CNR Institutional Research Information System

GAMBARDELLA, ANTONIO
 Distribuzione geografica
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Continente #
AS - Asia 3.967
NA - Nord America 1.671
SA - Sud America 764
EU - Europa 762
AF - Africa 69
OC - Oceania 10
Totale 7.243
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Nazione #
SG - Singapore 1.721
US - Stati Uniti d'America 1.580
CN - Cina 924
BR - Brasile 622
HK - Hong Kong 389
VN - Vietnam 375
FR - Francia 237
IT - Italia 186
KR - Corea 161
JP - Giappone 107
IN - India 68
NL - Olanda 66
DE - Germania 59
AR - Argentina 50
GB - Regno Unito 47
BD - Bangladesh 41
FI - Finlandia 41
CA - Canada 34
MX - Messico 33
IL - Israele 29
EC - Ecuador 28
ZA - Sudafrica 23
CO - Colombia 20
PL - Polonia 18
TR - Turchia 18
ID - Indonesia 17
UA - Ucraina 17
PH - Filippine 14
IQ - Iraq 13
UZ - Uzbekistan 12
VE - Venezuela 12
AT - Austria 11
ES - Italia 11
PE - Perù 11
CL - Cile 10
SA - Arabia Saudita 10
IE - Irlanda 9
AZ - Azerbaigian 8
MA - Marocco 8
RU - Federazione Russa 8
SE - Svezia 8
PK - Pakistan 7
PY - Paraguay 7
AU - Australia 6
EG - Egitto 6
KE - Kenya 6
AE - Emirati Arabi Uniti 5
DK - Danimarca 5
OM - Oman 5
CR - Costa Rica 4
DO - Repubblica Dominicana 4
DZ - Algeria 4
JO - Giordania 4
KZ - Kazakistan 4
LK - Sri Lanka 4
LT - Lituania 4
TN - Tunisia 4
AL - Albania 3
BG - Bulgaria 3
BY - Bielorussia 3
CZ - Repubblica Ceca 3
GE - Georgia 3
GR - Grecia 3
HN - Honduras 3
JM - Giamaica 3
KW - Kuwait 3
LV - Lettonia 3
MY - Malesia 3
NP - Nepal 3
NZ - Nuova Zelanda 3
PT - Portogallo 3
SN - Senegal 3
BB - Barbados 2
BN - Brunei Darussalam 2
BO - Bolivia 2
CI - Costa d'Avorio 2
CY - Cipro 2
EE - Estonia 2
HU - Ungheria 2
LA - Repubblica Popolare Democratica del Laos 2
LB - Libano 2
MD - Moldavia 2
NG - Nigeria 2
PS - Palestinian Territory 2
RO - Romania 2
SI - Slovenia 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
UY - Uruguay 2
AM - Armenia 1
AO - Angola 1
BW - Botswana 1
CM - Camerun 1
CU - Cuba 1
DJ - Gibuti 1
DM - Dominica 1
ET - Etiopia 1
GA - Gabon 1
Totale 7.227
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Città #
Singapore 977
Santa Clara 610
Hefei 386
Hong Kong 384
San Jose 197
Lauterbourg 185
Beijing 166
Seoul 161
Ho Chi Minh City 144
Ashburn 99
Hanoi 91
Tokyo 83
Los Angeles 60
São Paulo 47
New York 40
Dallas 36
Helsinki 31
Buffalo 29
Frankfurt am Main 26
Milan 24
Minamishinagawa 23
Curitiba 21
Rome 18
Warsaw 17
Orem 16
Porto Alegre 16
Rio de Janeiro 15
Bengaluru 14
Montreal 14
London 13
Haiphong 12
Phoenix 12
Brasília 11
Tashkent 11
Belo Horizonte 10
Chennai 10
Da Nang 10
Naples 10
Quito 10
Atlanta 9
Council Bluffs 9
Dublin 9
Goiânia 9
Guayaquil 9
Ankara 8
Baku 8
Biên Hòa 8
Campinas 8
Elk Grove Village 8
Johannesburg 8
Lima 8
Mexico City 8
Nuremberg 8
Brooklyn 7
Cape Town 7
Genoa 7
Guangzhou 7
Hyderabad 7
Munich 7
Paris 7
Recife 7
San Francisco 7
Anoia Superiore 6
Bologna 6
Catania 6
Chicago 6
Colombo 6
Guarulhos 6
Hải Dương 6
Jakarta 6
Lappeenranta 6
Rio Grande 6
Salvador 6
Stockholm 6
Thái Bình 6
Toronto 6
Verona 6
Vienna 6
Amsterdam 5
Boardman 5
Bắc Ninh 5
Denver 5
Houston 5
Manaus 5
Mumbai 5
Nairobi 5
San Martino in Rio 5
Shanghai 5
Shenzhen 5
Thái Nguyên 5
Amman 4
Baghdad 4
Bogotá 4
Brescia 4
Buenos Aires 4
Caxias do Sul 4
Charlotte 4
City of London 4
Dhaka 4
Duque de Caxias 4
Totale 4.415
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Nome #
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes 88
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis 84
Orbito-frontal thinning together with a somatoform dissociation might be the fingerprint of PNES 79
Contribution of Cerebrospinal Fluid Thymosin beta 4 Levels to the Clinical Differentiation of Creutzfeldt-Jakob Disease 77
Ataxia with oculomotor apraxia in a family from southern italy : a clinical and genetic study 76
Conventional MRI and NOTCH3 gene screening in sporadic CADASIL. 76
Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features. 75
Circulating microRNAs as Potential Novel Diagnostic Biomarkers to Predict Drug Resistance in Temporal Lobe Epilepsy: A Pilot Study 72
Serotonin receptor 2a gene variant influences age at onset but not cognitive performance in patients with temporal lobe epilepsy. 70
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis. 67
