PIACENTINI, SILVIA
 Distribuzione geografica
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Continente #
NA - Nord America 10.508
EU - Europa 5.576
AS - Asia 3.463
SA - Sud America 437
AF - Africa 113
OC - Oceania 85
Continente sconosciuto - Info sul continente non disponibili 62
Totale 20.244
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Nazione #
US - Stati Uniti d'America 10.360
RU - Federazione Russa 1.950
IT - Italia 1.117
SG - Singapore 925
HK - Hong Kong 745
CN - Cina 724
PL - Polonia 503
SE - Svezia 501
IE - Irlanda 493
VN - Vietnam 386
BR - Brasile 344
KR - Corea 283
DE - Germania 240
UA - Ucraina 230
FI - Finlandia 171
FR - Francia 151
GB - Regno Unito 142
IN - India 119
CA - Canada 88
AU - Australia 79
TR - Turchia 71
JO - Giordania 43
AR - Argentina 35
BD - Bangladesh 26
CI - Costa d'Avorio 22
ZA - Sudafrica 22
JP - Giappone 21
IQ - Iraq 19
MX - Messico 19
NL - Olanda 18
EC - Ecuador 17
ES - Italia 15
NG - Nigeria 13
ID - Indonesia 12
PK - Pakistan 12
CO - Colombia 11
SC - Seychelles 11
UZ - Uzbekistan 10
VE - Venezuela 10
BE - Belgio 9
KG - Kirghizistan 9
LT - Lituania 8
PE - Perù 8
PH - Filippine 8
TN - Tunisia 8
AE - Emirati Arabi Uniti 7
BH - Bahrain 6
JM - Giamaica 6
MA - Marocco 6
NZ - Nuova Zelanda 6
PR - Porto Rico 6
SN - Senegal 6
TT - Trinidad e Tobago 6
BG - Bulgaria 5
BJ - Benin 5
CR - Costa Rica 5
EG - Egitto 5
EU - Europa 5
KE - Kenya 5
NP - Nepal 5
OM - Oman 5
PY - Paraguay 5
SA - Arabia Saudita 5
UY - Uruguay 5
AZ - Azerbaigian 4
HN - Honduras 4
TH - Thailandia 4
BY - Bielorussia 3
GT - Guatemala 3
IL - Israele 3
MY - Malesia 3
PA - Panama 3
BS - Bahamas 2
CL - Cile 2
CW - ???statistics.table.value.countryCode.CW??? 2
CZ - Repubblica Ceca 2
DZ - Algeria 2
EE - Estonia 2
ET - Etiopia 2
KZ - Kazakistan 2
LY - Libia 2
MK - Macedonia 2
NO - Norvegia 2
RO - Romania 2
SV - El Salvador 2
TW - Taiwan 2
AI - Anguilla 1
AL - Albania 1
AM - Armenia 1
AT - Austria 1
BA - Bosnia-Erzegovina 1
BF - Burkina Faso 1
CG - Congo 1
CH - Svizzera 1
CU - Cuba 1
DO - Repubblica Dominicana 1
GA - Gabon 1
HU - Ungheria 1
LA - Repubblica Popolare Democratica del Laos 1
LI - Liechtenstein 1
Totale 20.181
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Città #
Santa Clara 1.883
Ashburn 939
Fairfield 900
Hong Kong 639
Chandler 609
Singapore 590
Warsaw 496
Dublin 491
Woodbridge 425
Cambridge 398
Seattle 383
Jacksonville 380
San Jose 339
Wilmington 328
Houston 313
Seoul 280
Beijing 244
Milan 238
Ann Arbor 161
Council Bluffs 158
Dearborn 158
Los Angeles 143
Dallas 141
Princeton 135
Ho Chi Minh City 133
Buffalo 123
Altamura 121
Lawrence 121
The Dalles 118
Rome 113
Lauterbourg 109
Boardman 96
Hanoi 87
Medford 80
Mumbai 80
Melbourne 78
Boston 72
Hefei 68
Moscow 61
Izmir 57
Florence 55
New York 52
San Diego 52
Munich 44
Phoenix 36
Chicago 32
Shanghai 32
Helsinki 31
Kent 31
Naples 30
Norwalk 29
São Paulo 28
Columbus 24
Da Nang 23
Abidjan 22
Bologna 22
Tokyo 20
Toronto 20
Turin 19
Bremen 18
Brooklyn 18
Guangzhou 18
Orem 18
London 17
Turku 17
Hillsboro 16
Palermo 16
Falls Church 15
Genoa 15
Auburn Hills 14
Jinan 13
Manchester 13
Montreal 13
Johannesburg 12
Nanjing 12
Washington 12
Abuja 11
Haiphong 11
Kunming 11
Verona 11
Andover 10
Charlotte 10
Yubileyny 10
Belo Horizonte 9
Bishkek 9
Biên Hòa 9
Brussels 9
Chennai 9
Denver 9
Frankfurt Am Main 9
Frankfurt am Main 9
Guayaquil 9
Salerno 9
Stockholm 9
Tashkent 9
Brasília 8
Catania 8
Dong Ket 8
Miano 8
Padua 8
Totale 13.369
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Nome #
NMDA receptor gene variations as modifiers in Huntington disease: a replication study. 356
Time perception impairment in early-to-moderate stages of Huntington's disease is related to memory deficits 333
Progression of brain atrophy in spinocerebellar ataxia type 2: A longitudinal tensor-based morphometry study 328
Suicidal ideation in a European Huntington's disease population 296
Huntington’s disease and Scalar Expectancy Theory: A memory-based time perception deficit 269
Trapianto intracerebrale di striato fetale nella malattia di Huntington: un aggiornamento dell'esperienza clinica italiana 256
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study 246
ADC mapping of neurodegeneration in the brainstem and cerebellum of patients with progressive ataxias. 226
Association analysis of the paraoxonase-1 gene with Alzheimer's disease 223
