IRIS
ROSSI, Settimio
 Distribuzione geografica
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Continente #
EU - Europa 4.102
NA - Nord America 3.781
AS - Asia 536
AF - Africa 12
SA - Sud America 12
Continente sconosciuto - Info sul continente non disponibili 8
OC - Oceania 4
Totale 8.455
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Nazione #
US - Stati Uniti d'America 3.772
IE - Irlanda 1.294
UA - Ucraina 623
IT - Italia 543
GB - Regno Unito 512
CN - Cina 352
DE - Germania 300
SE - Svezia 243
FR - Francia 227
FI - Finlandia 162
GR - Grecia 124
TR - Turchia 104
VN - Vietnam 42
BE - Belgio 32
IN - India 13
SC - Seychelles 10
EU - Europa 8
BR - Brasile 7
RO - Romania 7
AE - Emirati Arabi Uniti 5
ES - Italia 5
PL - Polonia 5
MD - Moldavia 4
NL - Olanda 4
AT - Austria 3
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
BD - Bangladesh 2
NZ - Nuova Zelanda 2
PH - Filippine 2
PR - Porto Rico 2
SA - Arabia Saudita 2
SG - Singapore 2
CZ - Repubblica Ceca 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
PE - Perù 1
PT - Portogallo 1
SI - Slovenia 1
TH - Thailandia 1
TW - Taiwan 1
ZA - Sudafrica 1
Totale 8.455
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Città #
Dublin 1.294
Jacksonville 943
Chandler 748
Princeton 184
Ann Arbor 155
Roxbury 128
Boardman 122
Bremen 115
Woodbridge 112
Medford 101
Cambridge 89
Wilmington 87
San Mateo 65
Beijing 64
Nanjing 60
Caserta 58
Ashburn 53
Dong Ket 42
Des Moines 39
Brussels 31
Mountain View 29
Rome 29
Jinan 26
Norwalk 24
New York 23
Düsseldorf 21
Naples 20
Napoli 20
Taiyuan 18
Kunming 16
Shenyang 16
Nanchang 15
Tianjin 15
Auburn Hills 14
Haikou 14
Aversa 13
Lanzhou 13
Los Angeles 13
Redwood City 12
Changsha 11
Falls Church 11
Hebei 11
Houston 11
Ningbo 10
Taizhou 10
Florence 9
Guangzhou 8
Hangzhou 8
Milan 8
Zhengzhou 8
Bologna 7
Jiaxing 7
Reggio Nell'emilia 7
Changchun 6
Helsinki 6
Salerno 6
Castelfranco Emilia 5
London 5
Pune 5
Avella 4
Baselicaduce 4
Catania 4
Fuzhou 4
Venice 4
Brampton 3
Castel Gandolfo 3
Dubai 3
Forlì 3
Genova 3
Montereale Valcellina 3
Mumbai 3
Munich 3
Portici 3
Redmond 3
Seattle 3
Seregno 3
Stockholm 3
Torre Del Greco 3
Torre del Greco 3
Amsterdam 2
Andover 2
Arzano 2
Atlanta 2
Bedford 2
Bischheim 2
Brescia 2
Budapest 2
Casoria 2
Castellammare Di Stabia 2
Cedar Knolls 2
Chicago 2
Citerna 2
Dallas 2
Edinburgh 2
Fairfield 2
Fiumefreddo Bruzio 2
Fumone 2
Gravina di Catania 2
Gurgaon 2
Hanover 2
Totale 5.107
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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 125
Analisi del gene della periferina/rds in famiglie con distrofia a pattern dell’epitelio pigmentato retinico 120
Caratterizzazione clinico-genetica di pazienti italiani con Distrofia Cristallina di Bietti 107
Sicurezza ed efficacia della terapia genica nell'Amaurosi Congenita di Leber: un anno di followup. 91
ESTRUSIONE DI PIOMBAGGIO? RUOLO DELL’ECOGRAFIA 85
Post-operative results of corneal collagen cross-linking for progressive keratoconus 79
Activation of Melanocortin Receptors MC1 and MC5 Attenuates Retinal Damage in Experimental Diabetic Retinopathy 78
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina. 76
Terapia del glaucoma: the cannabinoids way. 73
Identifying fallers among ophthalmic patients using classification tree methodology 73
Recombinant vectors based on porcine adeno-associated viral serotypes transduce the murine and pig retina 72
Evaluation of Italian Patients with Leber Congenital Amaurosis due to AIPL1 Mutations Highlights the Potential Applicability of Gene Therapy 72
Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with leber congenital amaurosis type 2 71
AAV-mediated photoreceptor transduction of the pig cone-enriched retina 71
Studio clinico genetico di pazienti con amaurosi congenita di Leber 71
Wearable Improved Vision System for Color Vision Deficiency Correction 71
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial 70
