IRIS
TESTA, Francesco
 Distribuzione geografica
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Continente #
EU - Europa 15.285
NA - Nord America 7.781
AS - Asia 5.978
SA - Sud America 876
AF - Africa 66
OC - Oceania 19
Continente sconosciuto - Info sul continente non disponibili 13
AN - Antartide 1
Totale 30.019
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Nazione #
RU - Federazione Russa 9.114
US - Stati Uniti d'America 7.653
SG - Singapore 2.008
IE - Irlanda 1.633
CN - Cina 1.375
IT - Italia 1.168
VN - Vietnam 876
UA - Ucraina 810
HK - Hong Kong 805
BR - Brasile 725
GB - Regno Unito 706
DE - Germania 459
FR - Francia 420
SE - Svezia 328
FI - Finlandia 235
IN - India 203
TR - Turchia 189
KR - Corea 184
GR - Grecia 161
JP - Giappone 147
CA - Canada 64
AR - Argentina 54
BE - Belgio 47
MX - Messico 33
AT - Austria 31
BD - Bangladesh 30
CZ - Repubblica Ceca 30
EC - Ecuador 27
ES - Italia 27
NL - Olanda 25
IQ - Iraq 24
ID - Indonesia 23
PL - Polonia 23
PK - Pakistan 19
AU - Australia 18
CH - Svizzera 17
CL - Cile 15
UZ - Uzbekistan 14
VE - Venezuela 14
PY - Paraguay 13
ZA - Sudafrica 13
EU - Europa 12
KE - Kenya 12
AE - Emirati Arabi Uniti 11
CO - Colombia 11
RO - Romania 11
SC - Seychelles 11
MA - Marocco 10
PE - Perù 10
SA - Arabia Saudita 10
LT - Lituania 8
GT - Guatemala 7
KZ - Kazakistan 7
DZ - Algeria 6
PH - Filippine 6
TH - Thailandia 6
AZ - Azerbaigian 5
BY - Bielorussia 5
JO - Giordania 5
NP - Nepal 5
UY - Uruguay 5
AL - Albania 4
EG - Egitto 4
JM - Giamaica 4
MD - Moldavia 4
BN - Brunei Darussalam 3
CR - Costa Rica 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
EE - Estonia 3
HN - Honduras 3
HR - Croazia 3
HU - Ungheria 3
KG - Kirghizistan 3
MY - Malesia 3
PA - Panama 3
BH - Bahrain 2
CU - Cuba 2
IL - Israele 2
IR - Iran 2
NG - Nigeria 2
OM - Oman 2
PT - Portogallo 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
SV - El Salvador 2
TN - Tunisia 2
TW - Taiwan 2
AO - Angola 1
AQ - Antartide 1
BB - Barbados 1
BO - Bolivia 1
CG - Congo 1
CI - Costa d'Avorio 1
CY - Cipro 1
DM - Dominica 1
ET - Etiopia 1
GE - Georgia 1
GY - Guiana 1
KW - Kuwait 1
Totale 30.008
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Città #
Moscow 3.227
Dublin 1.619
Jacksonville 1.203
Chandler 960
Santa Clara 934
Singapore 907
Hong Kong 781
San Jose 624
Ashburn 293
Ho Chi Minh City 272
Princeton 230
Boardman 208
Hanoi 206
Seoul 182
Roxbury 177
Ann Arbor 175
Hefei 160
Beijing 157
Woodbridge 140
Bengaluru 139
Bremen 128
Cambridge 120
Medford 119
Dallas 115
Los Angeles 107
The Dalles 101
Wilmington 101
New York 84
Rome 80
Nanjing 66
San Mateo 64
Da Nang 62
Caserta 60
Naples 60
Munich 58
Jinan 57
Des Moines 54
São Paulo 52
Memphis 51
Istanbul 47
Brussels 45
Dong Ket 42
Mountain View 40
Shenyang 37
Haiphong 36
Nuremberg 34
Taiyuan 34
Tianjin 32
Brno 30
Rio de Janeiro 30
Bologna 28
Council Bluffs 28
Milan 27
Chicago 26
Orem 26
Guangzhou 23
Haikou 23
Turku 23
Düsseldorf 22
London 22
Nanchang 22
Norwalk 21
Atlanta 20
Biên Hòa 20
San Francisco 20
Casoria 19
Changsha 19
Lanzhou 19
Belo Horizonte 18
Hebei 18
Taizhou 18
Aversa 17
Brasília 17
Helsinki 17
Redwood City 17
Tokyo 17
Toronto 17
Auburn Hills 16
Brooklyn 16
Hải Dương 16
Ningbo 16
Chennai 15
Napoli 15
Reggio Nell'emilia 15
Castelfranco Emilia 14
Frankfurt am Main 14
Mumbai 14
Vienna 14
Warsaw 14
Houston 13
Manchester 13
Tashkent 13
Zhengzhou 13
Bến Tre 12
Hangzhou 12
Perth 12
Guayaquil 11
Kunming 11
Padova 11
Baghdad 10
Totale 15.414
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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 240
An Alu-mediated duplication in NMNAT1, involved in NAD biosynthesis, causes a novel syndrome, SHILCA, affecting multiple tissues and organs 239
Caratteristiche cliniche e diagnosi della retinite pigmentosa monolaterale 230
Caratterizzazione clinico-genetica di pazienti italiani con Distrofia Cristallina di Bietti 222
Analisi del gene della periferina/rds in famiglie con distrofia a pattern dell’epitelio pigmentato retinico 215
Post-operative results of corneal collagen cross-linking for progressive keratoconus 201
Activation of Melanocortin Receptors MC1 and MC5 Attenuates Retinal Damage in Experimental Diabetic Retinopathy 199
A pilot study for development of a novel tool for clinical decision making to identify fallers among ophthalmic patients 198
Mutations in the PCYT1A gene are responsible for isolated forms of retinal dystrophy 195
