Antonio Gambardella
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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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(Suggest an Edit or Addition)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)
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- PRECLINICAL MARKERS OF NEUROPATHIC DAMAGE IN TYPE 1 DIABETES MELLITUS (2021) (0)
- 20. In vivo PET study of the mutated nicotinic receptors using [18F]-A-85380 in patients with autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) (2009) (0)
- Review for "Insights into déjà vu: Associations between the frequency of experience and amplitudes of low‐frequency oscillations in resting‐state fMRI" (2021) (0)
- Clinical importance of mimics (2021) (0)
- Parkinsonism and corticospinal tracts involvement in hepatic encephalopathy (2021) (0)
- Sensory evoked potentials in herpes simplex encephalitis (1991) (0)
- Identification of a new polymorphism (c134G>A) in the exon 2 of the myelin protein zero gene. (2000) (0)
- Asymmetry of Permutation Entropy in Early Creutzfeldt-Jakob Disease: A Clue to a Specific Pathological Process? (2015) (0)
- Natural clusters of tuberous sclerosis complex (TSC)-associated neuropsychiatric disorders (TAND): new findings from the TOSCA TAND research project (2020) (0)
- Huntington disease like 2 in Southern Iitaly: screening of JPH3 and other genes involved in huntington like phenotypes (2010) (0)
- [On a simple and exact method for the colorimetric determination of glucose in the cerebrospinal fluid]. (1960) (0)
- [Treatment of surgical meningitis]. (1950) (0)
- [COLLIQUATIVE AMEBIC HAPITITIS, WITH SECONDARY PULMONARY ABSCESS. ASSOCIATED CHLOROQUINE-EMETINE TREATMENT. RECOVERY]. (1963) (0)
- Structural network alterations in focal and generalized epilepsy follow axes of epilepsy risk gene expression: An ENIGMA study (2021) (0)
- Epidemiology and clinical studies of ischemic cardiopathy in the elderly (1991) (0)
- [Behavior of hemoglobin metabolism in leprosy]. (1951) (0)
- Correction: The landscape of epilepsy-related GATOR1 variants (2018) (0)
- 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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What Schools Are Affiliated With Antonio Gambardella?
Antonio Gambardella is affiliated with the following schools: