IRIS
TESTA, Francesco
 Distribuzione geografica
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Continente #
EU - Europa 15.600
NA - Nord America 9.691
AS - Asia 6.181
SA - Sud America 895
Continente sconosciuto - Info sul continente non disponibili 433
AF - Africa 67
OC - Oceania 19
AN - Antartide 1
Totale 32.887
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Nazione #
US - Stati Uniti d'America 9.518
RU - Federazione Russa 9.114
SG - Singapore 2.143
IE - Irlanda 1.633
IT - Italia 1.434
CN - Cina 1.397
VN - Vietnam 878
HK - Hong Kong 826
UA - Ucraina 812
BR - Brasile 732
GB - Regno Unito 724
DE - Germania 464
FR - Francia 422
SE - Svezia 328
FI - Finlandia 235
IN - India 208
TR - Turchia 190
KR - Corea 189
GR - Grecia 161
JP - Giappone 155
CA - Canada 80
AR - Argentina 56
BE - Belgio 47
MX - Messico 37
AT - Austria 31
BD - Bangladesh 30
CZ - Repubblica Ceca 30
EC - Ecuador 30
ES - Italia 29
NL - Olanda 27
ID - Indonesia 24
IQ - Iraq 24
PL - Polonia 24
PK - Pakistan 19
AU - Australia 18
RO - Romania 18
CH - Svizzera 17
CL - Cile 16
VE - Venezuela 15
CO - Colombia 14
UZ - Uzbekistan 14
PY - Paraguay 13
ZA - Sudafrica 13
AE - Emirati Arabi Uniti 12
EU - Europa 12
KE - Kenya 12
PE - Perù 12
SC - Seychelles 12
EE - Estonia 11
MA - Marocco 10
SA - Arabia Saudita 10
GT - Guatemala 9
CR - Costa Rica 8
LT - Lituania 8
JM - Giamaica 7
KZ - Kazakistan 7
DZ - Algeria 6
PH - Filippine 6
TH - Thailandia 6
AZ - Azerbaigian 5
BY - Bielorussia 5
HN - Honduras 5
JO - Giordania 5
MD - Moldavia 5
NP - Nepal 5
UY - Uruguay 5
AL - Albania 4
EG - Egitto 4
HR - Croazia 4
IL - Israele 4
TT - Trinidad e Tobago 4
BN - Brunei Darussalam 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
HU - Ungheria 3
KG - Kirghizistan 3
MY - Malesia 3
PA - Panama 3
SV - El Salvador 3
BB - Barbados 2
BH - Bahrain 2
CU - Cuba 2
IR - Iran 2
LC - Santa Lucia 2
NG - Nigeria 2
OM - Oman 2
PT - Portogallo 2
SK - Slovacchia (Repubblica Slovacca) 2
SN - Senegal 2
TN - Tunisia 2
TW - Taiwan 2
VI - Stati Uniti Isole Vergini 2
AO - Angola 1
AQ - Antartide 1
AW - Aruba 1
BO - Bolivia 1
CG - Congo 1
CI - Costa d'Avorio 1
CY - Cipro 1
DM - Dominica 1
Totale 32.450
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Città #
Moscow 3.227
Dublin 1.620
Jacksonville 1.204
Santa Clara 995
Chandler 960
Singapore 924
San Jose 918
Hong Kong 798
Ashburn 572
Council Bluffs 525
Ho Chi Minh City 272
Princeton 230
Boardman 208
Hanoi 208
Seoul 187
Roxbury 177
Ann Arbor 175
Beijing 174
Hefei 160
Woodbridge 140
Bengaluru 139
Bremen 128
Los Angeles 126
Dallas 122
Cambridge 121
Medford 119
Wilmington 102
The Dalles 101
Milan 97
Rome 94
New York 89
Naples 69
Nanjing 66
San Mateo 64
Da Nang 62
Caserta 60
Munich 58
Jinan 57
Des Moines 54
São Paulo 54
Memphis 51
Istanbul 48
Brussels 45
Dong Ket 42
Mountain View 40
Chicago 39
Shenyang 37
Haiphong 36
Nuremberg 34
Taiyuan 34
Tianjin 32
Bologna 31
Brno 30
Rio de Janeiro 30
Atlanta 29
Orem 27
Miano 26
San Francisco 25
Tokyo 25
Guangzhou 23
Haikou 23
Turku 23
Düsseldorf 22
London 22
Nanchang 22
Brooklyn 21
Norwalk 21
Biên Hòa 20
Houston 20
Brasília 19
Casoria 19
Changsha 19
Lanzhou 19
Belo Horizonte 18
Frankfurt am Main 18
Hebei 18
Taizhou 18
Toronto 18
Aversa 17
Helsinki 17
Redwood City 17
Auburn Hills 16
Hải Dương 16
Ningbo 16
Chennai 15
Napoli 15
Reggio Nell'emilia 15
Turin 15
Castelfranco Emilia 14
Manchester 14
Mumbai 14
Vienna 14
Warsaw 14
Denver 13
Florence 13
Tashkent 13
Zhengzhou 13
Buffalo 12
Bến Tre 12
Columbus 12
Totale 16.817
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Nome #
An Alu-mediated duplication in NMNAT1, involved in NAD biosynthesis, causes a novel syndrome, SHILCA, affecting multiple tissues and organs 253
