TEDDE, ANDREA
 Distribuzione geografica
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Continente #
NA - Nord America 6.517
EU - Europa 3.335
AS - Asia 2.075
SA - Sud America 254
AF - Africa 64
OC - Oceania 49
Continente sconosciuto - Info sul continente non disponibili 1
Totale 12.295
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Nazione #
US - Stati Uniti d'America 6.444
RU - Federazione Russa 1.184
IT - Italia 658
SG - Singapore 612
CN - Cina 492
HK - Hong Kong 363
SE - Svezia 317
IE - Irlanda 277
PL - Polonia 263
VN - Vietnam 219
BR - Brasile 193
DE - Germania 179
KR - Corea 164
UA - Ucraina 122
FR - Francia 109
FI - Finlandia 96
GB - Regno Unito 67
IN - India 58
AU - Australia 46
CA - Canada 38
TR - Turchia 31
JO - Giordania 23
AR - Argentina 21
IQ - Iraq 19
MX - Messico 14
BD - Bangladesh 13
BE - Belgio 11
CI - Costa d'Avorio 11
JP - Giappone 11
ZA - Sudafrica 11
NL - Olanda 10
ES - Italia 9
CO - Colombia 8
ID - Indonesia 8
CH - Svizzera 7
CL - Cile 7
EC - Ecuador 7
KE - Kenya 7
KG - Kirghizistan 7
PK - Pakistan 7
SA - Arabia Saudita 7
PH - Filippine 6
SC - Seychelles 6
VE - Venezuela 6
DZ - Algeria 5
EG - Egitto 5
LT - Lituania 5
NG - Nigeria 5
TH - Thailandia 5
TN - Tunisia 5
JM - Giamaica 4
MA - Marocco 4
PE - Perù 4
AT - Austria 3
AZ - Azerbaigian 3
BO - Bolivia 3
CR - Costa Rica 3
CZ - Repubblica Ceca 3
IL - Israele 3
MY - Malesia 3
NO - Norvegia 3
NP - Nepal 3
NZ - Nuova Zelanda 3
OM - Oman 3
PA - Panama 3
UY - Uruguay 3
AE - Emirati Arabi Uniti 2
BG - Bulgaria 2
BH - Bahrain 2
HN - Honduras 2
KZ - Kazakistan 2
LB - Libano 2
PR - Porto Rico 2
PY - Paraguay 2
RO - Romania 2
SV - El Salvador 2
TT - Trinidad e Tobago 2
AL - Albania 1
AM - Armenia 1
BJ - Benin 1
BY - Bielorussia 1
CG - Congo 1
CY - Cipro 1
DO - Repubblica Dominicana 1
EE - Estonia 1
ET - Etiopia 1
EU - Europa 1
GE - Georgia 1
GT - Guatemala 1
IR - Iran 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
LI - Liechtenstein 1
LV - Lettonia 1
LY - Libia 1
NI - Nicaragua 1
RS - Serbia 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
Totale 12.294
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Città #
Santa Clara 1.089
Ashburn 667
Fairfield 605
Singapore 428
Chandler 399
Hong Kong 310
Woodbridge 306
Dublin 276
Seattle 265
Warsaw 261
Cambridge 250
Houston 232
Dallas 222
Jacksonville 206
Wilmington 203
Beijing 165
Seoul 162
San Jose 159
Ann Arbor 139
Altamura 127
Milan 125
Dearborn 124
Lawrence 111
Buffalo 104
Princeton 80
The Dalles 77
Los Angeles 71
Ho Chi Minh City 68
Lauterbourg 67
Boardman 59
Rome 50
Boston 49
Hanoi 47
Melbourne 45
Munich 41
Medford 38
Hefei 35
Mumbai 35
San Diego 35
Florence 32
Moscow 32
New York 32
Bremen 27
Izmir 26
Shanghai 25
São Paulo 22
Naples 20
Orem 18
Kent 17
Council Bluffs 16
Turku 15
Auburn Hills 13
Norwalk 13
Bologna 12
Chicago 12
Helsinki 12
Paris 12
Abidjan 11
Brussels 11
Frankfurt am Main 11
London 11
Toronto 11
Figino 10
Guangzhou 10
Phoenix 10
Tokyo 10
Hillsboro 9
Miano 9
Montreal 9
Redondo Beach 9
Bari 8
Brooklyn 8
Da Nang 8
Haiphong 8
Pune 8
San Giuseppe Vesuviano 8
Turin 8
Verona 8
Bishkek 7
Biên Hòa 7
Cagliari 7
Clifton 7
Denver 7
Jinan 7
Kunming 7
Manchester 7
Bern 6
Catania 6
Nanjing 6
Palermo 6
Poplar 6
Rio de Janeiro 6
Yubileyny 6
Andover 5
Atlanta 5
Baghdad 5
Da Lat 5
Falls Church 5
Frankfurt Am Main 5
Fuzhou 5
Totale 8.416
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Nome #
Low Florbetapir PET Uptake and Normal Aβ1-42 Cerebrospinal Fluid in an APP Ala713Thr Mutation Carrier 336
Association Study of Genetic Variants in CDKN2A/CDKN2B genes/Loci with Late-Onset Alzheimer's Disease 298
