MARCON, GABRIELLA
 Distribuzione geografica
Continente #
NA - Nord America 5.834
AS - Asia 3.732
EU - Europa 1.915
SA - Sud America 950
Continente sconosciuto - Info sul continente non disponibili 211
AF - Africa 65
OC - Oceania 8
Totale 12.715
Nazione #
US - Stati Uniti d'America 5.738
SG - Singapore 1.490
BR - Brasile 761
VN - Vietnam 647
CN - Cina 486
HK - Hong Kong 428
IT - Italia 364
PL - Polonia 316
TR - Turchia 241
SE - Svezia 230
FR - Francia 213
KR - Corea 200
RU - Federazione Russa 142
UA - Ucraina 142
BG - Bulgaria 124
IE - Irlanda 121
AR - Argentina 71
DE - Germania 65
BD - Bangladesh 48
NL - Olanda 46
FI - Finlandia 41
ID - Indonesia 41
EC - Ecuador 39
GB - Regno Unito 35
CA - Canada 34
IN - India 32
MX - Messico 25
IQ - Iraq 21
BE - Belgio 19
ZA - Sudafrica 19
CO - Colombia 18
JP - Giappone 17
PY - Paraguay 17
CL - Cile 15
MA - Marocco 13
KE - Kenya 11
VE - Venezuela 11
ES - Italia 10
SA - Arabia Saudita 10
TN - Tunisia 9
AU - Australia 8
PH - Filippine 8
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
JM - Giamaica 6
TT - Trinidad e Tobago 6
AE - Emirati Arabi Uniti 5
CH - Svizzera 5
CR - Costa Rica 5
CZ - Repubblica Ceca 5
GR - Grecia 5
AL - Albania 4
AM - Armenia 4
BO - Bolivia 4
LT - Lituania 4
NP - Nepal 4
PA - Panama 4
RS - Serbia 4
BY - Bielorussia 3
DZ - Algeria 3
IL - Israele 3
KZ - Kazakistan 3
MY - Malesia 3
TH - Thailandia 3
CY - Cipro 2
GA - Gabon 2
HR - Croazia 2
JO - Giordania 2
KG - Kirghizistan 2
MD - Moldavia 2
NI - Nicaragua 2
OM - Oman 2
PT - Portogallo 2
RO - Romania 2
SV - El Salvador 2
TW - Taiwan 2
BH - Bahrain 1
BN - Brunei Darussalam 1
BZ - Belize 1
ET - Etiopia 1
EU - Europa 1
GE - Georgia 1
GT - Guatemala 1
HN - Honduras 1
IR - Iran 1
LA - Repubblica Popolare Democratica del Laos 1
LV - Lettonia 1
NO - Norvegia 1
PR - Porto Rico 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 12.506
Città #
Singapore 786
Ashburn 592
Fairfield 587
Hong Kong 425
Chandler 403
Warsaw 297
San Jose 287
Jacksonville 247
Princeton 244
Wilmington 241
Izmir 236
Woodbridge 225
Ho Chi Minh City 215
Seattle 197
Seoul 195
Cambridge 184
Boardman 180
Houston 176
Ann Arbor 153
Chicago 145
Hanoi 143
Beijing 132
Council Bluffs 129
Sofia 123
Dublin 121
Columbus 119
Lauterbourg 108
Los Angeles 100
Santa Clara 95
The Dalles 82
Moscow 80
Milan 70
São Paulo 65
Buffalo 58
San Diego 53
New York 39
Dongguan 34
Dallas 32
Trieste 32
Helsinki 31
Dearborn 27
Haiphong 27
Da Nang 26
Fremont 25
Frankfurt am Main 24
Rome 22
Norwalk 21
Curitiba 19
Biên Hòa 16
Quito 16
Rio de Janeiro 16
Brasília 15
Zgierz 15
Brooklyn 14
Brussels 14
Miano 14
Nanjing 14
Atlanta 13
Munich 13
Tokyo 13
Belo Horizonte 12
Hefei 12
London 12
Phoenix 12
Salvador 12
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
Turin 9
Jakarta 8
Manaus 8
Orem 8
Thái Bình 8
Toronto 8
Udine 8
Washington 8
Baku 7
Florence 7
Recife 7
Redwood City 7
Ribeirão Preto 7
Baghdad 6
Casablanca 6
Catania 6
Chennai 6
Dong Ket 6
Jeddah 6
Kunming 6
Mexico City 6
Montevideo 6
Montreal 6
Totale 8.372
Nome #
Cohort profile: ‘Centenari a Trieste’ (CaT), a study of the health status of centenarians in a small defined area of Italy 286
How experience modulates semantic memory for food: Evidence from elderly adults and centenarians 267
APE1/Ref-1 in Alzheimer's disease: An immunohistochemical study 258
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 255
APE1/Ref-1 regulates PTEN expression mediated by EGR-1 251
Echocardiographic evaluation of centenarians in Trieste 206
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant 176
Role of circulating factors in cardiac aging 165
A novel PSEN2 mutation associated with a peculiar phenotype 163
Serotoninergic fibres form dense synaptic contacts with Purkinje cells in the mouse cerebellar cortex - An immunohistochemical study 153
Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP 149
Risk of dementia and death in patients with atrial fibrillation: A competing risk analysis of a population-based cohort 142