Analisi di correlazione genotipo fenotipo in una famiglia con retinite pigmentosa autosomica dominante associata ad una nuova mutazione nel gene PRPF8 249
Caratteristiche cliniche e diagnosi della retinite pigmentosa monolaterale 237
Caratterizzazione clinico-genetica di pazienti italiani con Distrofia Cristallina di Bietti 237
Analisi del gene della periferina/rds in famiglie con distrofia a pattern dell’epitelio pigmentato retinico 222
Iatrogenic ophthalmic artery occlusion after platelet-rich plasma dermal filler documented with ultra-widefield imaging 221
Post-operative results of corneal collagen cross-linking for progressive keratoconus 213
A pilot study for development of a novel tool for clinical decision making to identify fallers among ophthalmic patients 209
Activation of Melanocortin Receptors MC1 and MC5 Attenuates Retinal Damage in Experimental Diabetic Retinopathy 207
Mutations in the PCYT1A gene are responsible for isolated forms of retinal dystrophy 206
AAV-mediated photoreceptor transduction of the pig cone-enriched retina 195
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial 194
Carbonic anhydrase inhibitors in patients with X-linked retinoschisis: effects on macular morphology and function 192
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy 190
Emeralopia stazionaria congenita. Caratteristiche cliniche e diagnosi differenziale 186
Clinical and Genetic Evaluation of a Cohort of Pediatric Patients with Severe Inherited Retinal Dystrophies 185
Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease 181
Prevalence of macular abnormalities assessed by Optical Coherence Tomography in patients with Usher Syndrome 181
Clinical and genetic analysis of a european cohort with pericentral retinitis pigmentosa 181
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene 180
Identifying fallers among ophthalmic patients using classification tree methodology 179
An Atypical Form of Bietti Crystalline Dystrophy 178
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation 175
Aspetti clinici dell’albinismo oculo-cutaneo correlato a mutazioninei geni TYR e MATP 174
Evaluation of ocular gene therapy in an italian patient affected by congenital leber amaurosis type 2 treated in both eyes 174
Biofeedback Rehabilitation in Patients with Stargardt disease: a randomized controlled trial 174
Association between genotype and disease progression in Italian stargardt patients: A retrospective natural history study 173
A novel mutation in the RDS gene in an Italian family with pattern dystrophy 172
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 172
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 171
Sicurezza ed efficacia della terapia genica nell'Amaurosi Congenita di Leber: un anno di followup. 170
High levels of serum ubiquitin and proteasome in a case of HLA-B27 uveitis 170
CHM/REP1 transcript expression and loss of visual function in patients affected by choroideremia 169
Photorefractive Keratectomy on Purely Refractive Accommodative Esotropia. 168
Union Makes Strength: A Worldwide Collaborative Genetic and Clinical Study to Provide a Comprehensive Survey of RD3 Mutations and Delineate the Associated Phenotype 166
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene. 165
Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with leber congenital amaurosis type 2 163
Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family 163
The role of optical coherence tomography in an atypical case of oculocutaneous albinism: A case report 161
Studio clinico sulla retinite pigmentosa pericentrale: confronto tra forme ereditarie e sporadiche 160
Diagnosi differenziale nelle forme atipiche di retinite pigmentosa 160
Clinical presentation and disease course in Choroideremia patients 160
