IRIS
ROSSI, Settimio
 Distribuzione geografica
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Continente #
EU - Europa 4.180
NA - Nord America 4.026
AS - Asia 874
SA - Sud America 12
AF - Africa 11
Continente sconosciuto - Info sul continente non disponibili 8
OC - Oceania 4
Totale 9.115
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Nazione #
US - Stati Uniti d'America 4.012
IE - Irlanda 1.293
UA - Ucraina 623
IT - Italia 587
GB - Regno Unito 515
CN - Cina 391
DE - Germania 313
SG - Singapore 257
SE - Svezia 240
FR - Francia 227
FI - Finlandia 164
TR - Turchia 132
GR - Grecia 124
VN - Vietnam 42
BE - Belgio 32
KR - Corea 19
CZ - Repubblica Ceca 18
IN - India 12
SC - Seychelles 10
EU - Europa 8
RO - Romania 8
BR - Brasile 7
AE - Emirati Arabi Uniti 5
ES - Italia 5
GT - Guatemala 5
NL - Olanda 5
PL - Polonia 5
AT - Austria 4
MD - Moldavia 4
CA - Canada 3
CH - Svizzera 3
CL - Cile 3
HU - Ungheria 3
IR - Iran 3
JP - Giappone 3
MX - Messico 3
RU - Federazione Russa 3
AU - Australia 2
DK - Danimarca 2
HK - Hong Kong 2
NZ - Nuova Zelanda 2
PH - Filippine 2
PR - Porto Rico 2
BD - Bangladesh 1
EC - Ecuador 1
ID - Indonesia 1
IL - Israele 1
KZ - Kazakistan 1
NO - Norvegia 1
PA - Panama 1
PE - Perù 1
PT - Portogallo 1
TH - Thailandia 1
TW - Taiwan 1
ZA - Sudafrica 1
Totale 9.115
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Città #
Dublin 1.293
Jacksonville 943
Chandler 748
Santa Clara 201
Princeton 184
Singapore 158
Boardman 157
Ann Arbor 155
Roxbury 128
Bremen 115
Woodbridge 112
Medford 101
Cambridge 89
Wilmington 87
San Mateo 65
Beijing 64
Nanjing 60
Caserta 58
Ashburn 54
Dong Ket 42
Naples 40
Des Moines 39
Brussels 31
Rome 31
Mountain View 29
Istanbul 28
Jinan 26
Norwalk 24
New York 23
Düsseldorf 21
Napoli 20
Seoul 19
Aversa 18
Taiyuan 18
Brno 17
Munich 17
Kunming 16
Shenyang 16
Nanchang 15
Tianjin 15
Auburn Hills 14
Haikou 14
Los Angeles 14
Lanzhou 13
Redwood City 12
Changsha 11
Falls Church 11
Hebei 11
Houston 11
Ningbo 10
Taizhou 10
Florence 9
Guangzhou 9
Milan 9
Hangzhou 8
Helsinki 8
Zhengzhou 8
Bologna 7
Jiaxing 7
Reggio Nell'emilia 7
Changchun 6
Salerno 6
Castelfranco Emilia 5
Guatemala City 5
London 5
Avella 4
Baselicaduce 4
Catania 4
Fuzhou 4
New Haven 4
Pune 4
Venice 4
Amsterdam 3
Brampton 3
Cassano delle Murge 3
Castel Gandolfo 3
Chicago 3
Dubai 3
Forlì 3
Genova 3
Lappeenranta 3
Montereale Valcellina 3
Mumbai 3
Padova 3
Portici 3
Redmond 3
Seattle 3
Seregno 3
Torre Del Greco 3
Torre del Greco 3
Vienna 3
Agerola 2
Andover 2
Arzano 2
Atlanta 2
Bassano del Grappa 2
Bedford 2
Bischheim 2
Brescia 2
Budapest 2
Totale 5.610
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Nome #
Analisi di correlazione genotipo fenotipo in una famiglia con retinite pigmentosa autosomica dominante associata ad una nuova mutazione nel gene PRPF8 131
Analisi del gene della periferina/rds in famiglie con distrofia a pattern dell’epitelio pigmentato retinico 128
Caratterizzazione clinico-genetica di pazienti italiani con Distrofia Cristallina di Bietti 114
Sicurezza ed efficacia della terapia genica nell'Amaurosi Congenita di Leber: un anno di followup. 94
ESTRUSIONE DI PIOMBAGGIO? RUOLO DELL’ECOGRAFIA 89
Activation of Melanocortin Receptors MC1 and MC5 Attenuates Retinal Damage in Experimental Diabetic Retinopathy 85
Post-operative results of corneal collagen cross-linking for progressive keratoconus 83
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina. 79
AAV-mediated photoreceptor transduction of the pig cone-enriched retina 78
Terapia del glaucoma: the cannabinoids way. 78
Recombinant vectors based on porcine adeno-associated viral serotypes transduce the murine and pig retina 76
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial 76
Identifying fallers among ophthalmic patients using classification tree methodology 76
Wearable Improved Vision System for Color Vision Deficiency Correction 76
Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with leber congenital amaurosis type 2 74
Evaluation of Italian Patients with Leber Congenital Amaurosis due to AIPL1 Mutations Highlights the Potential Applicability of Gene Therapy 74
Studio clinico genetico di pazienti con amaurosi congenita di Leber 74
Intravitreal Injections of Melanocortin Receptor 1, 5 Agonists Prevents Neovascularization in a VEGF165 Mouse Model of Retinopathy 74
