MARCON, Gabriella
 Distribuzione geografica
Continente #
NA - Nord America 4.931
EU - Europa 990
AS - Asia 429
Continente sconosciuto - Info sul continente non disponibili 5
SA - Sud America 4
AF - Africa 1
Totale 6.360
Nazione #
US - Stati Uniti d'America 4.885
UA - Ucraina 347
CN - Cina 272
DE - Germania 195
IT - Italia 118
IE - Irlanda 106
FI - Finlandia 89
VN - Vietnam 64
SE - Svezia 55
CA - Canada 46
TR - Turchia 37
GB - Regno Unito 29
IN - India 27
FR - Francia 23
BE - Belgio 13
IR - Iran 10
HK - Hong Kong 9
NL - Olanda 7
EU - Europa 5
MY - Malesia 5
BO - Bolivia 3
RU - Federazione Russa 3
TW - Taiwan 3
IL - Israele 2
CH - Svizzera 1
CL - Cile 1
ES - Italia 1
HR - Croazia 1
NO - Norvegia 1
RO - Romania 1
TG - Togo 1
Totale 6.360
Città #
Fairfield 613
Woodbridge 536
Houston 463
Ashburn 452
Dearborn 336
Chandler 295
Ann Arbor 293
Seattle 286
Wilmington 257
Jacksonville 247
Cambridge 230
Beijing 131
Princeton 111
Dublin 106
Dong Ket 63
San Diego 48
Ottawa 40
Izmir 37
Washington 28
Nanjing 24
Udine 24
Des Moines 21
Boardman 18
Kunming 18
Norwalk 18
Augusta 17
Venezia 16
Trieste 15
Hefei 14
Brussels 12
Ogden 12
Guangzhou 10
Leawood 9
Los Angeles 8
New York 8
Jinan 7
Nanchang 7
San Mateo 7
Grafing 6
Shanghai 6
Chengdu 5
Shenyang 5
Toronto 5
Chongqing 4
Ipoh 4
Isfahan 4
Monmouth Junction 4
Pavia 4
Phoenix 4
Xian 4
Ardabil 3
Codroipo 3
Harbin 3
Helsinki 3
Indiana 3
La Paz 3
Milan 3
Mumbai 3
Niccolo 3
Redwood City 3
Sabz 3
Taipei 3
Venice 3
Wuhan 3
Zhengzhou 3
Bhubaneswar 2
Bologna 2
Charlotte 2
Fuzhou 2
Hamburg 2
Hong Kong 2
Huzhou 2
Jerusalem 2
Magenta 2
Romainville 2
Saint Petersburg 2
Tavagnacco 2
Andover 1
Auburn Hills 1
Bangalore 1
Baotou 1
Bisenti 1
Cedar Knolls 1
Changsha 1
Côré 1
Dallas 1
Eindhoven 1
Fano 1
Hangzhou 1
Hanoi 1
Hebei 1
Kirkcaldy 1
Knoxville 1
Lausanne 1
Lomé 1
Montreal 1
Nanning 1
Ningbo 1
Oederan 1
Oslo 1
Totale 4.984
Nome #
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. 152
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. 144
Nicastrin gene in familial and sporadic Alzheimer's disease 133
ASSOCIATION BETWEEN 5-HT(2A) RECEPTOR POLYMORPHISM AND PSYCHOTIC SYMPTOMS IN ALZHEIMER'S DISEASE 131
Diagnosis of Alzheimer's disease 127
APE1/Ref-1 regulates PTEN expression mediated by EGR-1 126
Bilateral scopolamine mydriasis in a traveller 123
Role of circulating factors in cardiac aging 120
Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPSc 120
Doxycycline in Creutzfeldt-Jakob disease: A phase 2, randomised, double-blind, placebo-controlled trial 116
Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 gene 115
Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP 115
Cognitive deficits in familial Alzheimer's disease associated with M239V mutation of presenilin 2 115
Is Parkinson's Disease a Very Rare Pathology in Centenarians? A Clinical Study in a Cohort of Subjects. 115
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant 114
How experience modulates semantic memory for food: Evidence from elderly adults and centenarians 112
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 108
A betaPP peptide carboxyl-terminal to Abeta is neurotoxic 105
Factors associated with complex visual hallucinations during antidepressant treatment 103
Paraneoplastic cerebellar degeneration associated with anti-neuronal anti-Tr antibodies in a patient with Hodgkin's disease 102
Cohort profile: ‘Centenari a Trieste’ (CaT), a study of the health status of centenarians in a small defined area of Italy 102
Variability of the clinical phenotype in an Italian family with dementia associated with an intronic deletion in the GRN gene 101
Risk of dementia and death in patients with atrial fibrillation: A competing risk analysis of a population-based cohort 100
Demenze degenerative primarie 93
APE1/Ref-1 in Alzheimer's disease: An immunohistochemical study 92
HLA A2 allele is associated with age at onset of Alzheimer's disease 92
Guidelines for the diagnosis of dementia and Alzheimer’s disease 89
Memantine effects on behaviour in moderately severe to severe Alzheimer's disease: a post-marketing surveillance study. 88
Serotoninergic fibres form dense synaptic contacts with Purkinje cells in the mouse cerebellar cortex--an immunohistochemical study 84
Familial frontotemporal dementia associated with the novel MAPT mutation T427M 83
A novel PSEN2 mutation associated with a peculiar phenotype. 83
Atypical tauopathy with massive involvement of the white matter. 79
Are premorbid personality traits linked to the risk of Alzheimer's disease? A case series of subjects with familial mutation 77
Tetracyclines and prion infectivity 75
Regression of chronic posterior leukoencephalopathy after stop of methotrexate treatment. 74
Drug points: Bilateral scopolamine mydriasis in a traveller 73
Visual hallucinations with sertraline 72
Localisation of presenilin 2 in human and rodent pancreatic islet beta-cells; Met239Val presenilin 2 variant is not associated with diabetes in man 72
PEN-2 gene mutation in a familial Alzheimer's disease case 71
Late onset neurodegenerative diseases: A theoretical point of view 70
Mutant prion protein expression causes motor and memory deficits and abnormal sleep patterns in a transgenic mouse model. 70
Presenilin 2 mutation does not influence expression and concentration of APP forms in human platelets 68
Association between 5-HT2A receptor polymorphism and psychotic symptoms in Alzheimer’s disease 67
Experience with phosphatidylserine treatment of patients with cognitive and behavioral decline 65
Clinical phenotypic variability in an Italian family bearing the IVS6+ 5_8delGTGA mutation in PGRN gene 64
Amyotrophic Lateral Sclerosis, a Multisystem Pathology: Insights into the Role of TNFα 61
Differences in educational level and association with dementia prevalence in two centenarian cohorts in Italy: The Monzino 80-plus Study and the Centenari a Trieste Study 61
P4-136 Nicastrin mutation (N417Y) is a risk factor in Alzheimer's disease 61
Brainstem Sparing in Human Prion Disease: Sleep and Autonomic Function in a Long Survival Case Report 58
A novel Italian PSEN2 mutation with behavioral phenotype 54
Linkage Analysis in Italian Pedigrees with Autosomal Dominant Familial Alzheimer’s Disease 54
Implication of alpha1-antichymotrypsin polymorphism in familial Alzheimer's disease 53
IL TRATTAMENTO FARMACOLOGICO DELLA MALATTIA DI ALZHEIMER. 51
Neocortical Variation of Abeta Load in Fully Expressed, Pure Alzheimer's Disease 51
APOLIPOPROTEIN E AND INFLAMMATORY CYTOKINES PROMOTER GENOTYPING IN A GROUP OF CENTENARIANS FROM THE “CaT: Centenari a Trieste” ONGOING STUDY 49
ANALYSIS OF CHROMOSOME-21 LINKAGE IN FAMILIAL ALZHEIMERS-DISEASE 48
Angiotensin converting enzyme gene polymorphism in Presenilin linked Familial Alzhiemer’s Disease and Sporadic Alzheimer’s Disease 47
Association between 5-HT 2° receptor polymorphism and psychotic symptoms in Alzheimer’s Disease 46
Cognitive impairment and oral macrobiome analysis in centenarians from CaT Study: preliminary data 44
A novel missense mutation in PSEN2 gene associated with a clinical phenotype of frontotemporal dementia 43
Angiotensin converting enzyme gene polymorphism in Presenilin linked Familial Alzhiemer’s Disease and Sporadic Alzheimer’s Disease 43
Hereditary demyelinating neuropathies: autosomic recessive and sporadic forms 43
COVID-19 MORTALITY IN LOMBARDY: THE VULNERABILITY OF THE OLDEST OLD AND THE RESILIENCE OF MALE CENTENARIANS 41