A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia. 219
Huntington disease: Volumetric, diffusion-weighted, and magnetization transfer MR imaging of brain 218
Clinical and genetic characteristics of late-onset Huntington's disease 214
A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset. 211
Abnormalities of mitochondrial enzymes in hereditary ataxias. 207
Association of IL10 promoter polymorphism in Italian Alzheimer's disease. 207
Lack of efficacy of phosphatidylcholine in ataxias. 203
Abnormal platelet glutamate dehydrogenase activity and activation in dominant and nondominant olivopontocerebellar atrophy. 199
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion 199
Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Italy 195
Double-blind, crossover, placebo-controlled clinical trial with L-acetylcarnitine in patients with degenerative cerebellar ataxia. 193
Fragile X premutation with atypical symptoms at onset. 193
Alzheimer skin fibroblasts show increased susceptibility to free radicals. 191
No implication of apolipoprotein E polymorphism in Italian schizophrenic patients. 190
ApoE genotype and familial Alzheimer's disease: a possible influence on age of onset in APP717 Val-->Ile mutated families. 188
Influence of impaired T- and B-cell compartments on efficacy of IVIg in dysimmune neuropathies. 185
Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity 183
Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease 183
Atypical Friedreich ataxia with a very late onset and an unusual limited GAA repeat. 181
Implication of sex and SORL1 variants in italian patients with Alzheimer disease. 180
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant. 180
Assessment of brain white matter fiber bundle atrophy in patients with Friedreich ataxia. 180
Human fetal striatal transplantation in disease. First italian clinic trial at the University of Florence. Preliminare Report 179
Alterations in metabolic properties in fibroblasts in Alzheimer disease. 179
APP717 and Alzheimer's disease in Italy 178
Human striatal neuroblasts develop and build a striatal-like structure into the brain of Huntington's disease patients after transplantation. 178
Risperidone in idiopathic and symptomatic dystonia: preliminary experience. 177
Progranulin genetic screening in frontotemporal lobar degeneration patients from central Italy. 177
Neurodegeneration in Friedreich’s ataxia is associated with a mixed activation pattern of the brain. A fMRI study 177
Trapianto di tessuto striatale fetale umano nella malattia di Huntington. Primi risultati del trial clinico italiano 177
Implication of alpha1-antichymotrypsin polymorphism in familial Alzheimer's disease. 176
ApoE allele frequencies in Italian sporadic and familial Alzheimer's disease. 175
Absence of APP717 mutation in Italian FAD families 175
Presenilin-1 gene intronic polymorphism in sporadic and familial Alzheimer's disease. 174
Discrepancies in reporting the CAG repeat lengths for Huntington's disease 174
Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY. 173
ApoE as a prognostic factor for post-traumatic coma. 172
IgM monoclonal gammopathy-associated neuropathies with different IgM specificity. 172
Psychosis, serotonin receptor polymorphism and Alzheimer's disease 171
Free radical injury in skin cultured fibroblasts from Alzheimer's disease patients. 167
Neurochirurgia riparativa: trapianto caudato-putaminale di tessuto striatale fetale umano nella malattia di Huntington. Progetto dell'Università di Firenze 164
Altered hexokinase activity in skin cultured fibroblasts and leukocytes from Alzheimer's disease patients 164
Lactate production and glycolytic enzymes in sporadic and familial Alzheimer’s disease. 164
Molecular genetics of Alzheimer's disease in Italian families. 161
Apolipoprotein E and alpha1-antichymotrypsin polymorphism in Alzheimer's disease. 160
Insulin degrading enzyme and alpha-3 catenin polymorphisms in italian patients with Alzheimer disease 158
DAPK1 is Associated with FTD and not with Alzheimer's Disease 158
Alzheimer's disease and apolipoprotein E in Italy. 157
Cystatin C and apoe polymorphisms in Italian Alzheimer'sdisease. 157
The first Alzheimer disease case: a metachromatic leukodystrophy? 156
No association between the LRRK2 G2019S mutation and Alzheimer's disease in Italy. 156
