IRIS
ROSSI, Settimio
 Distribuzione geografica
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Continente #
EU - Europa 4.157
NA - Nord America 3.825
AS - Asia 734
AF - Africa 14
SA - Sud America 14
Continente sconosciuto - Info sul continente non disponibili 8
OC - Oceania 4
Totale 8.756
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Nazione #
US - Stati Uniti d'America 3.816
IE - Irlanda 1.294
UA - Ucraina 623
IT - Italia 559
GB - Regno Unito 516
CN - Cina 385
DE - Germania 311
SE - Svezia 245
FR - Francia 227
FI - Finlandia 163
SG - Singapore 158
GR - Grecia 124
TR - Turchia 104
VN - Vietnam 42
BE - Belgio 32
CZ - Repubblica Ceca 18
IN - India 13
SC - Seychelles 10
EU - Europa 8
RO - Romania 8
BR - Brasile 7
ES - Italia 7
AE - Emirati Arabi Uniti 6
PL - Polonia 5
AT - Austria 4
IR - Iran 4
MD - Moldavia 4
NL - Olanda 4
BD - Bangladesh 3
CA - Canada 3
CH - Svizzera 3
CL - Cile 3
HU - Ungheria 3
IQ - Iraq 3
JP - Giappone 3
MX - Messico 3
RU - Federazione Russa 3
SA - Arabia Saudita 3
AU - Australia 2
GH - Ghana 2
NZ - Nuova Zelanda 2
PE - Perù 2
PH - Filippine 2
PK - Pakistan 2
PR - Porto Rico 2
CO - Colombia 1
DK - Danimarca 1
DZ - Algeria 1
EC - Ecuador 1
ID - Indonesia 1
IL - Israele 1
KR - Corea 1
KZ - Kazakistan 1
NO - Norvegia 1
PA - Panama 1
PT - Portogallo 1
SI - Slovenia 1
TH - Thailandia 1
TW - Taiwan 1
ZA - Sudafrica 1
Totale 8.756
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Città #
Dublin 1.294
Jacksonville 943
Chandler 748
Princeton 184
Boardman 156
Ann Arbor 155
Roxbury 128
Bremen 115
Woodbridge 112
Medford 101
Cambridge 89
Singapore 87
Wilmington 87
San Mateo 65
Beijing 64
Nanjing 60
Caserta 58
Ashburn 54
Dong Ket 42
Des Moines 39
Brussels 31
Rome 31
Mountain View 29
Jinan 26
Naples 24
Norwalk 24
New York 23
Düsseldorf 21
Napoli 20
Brno 18
Taiyuan 18
Kunming 16
Shenyang 16
Nanchang 15
Tianjin 15
Auburn Hills 14
Aversa 14
Haikou 14
Munich 14
Lanzhou 13
Los Angeles 13
Redwood City 12
Changsha 11
Falls Church 11
Hebei 11
Houston 11
Ningbo 10
Taizhou 10
Florence 9
Milan 9
Guangzhou 8
Hangzhou 8
Zhengzhou 8
Bologna 7
Jiaxing 7
Reggio Nell'emilia 7
Changchun 6
Helsinki 6
Salerno 6
Castelfranco Emilia 5
London 5
Pune 5
Stockholm 5
Avella 4
Baselicaduce 4
Catania 4
Fuzhou 4
New Haven 4
Venice 4
Brampton 3
Castel Gandolfo 3
Chicago 3
Dubai 3
Erbil 3
Forlì 3
Genova 3
Lappeenranta 3
Montereale Valcellina 3
Mumbai 3
Padova 3
Portici 3
Redmond 3
Santa Clara 3
Seattle 3
Seregno 3
Torre Del Greco 3
Torre del Greco 3
Vienna 3
Accra 2
Amsterdam 2
Andover 2
Arzano 2
Atlanta 2
Bedford 2
Bischheim 2
Brescia 2
Budapest 2
Buffalo 2
Casoria 2
Castellammare Di Stabia 2
Totale 5.272
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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 128
Analisi del gene della periferina/rds in famiglie con distrofia a pattern dell’epitelio pigmentato retinico 125
Caratterizzazione clinico-genetica di pazienti italiani con Distrofia Cristallina di Bietti 110
Sicurezza ed efficacia della terapia genica nell'Amaurosi Congenita di Leber: un anno di followup. 92
ESTRUSIONE DI PIOMBAGGIO? RUOLO DELL’ECOGRAFIA 87
Post-operative results of corneal collagen cross-linking for progressive keratoconus 81
Activation of Melanocortin Receptors MC1 and MC5 Attenuates Retinal Damage in Experimental Diabetic Retinopathy 81
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina. 77
AAV-mediated photoreceptor transduction of the pig cone-enriched retina 75
Terapia del glaucoma: the cannabinoids way. 74
Identifying fallers among ophthalmic patients using classification tree methodology 74
Recombinant vectors based on porcine adeno-associated viral serotypes transduce the murine and pig retina 73
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial 73
Wearable Improved Vision System for Color Vision Deficiency Correction 73
Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with leber congenital amaurosis type 2 72
Evaluation of Italian Patients with Leber Congenital Amaurosis due to AIPL1 Mutations Highlights the Potential Applicability of Gene Therapy 72
