ArTS Archivio della ricerca di Trieste

MARCON, GABRIELLA
 Distribuzione geografica
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Continente #
NA - Nord America 5.209
AS - Asia 3.714
EU - Europa 1.785
SA - Sud America 935
AF - Africa 65
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 2
Totale 11.717
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Nazione #
US - Stati Uniti d'America 5.137
SG - Singapore 1.487
BR - Brasile 756
VN - Vietnam 644
CN - Cina 479
HK - Hong Kong 425
PL - Polonia 315
IT - Italia 247
TR - Turchia 241
SE - Svezia 230
FR - Francia 211
KR - Corea 200
RU - Federazione Russa 142
UA - Ucraina 140
BG - Bulgaria 124
IE - Irlanda 121
AR - Argentina 65
DE - Germania 60
BD - Bangladesh 48
NL - Olanda 46
FI - Finlandia 41
ID - Indonesia 41
EC - Ecuador 39
GB - Regno Unito 34
IN - India 31
CA - Canada 25
MX - Messico 22
IQ - Iraq 21
BE - Belgio 19
ZA - Sudafrica 19
JP - Giappone 17
PY - Paraguay 17
CL - Cile 15
CO - Colombia 14
MA - Marocco 13
KE - Kenya 11
VE - Venezuela 11
ES - Italia 10
SA - Arabia Saudita 10
TN - Tunisia 9
PH - Filippine 8
AU - Australia 7
AZ - Azerbaigian 7
DO - Repubblica Dominicana 7
EG - Egitto 7
PE - Perù 7
PK - Pakistan 7
UY - Uruguay 7
UZ - Uzbekistan 7
AT - Austria 6
AE - Emirati Arabi Uniti 5
CH - Svizzera 5
CZ - Repubblica Ceca 5
GR - Grecia 5
JM - Giamaica 5
AL - Albania 4
AM - Armenia 4
BO - Bolivia 4
LT - Lituania 4
NP - Nepal 4
PA - Panama 4
TT - Trinidad e Tobago 4
BY - Bielorussia 3
DZ - Algeria 3
IL - Israele 3
KZ - Kazakistan 3
MY - Malesia 3
RS - Serbia 3
TH - Thailandia 3
CR - Costa Rica 2
GA - Gabon 2
JO - Giordania 2
KG - Kirghizistan 2
MD - Moldavia 2
OM - Oman 2
PT - Portogallo 2
RO - Romania 2
TW - Taiwan 2
BH - Bahrain 1
BN - Brunei Darussalam 1
CY - Cipro 1
ET - Etiopia 1
EU - Europa 1
GE - Georgia 1
HN - Honduras 1
HR - Croazia 1
IR - Iran 1
LA - Repubblica Popolare Democratica del Laos 1
LV - Lettonia 1
NI - Nicaragua 1
NO - Norvegia 1
PS - Palestinian Territory 1
QA - Qatar 1
SK - Slovacchia (Repubblica Slovacca) 1
TC - Turks e Caicos 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 11.717
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Città #
Singapore 785
Fairfield 587
Ashburn 480
Hong Kong 422
Chandler 403
Warsaw 297
Jacksonville 246
Princeton 242
Wilmington 240
Izmir 236
Woodbridge 225
San Jose 220
Ho Chi Minh City 215
Seattle 197
Seoul 195
Cambridge 184
Boardman 180
Houston 176
Ann Arbor 153
Hanoi 141
Chicago 137
Beijing 129
Sofia 123
Dublin 121
Columbus 115
Lauterbourg 108
Los Angeles 93
Santa Clara 87
The Dalles 82
Moscow 80
São Paulo 65
Buffalo 58
San Diego 53
Dongguan 34
New York 34
Trieste 32
Helsinki 31
Dearborn 27
Haiphong 27
Milan 27
Da Nang 26
Dallas 26
Fremont 25
Frankfurt am Main 23
Norwalk 21
Curitiba 19
Biên Hòa 16
Quito 16
Brasília 15
Rio de Janeiro 15
Rome 15
Zgierz 15
Brussels 14
Nanjing 14
Munich 13
Tokyo 13
Belo Horizonte 12
Hefei 12
London 12
Salvador 12
Brooklyn 11
Can Tho 11
Dhaka 11
Goiânia 11
Guayaquil 11
Ninh Bình 11
Osasco 11
Porto Alegre 11
Asunción 10
Campinas 10
Hải Dương 10
Nairobi 10
Nuremberg 10
Jakarta 8
Manaus 8
Thái Bình 8
Toronto 8
Udine 8
Atlanta 7
Baku 7
Council Bluffs 7
Orem 7
Recife 7
Redwood City 7
Ribeirão Preto 7
Baghdad 6
Casablanca 6
Catania 6
Chennai 6
Dong Ket 6
Jeddah 6
Kunming 6
Montevideo 6
Montreal 6
Quảng Ngãi 6
Tashkent 6
Thái Nguyên 6
Turku 6
Volta Redonda 6
Betim 5
Totale 7.937
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Nome #
Cohort profile: ‘Centenari a Trieste’ (CaT), a study of the health status of centenarians in a small defined area of Italy 277
How experience modulates semantic memory for food: Evidence from elderly adults and centenarians 265
ICC-dementia (International Centenarian Consortium - dementia): an international consortium to determine the prevalence and incidence of dementia in centenarians across diverse ethnoracial and sociocultural groups 251
APE1/Ref-1 in Alzheimer's disease: An immunohistochemical study 251
APE1/Ref-1 regulates PTEN expression mediated by EGR-1 233
Echocardiographic evaluation of centenarians in Trieste 195
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant 172
Role of circulating factors in cardiac aging 162
A novel PSEN2 mutation associated with a peculiar phenotype 158