Neuropsychological and psychometric findings in a large Italian Family with the M239V mutation of the PSEN2 gene 40
Clinical and neuropathological findings of an Italian Family with Alzheimer’s disease and M239V mutation of PS2 gene 40
An Italian family with Alzhiemer’s disease and M239V mutation in PS2 40
DIFFERENTIAL EXPRESSION OF PERILIPINS IN HUMAN BRAIN DURING NORMAL AND PATHOLOGICAL AGING 39
Mental disorders associated with benzodiazepine use among older primary care attenders A regional survey 37
“CAT: CENTENARI A TRIESTE”: A STUDY FOR A CLINICAL-BIOLOGICAL AND PSYCHO-SOCIAL DATABASE OF THE CENTENARIAN POPULATION IN TRIESTE 37
PURE, ACUTE CEREBELAR SYNDROME ASSOCIATED WITH CYCLOSPORINE TREATMENT IN AN ADULT LIVER TRANSPLANT RECIPIENT 36
NEUROPATHOLOGIC FEATURES OF CENTENARIANS. 35
Clinical and neuropathologic phenotype of a large Italian kindred with presenilin2 mutation M239V 35
Angiotensin converting enzyme polymorphism in sporadic and presenilin-linked Alzheimer's disease families 35
null 34
Expression of c-sis oncogene products in peripheral nerve tissue 33
CaT “Centenari a Trieste” and Sardinian Longevity Blue Zones Studies: the creation of database and comparison between two Italian centenarian populations 32
Hypomyelination neuropathy in an adult 32
Clinical – neuropathological correlations in Alzheimer’s disease: description of seven cases 32
Cytoskeletal markers in developmental disorders of human CNS 31
PRION PROTEIN GENE ANALYSIS IN PRE-SENILE DEMENTING AND ATAXlC 31
Subacute spongiform encephalopaty assiciated with amyloid deposits 30
Lifestyle in middle age and dementia in centenarians in the CaT Study: a preliminary report. 29
Neuropsychological impairment in chronic brain diseases: comparison of metabolic encephalopahies with vascular encephalopahies and degenerative dementia 28
Expression of tumor necrosis factor-alfa and its receptors in amyotrophic lateral sclerosis 28
Expression of tumor necrosis factor- and its receptors in Amyotrophic Lateral Sclerosis 28
Enzyme polymorphism in presenilin linked Alzheimer’s disease families and sporadic Alzheimer’s disease 28
AD: role of clinical examinations in predicting neurpathological features 27
The Folding and Maturation of Amyloid Precursor Protein in ER Stress Conditions 27
Alzheimer disease: APP mutations are associated with high percentage of cerebral amyloid deposits containing Aβ40 27
Memantine in moderately-severe-to-severe Alzheimer's disease: a postmarketing surveillance study. 27
Neurotoxicity of a bPP peptide other than Ab 26
Clinico-Neuropathological correlations in AD 26
Implication of α1-antichimotrypsin polymorphism in familial Alazheimer’s disease 25
Prominent tau deposits in the white matter glia in an atypical sporadic tauopathy 25
The intronic polymorphism in presenilin-1 gene in familial Alzheimer’s disease with pathogenetic mutations in amyloid precursor protein and presenilin 1 and 2 genes 25
Neuropathologic features of two semi-supercentenarians 24
Presenilin gene analysis in Italian familieswith early-onset Alzheimer’s disease 24
Expression of activated caspase-3 in Alzheimer’s Disease and in Frontotemporal Dementia 24
Genetic and phenotypical analysis of presenilin genes-linked Familial Alzheimer’s disease in Italian kindreds 24
La terapia nella malattia di Alzheimer 24
Totale 6.433
Categoria #
all - tutte 23.304
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 23.304


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019133 0 0 0 0 0 0 0 0 0 0 0 133
2019/20202.285 295 155 91 258 189 398 277 196 144 147 40 95
2020/20211.059 49 81 52 139 38 118 53 131 112 38 141 107
2021/2022731 26 92 28 68 6 24 36 56 9 138 108 140
2022/2023735 119 58 8 77 77 226 0 34 89 12 14 21
2023/2024456 33 19 36 19 77 158 7 64 17 12 12 2
Totale 6.653