NACMIAS, BENEDETTA
 Distribuzione geografica
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Continente #
NA - Nord America 20.654
EU - Europa 11.815
AS - Asia 4.469
SA - Sud America 276
OC - Oceania 205
AF - Africa 88
Continente sconosciuto - Info sul continente non disponibili 3
Totale 37.510
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Nazione #
US - Stati Uniti d'America 20.595
RU - Federazione Russa 4.414
PL - Polonia 2.206
HK - Hong Kong 1.594
IT - Italia 1.348
IE - Irlanda 1.266
SG - Singapore 1.233
SE - Svezia 1.020
CN - Cina 836
DE - Germania 411
UA - Ucraina 305
FI - Finlandia 292
IN - India 273
BR - Brasile 252
GB - Regno Unito 213
AU - Australia 195
ID - Indonesia 128
JO - Giordania 125
FR - Francia 107
TR - Turchia 90
KR - Corea 54
VN - Vietnam 53
CI - Costa d'Avorio 48
CA - Canada 47
NL - Olanda 44
CH - Svizzera 30
AT - Austria 29
BE - Belgio 27
ES - Italia 24
SC - Seychelles 20
GR - Grecia 19
NZ - Nuova Zelanda 10
AZ - Azerbaigian 9
BG - Bulgaria 9
KG - Kirghizistan 9
CZ - Repubblica Ceca 8
JP - Giappone 8
LV - Lettonia 7
UZ - Uzbekistan 7
GE - Georgia 6
LT - Lituania 6
PK - Pakistan 6
AR - Argentina 5
BD - Bangladesh 5
IQ - Iraq 5
KZ - Kazakistan 5
EC - Ecuador 4
EG - Egitto 4
MU - Mauritius 4
MX - Messico 4
NO - Norvegia 4
PE - Perù 4
PH - Filippine 4
ZA - Sudafrica 4
AE - Emirati Arabi Uniti 3
AL - Albania 3
CL - Cile 3
CO - Colombia 3
EU - Europa 3
HU - Ungheria 3
IL - Israele 3
IR - Iran 3
KE - Kenya 3
MA - Marocco 3
PA - Panama 3
PT - Portogallo 3
RO - Romania 3
SK - Slovacchia (Repubblica Slovacca) 3
BO - Bolivia 2
BY - Bielorussia 2
DK - Danimarca 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
EE - Estonia 2
NP - Nepal 2
SA - Arabia Saudita 2
TW - Taiwan 2
AM - Armenia 1
BA - Bosnia-Erzegovina 1
CR - Costa Rica 1
HN - Honduras 1
IS - Islanda 1
JM - Giamaica 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LI - Liechtenstein 1
MK - Macedonia 1
PY - Paraguay 1
RS - Serbia 1
UY - Uruguay 1
VE - Venezuela 1
Totale 37.510
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Città #
Santa Clara 4.754
Fairfield 2.323
Warsaw 2.204
Ashburn 1.438
Hong Kong 1.324
Chandler 1.287
Dublin 1.262
Woodbridge 1.092
Seattle 998
Cambridge 928
Houston 870
Wilmington 770
Singapore 720
Altamura 525
Jacksonville 502
Lawrence 486
Dearborn 450
Ann Arbor 395
Princeton 343
Florence 251
Beijing 249
Mumbai 223
Boston 206
Boardman 200
Melbourne 190
Moscow 178
Medford 165
Buffalo 160
San Diego 145
Jakarta 125
Bremen 119
Shanghai 113
Los Angeles 97
Izmir 85
New York 77
Kent 74
Helsinki 68
Norwalk 64
Hefei 50
Paris 50
Falls Church 49
Abidjan 48
Seoul 48
Milan 44
Dong Ket 40
Pune 40
Toronto 38
Yubileyny 38
London 37
Rome 36
West Jordan 36
Hillsboro 34
Andover 30
Kunming 29
Nanjing 29
Guangzhou 28
Brussels 27
Auburn Hills 21
Bern 20
Jinan 19
Nuremberg 19
São Paulo 18
Barcelona 17
Lappeenranta 17
Phoenix 15
Fuzhou 13
Vienna 13
Frankfurt am Main 12
Redwood City 12
Frankfurt Am Main 11
Verona 11
Zurich 10
Belo Horizonte 9
Bishkek 9
Rio de Janeiro 9
Sofia 9
Wuhan 9
Nanchang 8
Newark 8
Umbertide 8
Auckland 7
Baku 7
Bari 7
Falkenstein 7
Riga 7
Shenzhen 7
The Dalles 7
Turin 7
Bologna 6
Castelliri 6
Chengdu 6
Chicago 6
Düsseldorf 6
Jiaxing 6
Lambeth 6
Laurel 6
Munich 6
Old Bridge 6
Prescot 6
Redmond 6
Totale 26.616
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Nome #
Clinical and neuroimaging profiles to identify C9orf72-FTD patients and serum Neurofilament to monitor the progression and the severity of the disease 307
Low Florbetapir PET Uptake and Normal Aβ1-42 Cerebrospinal Fluid in an APP Ala713Thr Mutation Carrier 267
Increased susceptibility to amyloid toxicity in familial Alzheimer's fibroblasts 262
Fat Mass and Obesity-Associated Gene (FTO) in Eating Disorders: Evidence for Association of the rs9939609 Obesity Risk Allele with Bulimia nervosa and Anorexia nervosa 255
Immunoproteasome LMP2 60HH variant alters MBP epitope generation and reduces the risk to develop multiple sclerosis in Italian female population. 253
FDG PET and the genetics of dementia 248
Lipid Rafts Mediate Amyloid-induced Calcium Dyshomeostasis and Oxidative Stress in Alzheimer's Disease. 246
Specific Silencing of L392V PSEN1 Mutant Allele by RNA Interference 235
Association Study of Genetic Variants in CDKN2A/CDKN2B genes/Loci with Late-Onset Alzheimer's Disease 235
Membrane cholesterol enrichment prevents Abeta-induced oxidative stress in Alzheimer's fibroblasts. 229
Fat mass and obesity-associated gene (FTO) is associated to eating disorders susceptibility and moderates the expression of psychopathological traits 229