Serotoninergic fibres form dense synaptic contacts with Purkinje cells in the mouse cerebellar cortex - An immunohistochemical study 150
Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP 143
Risk of dementia and death in patients with atrial fibrillation: A competing risk analysis of a population-based cohort 136
A novel mutation in a large italian pedigree 132
A family with Alzheimer’s Disease and parkinsonism associated with the novel A85V mutation of presenilin 2 gene 131
Visual hallucinations with sertraline 128
Mutant prion protein expression causes motor and memory deficits and abnormal sleep patterns in a transgenic mouse model 126
AD: role of clinical examinations in predicting neurpathological features 125
Analisi di linkage in Famiglie di Origine Italiana con Malattia di Alzheimer 125
A novel Italian PSEN2 mutation with behavioral phenotype 123
Presenilin 2 mutation does not influence expression and concentration of APP forms in human platelets 122
Doxycycline in Creutzfeldt-Jakob disease: A phase 2, randomised, double-blind, placebo-controlled trial 122
Guidelines for the diagnosis of dementia and Alzheimer’s disease 119
Are premorbid personality traits linked to the risk of Alzheimer's disease? A case series of subjects with familial mutation 119
Regression of chronic posterior leukoencephalopathy after stop of methotrexate treatment 117
PEN-2 gene mutation in a familial Alzheimer's disease case 117
Demenze degenerative primarie 117
Familial frontotemporal dementia associated with the novel MAPT mutation T427M 115
Alzheimer disease: APP mutations are associated with high percentage of cerebral amyloid deposits containing Aβ40 115
Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPSc 115
A betaPP peptide carboxyl-terminal to Abeta is neurotoxic 115
Nicastrin gene in familial and sporadic Alzheimer's disease 114
Angiotensin converting enzyme gene polymorphism in Presenilin linked Familial Alzhiemer’s Disease and Sporadic Alzheimer’s Disease 114
Panencephalopathic Creutzfeldt-Jakob disease with distinct pattern of prion protein deposition in a patient with D178N mutation and homozygosity for valine at codon 129 of the prion protein gene 113
Variability of the clinical phenotype in an Italian family with dementia associated with an intronic deletion in the GRN gene 113
An Italian family with Alzhiemer’s disease and M239V mutation in PS2 112
Absence of association between intronic polymorphism in PS-1 gene and Alzheimer’s disease in Italian patients 112
Diagnosis of Alzheimer's disease 112
Angiotensin converting enzyme gene polymorphism in Presenilin linked Familial Alzhiemer’s Disease and Sporadic Alzheimer’s Disease 111
Angiotensin Converting Enzyme polymorphism in sporadic and Presenilin linked Alzheimer’s disease families 109
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 109
Angiotensin converting enzyme gene polymorphism in Presenilin linked Familial Alzhiemer’s Disease and Sporadic Alzheimer’s Disease 108
Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 gene 108
Cognitive deficits in familial Alzheimer's disease associated with M239V mutation of presenilin 2 108
Late onset neurodegenerative diseases: A theoretical point of view 107
Paraneoplastic cerebellar degeneration associated with anti-neuronal anti-Tr antibodies in a patient with Hodgkin's disease 107
Tetracyclines and prion infectivity 106
Memantine effects on behaviour in moderately severe to severe Alzheimer's disease: a post-marketing surveillance study 106
ASSOCIATION BETWEEN 5-HT(2A) RECEPTOR POLYMORPHISM AND PSYCHOTIC SYMPTOMS IN ALZHEIMER'S DISEASE 106
Angiotensin converting enzyme gene polymorphism in Presenilin linked Familial Alzhiemer’s Disease and Sporadic Alzheimer’s Disease 105
HLA A2 allele is associated with age at onset of Alzheimer's disease 102
Factors associated with complex visual hallucinations during antidepressant treatment 100
Angiotensin converting enzyme gene polymorphism in Presenilin linked Familial Alzhiemer’s Disease and Sporadic Alzheimer’s Disease 100
Atypical tauopathy with massive involvement of the white matter 99
Oral microbiota profile is related to cognitive status in centenarians: a clinical and biological study 95
PURE, ACUTE CEREBELAR SYNDROME ASSOCIATED WITH CYCLOSPORINE TREATMENT IN AN ADULT LIVER TRANSPLANT RECIPIENT 92
