CNR Institutional Research Information System

ANDREOLI, VIRGINIA
 Distribuzione geografica
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Continente #
AS - Asia 2.368
NA - Nord America 1.206
EU - Europa 757
SA - Sud America 430
AF - Africa 36
OC - Oceania 6
Continente sconosciuto - Info sul continente non disponibili 2
Totale 4.805
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Nazione #
US - Stati Uniti d'America 1.141
SG - Singapore 1.022
CN - Cina 465
BR - Brasile 369
IT - Italia 256
VN - Vietnam 243
HK - Hong Kong 238
FR - Francia 169
NL - Olanda 154
JP - Giappone 111
KR - Corea 65
DE - Germania 45
IN - India 35
GB - Regno Unito 33
BD - Bangladesh 32
ID - Indonesia 29
AR - Argentina 24
TH - Thailandia 22
CA - Canada 21
MY - Malesia 19
MX - Messico 18
FI - Finlandia 17
IL - Israele 13
AT - Austria 11
EC - Ecuador 10
ES - Italia 10
TR - Turchia 10
CO - Colombia 9
PL - Polonia 9
SE - Svezia 9
ZA - Sudafrica 9
IQ - Iraq 8
PH - Filippine 8
PK - Pakistan 8
RU - Federazione Russa 8
CR - Costa Rica 7
JM - Giamaica 7
KE - Kenya 7
MA - Marocco 7
PY - Paraguay 7
UZ - Uzbekistan 7
UA - Ucraina 6
AE - Emirati Arabi Uniti 5
SA - Arabia Saudita 5
AU - Australia 4
CL - Cile 4
IE - Irlanda 4
TN - Tunisia 4
AL - Albania 3
DO - Repubblica Dominicana 3
JO - Giordania 3
KG - Kirghizistan 3
LT - Lituania 3
MT - Malta 3
PE - Perù 3
SK - Slovacchia (Repubblica Slovacca) 3
SN - Senegal 3
AZ - Azerbaigian 2
BB - Barbados 2
CZ - Repubblica Ceca 2
DZ - Algeria 2
HN - Honduras 2
HU - Ungheria 2
KZ - Kazakistan 2
LB - Libano 2
NZ - Nuova Zelanda 2
SV - El Salvador 2
UY - Uruguay 2
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
BQ - ???statistics.table.value.countryCode.BQ??? 1
BW - Botswana 1
BY - Bielorussia 1
BZ - Belize 1
CH - Svizzera 1
CI - Costa d'Avorio 1
EE - Estonia 1
ET - Etiopia 1
GE - Georgia 1
GR - Grecia 1
HR - Croazia 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
LV - Lettonia 1
MM - Myanmar 1
NP - Nepal 1
OM - Oman 1
PA - Panama 1
QA - Qatar 1
RS - Serbia 1
SI - Slovenia 1
TM - Turkmenistan 1
TT - Trinidad e Tobago 1
TZ - Tanzania 1
VE - Venezuela 1
XK - ???statistics.table.value.countryCode.XK??? 1
YE - Yemen 1
Totale 4.805
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Città #
Singapore 605
Santa Clara 421
Hong Kong 235
Hefei 148
San Jose 130
Lauterbourg 107
Tokyo 98
Ho Chi Minh City 92
Beijing 89
Ashburn 78
Seoul 65
Hanoi 56
Los Angeles 53
Dallas 35
Milan 33
São Paulo 29
Anoia Superiore 25
New York 23
Rome 22
Bangkok 20
Catanzaro 18
Naples 18
Frankfurt am Main 17
Jakarta 17
Buffalo 16
Orem 14
Amsterdam 11
Kuala Selangor 11
Bologna 10
Minamishinagawa 10
Atlanta 9
Guangzhou 9
Belo Horizonte 8
Helsinki 8
Hải Dương 8
Vienna 8
Brasília 7
Haiphong 7
Kuala Lumpur 7
Manila 7
Munich 7
Nuremberg 7
Washington 7
Bengaluru 6
Kingston 6
Nairobi 6
Padova 6
Porto Alegre 6
Rio de Janeiro 6
Rizziconi 6
San José 6
Stockholm 6
Tashkent 6
Toronto 6
Turin 6
Warsaw 6
Asunción 5
Biên Hòa 5
Bắc Giang 5
Bắc Ninh 5
Campinas 5
Chennai 5
Chicago 5
Luzzi 5
Montreal 5
Mumbai 5
Salvador 5
Santo André 5
Shanghai 5
Sydney 5
Turku 5
Bari 4
Bexley 4
Blumenau 4
Brooklyn 4
Bến Tre 4
Can Tho 4
Casablanca 4
Curitiba 4
Da Nang 4
Duque de Caxias 4
Goiânia 4
Guayaquil 4
Lappeenranta 4
London 4
Manaus 4
Messina 4
Modena 4
Newark 4
Phủ Lý 4
Volta Redonda 4
Ankara 3
Austin 3
Bekasi 3
Bishkek 3
Boardman 3
Bogotá 3
Cape Town 3
Catanduva 3
Cavallino 3
Totale 2.865
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Nome #
Climate and environmental changes in Italian mountains 139
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis 85
Lack of interaction between LRP1 and A2M polymorphisms for the risk of Alzheimer disease. 84
Associazione tra la subunità 2B del recettore NMDA (gene GRIN2B) e la malattia di Alzheimer 84
Relazione tecnica sui risultati dei monitoraggi del Mercurio in aria ambiente e nelle deposizioni 84
Cst3: fattore di rischio genetico per la Malattia di Alzheimer sporadica? 82
Genetic association of alpha2-macroglobulin polymorphisms with AD in southern Italy. 71
Contribution of volcanic and fumarolic emission to the aerosol in marine atmosphere in the central mediterranean sea: Results from med-oceanor 2017 cruise campaign 70
Caratterizzazione dell’Aerosol atmosferico presso l’Osservatorio Climatico-Ambientale di alta quota sito in Monte Curcio (Sila Grande, Calabria) 67
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man 65
