CNR Institutional Research Information System

GAMBARDELLA, ANTONIO
 Distribuzione geografica
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Continente #
AS - Asia 4.043
NA - Nord America 2.561
EU - Europa 912
SA - Sud America 811
AF - Africa 78
Continente sconosciuto - Info sul continente non disponibili 44
OC - Oceania 10
Totale 8.459
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Nazione #
US - Stati Uniti d'America 2.390
SG - Singapore 1.712
CN - Cina 919
BR - Brasile 634
HK - Hong Kong 388
VN - Vietnam 383
IT - Italia 317
FR - Francia 237
KR - Corea 160
BD - Bangladesh 103
JP - Giappone 103
NL - Olanda 70
IN - India 67
CA - Canada 59
DE - Germania 58
GB - Regno Unito 55
AR - Argentina 50
FI - Finlandia 41
EC - Ecuador 39
CO - Colombia 36
MX - Messico 35
IL - Israele 29
ID - Indonesia 25
ZA - Sudafrica 23
PL - Polonia 19
TR - Turchia 19
VE - Venezuela 19
PH - Filippine 17
UA - Ucraina 17
JM - Giamaica 16
IQ - Iraq 14
CR - Costa Rica 13
ES - Italia 13
UZ - Uzbekistan 12
AT - Austria 11
CL - Cile 11
HN - Honduras 11
PE - Perù 11
SA - Arabia Saudita 10
IE - Irlanda 9
MA - Marocco 9
MY - Malesia 9
AZ - Azerbaigian 8
RU - Federazione Russa 8
SE - Svezia 8
EG - Egitto 7
KE - Kenya 7
PK - Pakistan 7
PY - Paraguay 7
SV - El Salvador 7
TH - Thailandia 7
AU - Australia 6
JO - Giordania 6
AE - Emirati Arabi Uniti 5
BG - Bulgaria 5
DK - Danimarca 5
KZ - Kazakistan 5
SC - Seychelles 5
DO - Repubblica Dominicana 4
DZ - Algeria 4
GT - Guatemala 4
LK - Sri Lanka 4
LT - Lituania 4
NI - Nicaragua 4
OM - Oman 4
PT - Portogallo 4
TN - Tunisia 4
TT - Trinidad e Tobago 4
AL - Albania 3
BB - Barbados 3
BY - Bielorussia 3
CZ - Repubblica Ceca 3
EE - Estonia 3
GE - Georgia 3
GR - Grecia 3
KW - Kuwait 3
LV - Lettonia 3
NP - Nepal 3
NZ - Nuova Zelanda 3
PR - Porto Rico 3
RO - Romania 3
SN - Senegal 3
BN - Brunei Darussalam 2
BO - Bolivia 2
CI - Costa d'Avorio 2
CY - Cipro 2
HU - Ungheria 2
LA - Repubblica Popolare Democratica del Laos 2
LB - Libano 2
MD - Moldavia 2
NG - Nigeria 2
PS - Palestinian Territory 2
SI - Slovenia 2
SK - Slovacchia (Repubblica Slovacca) 2
TW - Taiwan 2
UY - Uruguay 2
AM - Armenia 1
AO - Angola 1
BW - Botswana 1
BZ - Belize 1
Totale 8.390
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Città #
Singapore 973
Santa Clara 617
Hefei 385
Hong Kong 383
San Jose 284
Lauterbourg 185
Beijing 165
Seoul 160
Ho Chi Minh City 150
Ashburn 136
Hanoi 94
Tokyo 79
Los Angeles 73
New York 48
São Paulo 46
Dallas 44
Milan 38
Buffalo 37
Helsinki 31
Rome 30
Council Bluffs 29
Frankfurt am Main 26
Minamishinagawa 23
Curitiba 22
Montreal 19
Chicago 18
Warsaw 18
Brasília 17
Orem 17
Atlanta 16
Phoenix 16
Porto Alegre 16
Rio de Janeiro 16
Naples 15
Bengaluru 14
Guayaquil 14
London 14
Quito 14
Charlotte 13
Houston 13
Haiphong 12
Bologna 11
San José 11
Tashkent 11
Belo Horizonte 10
Brooklyn 10
Chennai 10
Da Nang 10
Queens 10
The Bronx 10
Boardman 9
Dublin 9
Elk Grove Village 9
Genoa 9
Goiânia 9
Kingston 9
Toronto 9
Ankara 8
Baku 8
Birmingham 8
Biên Hòa 8
Bogotá 8
Campinas 8
Catania 8
Denver 8
Johannesburg 8
Lima 8
Nuremberg 8
Verona 8
Cape Town 7
Dhaka 7
Guangzhou 7
Hyderabad 7
Medellín 7
Mexico City 7
Munich 7
Palermo 7
Paris 7
Recife 7
Anoia Superiore 6
Colombo 6
Detroit 6
Fayetteville 6
Florence 6
Guarulhos 6
Hải Dương 6
Jakarta 6
Lappeenranta 6
Manaus 6
Miami 6
Nairobi 6
Rio Grande 6
Salvador 6
San Francisco 6
Shanghai 6
Stockholm 6
Thái Bình 6
Vienna 6
Alexandria 5
Amsterdam 5
Totale 4.766
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Nome #
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes 99
Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features. 96
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis 87
Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. 85
Conventional MRI and NOTCH3 gene screening in sporadic CADASIL. 84
Orbito-frontal thinning together with a somatoform dissociation might be the fingerprint of PNES 83
Contribution of Cerebrospinal Fluid Thymosin beta 4 Levels to the Clinical Differentiation of Creutzfeldt-Jakob Disease 82
Ataxia with oculomotor apraxia in a family from southern italy : a clinical and genetic study 81
Circulating microRNAs as Potential Novel Diagnostic Biomarkers to Predict Drug Resistance in Temporal Lobe Epilepsy: A Pilot Study 79
