VITALE, EMILIA
 Distribuzione geografica
Continente #
AS - Asia 1.296
NA - Nord America 652
EU - Europa 385
SA - Sud America 237
AF - Africa 25
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 1
Totale 2.599
Nazione #
US - Stati Uniti d'America 619
SG - Singapore 554
CN - Cina 306
BR - Brasile 189
VN - Vietnam 141
HK - Hong Kong 130
IT - Italia 129
FR - Francia 98
KR - Corea 55
DE - Germania 37
BD - Bangladesh 24
NL - Olanda 24
GB - Regno Unito 19
FI - Finlandia 18
JP - Giappone 17
AR - Argentina 15
CA - Canada 14
IN - India 13
AT - Austria 12
PL - Polonia 10
EC - Ecuador 8
IL - Israele 8
IQ - Iraq 8
ES - Italia 7
ID - Indonesia 7
MX - Messico 7
PK - Pakistan 7
ZA - Sudafrica 7
CO - Colombia 6
MA - Marocco 6
SA - Arabia Saudita 6
IE - Irlanda 5
PE - Perù 5
SE - Svezia 5
VE - Venezuela 5
KE - Kenya 4
PY - Paraguay 4
UA - Ucraina 4
BE - Belgio 3
PH - Filippine 3
RU - Federazione Russa 3
TR - Turchia 3
UZ - Uzbekistan 3
AZ - Azerbaigian 2
CR - Costa Rica 2
EG - Egitto 2
ET - Etiopia 2
HN - Honduras 2
HR - Croazia 2
LT - Lituania 2
NZ - Nuova Zelanda 2
RS - Serbia 2
TN - Tunisia 2
UY - Uruguay 2
AM - Armenia 1
AU - Australia 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
BS - Bahamas 1
BW - Botswana 1
CH - Svizzera 1
CI - Costa d'Avorio 1
CL - Cile 1
DO - Repubblica Dominicana 1
GE - Georgia 1
GI - Gibilterra 1
GY - Guiana 1
HT - Haiti 1
JM - Giamaica 1
JO - Giordania 1
LB - Libano 1
ME - Montenegro 1
MM - Myanmar 1
NI - Nicaragua 1
NP - Nepal 1
PA - Panama 1
PS - Palestinian Territory 1
SI - Slovenia 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
VC - Saint Vincent e Grenadine 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 2.599
Città #
Singapore 323
Santa Clara 206
Hong Kong 128
San Jose 127
Hefei 108
Beijing 85
Lauterbourg 71
Seoul 52
Ashburn 48
Ho Chi Minh City 48
Hanoi 35
Los Angeles 29
Naples 28
Rome 21
Dallas 19
São Paulo 18
Marigliano 13
Buffalo 11
Düsseldorf 11
Nuremberg 11
Tokyo 11
New York 10
Helsinki 9
Milan 8
Haiphong 7
Rio de Janeiro 7
Belo Horizonte 6
Brasília 6
Da Nang 6
Lappeenranta 6
Warsaw 6
Dublin 5
Frankfurt am Main 5
Jeddah 5
Minamishinagawa 5
Montreal 5
Baghdad 4
Chennai 4
Goiânia 4
Johannesburg 4
Medellín 4
Orem 4
Phoenix 4
Poplar 4
Thái Bình 4
Amsterdam 3
Asunción 3
Bắc Giang 3
Cagliari 3
Chicago 3
Dhaka 3
Guangzhou 3
Guarulhos 3
Houston 3
Lahore 3
Lima 3
Mogi das Cruzes 3
Nairobi 3
New Delhi 3
Ninh Bình 3
Ribeirão Preto 3
Roubaix 3
Seattle 3
Stockholm 3
Tashkent 3
Taubaté 3
Turku 3
Wroclaw 3
Addis Ababa 2
An Giang Province 2
Ankara 2
Atlanta 2
Avellino 2
Baku 2
Belgrade 2
Bengaluru 2
Brussels 2
Cairo 2
Can Tho 2
Cape Town 2
Caxias do Sul 2
Charlotte 2
City of London 2
Contagem 2
Council Bluffs 2
Denver 2
Durham 2
Embu das Artes 2
Falkenstein 2
Florence 2
Genoa 2
Guayaquil 2
Itaquaquecetuba 2
João Pessoa 2
Karachi 2
Lanús 2
London 2
Magé 2
Marabá 2
Montevideo 2
Totale 1.668
Nome #
Sustained Depolarization Induces Gene Expression Pattern Changes Related to Synaptic Plasticity in a Human Cholinergic Cellular Model 93
C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts 82
Give a selfie for women @CNR 73
300x100: Protagoniste per la ricerca 71
CD33 rs2455069 SNP: Correlation with Alzheimer’s Disease and Hypothesis of Functional Role 67
Gold nanoparticles (AuNPs) cause variation in the level of methylation in H3K4 and H3K9 58
Variants of ST8SIA1 are associated with risk of developing multiple sclerosis 58
Loss-of-function mutations of progranulin (PGRN) in siblings with familial FTLD 57
Molecular responses of cells to 2-mercapto-1-methylimidazole gold nanoparticles (AuNPs)-mmi: investigations of histone methylation changes 56
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia 56
Fertility in a case of isochromosome Xq Klinefelter Syndrome (KS) 55
GRN deletion in Familial Fronto-Temporal Dementia showing Association with clinical Variability in three familial cases 55
Uncommon PGRN deletion and FTD responsible for phenotype variability in three familial cases. 55
CD33 and SIGLECL1 Immunoglobulin Superfamily Involved in Dementia 54
Clinical and Molecular Characterization of a Novel Progranulin Deletion Associated with Different Phenotypes 52
Circulating levels of IL-1 family cytokines and receptors in Alzheimer's disease: new markers of disease progression? 52
Identification, Characterization, and Regulatory Mechanisms of a Novel EGR1 Splicing Isoform 51
Metabolic response of SH-SY5Y cells to gold nanoparticles by NMR-based metabolomics analyses 50
Imidazole-stabilized gold nanoparticles induce neuronal apoptosis: An in vitro and in vivo study 49
Imidazole-stabilized gold nanoparticles induce neuronal apoptosis: An in vitro and in vivo study 48
Donor splice-site mutation in CUL4B is likely cause of X-linked intellectual disability 45
Early molecular and cellular characterization of extraocular phototransductive elements in Hydra (Cnidraria, Hydrozoa) 44
Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 44
Linc00473 as an immediate early gene under the control of the egr1 transcription factor 44
Imidazole-stabilized gold nanoparticles induce neuronal apoptosis: an in vitro and in vivo study. 44
SH-imi-goldnanoparticles a possible drug target carrier: an evaluation using epigenetic histone dimethylation levels 43
Assignment of human aldolase C gene to chromosome 17, region cen→q21.1 43
Loss-of-function mutations of progranulin (PGRN) in a familial FTLD 41
Loss-of-function mutation of progranulin (PGRN) in a familial FTLD 41
Role of cytosolic calcium-dependent phospholipase A2 in Alzheimer's disease pathogenesis 41
Non visual photoreception in Hydra: Molecular and morpho-functional correlates of the signal transduction cascade, 34
Gold nanoparticles (AuNPs) in vivo and in vitro neuronal interaction 33
Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12. 32
Rs34424835 PGRN gene variation a possible modifier in Frontotemporal lobar degeneration (FTLD) 31
Microarray analysis identifies up-regulation of CD36 in human PBMC treated with endocannabinoids. 30
Characterization of a type II collagen gene (COL2A1) mutation identified in cultured chondrocytes from human hypochondrogenesis 30
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene 30
Clinical and genetic associations in Marfan syndrome and related disorders 30
Impaired Ganglioside synthesis involved with pathogenic mechanism in a familial form of multiple sclerosis. 29
PGRN exon 6 deletion G.101349_101355delCTGCTGT associated with Nonfluent primary progressive aphasia in a familial form of FTLD 29
Early molecular and cellular characterization of extraocular phototransductive elements in Hydra 29
Cortical Metabolic Deficits in a Rat Model of Cholinergic Basal Forebrain Degeneration 29
Second family with hearing impairment linked to 19q13 and refined DFNA4 localization. 28
Potential fertility in a case of isochromosome Xq Klinefelter syndrome (KS) due to maternal meiotic error:review of the i (Xq) KS casuistry. 26
Role of Cytosolic Calcium-Dependent Phospholipase A2 in Alzheimer's Disease Pathogenesis. 25
Genetic linkage of the marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5 25
A second Middle Eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9 25
Arvanil and anandamide up-regulate CD36 expression in human peripheral blood mononuclear cells 25
Genome Mapping of Multiple Sclerosis in alarge American pedigree. 25
Arvanil and anandamide up-regulate CD36 expression in human peripheral blood mononuclear cells. 24
Linkage studies of non syndromic recessive deafness in a Turkishkindred which segregates DFNB9. 24
Gold nanoparticles (AuNPs) cross the BBB and induce cytotoxicity in SH-SY5Y cells 24
ST8SIA1 gene variants associated with risk of developing multiple sclerosis 24
Novel X-Linked mental retardation syndrome with short stature maps to Xq24. 23
Crossing of BBB using gold nanoparticles (AuNPs) 23
Paraparesi spastica complicata da epilessia in due fratelli 23
Influence of Variations in Two Serotonin Genes and Gender Differences on Learning and Memory. 22
Gold nanoparticles (AuNPs) cross the blood brain barrier and induce cytotoxicity in human neuroblastoma cells SH-SY5Y: an in vivo and in vitro study 22
A familial form of multiple sclerosis showing impaired ganglioside synthesis. 22
Variants of Risk of ST8SIA1 are associated with the risk of developing multiple sclerosis 22
Structural chromosomal variations in neurological diseases 22
Genomic cloning and characterization of the human thrombin receptor gene: Structural similarity to the proteinase activated receptor-2 gene 21
Arvanil and anandamideup-regulate CD36 expression in human peripheral blood mononuclearcells. 21
Arvanil and anandamide up-regulate CD36 expression in human peripheral blood mononuclear cells 20
A novel frameshift mutation of FOXC2gene in a family with hereditary lymphedema-distichiasis syndrome associated with renal disease and diabetes mellitus 20
A previously unreportedsyndrome of X-linked mental retardation with short stature maps toXq24 20
Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes 20
Risk of developing multiple sclerosis is associated with variants in the ST8SIA1 gene 19
Crossing of BBB using gold nanoparticles (AuNPS) 19
Suggestive linkage of situs inversusand other left-right abnormalities to chromosome 6p. 18
Repating developmental expression of G-Hox 7, a novel homeobox-containing gene in the chicken 18
Characterization of the human MSX-1 promoter and an enhancer responsible for retinoic acid induction 17
Totale 2.655
Categoria #
all - tutte 8.096
article - articoli 5.262
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 13.358


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202412 0 0 0 0 0 0 0 0 2 4 4 2
2024/20251.049 3 3 67 35 198 78 13 67 49 39 262 235
2025/20261.594 109 139 152 249 267 81 243 108 92 92 62 0
Totale 2.655