CNR Institutional Research Information System

MANNA, IDA
 Distribuzione geografica
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Continente #
AS - Asia 2.417
NA - Nord America 1.096
EU - Europa 492
SA - Sud America 461
AF - Africa 37
OC - Oceania 3
Totale 4.506
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Nazione #
US - Stati Uniti d'America 1.052
SG - Singapore 990
CN - Cina 556
BR - Brasile 391
HK - Hong Kong 237
VN - Vietnam 211
FR - Francia 142
IT - Italia 130
KR - Corea 108
JP - Giappone 103
NL - Olanda 66
IN - India 36
BD - Bangladesh 34
AR - Argentina 29
DE - Germania 29
FI - Finlandia 28
ID - Indonesia 28
GB - Regno Unito 27
IL - Israele 16
EC - Ecuador 15
MX - Messico 14
MY - Malesia 14
UA - Ucraina 13
TH - Thailandia 12
CA - Canada 11
ZA - Sudafrica 11
TR - Turchia 10
SA - Arabia Saudita 9
CO - Colombia 8
IQ - Iraq 7
PH - Filippine 7
PY - Paraguay 7
SE - Svezia 7
IE - Irlanda 6
PK - Pakistan 6
ES - Italia 5
LT - Lituania 5
PL - Polonia 5
UZ - Uzbekistan 5
AT - Austria 4
AZ - Azerbaigian 4
KE - Kenya 4
MA - Marocco 4
PE - Perù 4
RO - Romania 4
RU - Federazione Russa 4
TN - Tunisia 4
AE - Emirati Arabi Uniti 3
AM - Armenia 3
BB - Barbados 3
CL - Cile 3
DZ - Algeria 3
JO - Giordania 3
KZ - Kazakistan 3
PR - Porto Rico 3
TT - Trinidad e Tobago 3
AL - Albania 2
BY - Bielorussia 2
EG - Egitto 2
HU - Ungheria 2
IM - Isola di Man 2
JM - Giamaica 2
KG - Kirghizistan 2
KW - Kuwait 2
NI - Nicaragua 2
NP - Nepal 2
NZ - Nuova Zelanda 2
SV - El Salvador 2
VE - Venezuela 2
AO - Angola 1
AU - Australia 1
BA - Bosnia-Erzegovina 1
BE - Belgio 1
BO - Bolivia 1
BZ - Belize 1
CD - Congo 1
DO - Repubblica Dominicana 1
EE - Estonia 1
ET - Etiopia 1
GH - Ghana 1
GM - Gambi 1
GP - Guadalupe 1
HN - Honduras 1
HR - Croazia 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LK - Sri Lanka 1
MD - Moldavia 1
MG - Madagascar 1
MM - Myanmar 1
MT - Malta 1
MU - Mauritius 1
NG - Nigeria 1
RS - Serbia 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
TM - Turkmenistan 1
TW - Taiwan 1
TZ - Tanzania 1
UY - Uruguay 1
Totale 4.506
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Città #
Singapore 583
Santa Clara 436
Hefei 256
Hong Kong 233
San Jose 148
Lauterbourg 113
Seoul 107
Ho Chi Minh City 93
Beijing 91
Tokyo 90
Ashburn 63
Los Angeles 60
Dallas 39
Hanoi 39
São Paulo 26
Buffalo 19
New York 19
Helsinki 16
Jakarta 16
Milan 16
Rome 16
Minamishinagawa 13
Rio de Janeiro 13
Frankfurt am Main 12
Bangkok 10
Bengaluru 9
Biên Hòa 9
Boardman 9
Haiphong 9
Kuala Selangor 9
Orem 9
Anoia Superiore 8
Belo Horizonte 8
Goiânia 8
Lappeenranta 8
Curitiba 7
Da Nang 7
San Martino in Rio 7
Brasília 6
Johannesburg 6
Manaus 6
Phoenix 6
São José do Rio Preto 6
Amsterdam 5
Atlanta 5
Brooklyn 5
Capua 5
Council Bluffs 5
Dublin 5
Guarulhos 5
Hải Dương 5
London 5
Manila 5
Montreal 5
Porto Alegre 5
Quito 5
Salvador 5
Stockholm 5
Venice 5
Asunción 4
Baku 4
Campinas 4
Chennai 4
Dhaka 4
Düsseldorf 4
Florence 4
Guangzhou 4
Kuala Lumpur 4
Lahore 4
Mumbai 4
Munich 4
New Delhi 4
Newark 4
Niterói 4
Nova Iguaçu 4
Nuremberg 4
Paris 4
Portsmouth 4
Ribeirão Preto 4
Riyadh 4
Santo André 4
Tashkent 4
Turku 4
Warsaw 4
Amman 3
Ankara 3
Baghdad 3
Blumenau 3
Bologna 3
Bridgetown 3
Bến Tre 3
Cabo Frio 3
Charlotte 3
Colombo 3
Cosenza 3
Denver 3
Duque de Caxias 3
Glasgow 3
Istanbul 3
Jeddah 3
Totale 2.892
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Nome #
Dropped head syndrome in a patient with FTD-ALS caused by abnormal expansion of C9orf72 gene. 115
Exosomal miRNAs as Potential Diagnostic Biomarkers in Alzheimer's Disease 91
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis 85
NOS2A AS CANDIDATE GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS: AN HAPLOTYPE STUDY BY USING A SUBSETS OF SNPs. 79
Contribution of Cerebrospinal Fluid Thymosin beta 4 Levels to the Clinical Differentiation of Creutzfeldt-Jakob Disease 78
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. 71
Serotonin transporter gene (5-Htt): association analysis with temporal lobe epilepsy. 71
Genetic association of alpha2-macroglobulin polymorphisms with AD in southern Italy. 71
Extracellular vesicles in Multiple Sclerosis: their significance in the development and possible applications as therapeutic agents and biomarkers 68
A Comprehensive Examination of the Role of Epigenetic Factors in Multiple Sclerosis 67