Serotonin receptor 2a gene variant influences age at onset but not cognitive performance in patients with temporal lobe epilepsy. 73
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis. 71
Hyper-religiosity and visual hallucinations in a patient with frontotemporal dementia carrying a double variant in GRN gene 71
FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis. 69
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man 69
Fukutin-Related Protein L276I mutation in Limb Girdle Muscular Dystrophy patients with a Duchenne/Becker like phenotype 66
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia 65
Anti-N-methyl-D-aspartate-glutamic-receptor encephalitis presenting as paroxysmal exercise-induced foot weakness. 64
Molecular studies of the PANK2 gene in patients with PKAN 64
Unilateral basal ganglia atrophy in a patient with tuberous sclerosis complex and hemichorea 64
NOTCH3 gene mutations in twins with CADASIL 62
Temporal lobe abnormalities on brain MRI in healthy volunteers: a prospective case-control study 62
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP. 62
Non-Coding RNAs: New Biomarkers and Therapeutic Targets for Temporal Lobe Epilepsy 62
Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease 62
"Schwann cells", a historical landmark in neurology 61
Tremor pattern differentiates drug-induced resting tremor from Parkinson disease 60
Climate change and hyponatremia‐related hospital admissions in people with focal epilepsy exposed to carbamazepine or its derivatives 60
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy. 60
Genetic analysis of SCA2 and SCA17 in familial Parkinson s disease. 58
CAV3 T78M MUTATION IN HETEROZYGOSIS IS NOT ASSOCIATED WITH LGMD1C IN SOUTHERN ITALY 58
Incidental evidence of hypointensity in brain grey nuclei on routine MR imaging: when to suspect a neurodegenerative disorder? 58
Mutational Analysis of the CHRNA4 and CHRNB2 genes in a family with autosomal dominant nocturnal frontal lobe epilepsy 57
Perampanel as only add-on epilepsy treatment in elderly: A subgroup analysis of real-world data from retrospective, multicenter, observational study 57
An SNP site in pri-miR-124, a brain expressed miRNA gene, no contribution to mesial temporal lobe epilepsy in an Italian sample 56
A common SCN1A polymorphisms does not influence drug responsiveness in Italian epilepsy patients. 55
Clinical and genetic study of an Italian family linked to SPG26 locus 55
A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy 55
NOTCH3 gene analysis in two couples of twins 54
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy 54
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man. 53
Epilepsy in "Sunflower syndrome": electroclinical features, therapeutic response, and long-term follow-up 53
Hypertension, seizures, and epilepsy: a review on pathophysiology and management 52
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 52
Atrophy of superior cerebellar peduncles in SCA7: a clinic-biological case report 51
Effects of levetiracetam on EEG abnormalities in juvenile myoclonic epilepsy. 51
Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus 49
Opicapone-induced reversible myopathy in a patient with advanced Parkinson's disease and familial hyperCKemia 49
Spastin Gene Mutations In Italian Patients With Pure And Complicated Forms Of Spastic Paraplegia 48
Contribution of Cerebrospinal fluid Thymosin ?4 levels to the clinical differentiation of Creutzfeldt-Jakob disease. 48
Effectiveness of Perampanel as the Only Add-on: Retrospective, Multicenter, Observational Real Life Study on epilepsy patients 48
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1 48
ADULT ONSET TAY-SACHS ASSOCIATED WITH -HEXOSAMINIDASE A DEFICIENCY: A CASE REPORT FROM SOUTH ITALY 47
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations 47
Proteomic profiling of cerebrospinal fluid in Creutzfeldt-Jakob disease 47
Creutzfeldt-Jakob disease and other dementia may be discriminated by Thymosin beta 4 levels in cerebrospinal fluid using MALDI-TOF MS. 47
Cerebellar Agenesis and Bilateral Polimicrogyria Associated with Rare Variants of CUB and Sushi Multiple Domains 1 Gene (CSMD1): A Longitudinal Neuropsychological and Neuroradiological Case Study 46
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3. 46
Detection of hippocampal atrophy in patients with temporal lobe epilepsy: A 3-Tesla MRI shape 46