Inhibition of Ocular Aldose Reductase by a New Benzofuroxane Derivative Ameliorates Rat Endotoxic Uveitis 73
Trattamento con acetazolamide dell’edema maculare cistoide in pazienti affetti da retinite pigmentosa. 72
A pilot study for development of a novel tool for clinical decision making to identify fallers among ophthalmic patients 72
The role of optical coherence tomography in an atypical case of oculocutaneous albinism: A case report 71
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene. 70
Strategie chirurgiche nella terapia genica 68
Efficacia della terapia genica per l’Amaurosi Congenita di Leber fino a tre anni dopo la somministrazione del vettore virale 68
A Phase I Safety Study in Subjects with Leber Congenital Amaurosis (LCA) Using Adeno-Associated Viral Vector to Deliver The Gene For Human Rpe65 Into The Retinal Pigment Epithelium (Rpe) [AAV.RPE65-101]: Treatment and Follow up of 3 Italian Patients 68
Genetic characterization of Italian patients with Bardet-Biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: Identification of eleven novel pathogenic sequence variants 68
Incidence of high myopia in italian patients with retinitis pigmentosa 67
Aspetti clinici dell’albinismo oculo-cutaneo correlato a mutazioninei geni TYR e MATP 66
Studio clinico-genetico di una famiglia con retinite pigmentosa autosomica dominante associata ad una nuova mutazione nel gene PRPF8. 66
Evaluation of ocular gene therapy in an italian patient affected by congenital leber amaurosis type 2 treated in both eyes 66
Analisi di mutazione del gene REP1 in famiglie Italiane affette da coroideremia 65
Effects of 5-perfluorophenyl/octyl/butyl-substituted derivatives of aromatic/heterocyclic sulfonamides on carbonic anhydrase II activity in vitro and on betamethasone-induced ocular hypertension in rabbits 63
Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family 63
Photorefractive Keratectomy on Purely Refractive Accommodative Esotropia. 63
VALUTAZIONE DELLA PRESSIONE INTRAOCULARE DOPO PRK IPERMETROPICA CON TONOMETRIA AD APPLANAZIONE E NON CONTACT 63
Hyperglycemia in streptozotocin-induced diabetes prolongs the inflammatory response of endotoxin-induced uveitis due to reduced ciliary body heme oxygenase-1 levels 63
Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration 62
MicroRNA-Restricted transgene expression in the retina 62
A novel mutation in the RDS gene in an Italian family with pattern dystrophy 62
Intrafamilial heterogeneity of congenital optic disc pit maculopathy 62
Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy. 61
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene 61
Antibiotic drug prescription in respiratory tract infections: A pharmacoepidemiological survey among general practitioners in a region of Italy 61
Pupillometric analysis for assessment of gene therapy in Leber Congenital Amaurosis patients 61
Differente espressione clinica in una famiglia italiana con mutazione nel gene RDS-periferina e distrofia dell'epitelio pigmentato retinico 61
An Atypical Form of Bietti Crystalline Dystrophy 60
Aspetti clinici delle carriers di coroideremia 60
Retinite pigmentosa autosomica dominante: correlazione genotipo fenotipo in una famiglia italiana con mutazione nel gene NRL 60
Malattia di Coats e retinite pigmentosa. Un caso clinico 59
Decorso clinico della Retinite Pigmentosa nelle varie forme genetiche 59
Phase I Safety Study In Subjects With Leber Congenital Amaurosis (Lca) Using Adeno-Associated Viral Vector To Deliver The Gene For Human Rpe65 Into The Retinal Pigment Epithelium (Rpe) [Aav.Rpe65-101]: Treatment And Follow Up Of 3 Italian Patients 59
Caso clinico di retinite pigmentosa e drusen della testa del nervo ottico 58
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 58
Severo fenotipo clinico in carriers di coroideremia associato ad una nuova mutazione del gene CHM 58
Association between genotype and disease progression in Italian stargardt patients: A retrospective natural history study 58
Effects of nebivolol on human platelet aggregation 57
Hyperglycemia in streptozotocin-induced diabetes leads to persistent inflammation and tissue damage following uveitis due to reduced levels of ciliary body heme oxygenase-1 57
A glucose biosensor operating under non-isothermal conditions: The dynamic response 56