Linkage Analysis in Italian Pedigrees with Autosomal Dominant Familial Alzheimer’s DiseaseCerebral Ischemia and Dementia 155
Genetics of Alzheimer's Disease and Frontotemporal Dementia 155
Clinical and genetic analysis of a Machado-Joseph Italian family 155
Development of human striatal anlagen after transplantation in a patient with Huntington's disease. 153
Congenital ocular Myastenia: case report 153
Absence of association between intronic polymorphism in PS-1 gene and alzheimer's disease in italian patients 152
Genetic and clinical analysis of SCA8 repeat expansion 151
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene 151
Occurrence of transketolase abnormalities in extracts of foreskin fibroblasts from patients with Alzheimer's disease 150
Epistatic effect of APP717 mutation and apolipoprotein E genotype in familial Alzheimer's disease. 150
Association between 5-HT2A receptor polymorphism and psychotic symptoms in Alzheimer’s disease 147
Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease-like and ataxia 146
Safety and tolerability of cyclophosphamide 'pulses' in multiple sclerosis: a prospective study in a clinical cohort. 145
A novel PS-1 mutation in an Italian AD family with psychotic symptoms at onset 145
La malattia di Alzheimer 143
Genetic Analysis of familial and sporadic cases of spinocerebellar ataxias in Italian patients 143
MRI and SPECT of midbrain and striatal degeneration in fragile X-associated tremor/ataxia syndrome. Journal of Neurology 142
Guidelines for the diagnosis of dementia and Alzheimer's disease 141
Clinical and genetic analysis of hereditary and sporadic ataxia in central Italy. 140
Regional distribution and clinical correlates of white matter structural damage in Huntington disease: a tract-based spatial statistics study. 140
Use of phosphatidylserine in sporadic and familial Alzheimer's disease 140
Implication of GAB2 Gene Polymorphism in Italian Patients with Alzheimer's Disease 139
Intralaminar distribution of neurotransmitter-related enzymes in cerebral cortex of Alzheimer's disease. 139
Linkage Analysis in familial Alzheimer's disease 139
Energy metabolism in demented brain. 138
Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder 137
Combining functional and structural brain magnetic resonance imaging in Huntington disease. 134
Activity of pyruvate de¬hydrogenase complex, glutamate dehydrogenase, lactete dehydrogenase, and choline acetyl¬transferase in rats after intracerebroventricular administration of bromopyruvate or AF64A 134
Inherent abnormalities in oxidative metabolism in Alzheimer's disease: interaction with vascular abnormalities. 133
Long-term evolution of anti-ganglioside antibody levels in patient with chronic dysimmune neuropathy under IVIg therapy. 132
The genetic defect causing familial Alzheimer's disease maps on chromosome 21 131
Gaze avoidance in subjects with extrapiramidal disorders 130
Protection from oxygen radical damage in human diploid fibroblasts by acetyl-L-carnitine 130
Normal lactate production and altered hexokinase activity in fibroblasts and leukocytes from familial Alzheimer's disease patients 129
Magnetization Transfer MR imaging demonstrates degeneration of the subcortical and cortical gray matter in Huntington’s disease 128
Brain white matter damage in SCA1 and SCA2. An in vivo study using voxel-based morphometry, histogram analysis of mean diffusivity and tract-based spatial statistics. 127
Competenze della funzione del setting percettivo dello sguardo nei disordini extrapiramidali dell'età evolutiva: metodologia di studio 125
Molecular genetic strategies in familial Alzheimer's disease. Theoretical and practical considerations. 122
Effetto del genotipo della Apolipoproteina E sulla evoluzione dello stato vegetativo post-traumatico 122
Chemical lateralization in human temporal cortex. 122
Totale 17.326
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Categoria #
all - tutte 56.856
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 56.856
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022637 0 0 0 29 38 25 40 53 37 22 157 236
2022/20232.254 225 381 71 232 181 427 301 115 229 12 70 10
2023/2024679 48 100 128 44 63 53 33 133 3 9 51 14
2024/20255.328 157 560 366 786 1.575 716 39 514 261 88 138 128
2025/20265.021 586 740 367 258 581 188 657 226 265 274 77 802
2026/2027910 147 232 526 5 0 0 0 0 0 0 0 0
Totale 20.244