Anti-N-methyl-D-aspartate-glutamic-receptor encephalitis presenting as paroxysmal exercise-induced foot weakness. 63
Unilateral basal ganglia atrophy in a patient with tuberous sclerosis complex and hemichorea 63
Fukutin-Related Protein L276I mutation in Limb Girdle Muscular Dystrophy patients with a Duchenne/Becker like phenotype 63
Molecular studies of the PANK2 gene in patients with PKAN 62
NOTCH3 gene mutations in twins with CADASIL 58
Hyper-religiosity and visual hallucinations in a patient with frontotemporal dementia carrying a double variant in GRN gene 58
Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease 57
Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. 57
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia 56
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man 56
Genetic analysis of SCA2 and SCA17 in familial Parkinson s disease. 55
CAV3 T78M MUTATION IN HETEROZYGOSIS IS NOT ASSOCIATED WITH LGMD1C IN SOUTHERN ITALY 55
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP. 55
Non-Coding RNAs: New Biomarkers and Therapeutic Targets for Temporal Lobe Epilepsy 54
Tremor pattern differentiates drug-induced resting tremor from Parkinson disease 53
Perampanel as only add-on epilepsy treatment in elderly: A subgroup analysis of real-world data from retrospective, multicenter, observational study 53
Mutational Analysis of the CHRNA4 and CHRNB2 genes in a family with autosomal dominant nocturnal frontal lobe epilepsy 52
Clinical and genetic study of an Italian family linked to SPG26 locus 52
"Schwann cells", a historical landmark in neurology 52
FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis. 51
NOTCH3 gene analysis in two couples of twins 50
A common SCN1A polymorphisms does not influence drug responsiveness in Italian epilepsy patients. 50
Climate change and hyponatremia‐related hospital admissions in people with focal epilepsy exposed to carbamazepine or its derivatives 50
An SNP site in pri-miR-124, a brain expressed miRNA gene, no contribution to mesial temporal lobe epilepsy in an Italian sample 49
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy. 49
A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy 48
Atrophy of superior cerebellar peduncles in SCA7: a clinic-biological case report 47
Temporal lobe abnormalities on brain MRI in healthy volunteers: a prospective case-control study 47
Incidental evidence of hypointensity in brain grey nuclei on routine MR imaging: when to suspect a neurodegenerative disorder? 47
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man. 46
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy 45
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations 44
Proteomic profiling of cerebrospinal fluid in Creutzfeldt-Jakob disease 43
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 43
Spastin Gene Mutations In Italian Patients With Pure And Complicated Forms Of Spastic Paraplegia 42
Contribution of Cerebrospinal fluid Thymosin ?4 levels to the clinical differentiation of Creutzfeldt-Jakob disease. 42
Gly269Ser mutation in compound heterozygosity with Leu127Arg is associated with adult onset of Tay-Sachs: a case report from south Italy 41
Babylonian knowledge about temporal lobe epilepsy: distinguishing mesial from lateral forms 41
Opicapone-induced reversible myopathy in a patient with advanced Parkinson's disease and familial hyperCKemia 41
ADULT ONSET TAY-SACHS ASSOCIATED WITH -HEXOSAMINIDASE A DEFICIENCY: A CASE REPORT FROM SOUTH ITALY 40
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy. 40
Advances in genetic testing and optimization of clinical management in children and adults with epilepsy 40
Management of status epilepticus in patients with liver or kidney disease: a narrative review 40
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1 40
Amyotrophic lateral sclerosis: a new missense mutation in the SOD1 gene. 40
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3. 39
Detection of hippocampal atrophy in patients with temporal lobe epilepsy: A 3-Tesla MRI shape 39
Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus 39
Failure to confirm association of a polymorphism in KCNMB4 gene with mesial temporal lobe epilepsy. 39
Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study. 38
Focal Neuromyotonia Associated With a C9ORF72 Expansion Mutation 38
No evidence for a role of the coding variant of the Toll-like receptor 4 gene in temporal lobe epilepsy 38
Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia 38
Colour vision in patients with Parkinson disease. Usefulness of three pseudoisochromatic tests 38
Creutzfeldt-Jakob disease and other dementia may be discriminated by Thymosin beta 4 levels in cerebrospinal fluid using MALDI-TOF MS. 38
Association of a GABA(B) gene haplotype and temporal lobe epilepsy. 37
Open label, long-term, pragmatic study on levetiracetam in the treatment of juvenile myoclonic epilepsy. 37
Vitamin E deficiency due to chylomicron retention disease in Marinesco-Sjogren Syndrome 37
Genetic analysis of TARDBP gene in a color of South Italian ALS patients 37
Thymosin beta 4 levels in cerebrospinal fluid: a new surrogate biomarker to discriminate Creutzfeldt-Jakob disease from other dementia 37
Familial Alzheimer's disease with amyloid precursor protein D678N mutation: a case report 37
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) 36
Epilepsy, Immunity and Neuropsychiatric Disorders 36
Association study between G-protein-coupled receptor kinase 5 gene and Parkinson s disease 36
Increased Risk for Alzheimer disease with the interaction of MPO and A2M Polymorphisms 36
Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis 36
Contribution of Cerebrospinal Fluid Thymosin ?4 Levels to the Clinical Differentiation of Creutzfeldt-Jakob Disease 35
Color vision inpatients with Parkinson disease. Usefulness of three pseudoisochromatic tests 35
Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study. 35
Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy. 35
Effectiveness of Perampanel as the Only Add-on: Retrospective, Multicenter, Observational Real Life Study on epilepsy patients 35
"Schwann cells", a historical landmark in neurology 35
The impact of one-year COVID-19 containment measures in patients with mesial temporal lobe epilepsy: A longitudinal survey-based study 35
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 34
The "minor" Alois Alzheimer before the discovery of the eponymous disorder 34
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis. 34
Sacsin-Related Spastic Ataxia Caused by a Novel Missense Mutation p.Arg272His in a Patient from Sicily, Southern Italy. 34
Combined use of cardiac m-i123-iodobenzylguanidine scintigraphy and (123) I-fp-cit single photon emission computed tomography in older adults with rapid eye movement sleep behavior disorder 34
Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene. 34
Clinical and genetic study of an Italian family with Autosomal Recessive Spastic Paraplegia associated with dysarthria and hearing loss. 33
Diffusivity of Cerebellar Hemispheres Enables Discrimination of Cerebellar or Parkinsonian Multiple System Atrophy from Progressive Supranuclear Palsy-Richardson Syndrome and Parkinson Disease. 33
The p.Arg416Cys mutation in SPG3a gene associated with a pure form of spastic paraplegia. 33
Epilepsy in "Sunflower syndrome": electroclinical features, therapeutic response, and long-term follow-up 33
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences. 33
Frequency and clinical features of progranulin mutation carriers in a series of patients affected by frontotemporal lobar degeneration: report of a novel mutation. 32
Vitamins prevent the neurological symptoms in their deficiency disorders 32
A familial t(4;8) translocation segregates with epilepsy and migraine with aura. 32
Dentatorubral-pallidoluysian atrophy: haplotype of Asian origin in 2 Italian families 32
Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification 32
Molecular analysis of the SCN1A gene in patients with Severe Myoclonic Epilepsy of Infancy 31
Totale 4.585
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Categoria #
all - tutte 24.389
article - articoli 17.350
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 41.739
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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
2024/20252.822 14 15 245 141 595 52 65 74 95 111 750 665
2025/20264.437 238 471 407 716 789 177 675 238 274 296 156 0
Totale 7.286