure and serum levels of the molar ratio of insulin-like growth factor-1 to its binding protein-3 in healthy centenarians. (1999) (20)
Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features (2018) (20)
Cardiac sympathetic index identifies patients with Parkinson's disease and REM behavior disorder. (2016) (20)
Temporal lobe abnormalities on brain MRI in healthy volunteers (2010) (20)
Integrity of the corpus callosum in patients with benign temporal lobe epilepsy (2016) (19)
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy (2008) (19)
Lacosamide monotherapy in clinical practice: A retrospective chart review (2018) (19)
Irinotecan plus leucovorin-modulated 5-fluorouracil I.V. bolus every other week may be a suitable therapeutic option also for elderly patients with metastatic colorectal carcinoma (2003) (19)
Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes. (2021) (19)
Association between the M129V variant allele of PRNP gene and mild temporal lobe epilepsy in women (2007) (19)
Treatment of palatal myoclonus with sumatriptan (1998) (18)
Family history and frontal lobe seizures predict long-term remission in newly diagnosed cryptogenic focal epilepsy (2013) (18)
Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer’s disease (2011) (18)
Circulating microRNAs as Potential Novel Diagnostic Biomarkers to Predict Drug Resistance in Temporal Lobe Epilepsy: A Pilot Study (2021) (18)
Psychopathological constellation in patients with PNES: A new hypothesis (2018) (18)
Non-paraneoplastic limbic encephalitis characterized by mesio-temporal seizures and extratemporal lesions: A case report (2010) (18)
The fragile X premutation presenting as postprandial hypotension (2004) (18)
Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy study (2021) (17)
Autonomic Nervous System and Cognitive Impairment in Older Patients: Evidence From Long-Term Heart Rate Variability in Real-Life Setting (2020) (17)
C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation. (2015) (17)
Tremor pattern differentiates drug-induced resting tremor from Parkinson disease. (2016) (17)
The role of calcium channel mutations in human epilepsy. (2014) (17)
Relationship between severity of migraine and vitamin D deficiency: a case-control study (2018) (17)
Prodynorphin Gene Promoter Polymorphism and Temporal Lobe Epilepsy (2003) (17)
An Italian multicentre study of perampanel in progressive myoclonus epilepsies (2019) (16)
An Embedded System for EEG Acquisition and Processing for Brain Computer Interface Applications (2010) (16)
Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies (2019) (16)
Novel spastin (SPG4) mutations in Italian patients with hereditary spastic paraplegia (2006) (16)
An SNP site in pri-miR-124, a brain expressed miRNA gene, no contribution to mesial temporal lobe epilepsy in an Italian sample (2016) (16)
Limited chronic focal encephalitis (2008) (16)
On the Classification of EEG Signal by Using an SVM Based Algorithm (2018) (16)
Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22 (2000) (15)
Leber’s hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man (2011) (15)
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 (2011) (15)
Hyperekplexia in a patient with a brainstem vascular anomaly (1999) (15)
Profile of brivaracetam and its potential in the treatment of epilepsy (2015) (15)
A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification. (2015) (15)
Kufs' disease presenting as late-onset epilepsia partialis continua (1998) (14)
Proteomic profiling of cerebrospinal fluid in Creutzfeldt–Jakob disease (2010) (14)
Brand‐to‐generic levetiracetam switching: a 4‐year prospective observational real‐life study (2018) (14)
Diagnostic Biomarkers of Epilepsy. (2018) (14)
Atlas of lesion locations and postsurgical seizure freedom in focal cortical dysplasia: A MELD study (2021) (14)
Epilepsy and sleep disorders improve in adolescents and adults with Angelman syndrome: A multicenter study on 46 patients (2017) (14)
Pharmacological modulation in mesial temporal lobe epilepsy: Current status and future perspectives. (2016) (14)
