PIACENTINI, SILVIA
 Distribuzione geografica
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Continente #
NA - Nord America 5.952
EU - Europa 3.202
AS - Asia 842
AF - Africa 32
Continente sconosciuto - Info sul continente non disponibili 5
OC - Oceania 5
Totale 10.038
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Nazione #
US - Stati Uniti d'America 5.934
RU - Federazione Russa 688
IE - Irlanda 494
SE - Svezia 492
PL - Polonia 486
IT - Italia 372
CN - Cina 230
UA - Ucraina 226
SG - Singapore 208
HK - Hong Kong 200
DE - Germania 177
FI - Finlandia 125
GB - Regno Unito 92
IN - India 72
TR - Turchia 62
JO - Giordania 38
FR - Francia 26
CI - Costa d'Avorio 21
KR - Corea 20
CA - Canada 18
SC - Seychelles 11
BE - Belgio 8
VN - Vietnam 8
ES - Italia 5
EU - Europa 5
NL - Olanda 5
NZ - Nuova Zelanda 4
TW - Taiwan 2
AU - Australia 1
BG - Bulgaria 1
CZ - Repubblica Ceca 1
IL - Israele 1
LI - Liechtenstein 1
MK - Macedonia 1
MY - Malesia 1
NO - Norvegia 1
RO - Romania 1
Totale 10.038
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Città #
Fairfield 900
Chandler 619
Dublin 493
Warsaw 486
Woodbridge 425
Ashburn 398
Cambridge 392
Seattle 378
Jacksonville 374
Wilmington 327
Houston 304
Ann Arbor 161
Dearborn 156
Singapore 137
Princeton 135
Altamura 121
Lawrence 121
Beijing 97
Boardman 96
Hong Kong 96
Medford 80
Mumbai 70
Boston 69
Buffalo 58
Izmir 56
San Diego 47
Florence 42
Shanghai 29
Los Angeles 27
Norwalk 27
Santa Clara 26
Kent 24
New York 23
Abidjan 21
Hefei 20
Seoul 19
Bremen 18
Milan 16
Falls Church 15
Hillsboro 15
Auburn Hills 14
Nanjing 11
Andover 10
Kunming 10
Toronto 10
Frankfurt Am Main 9
Jinan 9
London 9
Salerno 9
Verona 9
Brussels 8
Dong Ket 8
Guangzhou 8
Rome 8
Nanchang 6
Munich 5
Rockland 5
Fabriano 4
Fuzhou 4
Grezzana 4
Lucca 4
Old Bridge 4
Brooklyn 3
Edison 3
Hounslow 3
Phoenix 3
Prescot 3
Redwood City 3
Secaucus 3
Taiyuan 3
Albany 2
Ancona 2
Barcelona 2
Bari 2
Casorate Primo 2
Charlotte 2
Chengdu 2
Conegliano 2
Dallas 2
Helsinki 2
Islington 2
Kilburn 2
Menlo Park 2
Mogliano Veneto 2
Moscow 2
Naaldwijk 2
Origgio 2
Padova 2
Porto Ercole 2
Seano 2
Stia 2
Taipei 2
Trento 2
Trumbull 2
Turin 2
Xian 2
Acri 1
Acton 1
Ameno 1
Auckland 1
Totale 7.166
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Nome #
Time perception impairment in early-to-moderate stages of Huntington's disease is related to memory deficits 236
Progression of brain atrophy in spinocerebellar ataxia type 2: A longitudinal tensor-based morphometry study 234
Huntington’s disease and Scalar Expectancy Theory: A memory-based time perception deficit 183
NMDA receptor gene variations as modifiers in Huntington disease: a replication study. 173
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study 134
Association analysis of the paraoxonase-1 gene with Alzheimer's disease 120
A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset. 116
Abnormalities of mitochondrial enzymes in hereditary ataxias. 116
Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Italy 114
IgM monoclonal gammopathy-associated neuropathies with different IgM specificity. 114
Huntington disease: Volumetric, diffusion-weighted, and magnetization transfer MR imaging of brain 113
ADC mapping of neurodegeneration in the brainstem and cerebellum of patients with progressive ataxias. 113
Lack of efficacy of phosphatidylcholine in ataxias. 111
A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia. 110
Association of IL10 promoter polymorphism in Italian Alzheimer's disease. 110
No implication of apolipoprotein E polymorphism in Italian schizophrenic patients. 106
Fragile X premutation with atypical symptoms at onset. 106
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant. 105