The effects of BDNF Val(66)Met polymorphism on brain function in controls and patients with multiple sclerosis: An imaging genetic study. 65
Hyper-religiosity and visual hallucinations in a patient with frontotemporal dementia carrying a double variant in GRN gene 59
A novel mutation (Thr116Ile) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease. 58
Exosomal miRNA as peripheral biomarkers in Parkinson's disease and progressive supranuclear palsy: A pilot study 56
CAV3 T78M MUTATION IN HETEROZYGOSIS IS NOT ASSOCIATED WITH LGMD1C IN SOUTHERN ITALY 55
Non-Coding RNAs: New Biomarkers and Therapeutic Targets for Temporal Lobe Epilepsy 55
Serum MicroRNAs as Predictors of Diagnosis and Drug-resistance in Temporal Lobe Epilepsy: A Preliminary Study 54
A common SCN1A polymorphisms does not influence drug responsiveness in Italian epilepsy patients. 50
A family with dominant optic atrophy and deafness due to a novel Opa1 mutation. 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
Circulating microRNA: The potential novel diagnostic biomarkers to predict drug resistance in temporal lobe epilepsy, a pilot study. 49
A novel missense mutation of CAPN3 gene in a Italian patient with Limb Girdle Muscular Dystrophy 48
Circulating miRNAs in progressive supranuclear palsy: Recent evidence and future challenges 47
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy 47
Cognitive impairment and brain atrophy in patients with relapsing-remitting Multiple Sclerosis (RRMS): the role of brain derived neurotrophic factor (BDNF) gene. 46
Exosome-associated miRNA profile as a prognostic tool for therapy response monitoring in multiple sclerosis patients. 46
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 45
Dropped head syndrome in a patient with FTD-ALS caused by abnormal expansion of C9orf72 gene 45
Peripheral mRNA expression of brain-derived neurotrophic factor Val66Met polymorphism in patients with relapsing-remitting multiple sclerosis 45
Fas antigen and sporadic Alzheimer's disease in Southern Italy:evaluation of two polymorphisms in the TNFRSF6 gene. 44
Contribution of Cerebrospinal fluid Thymosin ?4 levels to the clinical differentiation of Creutzfeldt-Jakob disease. 42
Autosomal dominant lateral temporal epilepsy (ADLTE): Absence of chromosomal rearrangements in LGI1 gene 41
Brain-Derived Neurotrophic Factor Val66Met polymorphism and peripheral mrna expression in patients with Relapsing Remitting Multiple Sclerosis (RRMS). 40
Genetic association of α2-macroglobulin polymorphisms with AD in southern Italy 40
Potential Role of miRNAs as Theranostic Biomarkers of Epilepsy 40
Failure to confirm association of a polymorphism in KCNMB4 gene with mesial temporal lobe epilepsy. 40
Thymosin beta 4 levels in cerebrospinal fluid: a new surrogate biomarker to discriminate Creutzfeldt-Jakob disease from other dementia 39
Creutzfeldt-Jakob disease and other dementia may be discriminated by Thymosin beta 4 levels in cerebrospinal fluid using MALDI-TOF MS. 39
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms. 39
No evidence for a role of the coding variant of the Toll-like receptor 4 gene in temporal lobe epilepsy 38
Neuropatia ottica ereditaria di Leber s e Sclerosi Multipla: Harding s syndrome. 38
Association of a GABA(B) gene haplotype and temporal lobe epilepsy. 37
Preliminary evidences of a NOS2A protective effect from Relapsing-Remitting Multiple Sclerosis 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
PERIPHERAL MRNA EXPRESSION OF BRAIN-DERIVED NEUROTROPHIC FACTOR VAL66MET POLYMORPHISM IN PATIENTS WITH RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS). 35
Contribution of Cerebrospinal Fluid Thymosin ?4 Levels to the Clinical Differentiation of Creutzfeldt-Jakob Disease 35
Myocardial (123)I-MIBG scintigraphy for differentiation of Lewy bodies disease from FTD. 35
BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF) GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS): LONGITUDINAL EVALUATION 34
Ile587Val polymorphism of the eIF2B5 gene as susceptibility factor for multiple sclerosis. 34
Brain-derived Neurotrophic Factor Val66Met polimorphism and the cortical response to spatial working memory. 34
Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene. 34
Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinson s disease 33
Familial mesial temporal lobe epilepsy (FMTLE): a clinical and genetic study of 15 Italian families. 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
Trauma cranico e genotipo APO-E: causa o rischio di malatia di Alzheimer? 32
Screening for MELAS mutations in Italian patients having stroke-like episodes. 31
GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy. 31
Aspetti epidemiologici del deficit di G6PD in provincia di Cosenza. Dati preliminari 31
Huntington disease like 2 in Southern Italy: screening of JPH3 and other genes involved in huntington like phenotypes. 31
CA repeat estrogen receptor b gene polymorphism in patients with Multiple Sclerosis. 31
MUTATION AND PHENOTYPE SPECTRUM IN SPORADIC AND FAMILIAL 30
Preliminary evidences of a NOS2A protective effect from relapsing-remitting multiple sclerosis. 30
Brain-derived neurotrophic factor val66met polymorphysm and the cortical response to spatial working memory 30
ASSOCIATION OF A GABA(B) GENE HAPLOTYPE AND TEMPORAL LOBE EPILEPSY 30
Is M129V of the Prion protein gene ( PRNP) associated with mild temporal lobe epilepsy? 30
A novel mutation in FKRP gene in Italian patient with LGMD. 29
A Functional Genetic Variation of the 5-HTR2A Receptor Affects Age at Onset in Patients with Temporal Lobe Epilepsy. 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
Cognitive performances and brain volumes in patients with relapsing-remitting multiple sclerosis: investigating the role of BDNF Val66Met polymorphism. 28
A Novel Lys 130 Gln Mutation of the TAU gene. 28
Mutational screening of the CAPN3 in LGMD patients from Southern Italy. 28
A novel mutation (Thr116IIe) in the presenilin 1 gene in a patient with early-onset Alzheimer's disease 28
Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency in south-east Sicily. 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
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
A new human mtDNA polymorphism: MTND6: 14562 (C-->T). 26
Relationship between genetic variant in pre-microRNA-146a and genetic predisposition to temporal lobe epilepsy: a case-control study. 26
ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsy. 26
N-methyl-D-aspartate receptor subunit NR1 gene (GRIN1) and temporal lobe epilepsy: no evidence of association analysis for genetic variant in promoter region of the gene. 26
Investigation of the inducible nitric oxide synthase gene (NOS2A) polymorphisms in Multiple Sclerosis. 26
Apolipoprotein E polymorphisms and the risk of nonlesional temporal lobe epilepsy. 25
Association between Synapsin III gene promoter polymorphisms and multiple sclerosis. 25
Preliminary evidence of NOS2A protective effect in patients with Relapsing-Remitting Multiple Sclerosis 24
VLA-4 and Multiple Sclerosis in Italian population. 24
BK channel b4 subunit gene (KCNMB4) and Temporal Lobe Epilepsy 24
No association between estrogen receptor 1 gene polymorphisms and susceptibility to multiple sclerosis 24
The frequency of limb girdle muscular dystrophy 1c in southern Italy 24
Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinson s disease 24
Mitochondrial DNA tRNACys mutation in a family with Frontotemporal Dementia and Parkinson s disease 24
Investigation of the inducible nitric oxide synthase gene (NOS2A) polymorphisms in Multiple Sclerosis. 23
Genetic variation in the myeloperoxidase gene and cognitive impairment in multiple sclerosis 23
Associazione genetica tra un polimorfismo funzionale nel promotore del gene trasportatore della serotonina (5-HTT) e l epilessia del lobo temoprale: risultati di uno studio caso-controllo. 23
Association study between synapsin III gene and Multiple Sclerosis (MS). 22
Prodynorphin gene promoter polymorphism and temporal lobe epilepsy 22
Association between the M129V variant allele of PRNP gene andmild temporal lobe epilepsy in women 21
Totale 3.983
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Categoria #
all - tutte 15.127
article - articoli 9.607
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 24.734
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202424 0 0 0 0 0 0 0 0 6 0 14 4
2024/20251.771 16 7 122 93 453 26 30 44 60 87 439 394
2025/20262.766 147 292 274 441 443 105 413 143 196 172 95 45
2026/20277 7 0 0 0 0 0 0 0 0 0 0 0
Totale 4.568