IRIS
TESTA, Francesco
 Distribuzione geografica
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Continente #
EU - Europa 5.577
NA - Nord America 5.072
AS - Asia 1.080
SA - Sud America 18
AF - Africa 17
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 12
Totale 11.789
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Nazione #
US - Stati Uniti d'America 5.053
IE - Irlanda 1.631
IT - Italia 949
UA - Ucraina 793
GB - Regno Unito 629
CN - Cina 523
FR - Francia 376
DE - Germania 368
SE - Svezia 319
SG - Singapore 288
FI - Finlandia 207
TR - Turchia 178
GR - Grecia 160
BE - Belgio 42
VN - Vietnam 42
CZ - Repubblica Ceca 30
KR - Corea 22
RU - Federazione Russa 14
AU - Australia 13
IN - India 13
EU - Europa 12
SC - Seychelles 11
BR - Brasile 10
CH - Svizzera 10
CA - Canada 9
PL - Polonia 8
RO - Romania 8
AT - Austria 7
ES - Italia 7
NL - Olanda 6
CL - Cile 5
GT - Guatemala 5
HK - Hong Kong 4
MD - Moldavia 4
AE - Emirati Arabi Uniti 3
HU - Ungheria 3
MX - Messico 3
BY - Bielorussia 2
CU - Cuba 2
JP - Giappone 2
NG - Nigeria 2
ZA - Sudafrica 2
AL - Albania 1
AR - Argentina 1
DK - Danimarca 1
DZ - Algeria 1
EC - Ecuador 1
EE - Estonia 1
IL - Israele 1
IR - Iran 1
KE - Kenya 1
KZ - Kazakistan 1
NO - Norvegia 1
PE - Perù 1
PH - Filippine 1
PK - Pakistan 1
Totale 11.789
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Città #
Dublin 1.619
Jacksonville 1.197
Chandler 960
Santa Clara 257
Princeton 231
Boardman 208
Roxbury 178
Ann Arbor 175
Singapore 173
Woodbridge 138
Bremen 129
Cambridge 121
Medford 119
Wilmington 101
Beijing 67
Nanjing 65
San Mateo 64
Rome 63
Caserta 60
Ashburn 55
Jinan 53
Des Moines 52
Istanbul 46
Dong Ket 42
Brussels 41
Mountain View 40
Naples 35
Shenyang 34
Taiyuan 34
New York 33
Brno 30
Tianjin 25
Düsseldorf 22
Haikou 22
Munich 22
Nanchang 22
Seoul 22
Norwalk 21
Lanzhou 19
Bologna 18
Hebei 18
Los Angeles 18
Redwood City 17
Taizhou 17
Auburn Hills 16
Guangzhou 16
Ningbo 16
Changsha 15
Napoli 15
Reggio Nell'emilia 15
Castelfranco Emilia 14
Helsinki 14
Milan 13
Zhengzhou 12
Houston 11
Kunming 11
Perth 11
Padova 10
Aversa 8
Florence 8
Hangzhou 8
Jiaxing 7
Maletto 7
Portici 7
Washington 7
Collegeville 6
London 6
Salerno 6
Seattle 6
Torre del Greco 6
Vienna 6
Fairfield 5
Falls Church 5
Fuzhou 5
Guatemala City 5
Palermo 5
St Petersburg 5
Teramo 5
Avella 4
Avellino 4
Bari 4
Baselicaduce 4
Brescia 4
Catania 4
Changchun 4
Chicago 4
Edinburgh 4
Mumbai 4
New Haven 4
Peschiera Del Garda 4
Pozzuoli 4
Radomsko 4
Atella 3
Atlanta 3
Brampton 3
Budapest 3
Cassano delle Murge 3
Dubai 3
Fiumefreddo Bruzio 3
Forlì 3
Totale 7.075
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Nome #
Caratteristiche cliniche e diagnosi della retinite pigmentosa monolaterale 148
An Alu-mediated duplication in NMNAT1, involved in NAD biosynthesis, causes a novel syndrome, SHILCA, affecting multiple tissues and organs 131
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
Emeralopia stazionaria congenita. Caratteristiche cliniche e diagnosi differenziale 97
Diagnosi differenziale nelle forme atipiche di retinite pigmentosa 97
Sicurezza ed efficacia della terapia genica nell'Amaurosi Congenita di Leber: un anno di followup. 94
Studio clinico sulla retinite pigmentosa pericentrale: confronto tra forme ereditarie e sporadiche 87
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
Mutations in the PCYT1A gene are responsible for isolated forms of retinal dystrophy 83
Union Makes Strength: A Worldwide Collaborative Genetic and Clinical Study to Provide a Comprehensive Survey of RD3 Mutations and Delineate the Associated Phenotype 79
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
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
Studio di correlazione genotipo fenotipo in sindrome di Stargardt 75
Biofeedback Rehabilitation in Patients with Stargardt disease: a randomized controlled trial 75
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
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
Analisi molecolare del gene ABCR in famiglie con Sindrome di Stargardt 71
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene. 70
Valutazione della Progressione della Atrofia Corioretinica Pigmentata Paravenosa (PPRCA): Case Report 68
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
Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian population 67
Incidence of high myopia in italian patients with retinitis pigmentosa 67
Nuova mutazione del gene ABCR associata a distrofia dei coni 67
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 66
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