Anti-NMDA receptor encephalitis: a video case report. (2009) (14)
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson’s disease in Southern Italy (2011) (13)
3‐T magnetic resonance imaging simultaneous automated multimodal approach improves detection of ambiguous visual hippocampal sclerosis (2015) (13)
CAV3 T78M mutation as polymorphic variant in South Italy (2012) (13)
Neuro-anatomical differences among epileptic and non-epileptic déjà-vu (2015) (13)
Rosacea-like facial rash related to metformin administration in a young woman (2014) (13)
REM-Sleep Behavior Disorder in Patients With Essential Tremor: What Is Its Clinical Significance? (2019) (13)
Emotion‐Induced Myoclonic Absence‐Like Seizures in a Patient with Inv‐Dup(15) Syndrome: A Clinical, EEG, and Molecular Genetic Study (1999) (13)
Role of Pharmacogenomics in Antiepileptic Drug Therapy: Current Status and Future Perspectives. (2018) (13)
Low-Dose Iloprost Infusion Improves Insulin Action in Aged Healthy Subjects and NIDDM Patients (1995) (12)
Variable course of Unverricht-Lundborg disease (2017) (12)
Low fasting and insulin-mediated intracellular magnesium accumulation in hypertensive patients with left ventricular hypertrophy: role of insulin resistance. (1995) (12)
Anti–N‐methyl‐D‐aspartate‐glutamic‐receptor encephalitis presenting as paroxysmal exercise‐induced foot weakness (2013) (12)
Disappearance of periodic sharp wave complexes in Creutzfeldt-Jakob disease (1997) (12)
A systems-level analysis highlights microglial activation as a modifying factor in common forms of human epilepsy (2018) (12)
[Treatment of chronic constipation]. (1961) (12)
Contribution of cerebrospinal fluid thymosin β4 levels to the clinical differentiation of Creutzfeldt-Jakob disease. (2012) (11)
Startle epilepsy complicating aspartylglucosaminuria (2004) (11)
Chlorpromazine versus sleep deprivation in activation of EEG in adult-onset partial epilepsy (1994) (11)
Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22. (2000) (11)
Action palatal tremor in a patient with primary intestinal lymphoma (1997) (11)
Alexithymia and Cancer-Related Fatigue: A Controlled Cross-Sectional Study (2010) (11)
A novel ICA-based hardware system for reconfigurable and portable BCI (2009) (11)
Movement time and aging: a normative study in healthy subjects with the “Movement Time Analyzer®” (2005) (11)
A systems‐level analysis highlights microglial activation as a modifying factor in common epilepsies (2021) (10)
Value of Multimodal Imaging Approach to Diagnosis of Neurosarcoidosis (2019) (10)
A tailored regimen including capecitabine and oxaliplatin for treating elderly patients with metastatic colorectal carcinoma Southern Italy Cooperative Oncology Group trial 0108. (2005) (10)
The efficacy of perampanel as adjunctive therapy in drug-resistant focal epilepsy in a “real world” context: focus on temporal lobe epilepsy (2020) (10)
Combined Neurophysiological Studies in Creutzfeldt-Jakob Disease: A Case Report (1989) (10)
Lacosamide in patients with temporal lobe epilepsy: An observational multicentric open-label study (2016) (10)
Benign Partial Epilepsies of Adolescence: A Report of 37 New Cases (2001) (10)
Angiosarcoma of the breast: a new therapeutic approach? (2015) (10)
Negative Myoclonic Status Due to Antiepileptic Drug Tapering: Report of Three Cases (1997) (10)
Hepatonecrosis and cholangitis related to long-term phenobarbital therapy: An autopsy report of two patients (2007) (10)
Low-dose Iloprost infusion improves insulin action and non-oxidative glucose metabolism in hypertensive patients (2004) (9)
Photic‐Induced Epileptic Negative Myoclonus: A Case Report (1996) (9)
Autosomal Recessive Hereditary Motor and Sensory Neuropathy with Focally Folded Myelin Sheaths (CMT4B) (1999) (9)
PCDH19 mutations in female patients from Southern Italy (2015) (9)
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Sexual function and sex hormones in breast cancer patients (2018) (9)
