PIACENTINI, SILVIA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 8.979
EU - Europa 4.709
AS - Asia 2.740
SA - Sud America 397
AF - Africa 88
OC - Oceania 85
Continente sconosciuto - Info sul continente non disponibili 6
Totale 17.004
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 8.912
RU - Federazione Russa 1.962
SG - Singapore 750
HK - Hong Kong 736
CN - Cina 538
PL - Polonia 503
SE - Svezia 501
IE - Irlanda 497
IT - Italia 404
BR - Brasile 320
KR - Corea 283
DE - Germania 235
UA - Ucraina 229
FI - Finlandia 144
GB - Regno Unito 128
IN - India 103
VN - Vietnam 103
AU - Australia 79
TR - Turchia 70
JO - Giordania 41
FR - Francia 40
CA - Canada 36
AR - Argentina 27
CI - Costa d'Avorio 22
ZA - Sudafrica 19
BD - Bangladesh 18
IQ - Iraq 17
NL - Olanda 16
EC - Ecuador 15
JP - Giappone 15
MX - Messico 14
SC - Seychelles 11
ES - Italia 10
BE - Belgio 9
ID - Indonesia 9
PK - Pakistan 9
CO - Colombia 8
KG - Kirghizistan 8
LT - Lituania 8
PE - Perù 8
VE - Venezuela 8
UZ - Uzbekistan 7
MA - Marocco 6
NZ - Nuova Zelanda 6
TN - Tunisia 6
AE - Emirati Arabi Uniti 5
BG - Bulgaria 5
BH - Bahrain 5
BJ - Benin 5
CR - Costa Rica 5
EU - Europa 5
UY - Uruguay 5
EG - Egitto 4
KE - Kenya 4
PY - Paraguay 4
TT - Trinidad e Tobago 4
BY - Bielorussia 3
IL - Israele 3
OM - Oman 3
PA - Panama 3
SA - Arabia Saudita 3
SN - Senegal 3
AZ - Azerbaigian 2
CL - Cile 2
CZ - Repubblica Ceca 2
DZ - Algeria 2
MK - Macedonia 2
MY - Malesia 2
NG - Nigeria 2
NO - Norvegia 2
NP - Nepal 2
PR - Porto Rico 2
TW - Taiwan 2
AL - Albania 1
AM - Armenia 1
AT - Austria 1
CG - Congo 1
CH - Svizzera 1
DO - Repubblica Dominicana 1
EE - Estonia 1
ET - Etiopia 1
GA - Gabon 1
HN - Honduras 1
JM - Giamaica 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
LI - Liechtenstein 1
LK - Sri Lanka 1
LV - Lettonia 1
PH - Filippine 1
PS - Palestinian Territory 1
RO - Romania 1
RS - Serbia 1
SD - Sudan 1
SI - Slovenia 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 17.004
Salva come PNG Salva come JPEG
Città #
Santa Clara 1.875
Fairfield 900
Hong Kong 632
Ashburn 630
Chandler 619
Dublin 496
Warsaw 496
Woodbridge 425
Singapore 423
Cambridge 392
Seattle 379
Jacksonville 374
Wilmington 328
Houston 308
Seoul 282
Beijing 239
Ann Arbor 161
Dearborn 157
Princeton 135
Dallas 132
Los Angeles 123
Buffalo 122
Altamura 121
Lawrence 121
Boardman 96
Medford 80
Mumbai 79
Melbourne 77
Boston 72
Hefei 68
Moscow 60
Izmir 57
The Dalles 49
San Diego 47
Florence 45
New York 45
Munich 44
Ho Chi Minh City 43
Kent 31
Shanghai 31
Norwalk 27
São Paulo 27
Abidjan 22
Bremen 18
Hanoi 17
Milan 17
Turku 17
Falls Church 15
Hillsboro 15
Tokyo 15
Auburn Hills 14
London 14
Brooklyn 13
Chicago 13
Jinan 13
Toronto 13
Kunming 11
Nanjing 11
Rome 11
Andover 10
Genoa 10
Johannesburg 10
Yubileyny 10
Belo Horizonte 9
Brussels 9
Frankfurt Am Main 9
Guangzhou 9
Montreal 9
Salerno 9
Stockholm 9
Verona 9
Bishkek 8
Dong Ket 8
Manchester 8
Clifton 7
Frankfurt am Main 7
Guayaquil 7
Paris 7
Phoenix 7
Poplar 7
Rio de Janeiro 7
Secaucus 7
Baghdad 6
Brasília 6
Charlotte 6
Jakarta 6
Nanchang 6
Orem 6
Quito 6
Redondo Beach 6
Tashkent 6
Cape Town 5
Caracas 5
Chennai 5
Cotonou 5
Council Bluffs 5
Da Nang 5
Denver 5
Lahore 5
Rockland 5
Totale 11.388
Salva come PNG Salva come JPEG
Nome #
Time perception impairment in early-to-moderate stages of Huntington's disease is related to memory deficits 302
Progression of brain atrophy in spinocerebellar ataxia type 2: A longitudinal tensor-based morphometry study 299
Suicidal ideation in a European Huntington's disease population 250
Huntington’s disease and Scalar Expectancy Theory: A memory-based time perception deficit 244
NMDA receptor gene variations as modifiers in Huntington disease: a replication study. 243
Trapianto intracerebrale di striato fetale nella malattia di Huntington: un aggiornamento dell'esperienza clinica italiana 225
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study 206
ADC mapping of neurodegeneration in the brainstem and cerebellum of patients with progressive ataxias. 190
A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia. 190
Huntington disease: Volumetric, diffusion-weighted, and magnetization transfer MR imaging of brain 187
Association analysis of the paraoxonase-1 gene with Alzheimer's disease 187