Management of status epilepticus in patients with liver or kidney disease: a narrative review 46
Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia 46
Open label, long-term, pragmatic study on levetiracetam in the treatment of juvenile myoclonic epilepsy. 45
Babylonian knowledge about temporal lobe epilepsy: distinguishing mesial from lateral forms 45
Advances in genetic testing and optimization of clinical management in children and adults with epilepsy 45
Focal Neuromyotonia Associated With a C9ORF72 Expansion Mutation 45
Sacsin-Related Spastic Ataxia Caused by a Novel Missense Mutation p.Arg272His in a Patient from Sicily, Southern Italy. 45
Amyotrophic lateral sclerosis: a new missense mutation in the SOD1 gene. 45
Gly269Ser mutation in compound heterozygosity with Leu127Arg is associated with adult onset of Tay-Sachs: a case report from south Italy 44
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy. 44
Genetic analysis of TARDBP gene in a color of South Italian ALS patients 44
Increased Risk for Alzheimer disease with the interaction of MPO and A2M Polymorphisms 44
Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis 44
Association study between G-protein-coupled receptor kinase 5 gene and Parkinson s disease 43
Familial mesial temporal lobe epilepsy (FMTLE): a clinical and genetic study of 15 Italian families. 43
No evidence for a role of the coding variant of the Toll-like receptor 4 gene in temporal lobe epilepsy 43
Colour vision in patients with Parkinson disease. Usefulness of three pseudoisochromatic tests 43
Failure to confirm association of a polymorphism in KCNMB4 gene with mesial temporal lobe epilepsy. 43
Association of a GABA(B) gene haplotype and temporal lobe epilepsy. 42
Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study. 42
Contribution of Cerebrospinal Fluid Thymosin ?4 Levels to the Clinical Differentiation of Creutzfeldt-Jakob Disease 42
Gerstmann-Straussler-Scheinker disease with PRNP P102L heterozygous mutation presenting as progressive myoclonus epilepsy 42
Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification 42
A familial t(4;8) translocation segregates with epilepsy and migraine with aura. 41
Epilepsy, Immunity and Neuropsychiatric Disorders 41
Value of Clinical Features to Differentiate Refractory Epilepsy from Mimics A prospective longitudinal cohort study. 41
Familial Alzheimer's disease with amyloid precursor protein D678N mutation: a case report 41
The impact of first world war on post-traumatic psychiatric symptoms in soldiers. A retrospective study analysis of 498 soldiers admitted in the psychiatric hospital of Girifalco (Catanzaro) 40
Thymosin beta 4 levels in cerebrospinal fluid: a new surrogate biomarker to discriminate Creutzfeldt-Jakob disease from other dementia 40
Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy. 39
The p.Arg416Cys mutation in SPG3a gene associated with a pure form of spastic paraplegia. 39
Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene. 39
Color vision inpatients with Parkinson disease. Usefulness of three pseudoisochromatic tests 38
Molecular characterization of the APP gene in Italian patients with familial Alzheimer disease. 38
The "minor" Alois Alzheimer before the discovery of the eponymous disorder 38
Clinical and genetic study of an Italian family with Autosomal Recessive Spastic Paraplegia associated with dysarthria and hearing loss. 38
Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy. 38
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences. 38
Dentatorubral-pallidoluysian atrophy: haplotype of Asian origin in 2 Italian families 37
null 37
The impact of one-year COVID-19 containment measures in patients with mesial temporal lobe epilepsy: A longitudinal survey-based study 37
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1. 36
Totale 5.291
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Categoria #
all - tutte 30.403
article - articoli 21.798
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 52.201
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202427 0 0 0 0 0 0 0 0 4 0 17 6
2024/20252.794 14 15 242 139 585 52 64 74 95 110 743 661
2025/20264.559 236 469 404 710 782 174 668 238 270 291 172 145
2026/20271.079 258 245 576 0 0 0 0 0 0 0 0 0
Totale 8.459