SCALABRINI, DIEGO
 Distribuzione geografica
Continente #
EU - Europa 4.968
NA - Nord America 3.011
AS - Asia 1.519
SA - Sud America 86
OC - Oceania 3
AF - Africa 2
Continente sconosciuto - Info sul continente non disponibili 2
Totale 9.591
Nazione #
US - Stati Uniti d'America 2.851
GB - Regno Unito 1.866
DE - Germania 909
CN - Cina 708
SE - Svezia 594
IT - Italia 445
UA - Ucraina 316
FR - Francia 236
TR - Turchia 214
IN - India 196
KR - Corea 169
CA - Canada 157
SG - Singapore 153
EU - Europa 138
IE - Irlanda 137
RU - Federazione Russa 100
NL - Olanda 96
PL - Polonia 95
FI - Finlandia 92
CO - Colombia 83
GR - Grecia 42
HK - Hong Kong 24
VN - Vietnam 16
ID - Indonesia 15
BE - Belgio 13
DK - Danimarca 13
JP - Giappone 9
IR - Iran 7
UZ - Uzbekistan 4
ES - Italia 3
RO - Romania 3
AU - Australia 2
BR - Brasile 2
CZ - Repubblica Ceca 2
EG - Egitto 2
IL - Israele 2
MX - Messico 2
PT - Portogallo 2
TW - Taiwan 2
BA - Bosnia-Erzegovina 1
CR - Costa Rica 1
IS - Islanda 1
LV - Lettonia 1
MT - Malta 1
NZ - Nuova Zelanda 1
PE - Perù 1
Totale 9.727
Città #
Southend 1.678
Chandler 370
Jacksonville 271
Frankfurt am Main 248
Seattle 214
Beijing 202
Princeton 179
Milan 163
Wilmington 150
Dublin 134
Redmond 126
Ann Arbor 114
Somerville 114
Nanjing 99
Ashburn 97
Warsaw 94
Singapore 92
Mountain View 88
Kent 85
Bogotá 83
Sakarya 82
Serra 82
Andover 80
Toronto 79
Woodbridge 78
Ottawa 71
Bengaluru 66
Boardman 66
Des Moines 63
Dearborn 60
Berlin 59
New York 45
Jinan 44
Athens 41
Nanchang 39
Shenyang 38
Tianjin 33
Margão 32
Shanghai 31
Medford 26
Kiez 24
Zhengzhou 24
Phoenix 22
Houston 20
Jiaxing 20
Fairfield 19
Auburn Hills 18
Bitonto 18
Nürnberg 18
Hangzhou 17
Hebei 17
Lowell 17
Norwalk 16
Changsha 15
Santa Clara 14
Verona 14
Hong Kong 13
Odernheim 13
Kunming 12
Hamburg 11
Sunnyvale 11
Brussels 10
Dong Ket 10
Lanzhou 10
Los Angeles 10
Ningbo 10
Guangzhou 9
Palaiseau 9
San Diego 9
Seoul 9
Cambridge 8
Helsinki 8
Kwai Chung 8
Redwood City 8
San Jose 8
Taizhou 8
Bühl 7
Changchun 6
Atlanta 5
Cagliari 5
Collegno 5
Eitensheim 5
Fremont 5
Haikou 5
Piscataway 5
Taiyuan 5
Chicago 4
Fuzhou 4
Grafing 4
Hayward 4
Jakarta 4
Pskov 4
Washington 4
Boston 3
Buffalo 3
Costa Mesa 3
Dallas 3
Frankfurt 3
Kameoka 3
London 3
Totale 6.305
Nome #
The T-786C NOS3 polymorphism in Alzheimer's disease : association and influence on gene expression 222
NOS3 Glu298Asp polymorphism is a risk factor for frontotemporal lobar degeneration 222
P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosis 199
Rs5848 Variant Influences GRN mRNA Levels in Brain and Peripheral Mononuclear Cells in Patients with Alzheimer’s Disease 185
Progranulin gene mutation scanning in Alzheimer's disease and frontotemporal lobar degeneration: functional and phenotypic correlations. 172
Changes in vitamin B12 and tumour necrosis factor-a levels in cerebrospinal fluid of patients with different subtypes of multiple sclerosis 164
Genetic and functional analysis of progranulin gene variants in Alzheimer's disease. 160
Progranulin gene mutation scanning in multiple sclerosis patients with cognitive impairment 154
Loss of cobalamin-mediated regulation leads to decreased EGF and increased soluble CD40 levels in cerebrospinal fluid of patients with multiple sclerosis 152
Novel exon 1 progranulin gene variant in Alzheimer’s disease 152
Progranulin gene mutation scanning in Alzheimer's disease and Frontotemporal Lobar Degeneration: fuctional and phenotypic correlations 149
Neuronal Nitric Oxide Synthase C276T polymorphism increases the risk for Frontotemporal Lobar Degeneration 148
Chemokine serum levels in mild cognitive impairment and Alzheimer’s disease 146
Progranulin genetic variability in primary progressive multiple sclerosis. 144
Analisi genetica di molecole infiammatorie e di adesione coinvolte nella patogenesi della sclerosi multipla 139
Selectin gene cluster genetic variation: association study in two independent multiple sclerosis populations. 139
Progranulin gene mutation scanning in Multiple Sclerosis patiens with cognitive impairment. 139
Cerebrospinal fluid progranulin levels in patients with different multiple sclerosis subtypes 138
Absence of mutations in TREM-2 coding region in early onset dementia 136
Novel exon 1 progranulin gene variations in Alzheimer's disease and frontotemporal lobar degeneration 135
Absence of mutations in TREM-2 coding region in patients with early onset dementia 135
Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis 135
Candidate gene analysis of semaphorins in patients with Alzheimer's disease 135
Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to multiple sclerosis 134
Absence of TREM2 polymorphisms in patients with Alzheimer's disease and Frontotemporal Lobar Degeneration 134
Absence of mutations in TREM-2 coding region in early onset dementia 134
IP-10 haplotypes and multiple sclerosis : association and correlation with clinical course 134
Genetic and functional analysis of progranulin gene variants in patients with Alzheimer's disease 133
SELP and SELPLG single nucleotide polymorphisms in multiple sclerosis 132
DCUN1D1 is a risk factor for frontotemporal lobar degeneration 132
GRN variability contributes to sporadic frontotemporal lobar degeneration 132