A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset. 182
Lack of efficacy of phosphatidylcholine in ataxias. 181
Abnormalities of mitochondrial enzymes in hereditary ataxias. 178
Association of IL10 promoter polymorphism in Italian Alzheimer's disease. 177
Clinical and genetic characteristics of late-onset Huntington's disease 173
No implication of apolipoprotein E polymorphism in Italian schizophrenic patients. 171
Abnormal platelet glutamate dehydrogenase activity and activation in dominant and nondominant olivopontocerebellar atrophy. 170
Alzheimer skin fibroblasts show increased susceptibility to free radicals. 170
Fragile X premutation with atypical symptoms at onset. 167
Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Italy 165
ApoE genotype and familial Alzheimer's disease: a possible influence on age of onset in APP717 Val-->Ile mutated families. 162
Double-blind, crossover, placebo-controlled clinical trial with L-acetylcarnitine in patients with degenerative cerebellar ataxia. 161
Atypical Friedreich ataxia with a very late onset and an unusual limited GAA repeat. 158
Alterations in metabolic properties in fibroblasts in Alzheimer disease. 157
Influence of impaired T- and B-cell compartments on efficacy of IVIg in dysimmune neuropathies. 157
Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity 157
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion 157
Implication of alpha1-antichymotrypsin polymorphism in familial Alzheimer's disease. 155
Human striatal neuroblasts develop and build a striatal-like structure into the brain of Huntington's disease patients after transplantation. 154
Absence of APP717 mutation in Italian FAD families 153
APP717 and Alzheimer's disease in Italy 153
ApoE allele frequencies in Italian sporadic and familial Alzheimer's disease. 152
Progranulin genetic screening in frontotemporal lobar degeneration patients from central Italy. 152
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant. 152
Risperidone in idiopathic and symptomatic dystonia: preliminary experience. 151
Assessment of brain white matter fiber bundle atrophy in patients with Friedreich ataxia. 151
Free radical injury in skin cultured fibroblasts from Alzheimer's disease patients. 150
Psychosis, serotonin receptor polymorphism and Alzheimer's disease 150
ApoE as a prognostic factor for post-traumatic coma. 150
Human fetal striatal transplantation in disease. First italian clinic trial at the University of Florence. Preliminare Report 149
Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease 149
IgM monoclonal gammopathy-associated neuropathies with different IgM specificity. 149
Presenilin-1 gene intronic polymorphism in sporadic and familial Alzheimer's disease. 148
Lactate production and glycolytic enzymes in sporadic and familial Alzheimer’s disease. 146
Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY. 145
Altered hexokinase activity in skin cultured fibroblasts and leukocytes from Alzheimer's disease patients 144
Neurodegeneration in Friedreich’s ataxia is associated with a mixed activation pattern of the brain. A fMRI study 144
Implication of sex and SORL1 variants in italian patients with Alzheimer disease. 144
Insulin degrading enzyme and alpha-3 catenin polymorphisms in italian patients with Alzheimer disease 143
Discrepancies in reporting the CAG repeat lengths for Huntington's disease 143
Neurochirurgia riparativa: trapianto caudato-putaminale di tessuto striatale fetale umano nella malattia di Huntington. Progetto dell'Università di Firenze 142
Molecular genetics of Alzheimer's disease in Italian families. 138
Apolipoprotein E and alpha1-antichymotrypsin polymorphism in Alzheimer's disease. 137
Trapianto di tessuto striatale fetale umano nella malattia di Huntington. Primi risultati del trial clinico italiano 137
Occurrence of transketolase abnormalities in extracts of foreskin fibroblasts from patients with Alzheimer's disease 135
Linkage Analysis in Italian Pedigrees with Autosomal Dominant Familial Alzheimer’s DiseaseCerebral Ischemia and Dementia 135
No association between the LRRK2 G2019S mutation and Alzheimer's disease in Italy. 135
Alzheimer's disease and apolipoprotein E in Italy. 134