Studio clinico genetico di pazienti con amaurosi congenita di Leber 72
The role of optical coherence tomography in an atypical case of oculocutaneous albinism: A case report 70
Trattamento con acetazolamide dell’edema maculare cistoide in pazienti affetti da retinite pigmentosa. 70
Intravitreal Injections of Melanocortin Receptor 1, 5 Agonists Prevents Neovascularization in a VEGF165 Mouse Model of Retinopathy 70
Inhibition of Ocular Aldose Reductase by a New Benzofuroxane Derivative Ameliorates Rat Endotoxic Uveitis 69
A pilot study for development of a novel tool for clinical decision making to identify fallers among ophthalmic patients 69
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene. 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 67
Incidence of high myopia in italian patients with retinitis pigmentosa 65
Efficacia della terapia genica per l’Amaurosi Congenita di Leber fino a tre anni dopo la somministrazione del vettore virale 65
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 65
Studio clinico-genetico di una famiglia con retinite pigmentosa autosomica dominante associata ad una nuova mutazione nel gene PRPF8. 64
Aspetti clinici dell’albinismo oculo-cutaneo correlato a mutazioninei geni TYR e MATP 63
Strategie chirurgiche nella terapia genica 63
Photorefractive Keratectomy on Purely Refractive Accommodative Esotropia. 62
Analisi di mutazione del gene REP1 in famiglie Italiane affette da coroideremia 62
Evaluation of ocular gene therapy in an italian patient affected by congenital leber amaurosis type 2 treated in both eyes 62
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 61
Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family 61
MicroRNA-Restricted transgene expression in the retina 61
VALUTAZIONE DELLA PRESSIONE INTRAOCULARE DOPO PRK IPERMETROPICA CON TONOMETRIA AD APPLANAZIONE E NON CONTACT 61
Hyperglycemia in streptozotocin-induced diabetes prolongs the inflammatory response of endotoxin-induced uveitis due to reduced ciliary body heme oxygenase-1 levels 61
Intrafamilial heterogeneity of congenital optic disc pit maculopathy 61
Elective surgery system strengthening: development, measurement, and validation of the surgical preparedness index across 1632 hospitals in 119 countries 61
Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration 60
Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy. 60
A novel mutation in the RDS gene in an Italian family with pattern dystrophy 60
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene 59
Pupillometric analysis for assessment of gene therapy in Leber Congenital Amaurosis patients 59
Antibiotic drug prescription in respiratory tract infections: A pharmacoepidemiological survey among general practitioners in a region of Italy 58
Malattia di Coats e retinite pigmentosa. Un caso clinico 58
Retinite pigmentosa autosomica dominante: correlazione genotipo fenotipo in una famiglia italiana con mutazione nel gene NRL 58
Caso clinico di retinite pigmentosa e drusen della testa del nervo ottico 57
Decorso clinico della Retinite Pigmentosa nelle varie forme genetiche 57
Aspetti clinici delle carriers di coroideremia 57
Differente espressione clinica in una famiglia italiana con mutazione nel gene RDS-periferina e distrofia dell'epitelio pigmentato retinico 57
An Atypical Form of Bietti Crystalline Dystrophy 56
Hyperglycemia in streptozotocin-induced diabetes leads to persistent inflammation and tissue damage following uveitis due to reduced levels of ciliary body heme oxygenase-1 56
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 56
Severo fenotipo clinico in carriers di coroideremia associato ad una nuova mutazione del gene CHM 56
Association between genotype and disease progression in Italian stargardt patients: A retrospective natural history study 56
Studio dei polimorfismi del gene paraoxonasi nella degenerazione maculare senile 55
Standard versus trans-epithelial collagen cross-linking in keratoconus patients suitable for standard collagen cross-linking 55
Effects of nebivolol on human platelet aggregation 54