A family with Alzheimer’s Disease and parkinsonism associated with the novel A85V mutation of presenilin 2 gene 140
A novel mutation in a large italian pedigree 140
Guidelines for the diagnosis of dementia and Alzheimer’s disease 135
A novel Italian PSEN2 mutation with behavioral phenotype 133
Visual hallucinations with sertraline 132
AD: role of clinical examinations in predicting neurpathological features 132
Mutant prion protein expression causes motor and memory deficits and abnormal sleep patterns in a transgenic mouse model 132
Doxycycline in Creutzfeldt-Jakob disease: A phase 2, randomised, double-blind, placebo-controlled trial 132
Analisi di linkage in Famiglie di Origine Italiana con Malattia di Alzheimer 132
Cognitive deficits in familial Alzheimer's disease associated with M239V mutation of presenilin 2 126
Are premorbid personality traits linked to the risk of Alzheimer's disease? A case series of subjects with familial mutation 125
An Italian family with Alzhiemer’s disease and M239V mutation in PS2 123
Alzheimer disease: APP mutations are associated with high percentage of cerebral amyloid deposits containing Aβ40 123
Presenilin 2 mutation does not influence expression and concentration of APP forms in human platelets 123
Angiotensin converting enzyme gene polymorphism in Presenilin linked Familial Alzhiemer’s Disease and Sporadic Alzheimer’s Disease 122
Absence of association between intronic polymorphism in PS-1 gene and Alzheimer’s disease in Italian patients 121
Regression of chronic posterior leukoencephalopathy after stop of methotrexate treatment 121
Variability of the clinical phenotype in an Italian family with dementia associated with an intronic deletion in the GRN gene 121
Demenze degenerative primarie 121
PEN-2 gene mutation in a familial Alzheimer's disease case 120
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 119
Nicastrin gene in familial and sporadic Alzheimer's disease 117
Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPSc 117
Angiotensin converting enzyme gene polymorphism in Presenilin linked Familial Alzhiemer’s Disease and Sporadic Alzheimer’s Disease 117
A betaPP peptide carboxyl-terminal to Abeta is neurotoxic 117
Familial frontotemporal dementia associated with the novel MAPT mutation T427M 116
Angiotensin converting enzyme gene polymorphism in Presenilin linked Familial Alzhiemer’s Disease and Sporadic Alzheimer’s Disease 116
Angiotensin Converting Enzyme polymorphism in sporadic and Presenilin linked Alzheimer’s disease families 115
Diagnosis of Alzheimer's disease 115
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 113
Memantine effects on behaviour in moderately severe to severe Alzheimer's disease: a post-marketing surveillance study 111
Angiotensin converting enzyme gene polymorphism in Presenilin linked Familial Alzhiemer’s Disease and Sporadic Alzheimer’s Disease 111
Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 gene 111
ASSOCIATION BETWEEN 5-HT(2A) RECEPTOR POLYMORPHISM AND PSYCHOTIC SYMPTOMS IN ALZHEIMER'S DISEASE 111
Late onset neurodegenerative diseases: A theoretical point of view 110
Tetracyclines and prion infectivity 109
Angiotensin converting enzyme gene polymorphism in Presenilin linked Familial Alzhiemer’s Disease and Sporadic Alzheimer’s Disease 109
Paraneoplastic cerebellar degeneration associated with anti-neuronal anti-Tr antibodies in a patient with Hodgkin's disease 108
Factors associated with complex visual hallucinations during antidepressant treatment 105
Oral microbiota profile is related to cognitive status in centenarians: a clinical and biological study 104
HLA A2 allele is associated with age at onset of Alzheimer's disease 104
Atypical tauopathy with massive involvement of the white matter 102
PURE, ACUTE CEREBELAR SYNDROME ASSOCIATED WITH CYCLOSPORINE TREATMENT IN AN ADULT LIVER TRANSPLANT RECIPIENT 96
Il polimorfismo dell’ alfa-1 antichimotripsina nella forma familiare della Malattia di Alzheimer 96