Donor-specific anti-HLA antibodies in Huntington’s disease recipients of human fetal striatal grafts 224
Evidence for sub-haplogroup h5 of mitochondrial DNA as a risk factor for late onset Alzheimer's disease 222
A Pilot Study Evaluating the Contribution of SLC19A1 (RFC-1) 80G>A Polymorphism to Alzheimer’s Disease in Italian Caucasians 212
Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease 203
A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia 203
Analyses of the role of the glucocorticoid receptor gene polymorphism (rs41423247) as a potential moderator in the association between childhood overweight, psychopathology, and clinical outcomes in Eating Disorders patients: A 6 years follow up study. 181
Lipid rafts are primary mediators of amyloid oxidative attack on plasma membrane 173
Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies 172
Tumor necrosis factor α influences phenotypic plasticity and promotes epigenetic changes in human basal forebrain cholinergic neuroblasts 166
A2 macroglobulin polymorphisms in Italian sporadic and familial Alzheimer’s disease 160
Impact of demography and population dynamics on the genetic architecture of human longevity 157
Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline 155
Alzheimer's Disease Progression: Factors Influencing Cognitive Decline 154
5-HT2A receptor gene polymorphism and eating disorders. 149
The implication of BDNF Val66Met polymorphism in progression from subjective cognitive decline to mild cognitive impairment and Alzheimer's disease: a 9-year follow-up study 149
Genetics of vascular dementia - review from the ICVD working group 148
Cognitive reserve and TMEM106B genotype modulate brain damage in presymptomatic frontotemporal dementia: a GENFI study 148
No implication of apolipoprotein E polymorphism in Italian schizophrenic patients. 147
Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Italy 147
Association analysis of the paraoxonase-1 gene with Alzheimer's disease 146
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study 146
Ataxia-telangiectasia mutated (ATM) genetic variant in Italian centenarians 145
Brain-derived neurotrophic factor, apolipoprotein E genetic variants and cognitive performance in Alzheimer's disease. 144
A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia. 144
A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset. 142
Spatiotemporal analysis for detection of pre-symptomatic shape changes in neurodegenerative diseases: Initial application to the GENFI cohort 142
Association of IL10 promoter polymorphism in Italian Alzheimer's disease. 142
Comparative effects on tumor induction and root differentiation in potato tuber disks of the physiological state and its modification by DMSO treatment and infection with mutant A. tumefaciens strains. 142
A case of atypical early-onset Alzheimer’s disease carrying the missense mutation Thr354Ile in exon 10 of the PSEN1 gene 141
From Subjective Cognitive Decline to Alzheimer's Disease: The Predictive Role of Neuropsychological Assessment, Personality Traits, and Cognitive Reserve. A 7-Year Follow-Up Study 139
Association of the Variant Cys139Arg at GRN Gene to the Clinical Spectrum of Frontotemporal Lobar Degeneration 137
5-HT2A promoter polymorphism in anorexia nervosa. 137
Biomarkers study in atypical dementia: proof of a diagnostic work-up 136
Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa. 136
Pattern and progression of cognitive decline in Alzheimer's disease:role of premorbid intelligence and ApoE genotype 136
Association between serotonin transporter gene polymorphism and eating disorders outcome: A 6-year follow-up study. 136
Cerebral perfusion changes in presymptomatic genetic frontotemporal dementia: a GENFI study 135
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study 135
Age and ApoE genotype interaction in Alzheimer's disease: an FDG-PET study 134
Monomeric ß-amyloid interacts with type-1 insulin-like growth factor receptors to provide energy supply to neurons 134
Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease 134
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa 134
Fragile X premutation with atypical symptoms at onset. 133
Alzheimer's disease: role of size and location of white matter changes in determining cognitive deficits. 132
KIBRA T allele influences memory performance and progression of cognitive decline: a 7-year follow-up study in subjective cognitive decline and mild cognitive impairment 132
Primary Progressive Aphasia: Natural History in an Italian Cohort 132