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. 251
A2 macroglobulin polymorphisms in Italian sporadic and familial Alzheimer’s disease 226
Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline 220
Association analysis of the paraoxonase-1 gene with Alzheimer's disease 216
A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia. 212
Association of the Variant Cys139Arg at GRN Gene to the Clinical Spectrum of Frontotemporal Lobar Degeneration 212
Ataxia-telangiectasia mutated (ATM) genetic variant in Italian centenarians 211
A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset. 207
Screening for mutations in the neurofibromatosis type 2 (NF2) gene in sporadic meningiomas. 207
Brain-derived neurotrophic factor, apolipoprotein E genetic variants and cognitive performance in Alzheimer's disease. 203
A case of atypical early-onset Alzheimer’s disease carrying the missense mutation Thr354Ile in exon 10 of the PSEN1 gene 203
Association of IL10 promoter polymorphism in Italian Alzheimer's disease. 201
5-HT2A receptor gene polymorphisms in anorexia nervosa and bulimia nervosa 200
Analysis of the neurofibromatosis type 2 gene in different human tumors of neuroectodermal origin. 198
Identification of new presenilin gene mutations in early-onset familial Alzheimer disease 194
5-HT2A promoter polymorphism in anorexia nervosa. 189
Fragile X premutation with atypical symptoms at onset. 186
Implication of serotonin-transporter (5-HTT) gene polymorphism in subjective memory complaints and mild cognitive impairment (MCI). 185
Cathepsin D polymorphism in Italian sporadic and familial Alzheimer's disease. 183
No implication of apolipoprotein E polymorphism in Italian schizophrenic patients. 181
Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity 175
Imaging and Cognitive Reserve Studies Predict Dementia in Presymptomatic Alzheimer's Disease Subjects. 175
Progranulin genetic screening in frontotemporal lobar degeneration patients from central Italy. 174
Implication of sex and SORL1 variants in italian patients with Alzheimer disease. 173
Glucocorticoid receptor gene polymorphisms in Italian patients with eating disorders and obesity. 171
Implication of alpha1-antichymotrypsin polymorphism in familial Alzheimer's disease. 169
Lack of SOD1 gene mutations and activity alterations in two Italian families with amyotrophic lateral sclerosis 169
Psychosis, serotonin receptor polymorphism and Alzheimer's disease 168
Presenilin-1 gene intronic polymorphism in sporadic and familial Alzheimer's disease. 166
Cholesteryl ester transfer protein (CETP) I405V polymorphism and longevity in Italian centenarians. 166
Brain metabolic decreases related to the dose of the ApoE e4 allele in Alzheimer's disease. 164
Analysis of apolipoprotein E, alpha1-antichymotrypsin and presenilin-1 genes polymorphisms in dementia caused by normal pressure hydrocephalus in man. 162
Brain-derived neurotrophic factor genetic variants are notsusceptibility factors to Alzheimer's disease in Italy. 162
Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease. 161
Lack of association between the CYP46 gene polymorphism and Italian late-onset sporadic Alzheimer's disease 161
Psychopathological traits and 5-HT2A receptor promoter polymorphism (-1438 G/A) in patients suffering from Anorexia Nervosa and Bulimia Nervosa. 158
The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer's disease 155
Semantic dementia associated with mutation V363I in the tau gene. 153
