IRIS
TESTA, Francesco
 Distribuzione geografica
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Continente #
NA - Nord America 5.750
EU - Europa 5.651
AS - Asia 1.640
SA - Sud America 58
AF - Africa 19
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 12
Totale 13.143
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Nazione #
US - Stati Uniti d'America 5.720
IE - Irlanda 1.630
IT - Italia 979
UA - Ucraina 796
GB - Regno Unito 633
CN - Cina 552
HK - Hong Kong 456
DE - Germania 382
FR - Francia 377
SG - Singapore 341
SE - Svezia 320
FI - Finlandia 208
TR - Turchia 179
GR - Grecia 160
BR - Brasile 48
BE - Belgio 45
VN - Vietnam 42
CZ - Repubblica Ceca 30
KR - Corea 22
RU - Federazione Russa 20
CA - Canada 17
AU - Australia 13
IN - India 13
AT - Austria 12
EU - Europa 12
SC - Seychelles 11
CH - Svizzera 10
AE - Emirati Arabi Uniti 8
NL - Olanda 8
PL - Polonia 8
RO - Romania 8
ES - Italia 7
ID - Indonesia 7
CL - Cile 5
GT - Guatemala 5
KZ - Kazakistan 4
MD - Moldavia 4
HU - Ungheria 3
IQ - Iraq 3
LT - Lituania 3
MX - Messico 3
PK - Pakistan 3
AL - Albania 2
AR - Argentina 2
BY - Bielorussia 2
CU - Cuba 2
JP - Giappone 2
MA - Marocco 2
NG - Nigeria 2
PA - Panama 2
ZA - Sudafrica 2
AZ - Azerbaigian 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EC - Ecuador 1
EE - Estonia 1
GE - Georgia 1
IL - Israele 1
IR - Iran 1
KE - Kenya 1
NO - Norvegia 1
NP - Nepal 1
PE - Perù 1
PH - Filippine 1
PT - Portogallo 1
SA - Arabia Saudita 1
UZ - Uzbekistan 1
VE - Venezuela 1
Totale 13.143
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Città #
Dublin 1.618
Jacksonville 1.197
Chandler 960
Santa Clara 892
Hong Kong 455
Princeton 230
Singapore 209
Boardman 208
Roxbury 177
Ann Arbor 175
Woodbridge 138
Bremen 128
Cambridge 120
Medford 119
Wilmington 101
Beijing 67
Rome 67
Nanjing 65
San Mateo 64
Caserta 60
Ashburn 55
Jinan 53
Des Moines 52
Istanbul 46
Brussels 44
Dong Ket 42
Mountain View 40
Naples 35
Shenyang 34
Taiyuan 34
New York 33
Brno 30
Tianjin 25
Los Angeles 24
Düsseldorf 22
Haikou 22
Munich 22
Nanchang 22
Seoul 22
Norwalk 21
Lanzhou 19
Bologna 18
Hebei 18
Redwood City 17
Taizhou 17
Auburn Hills 16
Changsha 16
Guangzhou 16
Milan 16
Ningbo 16
Aversa 15
Napoli 15
Reggio Nell'emilia 15
Castelfranco Emilia 14
Helsinki 14
Zhengzhou 12
Houston 11
Kunming 11
Perth 11
Florence 10
Padova 10
Hangzhou 8
London 8
Nuremberg 8
São Paulo 8
Toronto 8
Falkenstein 7
Jakarta 7
Jiaxing 7
Maletto 7
Portici 7
Washington 7
Collegeville 6
Fuzhou 6
Salerno 6
Seattle 6
St Petersburg 6
Torre del Greco 6
Vienna 6
Dubai 5
Fairfield 5
Falls Church 5
Guatemala City 5
Palermo 5
Teramo 5
Almaty 4
Avella 4
Avellino 4
Bari 4
Baselicaduce 4
Brescia 4
Catania 4
Changchun 4
Chicago 4
Edinburgh 4
Ercolano 4
Mumbai 4
New Haven 4
Nizhniy Novgorod 4
Peschiera Del Garda 4
Totale 8.249
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Nome #
Caratteristiche cliniche e diagnosi della retinite pigmentosa monolaterale 154
An Alu-mediated duplication in NMNAT1, involved in NAD biosynthesis, causes a novel syndrome, SHILCA, affecting multiple tissues and organs 140
Analisi di correlazione genotipo fenotipo in una famiglia con retinite pigmentosa autosomica dominante associata ad una nuova mutazione nel gene PRPF8 133
Analisi del gene della periferina/rds in famiglie con distrofia a pattern dell’epitelio pigmentato retinico 131
Caratterizzazione clinico-genetica di pazienti italiani con Distrofia Cristallina di Bietti 121
Emeralopia stazionaria congenita. Caratteristiche cliniche e diagnosi differenziale 102
Diagnosi differenziale nelle forme atipiche di retinite pigmentosa 100
Sicurezza ed efficacia della terapia genica nell'Amaurosi Congenita di Leber: un anno di followup. 99
Activation of Melanocortin Receptors MC1 and MC5 Attenuates Retinal Damage in Experimental Diabetic Retinopathy 94
Studio clinico sulla retinite pigmentosa pericentrale: confronto tra forme ereditarie e sporadiche 91