Neurochirurgia riparativa: trapianto caudato-putaminale di tessuto striatale fetale umano nella malattia di Huntington. Progetto dell'Università di Firenze 102
Alzheimer skin fibroblasts show increased susceptibility to free radicals. 102
Alterations in metabolic properties in fibroblasts in Alzheimer disease. 102
Abnormal platelet glutamate dehydrogenase activity and activation in dominant and nondominant olivopontocerebellar atrophy. 99
ApoE as a prognostic factor for post-traumatic coma. 97
Insulin degrading enzyme and alpha-3 catenin polymorphisms in italian patients with Alzheimer disease 96
ApoE genotype and familial Alzheimer's disease: a possible influence on age of onset in APP717 Val-->Ile mutated families. 96
Double-blind, crossover, placebo-controlled clinical trial with L-acetylcarnitine in patients with degenerative cerebellar ataxia. 96
Free radical injury in skin cultured fibroblasts from Alzheimer's disease patients. 96
Molecular genetics of Alzheimer's disease in Italian families. 96
Occurrence of transketolase abnormalities in extracts of foreskin fibroblasts from patients with Alzheimer's disease 94
ApoE allele frequencies in Italian sporadic and familial Alzheimer's disease. 92
Influence of impaired T- and B-cell compartments on efficacy of IVIg in dysimmune neuropathies. 92
Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity 92
Human striatal neuroblasts develop and build a striatal-like structure into the brain of Huntington's disease patients after transplantation. 92
Safety and tolerability of cyclophosphamide 'pulses' in multiple sclerosis: a prospective study in a clinical cohort. 91
Epistatic effect of APP717 mutation and apolipoprotein E genotype in familial Alzheimer's disease. 91
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion 90
Lactate production and glycolytic enzymes in sporadic and familial Alzheimer’s disease. 90
Atypical Friedreich ataxia with a very late onset and an unusual limited GAA repeat. 90
Inherent abnormalities in oxidative metabolism in Alzheimer's disease: interaction with vascular abnormalities. 90
Risperidone in idiopathic and symptomatic dystonia: preliminary experience. 89
The first Alzheimer disease case: a metachromatic leukodystrophy? 89
Progranulin genetic screening in frontotemporal lobar degeneration patients from central Italy. 89
Neurodegeneration in Friedreich’s ataxia is associated with a mixed activation pattern of the brain. A fMRI study 89
DAPK1 is Associated with FTD and not with Alzheimer's Disease 89
Intralaminar distribution of neurotransmitter-related enzymes in cerebral cortex of Alzheimer's disease. 89
Clinical and genetic characteristics of late-onset Huntington's disease 88
Assessment of brain white matter fiber bundle atrophy in patients with Friedreich ataxia. 87
Suicidal ideation in a European Huntington's disease population 87
No association between the LRRK2 G2019S mutation and Alzheimer's disease in Italy. 85
Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease 85
Trapianto di tessuto striatale fetale umano nella malattia di Huntington. Primi risultati del trial clinico italiano 85
Altered hexokinase activity in skin cultured fibroblasts and leukocytes from Alzheimer's disease patients 83
APP717 and Alzheimer's disease in Italy 83
Genetics of Alzheimer's Disease and Frontotemporal Dementia 83
Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease-like and ataxia 82
Absence of APP717 mutation in Italian FAD families 82
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene 81
Effect of phosphatidylserine on free radical susceptibility in human diploid fibroblasts. 80
Long-term evolution of anti-ganglioside antibody levels in patient with chronic dysimmune neuropathy under IVIg therapy. 80
Alzheimer's disease and apolipoprotein E in Italy. 79
Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder 79
Human fetal striatal transplantation in disease. First italian clinic trial at the University of Florence. Preliminare Report 78
Clinical and genetic analysis of hereditary and sporadic ataxia in central Italy. 78
Implication of sex and SORL1 variants in italian patients with Alzheimer disease. 78
Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY. 78
Psychosis, serotonin receptor polymorphism and Alzheimer's disease 77
Energy metabolism in demented brain. 77
Development of human striatal anlagen after transplantation in a patient with Huntington's disease. 76
Cystatin C and apoe polymorphisms in Italian Alzheimer'sdisease. 76
Discrepancies in reporting the CAG repeat lengths for Huntington's disease 76
Implication of alpha1-antichymotrypsin polymorphism in familial Alzheimer's disease. 75
Presenilin-1 gene intronic polymorphism in sporadic and familial Alzheimer's disease. 75
Combining functional and structural brain magnetic resonance imaging in Huntington disease. 75
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. 74
Regional distribution and clinical correlates of white matter structural damage in Huntington disease: a tract-based spatial statistics study. 72
Trapianto intracerebrale di striato fetale nella malattia di Huntington: un aggiornamento dell'esperienza clinica italiana 71
Apolipoprotein E and alpha1-antichymotrypsin polymorphism in Alzheimer's disease. 71
Use of phosphatidylserine in sporadic and familial Alzheimer's disease 71
PET study in subjects from two Italian FAD families with APP717 Val to Ileu mutation 71
Molecular genetic strategies in familial Alzheimer's disease. Theoretical and practical considerations. 70
Chemical lateralization in human temporal cortex. 70
Normal lactate production and altered hexokinase activity in fibroblasts and leukocytes from familial Alzheimer's disease patients 70
Brain structural damage in Friedreich's ataxia. 69
The genetic defect causing familial Alzheimer's disease maps on chromosome 21 68
Kinetic studies of the mouse brain transketolase. 66
Linkage Analysis in Italian Pedigrees with Autosomal Dominant Familial Alzheimer’s DiseaseCerebral Ischemia and Dementia 66
Linkage Analysis in familial Alzheimer's disease 65
Implication of GAB2 Gene Polymorphism in Italian Patients with Alzheimer's Disease 64
Protection from oxygen radical damage in human diploid fibroblasts by acetyl-L-carnitine 64
Deficiency of a specific diaphorase in Luft disease fibroblasts 62
Congenital ocular Myastenia: case report 61
ENZYMES OF ENERGY METABOLISM IN DEMENTED BRAIN 59
Association between 5-HT2A receptor polymorphism and psychotic symptoms in Alzheimer’s disease 59
Missense mutation of S182 gene in Italian families with early-onset Alzheimer's disease. 58
Enzymes of energy metabolism in demented brain 58
Gaze avoidance in subjects with extrapiramidal disorders 57
La malattia di Alzheimer 57
Activity of pyruvate de¬hydrogenase complex, glutamate dehydrogenase, lactete dehydrogenase, and choline acetyl¬transferase in rats after intracerebroventricular administration of bromopyruvate or AF64A 56
Genetic Analysis of familial and sporadic cases of spinocerebellar ataxias in Italian patients 55
CO2-laser and electric somatosensory evoked potentials in Friedreich's ataxia. 53
Totale 8.919
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Categoria #
all - tutte 29.693
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 29.693
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.935 0 0 52 185 218 325 342 286 204 135 155 33
2020/20211.103 116 66 108 92 22 165 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
2024/20251.085 159 564 362 0 0 0 0 0 0 0 0 0
Totale 10.092