A glucose biosensor operating under non-isothermal conditions: The dynamic response 54
CAN WE UTILIZE PRK TO IMPROVE VISUAL ACUITY IN ADULT AMBLIOPIC EYES? 54
Emangioma capillare del disco ottico: 6 anni di Follow-up ecografico 54
Sindrome di Usher: una valutazione clinica 53
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina 53
TRATTAMENTO FOTOREFRATTIVO DELL’ASTIGMATISMO CON LA TECNICA DEI CILINDRI CROCIATI: STUDIO CLINICO 53
Effects of docosahexaenoic acid on [Ca2+]i increase induced by doxorubicin in ventricular rat cardiomyocytes 52
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 52
Molecular and clinical characterization of albinism in a large cohort of Italian patients 51
Clinical and genetic features in Italian Bietti crystalline dystrophy patients 51
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 51
CLINICAL PRESENTATION and DISEASE COURSE of USHER SYNDROME because of MUTATIONS in MYO7A or USH2A 51
High levels of serum ubiquitin and proteasome in a case of HLA-B27 uveitis 51
Efficient gene delivery to the cone-enriched pig retina by dual AAV vectors. 50
Cannabinoid CB2 receptor activation reduces mouse myocardial ischemia-reperfusion injury: involvement of cytokine/chemokines and PMN 50
Intrafamilial clinical heterogeneity associated with a novel mutation of the retinal degeneration slow/peripherin gene 49
Clinical pharmacology of nebivolol 49
Cannabinoid CB2 receptor activation reduces mouse myocardial ischemia-reperfusion injury: involvement of cytokine/chemokine and PMN 49
Correlazione tra spessore maculare ed acutezza visiva centrale in pazienti affetti da retinite pigmentosa. 49
Studio multicentrico nell’amaurosi congenita di leber: aspetti clinici e genetici 49
New Insight in Retinal Phenotype of Patient with AIPL1 Mutations 49
Management of hypertension by general practitioners: an Italian observational study 48
Dopaminergic dysfunction is associated with IL-1β-dependent mood alterations in experimental autoimmune encephalomyelitis. 48
CAPILLARY HEMANGIOMA OF THE OPTIC DISC: SIX-YEAR ECHO GRAPHIC FOLLOW-UP 48
Reproducibility of en-face Optical Coherence Tomography Imaging for Macular Atrophy Area Evaluation in Juvenile Macular Degeneration 48
Effective delivery of large genes to the retina by dual AAV vectors. 47
Genotype-phenotype correlation in Italian families with Stargardt disease 47
Can we utilize photorefractive keratectomy to improve visual acuity in adult amblyopic eyes? 47
Trattamento farmacologico del glaucoma: prospettive terapeutiche. 47
Prevalence of macular abnormalities assessed by optical coherence tomography in patients with Usher syndrome 47
Macular abnormalities in Italian patients with retinitis pigmentosa. 47
Studio clinico genetico in pazienti con degenerazione maculare senile 47
Una rara metastasi coroideale: descrizione di un caso 47
Prevalence of macular abnormalities assessed by Optical Coherence Tomography in patients with Usher Syndrome 47
Hyaluronan-induced stimulation of corneal wound healing is a pure pharmacological effect 46
Correlazione tra l’integrità dello strato dei fotorecettori retinici e la funzione visiva in pazienti affetti da Degenerazione maculare giovanile di Stargardt 46
Macular Function and Morphologic Features in Juvenile Stargardt Disease Longitudinal Study 46
ARPE-19-derived VEGF-containing exosomes promote neovascularization in HUVEC: the role of the melanocortin receptor 5 46
Clinical expression of cone dystrophy associated with a novel deleterious ABCR (ABCA4) mutation in an italian family 45
Evaluation of central cloudy distrophy with in vivo confocal microscopy 45
Totale 6.027
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Categoria #
all - tutte 33.951
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 33.951
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.069 185 181 38 23 176 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
2022/20232.684 219 81 36 217 339 239 14 152 1.250 27 61 49
2023/2024981 87 38 34 85 313 36 17 27 3 45 88 208
2024/202511 11 0 0 0 0 0 0 0 0 0 0 0
Totale 9.063