Intravitreal Injections of Melanocortin Receptor 1, 5 Agonists Prevents Neovascularization in a VEGF165 Mouse Model of Retinopathy 69
Inhibition of Ocular Aldose Reductase by a New Benzofuroxane Derivative Ameliorates Rat Endotoxic Uveitis 68
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene. 68
The role of optical coherence tomography in an atypical case of oculocutaneous albinism: A case report 68
Trattamento con acetazolamide dell’edema maculare cistoide in pazienti affetti da retinite pigmentosa. 68
A pilot study for development of a novel tool for clinical decision making to identify fallers among ophthalmic patients 65
Studio clinico-genetico di una famiglia con retinite pigmentosa autosomica dominante associata ad una nuova mutazione nel gene PRPF8. 64
Efficacia della terapia genica per l’Amaurosi Congenita di Leber fino a tre anni dopo la somministrazione del vettore virale 64
Incidence of high myopia in italian patients with retinitis pigmentosa 63
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 63
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
Strategie chirurgiche nella terapia genica 61
Photorefractive Keratectomy on Purely Refractive Accommodative Esotropia. 60
Aspetti clinici dell’albinismo oculo-cutaneo correlato a mutazioninei geni TYR e MATP 60
VALUTAZIONE DELLA PRESSIONE INTRAOCULARE DOPO PRK IPERMETROPICA CON TONOMETRIA AD APPLANAZIONE E NON CONTACT 60
Analisi di mutazione del gene REP1 in famiglie Italiane affette da coroideremia 60
Hyperglycemia in streptozotocin-induced diabetes prolongs the inflammatory response of endotoxin-induced uveitis due to reduced ciliary body heme oxygenase-1 levels 60
Evaluation of ocular gene therapy in an italian patient affected by congenital leber amaurosis type 2 treated in both eyes 60
Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration 59
MicroRNA-Restricted transgene expression in the retina 59
A novel mutation in the RDS gene in an Italian family with pattern dystrophy 59
Intrafamilial heterogeneity of congenital optic disc pit maculopathy 59
Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy. 58
Pupillometric analysis for assessment of gene therapy in Leber Congenital Amaurosis patients 58
Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family 57
Malattia di Coats e retinite pigmentosa. Un caso clinico 57
Decorso clinico della Retinite Pigmentosa nelle varie forme genetiche 57
Retinite pigmentosa autosomica dominante: correlazione genotipo fenotipo in una famiglia italiana con mutazione nel gene NRL 57
Antibiotic drug prescription in respiratory tract infections: A pharmacoepidemiological survey among general practitioners in a region of Italy 56
Aspetti clinici delle carriers di coroideremia 56
Differente espressione clinica in una famiglia italiana con mutazione nel gene RDS-periferina e distrofia dell'epitelio pigmentato retinico 56
Severo fenotipo clinico in carriers di coroideremia associato ad una nuova mutazione del gene CHM 56
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 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 55
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene 54
Effects of nebivolol on human platelet aggregation 54
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 54
CAN WE UTILIZE PRK TO IMPROVE VISUAL ACUITY IN ADULT AMBLIOPIC EYES? 54
Studio dei polimorfismi del gene paraoxonasi nella degenerazione maculare senile 54
Standard versus trans-epithelial collagen cross-linking in keratoconus patients suitable for standard collagen cross-linking 54
Caso clinico di retinite pigmentosa e drusen della testa del nervo ottico 53
A glucose biosensor operating under non-isothermal conditions: The dynamic response 53
Emangioma capillare del disco ottico: 6 anni di Follow-up ecografico 53
TRATTAMENTO FOTOREFRATTIVO DELL’ASTIGMATISMO CON LA TECNICA DEI CILINDRI CROCIATI: STUDIO CLINICO 53