IL TRATTAMENTO FARMACOLOGICO DELLA MALATTIA DI ALZHEIMER 88
Subacute spongiform encephalopaty assiciated with amyloid deposits 87
Il polimorfismo dell’ alfa-1 antichimotripsina nella forma familiare della Malattia di Alzheimer 87
Le angioti isolate del Sistema Nervoso Centrale (AIC) considerazioni clinico-radiologiche 86
Il polimorfismo dell’α1-antichimotripsina nella forma familiare della Malattia di Alzheimer 86
Presenilin genes analysis in Italian families with early-onset Alzheimer’s Disease 85
Degenerazione paraneoplastica cerebellare in un caso di linfoma di Hodgkin in remissione completa 85
Linkage Analysis in familial Alzheimer Disease 84
What do we learn from the clinical and biological evaluation of the oral cavity in centenarians? 84
Presenilin gene analysis in Italian familieswith early-onset Alzheimer’s disease 83
Pure acute cerebellar syndrome associated with cyclosporine treatmentin an adult liver transplant recipient 80
Localisation of presenilin 2 in human and rodent pancreatic islet beta-cells; Met239Val presenilin 2 variant is not associated with diabetes in man 80
Cytoskeletal markers in developmental disorders of human CNS 79
Le Sinucleinopatie 78
Presenilin genes analysis in Italian families with early onset Alzheimer’s disease 78
Influence of masticatory function on food preferences and cognitive performance in centenarians: an observational study 78
Presenilin genes and Alzheimer’s disease 77
bPP and Tau interaction in vitro 76
No association between 2 Macroglobulin DNA polymorphism and sporadic Alzheimer’s Disease in Italy 75
La Malattia di Alzheimer ad insorgenza precoce e tardiva: analisi di linkage con marker anonimi del cromosoma 21 74
La depressione nelle malattie di Alzheimer e di Parkinson. 73
Encefalopatia acuta convulsivante dopo iniezione con Anatetall 72
Neocortical Variation of Abeta Load in Fully Expressed, Pure Alzheimer's Disease 71
The Folding and Maturation of Amyloid Precursor Protein in ER Stress Conditions 71
Expression of c-sis oncogene products in peripheral nerve tissue 71
Hereditary demyelinating neuropathies: autosomic recessive and sporadic forms 71
Presenilin genes and Alzheimer’s disease 71
Hypomyelination neuropathy in an adult 70
Experience with phosphatidylserine treatment of patients with cognitive and behavioral decline 69
Mutation analysis in familial Alzheimer’s disease 69
Expression of tumor necrosis factor- and its receptors in Amyotrophic Lateral Sclerosis 69
Implication of α1-antichimotrypsin polymorphism in familial Alazheimer’s disease 67
Clinical and neuropathologic phenotype of a large Italian kindred with presenilin2 mutation M239V 67
Bilateral scopolamine mydriasis in a traveller 67
Enzyme polymorphism in presenilin linked Alzheimer’s disease families and sporadic Alzheimer’s disease 67
Correlati neuropsicologici e personologici premorbosi in una famiglia Italiana con Malattia di Alzheimer con mutazione M239V nel gene PS-2 66
Genetic and phenotypical analysis of presenilin genes-linked Familial Alzheimer’s disease in Italian kindreds 66
Clinical – neuropathological correlations in Alzheimer’s disease: description of seven cases 66
Presenilin analysis in Italian families with early-onset Alzheimer’s disease 66
Association between 5-HT2A receptor polymorphism and psychotic symptoms in Alzheimer’s disease 65
Correlati neuropsicologici e personologici premorbosi in una famiglia Italiana con Malattia di Alzheimer con mutazione M239V nel gene PS-2 65
Due casi familiari di parkinsonismi primari 65
Clinical and neuropathological findings of an Italian Family with Alzheimer’s disease and M239V mutation of PS2 gene 64
Clinico-Neuropathological correlations in AD 64
Association between 5-HT 2° receptor polymorphism and psychotic symptoms in Alzheimer’s Disease 64
Totale 10.570
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Categoria #
all - tutte 45.003
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 45.003
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021143 0 0 0 0 0 0 0 0 0 0 0 143
2021/2022829 30 101 18 26 13 31 18 34 153 109 91 205
2022/20231.106 126 89 75 158 143 224 5 95 131 4 40 16
2023/2024629 30 41 11 16 38 109 44 186 16 7 68 63
2024/20251.808 5 47 382 127 154 105 91 113 183 318 149 134
2025/20264.501 290 239 387 922 377 226 502 208 509 624 135 82
Totale 11.926