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Spontaneous obliteration of MRI-silent cerebral angiomatosis revealed by CT angiography in a patient with Sturge–Weber syndrome (2008) (8)
Rare manifestations and malignancies in tuberous sclerosis complex: findings from the TuberOus SClerosis registry to increAse disease awareness (TOSCA) (2021) (8)
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Blocking out the real diagnosis (2011) (6)
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A System for the Analysis of Snore Signals (2011) (6)
Autosornal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (1996) (6)
ADAM23, a Gene Related to LGI1, Is Not Linked to Autosomal Dominant Lateral Temporal Epilepsy (2010) (6)
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A Functional Genetic Variation of the 5‐HTR2A Receptor Affects Age at Onset in Patients with Temporal Lobe Epilepsy (2012) (5)
Psychiatric Assessment in Patients with Mild Temporal Lobe Epilepsy (2019) (5)
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Insulin Resistance and Hypertension in the Elderly (1994) (4)
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Sacsin-Related Spastic Ataxia Caused by a Novel Missense Mutation p.Arg272His in a Patient from Sicily, Southern Italy (2013) (4)
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Failure to confirm association of a polymorphism in KCNMB4 gene with mesial temporal lobe epilepsy (2013) (4)
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Ile587Val Polymorphism of the eIF2B5 Gene as Susceptibility Factor for Multiple Sclerosis (2011) (3)
Progressive Myoclonus Epilepsies (2021) (3)
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A Family With a Complex Phenotype Caused by Two Different Rare Metabolic Disorders: GLUT1 and Very-Long-Chain Fatty Acid Dehydrogenase (VLCAD) Deficiencies (2020) (2)
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The Aging Heart (1998) (0)
Assessment and treatment of elderly people with cancer: Italian (AIOM–SIGG) onco-geriatric survey results (2012) (0)
Clinical Observations on the Treatment of Amoebic Colitis with Di-iodohydroxyquinoline. (1954) (0)
[ON AUTOIMMUNE ETIOPATHOGENESIS OF IDIOPATHIC ULCERATIVE COLITIS]. (1963) (0)
P2.1 Usefulness of EC2 paste for scalp electrodes in long-term video EEG monitoring (2011) (0)
[Results of the use of the color pyramid test with a group of epileptics]. (1960) (0)
The one-and-a-half syndrome: a distinctive clinical finding in a patient with multiple sclerosis. (2023) (0)
Babylonian knowledge about temporal lobe epilepsy: distinguishing mesial from lateral forms (2022) (0)
[Study on a case of chronic polyarthritis treated with DOCA and ascorbic acid, cortisone per os, parenteral cortisone, and ACTH; considerations on so-called suspension syndrome]. (1952) (0)
Epilessia frontale notturna familiare (2002) (0)
LETTERS TO THE EDITOR AMYLOID POLYNEUROPATHY FOLLOWING DOMINO LIVER TRANSPLANTATION (2012) (0)
Thalamotemporal impairment in benign temporal lobe epilepsy: Same hypotheses? (2014) (0)
Two cases of unilateral wasting and weakness of distal upper limb: Similar onset and different diagnosis in young patients (2021) (0)
End of dose interval (EDI) symptoms in patients undergoing treatment with natalizumab (2021) (0)
Cannabidiol use in patients with Dravet syndrome and Lennox-Gastaut syndrome: experts’ opinions using a nominal group technique (NGT) approach (2023) (0)
Neurological manifestations in patients and disease carriers in an Italian family with osteosclerosis (2022) (0)
Correction: Perampanel as first add-on antiseizure medication: Italian consensus clinical practice statements (2022) (0)
Colliquative Amoebic Hepatitis with Secondary Pulmonary Manifestations. Successful Combined Treatment with Chloroquine and Emetine. (1963) (0)
Sorafenib (SFB) treated elderly patients (E) with hepatocellular carcinoma (HCC): Chromogranine A (CGA) plus vascular endothelial growth factor (VEGF) as predicting factors (PF) of treatment outcome. (2012) (0)

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