Particulate Matter Ionic and Elemental Composition during the Winter Season: A Comparative Study among Rural, Urban and Remote Sites in Southern Italy 64
Fukutin-Related Protein L276I mutation in Limb Girdle Muscular Dystrophy patients with a Duchenne/Becker like phenotype 63
Apolipoprotein E genotype does not influence the progression of multiple sclerosis. 60
Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease 59
Ruolo del gene Neuregulin 1 (NRG1) nella Sclerosi Multipla 56
CAV3 T78M MUTATION IN HETEROZYGOSIS IS NOT ASSOCIATED WITH LGMD1C IN SOUTHERN ITALY 55
Inter-Comparison of Carbon Content in PM2.5 and PM10 Collected at Five Measurement Sites in Southern Italy 53
Presenilin-2 gene mutation presenting as Lewy Body dementia? 52
Analytical study on the primary and secondary organic carbon and elemental carbon in the particulate matter at the high-altitude Monte Curcio GAW station, Italy 52
Seasonal patterns of Saharan Dust detected over the central Mediterranean basin, at the High-altitude Monte Curcio GAW Station 52
Role of the Neuregulin 1 gene (NRG1) in multiple sclerosis 52
Analytical study on the primary and secondary organic carbon and elemental carbon in the particulate matter at the high-altitude Monte Curcio GAW station, Italy 52
A family with dominant optic atrophy and deafness due to a novel Opa1 mutation. 51
A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy 50
Carbonaceous aerosols collected at the observatory of Monte Curcio in the Southern Mediterranean Basin 49
Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man. 48
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 47
Caratterizzazione chimica invernale di PM2.5 e PM10 presso cinque siti di misura nell'Italia Meridionale 47
Establishing a national network for atmospheric mercury monitoring: preliminary spatial and temporal insights from Italy 45
GENETIC VARIABILITY IN SUSCEPTIBILITY AND RESPONSE TO MERCURY TOXICITY: SPECIAL CONSIDERATIONS 45
Mutation analysis of the GRIN2B gene in Alzheimer's disease 45
Fas antigen and sporadic Alzheimer's disease in Southern Italy:evaluation of two polymorphisms in the TNFRSF6 gene. 44
Analisi dell'impatto dei nuovi sistemi osservativi sui vari servizi e verifica della compatibilità delle catene di acquisizione e processamento richieste da essi 44
DRD2 gene polymorphism and the risk of peak-dose dyskinesias in Parkinson's disease. 42
Molecular characterization of the APP gene in italian patients with familial Alzheimer disease. 41
Investigation of the chemical contribution of volcanic and fumarolic emission to the marine aerosol in the central Mediterranean Sea: results from Med-Oceanor 2017 cruise campaign 41
Sviluppo degli algoritmi necessari per la full exploitation dei sensori utilizzati e sulla definizione delle catene di processamento dei dati acquisiti dai nuovi sensori 41
Presenilin enhancer-2 gene: Identification of a novel promoter mutation in a patient with early-onset familial Alzheimer's disease 40
D678N mutation in a patient with an early-onset Alzheimer's Disease 40
Concentration of trace elements in fine and coarse aerosol over the Mediterranean basin during the Urania 2011 and 2012 cruise campaigns. 40
Genetic association of α2-macroglobulin polymorphisms with AD in southern Italy 40
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms. 40
CASP-9 : a susceptibility locus for multiple sclerosis in Italy. 39
Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study. 39
Neuropatia ottica ereditaria di Leber s e Sclerosi Multipla: Harding s syndrome. 39
Apo-1/Fas gene polymorphisms and multiple sclerosis in Southern Italy. 37
APP gene mutation (D678N) in a patient with an Early-Onset Alzheimer's Disease 37
Chemical characterization of pm2.5 and pm10 at five sites in Southern Italy during wintertime and spring. 37
Familial Alzheimer's disease with amyloid precursor protein D678N mutation: a case report 37
Two SNPs in the Fas gene on chromosome 10 are not associated with Italian Sporadic Alzheimer s Disease. 36
Report sull'analisi dei gap da colmare nell'erogazione di servizi per il risk management, evidenziando il rapporto con gli obiettivi e le linee guida di Horizon 2020 36
A phenotyphic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation. 36
Increased Risk for Alzheimer disease with the interaction of MPO and A2M Polymorphisms 36
Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study. 35
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis. 35