ApoE genotype and familial Alzheimer's disease: a possible influence on age of onset in APP717 Val-->Ile mutated families. 131
Molecular genetics of Alzheimer's disease. 131
Distinct patterns of brain atrophy in Genetic Frontotemporal Dementia Initiative (GENFI) cohort revealed by visual rating scales 131
Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease. 131
Advances in imaging-genetic relationships for Alzheimer's disease: clinical implications. 131
MCI conversion to dementia and the APOE genotype: a prediction study with FDG-PET 130
A new social-family model for eating disorders: A European multicentre project using a case-control design 130
Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation 130
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant. 130
Associations of individual and family eating patterns during childhood and early adolescence: a multicentre European study of associated eating disorder factors. 130
Lactate production and glycolytic enzymes in sporadic and familial Alzheimer’s disease. 129
Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: A cross-sectional analysis 129
Oxidative stress and reduced antioxidant defenses in peripheral cells from familial Alzheimer's patients. 129
Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study 129
5-HT2A receptor gene polymorphisms in anorexia nervosa and bulimia nervosa 128
Comparison of arterial spin labeling registration strategies in the multi-center GENetic frontotemporal dementia initiative (GENFI) 128
ApoE as a prognostic factor for post-traumatic coma. 128
Novel S-acyl glutathione derivatives prevent amyloid oxidative stress and cholinergic dysfunction in Alzheimer disease models. Free Radic Biol Med. 128
Cholesteryl ester transfer protein (CETP) I405V polymorphism and longevity in Italian centenarians. 127
Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (Scientific Reports (2017) DOI: 10.1038/s41598-017-09320-z) 126
APP717 and Alzheimer's disease in Italy 125
Implication of alpha1-antichymotrypsin polymorphism in familial Alzheimer's disease. 124
Plasma Membrane Injury Depends on Bilayer Lipid Composition in Alzheimer’s Disease 124
A case of limbic encephalitis evolving into a frontotemporal dementia-like picture 124
Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders. 124
Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in Italy 124
Implication of serotonin-transporter (5-HTT) gene polymorphism in subjective memory complaints and mild cognitive impairment (MCI). 123
Identification of new presenilin gene mutations in early-onset familial Alzheimer disease 122
Cathepsin D polymorphism in Italian sporadic and familial Alzheimer's disease. 122
Protective effect of new S-acylglutathione derivatives against amyloid induced oxidative stress 122
Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa 122
The dual role of cognitive reserve in subjective cognitive decline and mild cognitive impairment: a 7-year follow-up study 122
Lack of association between NOS3 poly morphism and Italian sporadic and familial Alzheimer's disease. 122
Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference 122
Assessing the effectiveness of subjective cognitive decline plus criteria in predicting the progression to Alzheimer’s disease: an 11-year follow-up study 122
Insulin degrading enzyme and alpha-3 catenin polymorphisms in italian patients with Alzheimer disease 121
Absence of APP717 mutation in Italian FAD families 121
High Frequency of Crossed Aphasia in Dextral in an Italian Cohort of Patients with Logopenic Primary Progressive Aphasia 121
Case-control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosa. 121
Metabolic interaction between ApoE genotype and onset age in Alzheimer's disease: implications for brain reserve. 120
ApolipoproteinE epsilon 4 allele is not associated with disease course and severity in multiple sclerosis. 120
Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity 120
Psychosis, serotonin receptor polymorphism and Alzheimer's disease 120
Totale 15.156
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Categoria #
all - tutte 118.482
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 118.482
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020836 0 0 0 0 0 0 0 0 0 354 370 112
2020/20212.894 278 252 218 306 112 287 104 257 277 413 177 213
2021/20222.236 55 161 209 72 78 106 102 190 118 89 387 669
2022/20235.947 597 1.343 206 556 382 1.037 775 278 551 34 133 55
2023/20242.505 111 219 371 130 167 234 111 720 56 144 173 69
2024/202514.222 533 1.794 1.079 2.418 4.186 2.014 222 929 826 221 0 0
Totale 37.941