BIANCHI, SILVIA
 Distribuzione geografica
Continente #
NA - Nord America 3.767
EU - Europa 2.628
AS - Asia 417
Continente sconosciuto - Info sul continente non disponibili 5
OC - Oceania 5
AF - Africa 4
SA - Sud America 1
Totale 6.827
Nazione #
US - Stati Uniti d'America 3.755
GB - Regno Unito 973
IE - Irlanda 440
CN - Cina 326
UA - Ucraina 274
SE - Svezia 234
IT - Italia 211
DE - Germania 134
FR - Francia 120
FI - Finlandia 79
RU - Federazione Russa 70
SG - Singapore 37
ES - Italia 23
TR - Turchia 21
BE - Belgio 18
NL - Olanda 16
CA - Canada 10
IN - India 10
CZ - Repubblica Ceca 8
VN - Vietnam 6
BG - Bulgaria 5
AU - Australia 4
EU - Europa 4
GR - Grecia 4
JP - Giappone 3
PL - Polonia 3
AT - Austria 2
EG - Egitto 2
HU - Ungheria 2
IL - Israele 2
IR - Iran 2
LU - Lussemburgo 2
PT - Portogallo 2
RO - Romania 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
AL - Albania 1
AR - Argentina 1
BN - Brunei Darussalam 1
DK - Danimarca 1
GL - Groenlandia 1
HR - Croazia 1
JM - Giamaica 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
LV - Lettonia 1
MM - Myanmar 1
MY - Malesia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PK - Pakistan 1
RS - Serbia 1
SA - Arabia Saudita 1
TN - Tunisia 1
UZ - Uzbekistan 1
ZA - Sudafrica 1
Totale 6.827
Città #
Southend 906
Menlo Park 838
Fairfield 454
Dublin 438
Chandler 315
Ashburn 245
Jacksonville 240
Woodbridge 211
Wilmington 174
Seattle 171
Houston 164
Cambridge 158
Ann Arbor 147
Princeton 93
Beijing 77
Nanjing 72
Siena 61
Nanchang 38
Helsinki 37
Boardman 34
San Mateo 32
New York 28
San Diego 28
Singapore 25
Shenyang 24
Moscow 22
Málaga 21
Izmir 19
Düsseldorf 18
Venezia 17
Shanghai 16
Changsha 14
Lancaster 13
Jinan 11
Milan 11
Florence 10
Hebei 10
Norwalk 10
Waanrode 10
Kunming 9
Brussels 8
Dearborn 8
Tianjin 8
Washington 8
Zhengzhou 8
Mestre 7
Ningbo 7
Hangzhou 6
Jiaxing 6
Renton 6
Auburn Hills 5
Dong Ket 5
Fremont 5
London 5
Redwood City 5
San Francisco 5
Sofia 5
Amsterdam 4
Guangzhou 4
Palermo 4
Toronto 4
Bologna 3
Brno 3
Brugherio 3
Dallas 3
Fuzhou 3
Haikou 3
Los Angeles 3
Munich 3
Prague 3
Sassari 3
Tappahannock 3
Tokyo 3
Warsaw 3
Bacoli 2
Budapest 2
Cairo 2
Calco 2
Changchun 2
Edinburgh 2
Florham Park 2
Leawood 2
Livorno 2
Loreggia 2
Luxembourg 2
Melbourne 2
Montreal 2
Naples 2
Olomouc 2
Padova 2
Phoenix 2
Ribolla 2
Saint Petersburg 2
San Giovanni Valdarno 2
Sant'Angelo in Pontano 2
Scottsdale 2
Southwark 2
Stoney Creek 2
Zanjan 2
Almere Stad 1
Totale 5.434
Nome #
Two novel HTRA1 mutations in a European CARASIL patient. 212
Adult Alexander disease with de novo c.1193C>T heterozygous variant in GFAP gene 207
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: Update on clinical, diagnostic, and management aspects 202
Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R gene 188
Visual System Involvement in CADASIL. 188
Toscana itaca (Italian CADASIL) registry: an implementable online database for CADASIL (Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy). 187
Homozygosity and severity of phenotypic presentation in a CADASIL family 183
null 182
Human peripheral blood lymphocytes and fibroblasts as Notch3 expression models. 180
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families 179
Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease 173
First report of a pathogenic mutation on exon 24 of the NOTCH3 gene in a CADASIL family. 172
Diagnostic value of ultrastructural skin biopsy studies in CADASIL 171
CADASIL in central Italy: a retrospective clinical and genetic study in 229 patients 167
First report of an Iraqi Kurdish CADASIL patient. 166
Ataxia with vitamin E deficiency: update of molecular diagnosis 162
Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 156
Cerebral hemorrhages in CADASIL: Report of four cases and a brief review. 155
A new family with CADASIL: presentation of an homozygous patient and comparison with heterozigous phenotypes. 151
Blood–brain barrier permeability in a patient with Labrune syndrome due to SNORD118 mutations 149
Hereditary cerebral small vessel diseases: A review. 146
Right-to-left shunt in CADASIL patients: prevalence and correlation with clinical and MRI findings 145
CADASIL and cerebrovascular diseases 143
Alu-element insertion in the OPA1 intron sequence associated with ADOA. 141
Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients. 140
Influence of vascular risk factors and neuropsychological profile on functional performances in CADASIL: results from the MIcrovascular LEukoencephalopathy Study (MILES). 140
The spectrum of NOTCH3 mutation and phonotype variability in fourteen Italian families with CADASIL. 133
Alu-Element Insertion In The Opa1 Intron Sequence Associated With ADOA 133
Bone Marrow-Derived Progenitor Cells in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy 131
A pathogenic mutation on exon 21 of the NOTCH3 gene causing CADASIL in an octogenarian paucisymptomatic patient 129
Location, number and factors associated with cerebral microbleeds in an Italian-British cohort of CADASIL patients 126
Neuro-Ophthalmological implications of CADASIL 124
The Cerebral Autosomal-Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale: A Screening Tool to Select Patients for NOTCH3 Gene Analysis. 123
Peripheral neuropathy in CADASIL 122
Screening for CADASIL mutation in Leukoencephalopathies. 122
Evidence of apoptosis via TUNEL staining in muscle biopsy from patients with mitochondrial encephaloneuromyopathies 115
Neuro-ophthalmologic aspects of CADASIL. 112
The first deep intronic mutation in the NOTCH3 gene in a family with late-onset CADASIL. 112
Acute visual loss due to anterior ischemic optic neuropathy as first symptom in a patient with CADASIL 110
null 108
null 107
The spectrum of Notch3 mutations in 28 italian CADASIL families 104
Neuro-opthalmological implications of Cadasil. 104
Anterior ischemic optic neuropathy as first symptom in a patient with CADASIL. 98
The neuro-Ophthalmology of CADASIL. 97
Pregnancy in CADASIL 93
Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL, exon 2 mutation. 84
Vitamin D levels in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) 43
A Novel CSF1R Mutation in a Patient with Clinical and Neuroradiological Features of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids 41
Circulating Biomarkers in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Patients 38
Totale 6.894
Categoria #
all - tutte 18.067
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 18.067


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.122 0 44 101 203 75 102 95 159 123 98 45 77
2020/2021848 39 97 25 70 35 96 44 147 89 53 91 62
2021/2022623 55 78 43 37 42 17 25 21 28 59 79 139
2022/2023976 54 82 129 135 104 177 16 88 98 32 50 11
2023/2024662 26 11 55 26 29 203 222 21 8 9 6 46
2024/202576 19 57 0 0 0 0 0 0 0 0 0 0
Totale 6.894