CAN WE UTILIZE PRK TO IMPROVE VISUAL ACUITY IN ADULT AMBLIOPIC EYES? 56
Emangioma capillare del disco ottico: 6 anni di Follow-up ecografico 56
Studio dei polimorfismi del gene paraoxonasi nella degenerazione maculare senile 56
Standard versus trans-epithelial collagen cross-linking in keratoconus patients suitable for standard collagen cross-linking 56
Sindrome di Usher: una valutazione clinica 55
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 55
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina 55
TRATTAMENTO FOTOREFRATTIVO DELL’ASTIGMATISMO CON LA TECNICA DEI CILINDRI CROCIATI: STUDIO CLINICO 55
Cannabinoid CB2 receptor activation reduces mouse myocardial ischemia-reperfusion injury: involvement of cytokine/chemokines and PMN 54
Effects of docosahexaenoic acid on [Ca2+]i increase induced by doxorubicin in ventricular rat cardiomyocytes 54
Molecular and clinical characterization of albinism in a large cohort of Italian patients 53
CLINICAL PRESENTATION and DISEASE COURSE of USHER SYNDROME because of MUTATIONS in MYO7A or USH2A 53
Clinical and genetic features in Italian Bietti crystalline dystrophy patients 52
Hyaluronan-induced stimulation of corneal wound healing is a pure pharmacological effect 52
High levels of serum ubiquitin and proteasome in a case of HLA-B27 uveitis 52
Efficient gene delivery to the cone-enriched pig retina by dual AAV vectors. 51
Dopaminergic dysfunction is associated with IL-1β-dependent mood alterations in experimental autoimmune encephalomyelitis. 51
Intrafamilial clinical heterogeneity associated with a novel mutation of the retinal degeneration slow/peripherin gene 51
Clinical pharmacology of nebivolol 51
Cannabinoid CB2 receptor activation reduces mouse myocardial ischemia-reperfusion injury: involvement of cytokine/chemokine and PMN 51
Correlazione tra spessore maculare ed acutezza visiva centrale in pazienti affetti da retinite pigmentosa. 51
New Insight in Retinal Phenotype of Patient with AIPL1 Mutations 51
Two-year macular volume assessment in multiple sclerosis patients treated with fingolimod 51
Management of hypertension by general practitioners: an Italian observational study 50
Genotype-phenotype correlation in Italian families with Stargardt disease 50
Macular abnormalities in Italian patients with retinitis pigmentosa. 50
CAPILLARY HEMANGIOMA OF THE OPTIC DISC: SIX-YEAR ECHO GRAPHIC FOLLOW-UP 50
Studio multicentrico nell’amaurosi congenita di leber: aspetti clinici e genetici 50
Reproducibility of en-face Optical Coherence Tomography Imaging for Macular Atrophy Area Evaluation in Juvenile Macular Degeneration 50
Prevalence of macular abnormalities assessed by Optical Coherence Tomography in patients with Usher Syndrome 50
Effective delivery of large genes to the retina by dual AAV vectors. 49
Can we utilize photorefractive keratectomy to improve visual acuity in adult amblyopic eyes? 49
Prevalence of macular abnormalities assessed by optical coherence tomography in patients with Usher syndrome 49
Studio clinico genetico in pazienti con degenerazione maculare senile 49
Una rara metastasi coroideale: descrizione di un caso 49
Macular Function and Morphologic Features in Juvenile Stargardt Disease Longitudinal Study 49
Trattamento farmacologico del glaucoma: prospettive terapeutiche. 48
Clinical expression of cone dystrophy associated with a novel deleterious ABCR (ABCA4) mutation in an italian family 48
Correlazione tra l’integrità dello strato dei fotorecettori retinici e la funzione visiva in pazienti affetti da Degenerazione maculare giovanile di Stargardt 47
Evaluation of central cloudy distrophy with in vivo confocal microscopy 47
ARPE-19-derived VEGF-containing exosomes promote neovascularization in HUVEC: the role of the melanocortin receptor 5 47
Totale 6.249
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Categoria #
all - tutte 39.529
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 39.529
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020642 0 0 0 0 176 36 187 47 74 59 47 16
2020/20211.568 101 5 166 182 240 9 185 159 22 214 186 99
2021/20221.218 84 5 19 26 374 16 39 35 42 126 105 347
2022/20232.678 219 81 36 217 341 239 9 152 1.247 27 61 49
2023/2024940 87 39 34 86 314 34 17 27 3 29 65 205
2024/2025420 8 35 36 94 247 0 0 0 0 0 0 0
Totale 9.425