Screening for MELAS mutations in Italian patients having stroke-like episodes. 34
Amyloid beta precursor protein mutation (D678N) in a patient with early-onset familial Alzheimer's disease: clinical characteristics and genetic identification 34
Leber s hereditary optic neuropathy and Multiple Sclerosis: Harding's syndrome. 33
CA repeat estrogen receptor b gene polymorphism in patients with Multiple Sclerosis. 33
Two SNPs in the Fas gene on chromosome 10 are not associated with Sporadic Alzheimer s Disease in southern Italy. 33
Molecular characterization of the APP gene in Italian patients with familial Alzheimer disease. 32
GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy. 32
Analisi molecolare del promotore del gene PSEN-2 nella Malattia di Alzheimer: uno studio di associazione nella popolazione calabrese 32
Trauma cranico e genotipo APO-E: causa o rischio di malatia di Alzheimer? 32
NOTCH3 gene mutations and mtDNA variations 32
Genetic association of a cystatin C gene polymorphism with late-onset Alzheimer disease. 32
The association of the regulatory region of the PS-2 gene with Alzheimer s disease. 31
Leber s hereditary optic neuropathy associated with multiple sclerosis like picture in a man. 31
Presenilin Enhancer-2 Gene mutations and Familial Alzheimer s Disease 31
Alzheimer s Disease and the Cystatin C gene polymorphism: an association study. 31
Genetic Aspects of Susceptibility to Mercury Toxicity: An Overview. 31
Genetic screening of Alzheimer's disease genes in Italian samples yields novel mutations in Presenilin-enhancer 2. 30
A novel mutation in FKRP gene in Italian patient with LGMD. 29
LRP1- LRPAP1 polymorphisms and risk of sporadic Alzheimer s disease. 29
Analisi mutazionale del gene OPA1 in una famiglia affetta da atrofia ottica autosomica dominante. 29
The frequency of Limb Girdle Muscular Dystrophy 1C in southern Italy 29
Elam-1 genotyping in Italian population with Multiple Sclerosis : molecular characterization of A561C variation. 28
A Novel Lys 130 Gln Mutation of the TAU gene. 28
Duchenne/Becker like phenotype and L276I mutation in FKRP gene 28
Mutational analysis of the mitochondrial tRNAleu gene In Italian patients with stroke-like episodes of undetermined origin. 28
Mutational screening of the CAPN3 in LGMD patients from Southern Italy. 28
Association between Synapsin III gene promoter polymorphisms and multiple sclerosis. 28
Caspase-9 gene C93T polymorphism and Multiple Sclerosis patients from Southern Italy 28
A new human mtDNA polymorphism: MTND6: 14562 (C-->T). 27
Gaba(b) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy 27
Mitochondrial mutations of Leber s hereditary optic neuropathy : a risk factor for multiple sclerosis? 27
Variations in two lipid metabolizing genes and susceptibility to sporadic Alzheimer s disease. 27
Identificazione di marcatori nel gene della presenilina-2 predittivi di malattia di alzheimer familiare. 27
Identification of Pen-2 gene mutations in Italian patients with Familial Alzheimer s Disease 27
Identificazione di una nuova mutazione nel gene OPA1 in una famiglia affetta da atrofia ottica e sordità. 27
Gene symbol: PSEN2. Disease: Alzheimer disease. 26
Two snps in the Fas gene on chromosome 10 are not associated with sporadic Alzheimer s disease. 26
VLA-4 and Multiple Sclerosis in Italian population. 26
The association of single nucleotide E-selectin gene polymorphism with Multiple Sclerosis . 25
CAV3 T78M mutation as polymorphic variant in South Italy 25
Severe erythrocyte adenylate kinase deficiency due to homozygous A -> G substitution at codon 164 of human AK1 gene associated with chronic haemolytic anaemia 24
Molecular characterization of the Presenilin-2 gene in Italian patients with familial Alzheimer Disease. 24
No association between estrogen receptor 1 gene polymorphisms and susceptibility to multiple sclerosis 24
Genetic variation in the myeloperoxidase gene and cognitive impairment in multiple sclerosis 24
The frequency of limb girdle muscular dystrophy 1c in southern Italy 24
Totale 4.153
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Categoria #
all - tutte 16.161
article - articoli 8.692
book - libri 383
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 25.236
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202419 0 0 0 0 0 0 0 0 4 1 13 1
2024/20251.939 7 8 140 77 423 30 52 91 62 158 468 423
2025/20262.790 117 235 225 395 500 148 432 177 230 207 75 49
2026/202796 96 0 0 0 0 0 0 0 0 0 0 0
Totale 4.844