AAV-mediated photoreceptor transduction of the pig cone-enriched retina 187
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial 183
Emeralopia stazionaria congenita. Caratteristiche cliniche e diagnosi differenziale 179
Carbonic anhydrase inhibitors in patients with X-linked retinoschisis: effects on macular morphology and function 178
Clinical and genetic analysis of a european cohort with pericentral retinitis pigmentosa 174
Clinical and Genetic Evaluation of a Cohort of Pediatric Patients with Severe Inherited Retinal Dystrophies 173
Prevalence of macular abnormalities assessed by Optical Coherence Tomography in patients with Usher Syndrome 172
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy 171
Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease 169
Identifying fallers among ophthalmic patients using classification tree methodology 169
Aspetti clinici dell’albinismo oculo-cutaneo correlato a mutazioninei geni TYR e MATP 167
Biofeedback Rehabilitation in Patients with Stargardt disease: a randomized controlled trial 167
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation 166
An Atypical Form of Bietti Crystalline Dystrophy 165
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene 164
Association between genotype and disease progression in Italian stargardt patients: A retrospective natural history study 164
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 162
Evaluation of ocular gene therapy in an italian patient affected by congenital leber amaurosis type 2 treated in both eyes 162
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 162
High levels of serum ubiquitin and proteasome in a case of HLA-B27 uveitis 160
A novel mutation in the RDS gene in an Italian family with pattern dystrophy 159
Union Makes Strength: A Worldwide Collaborative Genetic and Clinical Study to Provide a Comprehensive Survey of RD3 Mutations and Delineate the Associated Phenotype 156
Sicurezza ed efficacia della terapia genica nell'Amaurosi Congenita di Leber: un anno di followup. 156
Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family 155
Photorefractive Keratectomy on Purely Refractive Accommodative Esotropia. 155
Diagnosi differenziale nelle forme atipiche di retinite pigmentosa 154
CHM/REP1 transcript expression and loss of visual function in patients affected by choroideremia 154
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene. 152
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 152
The role of optical coherence tomography in an atypical case of oculocutaneous albinism: A case report 151
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 151
Caso clinico di retinite pigmentosa e drusen della testa del nervo ottico 149
Clinical presentation and disease course in Choroideremia patients 149
Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with leber congenital amaurosis type 2 148
Studio clinico sulla retinite pigmentosa pericentrale: confronto tra forme ereditarie e sporadiche 148
Aspetti clinici delle carriers di coroideremia 147
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy 146
Clinical and genetic features in Italian Bietti crystalline dystrophy patients 146
Analisi di mutazione del gene REP1 in famiglie Italiane affette da coroideremia 146
Mild clinical presentation of joubert syndrome in a male adult carrying biallelic mks1 truncating variants 146
Age related macular degeneration 145
Intrafamilial heterogeneity of congenital optic disc pit maculopathy 145
Incidence of high myopia in italian patients with retinitis pigmentosa 144
Prevalence of macular abnormalities assessed by optical coherence tomography in patients with Usher syndrome 143
Valutazione della Progressione della Atrofia Corioretinica Pigmentata Paravenosa (PPRCA): Case Report 142
Pupillometric analysis for assessment of gene therapy in Leber Congenital Amaurosis patients 142
Melanocortin receptor agonists MCR1-5 protect photoreceptors from high-glucose damage and restore antioxidant enzymes in primary retinal cell culture 141
Wearable Improved Vision System for Color Vision Deficiency Correction 141
A Novel Variant in TUBB4B Causes Progressive Cone‐Rod Dystrophy and Early Onset Sensorineural Hearing Loss 140
Visual function and retinal changes after voretigene neparvovec treatment in children with biallelic RPE65-related inherited retinal dystrophy 140