Clinical and Genetic Evaluation of a Cohort of Pediatric Patients with Severe Inherited Retinal Dystrophies 66
Clinical and genetic analysis of a european cohort with pericentral retinitis pigmentosa 66
Trattamento dell'edema maculare cistoide in pazienti con retinite pigmentosa 65
Analisi di mutazione del gene REP1 in famiglie Italiane affette da coroideremia 65
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation 65
XXIII International Congress of Ophthalmology 64
Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family 63
Molecular epidemiology of Usher syndrome in Italy 63
Photorefractive Keratectomy on Purely Refractive Accommodative Esotropia. 63
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy 63
Cone-rod dystrophy phenotype associated with ABCA4 (ABCR) gene mutation 63
Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration 62
A novel mutation in the RDS gene in an Italian family with pattern dystrophy 62
Apolipoprotein E polymorphisms in age-related macular degeneration in an Italian population 62
Studio clinico in una carrier di coroideremia con una manifestazione completa della malattia 62
Aspetti clinici e genetici nella malattia di Best 62
Intrafamilial heterogeneity of congenital optic disc pit maculopathy 62
Carbonic anhydrase inhibitors in patients with X-linked retinoschisis: effects on macular morphology and function 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
Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa 61
Pupillometric analysis for assessment of gene therapy in Leber Congenital Amaurosis patients 61
Age related macular degeneration 61
Differente espressione clinica in una famiglia italiana con mutazione nel gene RDS-periferina e distrofia dell'epitelio pigmentato retinico 61
X-lnked retinitis pigmentosa (RP3): screening for new mutations and promoter analysis of RPGR gene 61
Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease 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
Retinite pigmentosa X-linked (RP3): ricerca di nuove mutazioni ed analisi del promotore del gene RPGR 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
Analisi molecolare del gene RPGR in pazienti affetti da retinite pigmentosa X-linked 59
Analisi molecolare del gene ABCR in famiglie con Sindrome di Stargardt 59
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity 58
A novel mutation in the VMD2 gene in an Italian family with Best maculopathy 58
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
Aspetti ecografici della retinoschisi X-linked congenita 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
X-lnked retinitis pigmentosa (RP3): screening for new mutations and promoter analysis of RPGR gene 57
Analisi di mutazione del gene XLRS1 in famiglie Italiane affette da retinoschisi X-linked congenita 56
Mutation analysis of RPGR gene in patients with X-linked Retinitis Pigmentosa (RP3) 56
Studio dei polimorfismi del gene paraoxonasi nella degenerazione maculare senile 56
Analisi molecolare di mutazioni in pazienti affettti da retinite pigmentosa associata al cromosoma X 56
New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease 55
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
Analisi dei polimorfismi del gene paraoxonasi in pazienti affetti da degenerazione maculare senile 55
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina 55
Correlazione genotipo fenotipo in famiglie con coroideremia 55
Genotyping microarray (gene chip) for the ABCR (ABCA4) gene 54
Molecular and clinical characterization of albinism in a large cohort of Italian patients 53
Analisi molecolare del gene RP2 in famiglie affette da retinite pigmentosa associata al cromosoma X 53
CLINICAL PRESENTATION and DISEASE COURSE of USHER SYNDROME because of MUTATIONS in MYO7A or USH2A 53
Identification and characterization of C1orf36, a transcript highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa 52
Clinical and genetic features in Italian Bietti crystalline dystrophy patients 52
High levels of serum ubiquitin and proteasome in a case of HLA-B27 uveitis 52
Totale 6.823
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Categoria #
all - tutte 49.459
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 49.459
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020883 0 0 0 0 221 54 247 82 100 86 57 36
2020/20212.114 136 10 211 318 325 13 238 202 32 267 241 121
2021/20221.551 87 8 39 29 467 16 28 99 62 141 110 465
2022/20233.314 274 117 38 273 389 304 2 191 1.559 28 69 70
2023/20241.243 117 45 45 108 410 52 14 55 2 34 72 289
2024/2025530 20 54 45 125 286 0 0 0 0 0 0 0
Totale 12.170