Sindrome di Usher: una valutazione clinica 52
Molecular and clinical characterization of albinism in a large cohort of Italian patients 51
An Atypical Form of Bietti Crystalline Dystrophy 51
Effects of docosahexaenoic acid on [Ca2+]i increase induced by doxorubicin in ventricular rat cardiomyocytes 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
Association between genotype and disease progression in Italian stargardt patients: A retrospective natural history study 51
Clinical and genetic features in Italian Bietti crystalline dystrophy patients 50
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina 50
CLINICAL PRESENTATION and DISEASE COURSE of USHER SYNDROME because of MUTATIONS in MYO7A or USH2A 50
High levels of serum ubiquitin and proteasome in a case of HLA-B27 uveitis 50
Efficient gene delivery to the cone-enriched pig retina by dual AAV vectors. 49
Intrafamilial clinical heterogeneity associated with a novel mutation of the retinal degeneration slow/peripherin gene 49
Clinical pharmacology of nebivolol 49
Studio multicentrico nell’amaurosi congenita di leber: aspetti clinici e genetici 49
New Insight in Retinal Phenotype of Patient with AIPL1 Mutations 49
Cannabinoid CB2 receptor activation reduces mouse myocardial ischemia-reperfusion injury: involvement of cytokine/chemokines and PMN 48
Dopaminergic dysfunction is associated with IL-1β-dependent mood alterations in experimental autoimmune encephalomyelitis. 48
Correlazione tra spessore maculare ed acutezza visiva centrale in pazienti affetti da retinite pigmentosa. 48
Management of hypertension by general practitioners: an Italian observational study 47
Genotype-phenotype correlation in Italian families with Stargardt disease 47
Cannabinoid CB2 receptor activation reduces mouse myocardial ischemia-reperfusion injury: involvement of cytokine/chemokine and PMN 47
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 47
CAPILLARY HEMANGIOMA OF THE OPTIC DISC: SIX-YEAR ECHO GRAPHIC FOLLOW-UP 47
Una rara metastasi coroideale: descrizione di un caso 47
Reproducibility of en-face Optical Coherence Tomography Imaging for Macular Atrophy Area Evaluation in Juvenile Macular Degeneration 47
Effective delivery of large genes to the retina by dual AAV vectors. 46
Can we utilize photorefractive keratectomy to improve visual acuity in adult amblyopic eyes? 46
Trattamento farmacologico del glaucoma: prospettive terapeutiche. 46
Macular abnormalities in Italian patients with retinitis pigmentosa. 46
Prevalence of macular abnormalities assessed by optical coherence tomography in patients with Usher syndrome 45
Hyaluronan-induced stimulation of corneal wound healing is a pure pharmacological effect 45
Correlazione tra l’integrità dello strato dei fotorecettori retinici e la funzione visiva in pazienti affetti da Degenerazione maculare giovanile di Stargardt 45
Macular Function and Morphologic Features in Juvenile Stargardt Disease Longitudinal Study 45
Clinical expression of cone dystrophy associated with a novel deleterious ABCR (ABCA4) mutation in an italian family 44
Evaluation of the effect of Acetazolamide on cystoid macular edema in retinitis pigmentosa 44
Studio clinico genetico in pazienti con degenerazione maculare senile 44
Evaluation of central cloudy distrophy with in vivo confocal microscopy 44
Prevalence of macular abnormalities assessed by Optical Coherence Tomography in patients with Usher Syndrome 44
ARPE-19-derived VEGF-containing exosomes promote neovascularization in HUVEC: the role of the melanocortin receptor 5 44
Totale 5.851
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Categoria #
all - tutte 30.044
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 30.044
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201947 0 0 0 0 0 0 0 0 0 0 18 29
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
2023/2024690 87 38 34 85 313 36 17 27 3 45 5 0
Totale 8.761