Aspetti clinici e genetici nella malattia di Best 140
Studio clinico genetico di pazienti con amaurosi congenita di Leber 140
Efficacia della terapia genica per l’Amaurosi Congenita di Leber fino a tre anni dopo la somministrazione del vettore virale 140
Biofeedback rehabilitation and visual cortex response in stargardt’s disease: A randomized controlled trial 140
Choroidal vascularity features in patients with choroideremia and cystoid spaces 139
Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration 138
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina. 138
A novel mutation in the VMD2 gene in an Italian family with Best maculopathy 137
Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease (Genetics in Medicine, (2018), 10.1038/s41436-018-0345-5) 137
Clinical expression of juvenile x-linked retinoschisis in Italian families with mutations in the XLRS1 gene 136
Trattamento con acetazolamide dell’edema maculare cistoide in pazienti affetti da retinite pigmentosa. 136
X-lnked retinitis pigmentosa (RP3): screening for new mutations and promoter analysis of RPGR gene 136
X-lnked retinitis pigmentosa (RP3): screening for new mutations and promoter analysis of RPGR gene 136
Clinical and molecular characterization of achromatopsia patients: A longitudinal study 136
Evaluation of Italian Patients with Leber Congenital Amaurosis due to AIPL1 Mutations Highlights the Potential Applicability of Gene Therapy 135
Voretigene neparvovec gene therapy in clinical practice: treatment of the first two italian pediatric patients 135
Baseline characteristics of patients with Usher Syndrome due to MYO7A mutations enrolled in a prospective natural history study 135
Characterization of Italian Bietti Crystalline Dystrophy Patients with CYP4V2 Mutations 134
Clinical expression of cone dystrophy associated with a novel deleterious ABCR (ABCA4) mutation in an italian family 134
Analisi di mutazione del gene XLRS1 in famiglie Italiane affette da retinoschisi X-linked congenita 134
Whole genome sequencing identifies elusive variants in genetically unsolved Italian inherited retinal disease patients 133
Analisi molecolare del gene ABCR in famiglie con Sindrome di Stargardt 133
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients 133
Spectrum of Disease Severity in Patients With X-Linked Retinitis Pigmentosa Due to RPGR Mutations 132
Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian population 130
Analisi dei polimorfismi del gene paraoxonasi in pazienti affetti da degenerazione maculare senile 130
An Italian family affected by autosomal dominant microcephaly with chorioretinal degeneration 130
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity 129
Trattamento dell'edema maculare cistoide in pazienti con retinite pigmentosa 129
Decorso clinico della Retinite Pigmentosa nelle varie forme genetiche 129
Interplay between Intravitreal RvD1 and Local Endogenous Sirtuin-1 in the Protection from Endotoxin-Induced Uveitis in Rats. 129
Iatrogenic ophthalmic artery occlusion after platelet-rich plasma dermal filler documented with ultra-widefield imaging 129
Pericentral Retinitis Pigmentosa is associated with a high prevalence of USH2A pathogenic variants in an Italian cohort of patients 128
Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy. 127
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 127
Molecular epidemiology of Usher syndrome in Italy 127
A multidisciplinary approach to inherited retinal dystrophies from diagnosis to initial care: a narrative review with inputs from clinical practice 125
Clinical case of retinitis pigmentosa and drusen of the head of the optical nerve 125
Autosomal recessive retinitis pigmentosa gene analysis in Italian patients 125
Studio clinico-genetico di una famiglia con retinite pigmentosa autosomica dominante associata ad una nuova mutazione nel gene PRPF8. 125
XXIII International Congress of Ophthalmology 125
Totale 15.212
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Categoria #
all - tutte 97.314
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 97.314
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021121 0 0 0 0 0 0 0 0 0 0 0 121
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
2024/20253.610 20 54 45 125 549 506 443 366 431 448 333 290
2025/202615.198 569 761 664 669 1.214 8.525 989 601 533 356 296 21
Totale 30.437