DAPK1 is Associated with FTD and not with Alzheimer's Disease 153
Insulin degrading enzyme and alpha-3 catenin polymorphisms in italian patients with Alzheimer disease 152
No association between the LRRK2 G2019S mutation and Alzheimer's disease in Italy. 152
Genetics of Alzheimer's Disease and Frontotemporal Dementia 151
Lack of association between NOS3 poly morphism and Italian sporadic and familial Alzheimer's disease. 151
Apolipoprotein E and alpha1-antichymotrypsin polymorphism in Alzheimer's disease. 150
Fibroblasts from PS1 mutated pre-symptomatic subjects and Alzheimer's disease patients share a unique protein levels profile 148
Cystatin C and apoe polymorphisms in Italian Alzheimer'sdisease. 148
Interleukin-10 promoter polymorphisms influence susceptibility to ulcerative colitis in a gender-specific manner. 148
Genetic risk factors in familial Alzheimer's disease 148
The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family 147
KIBRA gene variants are associated with episodic memory performance in subjective memory complaints. 145
Absence of association between intronic polymorphism in PS-1 gene and alzheimer's disease in italian patients 144
Association between 5-HT2A receptor polymorphism and psychotic symptoms in Alzheimer’s disease 141
Novel presenilin 1 mutation (Ile408Thr) in an Italian family with late-onset Alzheimer's disease 141
Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease-like and ataxia 140
Suitability of neuropsychological tests in patients with vascular dementia (VaD). 140
Mutation analysis of patients with neurodegenerative disorders using NeuroX array 137
Different implication of NEDD9 genetic variant in early and late-onset Alzheimer's disease 137
Genetic Analysis of familial and sporadic cases of spinocerebellar ataxias in Italian patients 137
Implication of GAB2 Gene Polymorphism in Italian Patients with Alzheimer's Disease 135
Clinical and genetic analysis of hereditary and sporadic ataxia in central Italy. 134
Epigenetic modifications in Alzheimer's disease: Cause or effect? 132
Clinical and genetic analysis of a Machado-Joseph Italian family 130
A novel PS-1 mutation in an Italian AD family with psychotic symptoms at onset 129
Genetica della malattia di Alzheimer 128
Mutational screening analysis of DHCR24/seladin-1 gene in Italian familial Alzheimer's disease. 128
Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis 127
Tomm40 polymorphisms in Italian Alzheimer’s disease and frontotemporal dementia patients 127
Cholesteryl ester transfer protein (CETP) I405V polymorphism in Italian memory complainers 126
SNPs in neurotrophin system genes and Alzheimer's disease in an Italian population. 125
Lack of association between TNF-alpha polymorphisms and Alzheimer's disease in an Italian cohort 114
Genetic and clinical analysis of SCA8 repeat expansion 109
Implication of a genetic variant at PICALM in Alzheimer’s disease patients and centenarians 94
Common phenotypes in Huntington’s disease like and spinocerebellar ataxia type 17 patients 19
Totale 12.368
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Categoria #
all - tutte 34.662
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 34.662
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022565 28 62 48 20 6 13 34 40 7 16 133 158
2022/20231.511 132 332 46 186 94 271 170 79 139 11 33 18
2023/2024400 24 49 67 26 42 38 22 88 5 2 30 7
2024/20253.125 95 340 228 467 910 450 22 246 129 66 92 80
2025/20263.358 390 460 345 167 413 149 422 131 184 203 46 448
2026/202757 57 0 0 0 0 0 0 0 0 0 0 0
Totale 12.368