Subacute spongiform encephalopaty assiciated with amyloid deposits 93
Le angioti isolate del Sistema Nervoso Centrale (AIC) considerazioni clinico-radiologiche 92
Presenilin genes analysis in Italian families with early-onset Alzheimer’s Disease 92
Degenerazione paraneoplastica cerebellare in un caso di linfoma di Hodgkin in remissione completa 91
Il polimorfismo dell’α1-antichimotripsina nella forma familiare della Malattia di Alzheimer 91
IL TRATTAMENTO FARMACOLOGICO DELLA MALATTIA DI ALZHEIMER 90
Linkage Analysis in familial Alzheimer Disease 90
Presenilin gene analysis in Italian familieswith early-onset Alzheimer’s disease 89
Pure acute cerebellar syndrome associated with cyclosporine treatmentin an adult liver transplant recipient 89
What do we learn from the clinical and biological evaluation of the oral cavity in centenarians? 89
Cytoskeletal markers in developmental disorders of human CNS 88
Influence of masticatory function on food preferences and cognitive performance in centenarians: an observational study 87
Presenilin genes and Alzheimer’s disease 83
Expression of c-sis oncogene products in peripheral nerve tissue 83
bPP and Tau interaction in vitro 83
Neocortical Variation of Abeta Load in Fully Expressed, Pure Alzheimer's Disease 82
No association between 2 Macroglobulin DNA polymorphism and sporadic Alzheimer’s Disease in Italy 82
Localisation of presenilin 2 in human and rodent pancreatic islet beta-cells; Met239Val presenilin 2 variant is not associated with diabetes in man 81
Presenilin genes analysis in Italian families with early onset Alzheimer’s disease 81
Hereditary demyelinating neuropathies: autosomic recessive and sporadic forms 81
Prominent tau deposits in the white matter glia in an atypical sporadic tauopathy 81
Le Sinucleinopatie 80
La Malattia di Alzheimer ad insorgenza precoce e tardiva: analisi di linkage con marker anonimi del cromosoma 21 80
The Folding and Maturation of Amyloid Precursor Protein in ER Stress Conditions 79
Enzyme polymorphism in presenilin linked Alzheimer’s disease families and sporadic Alzheimer’s disease 79
Presenilin genes and Alzheimer’s disease 79
Encefalopatia acuta convulsivante dopo iniezione con Anatetall 78
Expression of tumor necrosis factor- and its receptors in Amyotrophic Lateral Sclerosis 78
Hypomyelination neuropathy in an adult 76
La depressione nelle malattie di Alzheimer e di Parkinson. 76
Experience with phosphatidylserine treatment of patients with cognitive and behavioral decline 75
Association between 5-HT2A receptor polymorphism and psychotic symptoms in Alzheimer’s disease 75
Mutation analysis in familial Alzheimer’s disease 74
Clinical – neuropathological correlations in Alzheimer’s disease: description of seven cases 74
Familial Frontotemporal Dementia Associated with Novel Tau Mutation T427M 74
Genetic and phenotypical analysis of presenilin genes-linked Familial Alzheimer’s disease in Italian kindreds 73
Clinical and neuropathological findings of an Italian Family with Alzheimer’s disease and M239V mutation of PS2 gene 73
Caspase-3 is activated in Alzheimer’s disease but not in Frontotemporal Dementia 73
Correlati neuropsicologici e personologici premorbosi in una famiglia Italiana con Malattia di Alzheimer con mutazione M239V nel gene PS-2 72
Bilateral scopolamine mydriasis in a traveller 72
Due casi familiari di parkinsonismi primari 72
Neuropsychological impairment in chronic brain diseases: comparison of metabolic encephalopahies with vascular encephalopahies and degenerative dementia 72
Nicastrin gene in familial Alzheimer’s Disease 72
Implication of α1-antichimotrypsin polymorphism in familial Alazheimer’s disease 71
Totale 11.219
Categoria #
all - tutte 48.346
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 48.346


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022698 0 0 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
2025/20264.519 290 239 387 922 377 226 502 208 509 624 135 100
2026/2027771 192 188 391 0 0 0 0 0 0 0 0 0
Totale 12.715