PASSERINI, ILARIA
 Distribuzione geografica
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Continente #
NA - Nord America 1.881
EU - Europa 991
AS - Asia 315
AF - Africa 16
SA - Sud America 3
Totale 3.206
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Nazione #
US - Stati Uniti d'America 1.875
RU - Federazione Russa 467
IE - Irlanda 127
CN - Cina 118
IT - Italia 109
SE - Svezia 93
PL - Polonia 88
SG - Singapore 79
CH - Svizzera 50
HK - Hong Kong 46
JO - Giordania 43
IN - India 22
DE - Germania 18
GB - Regno Unito 18
CI - Costa d'Avorio 13
FI - Finlandia 7
CA - Canada 6
NL - Olanda 5
UA - Ucraina 5
TR - Turchia 3
AO - Angola 2
BE - Belgio 2
BR - Brasile 2
VN - Vietnam 2
EC - Ecuador 1
FR - Francia 1
IR - Iran 1
JP - Giappone 1
MU - Mauritius 1
NO - Norvegia 1
Totale 3.206
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Città #
Santa Clara 282
Fairfield 246
Chandler 150
Woodbridge 129
Dublin 127
Seattle 118
Houston 112
Ashburn 110
Warsaw 88
Cambridge 83
Singapore 67
Wilmington 67
Bern 49
Beijing 45
Ann Arbor 43
Lawrence 40
Princeton 33
Moscow 32
Altamura 31
Boardman 27
Boston 25
Kent 25
Hong Kong 22
Mumbai 22
Buffalo 20
San Diego 19
Florence 17
Shanghai 16
Abidjan 13
New York 12
Redwood City 11
Medford 10
Nanjing 9
Guangzhou 7
Arezzo 6
Hillsboro 6
Jacksonville 6
Norwalk 5
Ameno 4
Andover 4
Milan 4
Toronto 4
Chengdu 3
Falls Church 3
Hangzhou 3
Izmir 3
Redmond 3
Brussels 2
Dong Ket 2
Laurel 2
Luanda 2
Montespertoli 2
Montréal 2
Munich 2
Rome 2
Shenzhen 2
Siena 2
Southwark 2
Stockholm 2
Yubileyny 2
Acquaviva Picena 1
Atlanta 1
Esslingen am Neckar 1
Euskirchen 1
Fremont 1
Genova 1
Gerlafingen 1
Grafing 1
Greenwich 1
Hebei 1
Legnago 1
London 1
Los Angeles 1
Loughborough 1
Lucca 1
Lund 1
Margherita Di Savoia 1
Mestrino 1
Napoli 1
New Bedfont 1
New Haven 1
Nuremberg 1
Old Bridge 1
Phoenix 1
Pignataro Maggiore 1
Polesella 1
Prescot 1
Quito 1
Reggio Nell'emilia 1
Santa Maria 1
Shaoxing 1
Shenyang 1
São Paulo 1
Tamm 1
Tønsberg 1
Verona 1
Washington 1
Wuhan 1
Wuxi 1
Yiwu 1
Totale 2.227
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Nome #
EDI OCT evaluation of choroidal thickness in stargardt disease 211
Long-term follow-up of a CRB1-associated maculopathy 135
Multimodal imaging of benign yellow dot maculopathy 133
Near-infrared autofluorescence in young Choroideremia patients 132
Novel clinical findings in autosomal recessive NR2E3-related retinal dystrophy 130
CFH Y402H polymorphism in Italian patients with age-related macular degeneration, retinitis pigmentosa, and Stargardt disease 125
OCTA Imaging of Choroidal Neovascularization Treated Using Photodynamic Therapy in a Young Patient With Best Macular Dystrophy 122
Retinal dystrophy and subretinal drusenoid deposits in female choroideremia carriers 112
EDI-OCT evaluation of choroidal thickness in retinitis pigmentosa 111
Long-Term Results of Photodynamic Therapy for Choroidal Neovascularization in Pediatric Patients with Best Vitelliform Macular Dystrophy 108
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene. 108
Novel RDH12 sequence variations in Leber congenital amaurosis. 107
Fundus phenotype in retinitis pigmentosa associated with EYS mutations 106
A novel GRK1 mutation in an Italian patient with Oguchi disease 103
Peculiar Clinical Findings in Young Choroideremia Patients: A Retrospective Case Review 99
A novel mutation in the VMD2 gene in an Italian family with Best maculopathy. 98
En face OCT in choroideremia 98
Correlation between Photoreceptor Layer Integrity and Visual Function in Patients with Stargardt Disease: Implications for Gene Therapy. 96
Optical Coherence Tomography Angiography (OCT-A) in young choroideremia (CHM) patients 91
Different patterns of fundus autofluorescence related to ABCA4 gene mutations in Stargardt disease. 90
Retinal astrocytic hamartoma and Stargardt's disease: unusual association in a patient with ABCR mutation without phacomatosis. 87
Choroidal Vascularity Index in young Choroideremia patients 82
Clinical and molecular findings in patients with Pattern Dystrophy 81
Inherited retinal diseases due to rpe65 variants: From genetic diagnostic management to therapy 77
Optical Coherence Tomography Angiography cyclic remodeling of CNV in patients affected by BEST Macular Dystrophy 76
MYO7A and USH2A gene sequence variants in Italian patients with Usher syndrome 73
Acquired retinoschisis and vitreous hemorrhage as unusual findings in Choroideremia: case report 71
Outer nuclear layer relevance in visual function correlated to quantitative enface OCT parameters in Stargardt disease 71
Optical Coherence Tomography Angiography (OCT-A) in Choroideremia (CHM) carriers 68
Choroidal Vascularity Index in CHM Carriers 68
Choroidal Caverns in Stargardt Disease 66
Lamellar Hole-associated Epiretinal Proliferation in choroideremia: a case report 64
Ocular phenothypes associated with biallelic mutations in BEST in Italian patients 45
Totale 3.244
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Categoria #
all - tutte 10.235
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 10.235
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020454 0 0 0 0 72 58 66 64 75 54 48 17
2020/2021252 30 30 11 27 12 18 16 25 24 29 20 10
2021/2022241 10 13 28 14 3 10 9 23 12 11 42 66
2022/2023697 63 120 36 18 57 101 76 50 93 6 26 51
2023/2024231 6 29 37 11 6 19 14 40 2 20 29 18
2024/2025964 71 176 115 255 347 0 0 0 0 0 0 0
Totale 3.244