Post-operative results of corneal collagen cross-linking for progressive keratoconus 90
Mutations in the PCYT1A gene are responsible for isolated forms of retinal dystrophy 90
Union Makes Strength: A Worldwide Collaborative Genetic and Clinical Study to Provide a Comprehensive Survey of RD3 Mutations and Delineate the Associated Phenotype 88
AAV-mediated photoreceptor transduction of the pig cone-enriched retina 85
Identifying fallers among ophthalmic patients using classification tree methodology 85
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina. 84
A pilot study for development of a novel tool for clinical decision making to identify fallers among ophthalmic patients 84
Wearable Improved Vision System for Color Vision Deficiency Correction 82
Biofeedback Rehabilitation in Patients with Stargardt disease: a randomized controlled trial 82
Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with leber congenital amaurosis type 2 80
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial 80
Studio clinico genetico di pazienti con amaurosi congenita di Leber 80
Evaluation of Italian Patients with Leber Congenital Amaurosis due to AIPL1 Mutations Highlights the Potential Applicability of Gene Therapy 78
The role of optical coherence tomography in an atypical case of oculocutaneous albinism: A case report 78
Trattamento con acetazolamide dell’edema maculare cistoide in pazienti affetti da retinite pigmentosa. 78
Studio di correlazione genotipo fenotipo in sindrome di Stargardt 78
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy 76
Incidence of high myopia in italian patients with retinitis pigmentosa 76
Analisi molecolare del gene ABCR in famiglie con Sindrome di Stargardt 76
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 75
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation 75
Clinical and genetic analysis of a european cohort with pericentral retinitis pigmentosa 75
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene. 74
Valutazione della Progressione della Atrofia Corioretinica Pigmentata Paravenosa (PPRCA): Case Report 74
Trattamento dell'edema maculare cistoide in pazienti con retinite pigmentosa 74
Strategie chirurgiche nella terapia genica 74
Efficacia della terapia genica per l’Amaurosi Congenita di Leber fino a tre anni dopo la somministrazione del vettore virale 74
Studio clinico-genetico di una famiglia con retinite pigmentosa autosomica dominante associata ad una nuova mutazione nel gene PRPF8. 73
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 73
Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian population 72
Aspetti clinici dell’albinismo oculo-cutaneo correlato a mutazioninei geni TYR e MATP 72
Nuova mutazione del gene ABCR associata a distrofia dei coni 72
Clinical and Genetic Evaluation of a Cohort of Pediatric Patients with Severe Inherited Retinal Dystrophies 72
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 71
Photorefractive Keratectomy on Purely Refractive Accommodative Esotropia. 71
Evaluation of ocular gene therapy in an italian patient affected by congenital leber amaurosis type 2 treated in both eyes 71
Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family 70
Carbonic anhydrase inhibitors in patients with X-linked retinoschisis: effects on macular morphology and function 70
Apolipoprotein E polymorphisms in age-related macular degeneration in an Italian population 69
Pupillometric analysis for assessment of gene therapy in Leber Congenital Amaurosis patients 69
XXIII International Congress of Ophthalmology 69
Analisi di mutazione del gene REP1 in famiglie Italiane affette da coroideremia 69
Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration 68
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene 68
Molecular epidemiology of Usher syndrome in Italy 68
Age related macular degeneration 68
Aspetti clinici e genetici nella malattia di Best 68
Association between genotype and disease progression in Italian stargardt patients: A retrospective natural history study 68