GRN rs5848 in neurodegeneration: a role in axonal damage? 129
Intrathecal levels of IL-6, IL-11, LIF, and A42, tau and phosphotau biomarkers in Alzheimer’s disease and Frontotemporal Lobar Degeneration. 127
IP-10 haplotypes and multiple sclerosis : association and correlation with clinical course 127
Progranulin gene variability in a population of 239 patients with primary progressive multiple sclerosis 126
Gender-specific influence of the chromosome 16 gene cluster on the susceptibility to multiple sclerosis 121
Chemokine serum levels in mild cognitive impairment and Alzheimer’s disease 120
CXCL10 haplotypes and multiple sclerosis : association and correlation with clinical course 119
SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosis 119
CDKN2A and CDKN2B genetic variability in Alzheimer's disease patients. 119
Progranulin gene variability increases the risk for primary progressive multiple sclerosis in males 119
MDC/CCL22 intrathecal levels in patients with multiple sclerosis 118
CSF levels of IL-6, IL-11, LIF, A42, TAU and phospoTAU biomarkers in Alzheimer’s disease and Frontotemporal Lobar Degeneration 117
CHMP5 and BAG1 are protective factors for sporadic frontotemporal lobar degeneration 116
Genetic and functional analysis of progranulin gene variants in Alzheimer's disease 115
Progranulin gene mutation scanning and expression analysis in patients with Alzheimer's disease 114
The NOS G894T (Glu298Asp) polymorphism is a risk for frontotemporal lobar degeneration 113
rs 5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells from patients with Alzheimer's disease 112
The MCP-1 A-2518G polymorphism acts as proctective factor for frontotemporal lobar degeneration 112
Selectin gene cluster genetic variation: association study in two independent multiple sclerosis populations. 112
PGRN polymorphisms influence the susceptibility for Alzheimer’s disease 111
Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to multiple sclerosis 111
Serum MCP-1 levels are increased in mild cognitive impairment and mild Alzheimer's disease 109
Progranulin gene mutation scanning in Italian Alzheimer's disease population 109
PGRN genetic variability in Alzheimer's disease: effect on susceptibility, age at onset and mRNS levels 109
Expression profile of miRNAs involved in CD4+ lymphocyte activation and differentiation in patients with multiple sclerosis 108
Neuronal nitric oxide synthase C276T polymorphism increases the risk for Frontotemporal Lobar Degeneration 107
The MCP-1 A-2518G polymorphism acts as protective factor for frontotemporal lobar degeneration 107
Gender-specific influence of the chromosome 16 chemokine genecluster on the susceptibility to Multiple Sclerosis 106
MCP-1 A-2518G polymorphism: effect on sysceptibility for Frontotemporel Lobar Degeneration and on cerebrospina fluid MCP-1 levels. 106
Is KIF24 a genetic risk factor for Frontotemporal Lobar degeneration? 106
CXCL10 haplotypes and multiple sclerosis : association and correlation with clinical course 104
Chemokine serum levels in mild cognitive impairment and Alzheimer’s disease 104
Chemokine serum levels in mild cognitive impairment as Alzheimer's disease early biomarkers 103
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration 103
GRN rs5848 polymorphism: a role in neurodegeneration? 103
GSK3β genetic variability in patients with Multiple Sclerosis 103
Neural nitric oxide Synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration 101
Novel exon 1 progranulin gene variant in Alzheimer's disease. 101
rs5848 variant influences GRN mRNA levels in patients with Alzheimer's Disease. 101
Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to multiple sclerosis 100
Progranulin gene variations associted with Alzheimer’s disease 98
MCP-1 A-2518G polymorphism : effect on susceptibility for Frontotemporal Lobar Degeneration and on cerebrospinal fluid MCP-1 level 97
Loss of epidermal growth factor regulation by cobalamin in multiple sclerosis 97
Candidate gene analysis of IP-10 gene in patients with Alzheimer's disease 96
IP-10 serum levels are not increased in mild cognitive impairment and Alzheimer's disease 95
The MCP-1 A-2518G polymorphism acts as protective factor for Frontotemporal Lobar Degeneration 94
Intrathecal levels of IL-6, IL-11 and LIF in Alzheimer's disease and frontotemporal lobar degeneration 94
Haplotypes in IP-10 gene and multiple sclerosis : association and correlation with clinical course 92
KIF24 single nucleotide polymorphism is a risk factor for sporadic frontemporal lobar degeneration 88
KIF24 gene is associated with frontotemporal lobar degeneration. 87
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for Frontotemporal Lobar Degeneration 85
Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort 85
Totale 10.240
Categoria #
all - tutte 29.615
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 29.615


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.025 120 56 64 40 59 103 85 32 178 191 72 25
2020/20211.206 58 124 130 2 109 66 65 43 137 90 302 80
2021/2022729 42 19 7 19 49 23 108 21 101 85 65 190
2022/20231.204 144 144 102 134 163 239 32 67 133 5 31 10
2023/2024903 18 62 33 56 362 40 26 32 23 97 67 87
2024/202520 20 0 0 0 0 0 0 0 0 0 0 0
Totale 10.240