Epistatic effect of APP717 mutation and apolipoprotein E genotype in familial Alzheimer's disease. 133
Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease-like and ataxia 131
Development of human striatal anlagen after transplantation in a patient with Huntington's disease. 131
Association between 5-HT2A receptor polymorphism and psychotic symptoms in Alzheimer’s disease 129
Genetics of Alzheimer's Disease and Frontotemporal Dementia 128
DAPK1 is Associated with FTD and not with Alzheimer's Disease 128
Cystatin C and apoe polymorphisms in Italian Alzheimer'sdisease. 128
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene 127
The first Alzheimer disease case: a metachromatic leukodystrophy? 125
Safety and tolerability of cyclophosphamide 'pulses' in multiple sclerosis: a prospective study in a clinical cohort. 125
Intralaminar distribution of neurotransmitter-related enzymes in cerebral cortex of Alzheimer's disease. 125
Absence of association between intronic polymorphism in PS-1 gene and alzheimer's disease in italian patients 123
Congenital ocular Myastenia: case report 123
Regional distribution and clinical correlates of white matter structural damage in Huntington disease: a tract-based spatial statistics study. 121
La malattia di Alzheimer 119
Inherent abnormalities in oxidative metabolism in Alzheimer's disease: interaction with vascular abnormalities. 119
Genetic Analysis of familial and sporadic cases of spinocerebellar ataxias in Italian patients 119
Clinical and genetic analysis of hereditary and sporadic ataxia in central Italy. 115
Implication of GAB2 Gene Polymorphism in Italian Patients with Alzheimer's Disease 115
Activity of pyruvate de¬hydrogenase complex, glutamate dehydrogenase, lactete dehydrogenase, and choline acetyl¬transferase in rats after intracerebroventricular administration of bromopyruvate or AF64A 115
Energy metabolism in demented brain. 115
Use of phosphatidylserine in sporadic and familial Alzheimer's disease 115
Long-term evolution of anti-ganglioside antibody levels in patient with chronic dysimmune neuropathy under IVIg therapy. 114
Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder 114
Guidelines for the diagnosis of dementia and Alzheimer's disease 113
MRI and SPECT of midbrain and striatal degeneration in fragile X-associated tremor/ataxia syndrome. Journal of Neurology 113
The genetic defect causing familial Alzheimer's disease maps on chromosome 21 111
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. 111
Gaze avoidance in subjects with extrapiramidal disorders 110
Combining functional and structural brain magnetic resonance imaging in Huntington disease. 109
Molecular genetic strategies in familial Alzheimer's disease. Theoretical and practical considerations. 109
Competenze della funzione del setting percettivo dello sguardo nei disordini extrapiramidali dell'età evolutiva: metodologia di studio 108
Linkage Analysis in familial Alzheimer's disease 108
Chemical lateralization in human temporal cortex. 107
Effect of phosphatidylserine on free radical susceptibility in human diploid fibroblasts. 105
Protection from oxygen radical damage in human diploid fibroblasts by acetyl-L-carnitine 104
PET study in subjects from two Italian FAD families with APP717 Val to Ileu mutation 104
Effetto del genotipo della Apolipoproteina E sulla evoluzione dello stato vegetativo post-traumatico 102
Normal lactate production and altered hexokinase activity in fibroblasts and leukocytes from familial Alzheimer's disease patients 102
Magnetization Transfer MR imaging demonstrates degeneration of the subcortical and cortical gray matter in Huntington’s disease 101
Enzymes of energy metabolism in demented brain 100
Totale 14.640
Salva come PNG Salva come JPEG
Categoria #
all - tutte 46.978
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 46.978
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021699 0 0 0 0 0 165 26 111 100 144 67 86
2021/2022828 20 99 72 29 38 25 40 53 37 22 157 236
2022/20232.271 225 381 71 236 183 431 303 119 230 12 70 10
2023/2024684 48 102 129 44 63 55 33 133 3 9 51 14
2024/20255.361 159 564 368 791 1.585 721 39 517 261 90 138 128
2025/20262.690 590 743 368 258 584 147 0 0 0 0 0 0
Totale 17.058