A novel mutation in the RDS gene in an Italian family with pattern dystrophy 67
Studio clinico in una carrier di coroideremia con una manifestazione completa della malattia 67
Differente espressione clinica in una famiglia italiana con mutazione nel gene RDS-periferina e distrofia dell'epitelio pigmentato retinico 67
Cone-rod dystrophy phenotype associated with ABCA4 (ABCR) gene mutation 67
X-lnked retinitis pigmentosa (RP3): screening for new mutations and promoter analysis of RPGR gene 67
Intrafamilial heterogeneity of congenital optic disc pit maculopathy 67
Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease 67
An Atypical Form of Bietti Crystalline Dystrophy 66
Caso clinico di retinite pigmentosa e drusen della testa del nervo ottico 66
Aspetti clinici delle carriers di coroideremia 66
Retinite pigmentosa autosomica dominante: correlazione genotipo fenotipo in una famiglia italiana con mutazione nel gene NRL 65
Malattia di Coats e retinite pigmentosa. Un caso clinico 64
Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa 64
Decorso clinico della Retinite Pigmentosa nelle varie forme genetiche 64
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 64
Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy. 63
Analisi molecolare del gene ABCR in famiglie con Sindrome di Stargardt 63
Sindrome di Usher: una valutazione clinica 62
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 62
Retinite pigmentosa X-linked (RP3): ricerca di nuove mutazioni ed analisi del promotore del gene RPGR 62
Analisi di mutazione del gene XLRS1 in famiglie Italiane affette da retinoschisi X-linked congenita 62
X-lnked retinitis pigmentosa (RP3): screening for new mutations and promoter analysis of RPGR gene 62
Analisi molecolare del gene RPGR in pazienti affetti da retinite pigmentosa X-linked 62
Severo fenotipo clinico in carriers di coroideremia associato ad una nuova mutazione del gene CHM 62
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity 61
A novel mutation in the VMD2 gene in an Italian family with Best maculopathy 61
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 61
Analisi dei polimorfismi del gene paraoxonasi in pazienti affetti da degenerazione maculare senile 61
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina 61
Aspetti ecografici della retinoschisi X-linked congenita 61
Studio dei polimorfismi del gene paraoxonasi nella degenerazione maculare senile 61
Analisi molecolare di mutazioni in pazienti affettti da retinite pigmentosa associata al cromosoma X 61
High levels of serum ubiquitin and proteasome in a case of HLA-B27 uveitis 60
Prevalence of macular abnormalities assessed by optical coherence tomography in patients with Usher syndrome 59
Mutation analysis of RPGR gene in patients with X-linked Retinitis Pigmentosa (RP3) 59
Correlazione genotipo fenotipo in famiglie con coroideremia 59
Prevalence of macular abnormalities assessed by Optical Coherence Tomography in patients with Usher Syndrome 59
New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease 58
Molecular and clinical characterization of albinism in a large cohort of Italian patients 58
Genotyping microarray (gene chip) for the ABCR (ABCA4) gene 58
Clinical and genetic features in Italian Bietti crystalline dystrophy patients 58
CLINICAL PRESENTATION and DISEASE COURSE of USHER SYNDROME because of MUTATIONS in MYO7A or USH2A 58
Totale 7.403
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Categoria #
all - tutte 55.293
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 55.293
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020361 0 0 0 0 0 0 0 82 100 86 57 36
2020/20212.114 136 10 211 318 325 13 238 202 32 267 241 121
2021/20221.548 87 8 39 29 467 16 28 99 62 141 109 463
2022/20233.309 273 117 38 273 388 304 2 191 1.556 28 69 70
2023/20241.240 117 45 45 108 408 52 14 55 2 34 72 288
2024/20251.922 20 54 45 125 549 506 445 178 0 0 0 0
Totale 13.551