Caso clinico di retinite pigmentosa e drusen della testa del nervo ottico 159
A Novel Variant in TUBB4B Causes Progressive Cone‐Rod Dystrophy and Early Onset Sensorineural Hearing Loss 158
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 158
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 158
Mild clinical presentation of joubert syndrome in a male adult carrying biallelic mks1 truncating variants 157
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy 156
Valutazione della Progressione della Atrofia Corioretinica Pigmentata Paravenosa (PPRCA): Case Report 156
Incidence of high myopia in italian patients with retinitis pigmentosa 155
Clinical and genetic features in Italian Bietti crystalline dystrophy patients 155
Aspetti clinici delle carriers di coroideremia 155
Age related macular degeneration 154
Intrafamilial heterogeneity of congenital optic disc pit maculopathy 154
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina. 153
Analisi di mutazione del gene REP1 in famiglie Italiane affette da coroideremia 153
Wearable Improved Vision System for Color Vision Deficiency Correction 152
Visual function and retinal changes after voretigene neparvovec treatment in children with biallelic RPE65-related inherited retinal dystrophy 151
Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration 151
Prevalence of macular abnormalities assessed by optical coherence tomography in patients with Usher syndrome 151
Pupillometric analysis for assessment of gene therapy in Leber Congenital Amaurosis patients 150
Aspetti clinici e genetici nella malattia di Best 150
A novel mutation in the VMD2 gene in an Italian family with Best maculopathy 148
Studio clinico genetico di pazienti con amaurosi congenita di Leber 148
X-lnked retinitis pigmentosa (RP3): screening for new mutations and promoter analysis of RPGR gene 148
Melanocortin receptor agonists MCR1-5 protect photoreceptors from high-glucose damage and restore antioxidant enzymes in primary retinal cell culture 148
Choroidal vascularity features in patients with choroideremia and cystoid spaces 148
Efficacia della terapia genica per l’Amaurosi Congenita di Leber fino a tre anni dopo la somministrazione del vettore virale 147
Biofeedback rehabilitation and visual cortex response in stargardt’s disease: A randomized controlled trial 147
Trattamento con acetazolamide dell’edema maculare cistoide in pazienti affetti da retinite pigmentosa. 146
Evaluation of Italian Patients with Leber Congenital Amaurosis due to AIPL1 Mutations Highlights the Potential Applicability of Gene Therapy 145
Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian population 144
Characterization of Italian Bietti Crystalline Dystrophy Patients with CYP4V2 Mutations 144
X-lnked retinitis pigmentosa (RP3): screening for new mutations and promoter analysis of RPGR gene 144
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) 144
Whole genome sequencing identifies elusive variants in genetically unsolved Italian inherited retinal disease patients 143
Trattamento dell'edema maculare cistoide in pazienti con retinite pigmentosa 143
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 142
Clinical expression of juvenile x-linked retinoschisis in Italian families with mutations in the XLRS1 gene 142
Analisi di mutazione del gene XLRS1 in famiglie Italiane affette da retinoschisi X-linked congenita 142
Analisi molecolare del gene ABCR in famiglie con Sindrome di Stargardt 142
Clinical and molecular characterization of achromatopsia patients: A longitudinal study 142
Voretigene neparvovec gene therapy in clinical practice: treatment of the first two italian pediatric patients 142
Baseline characteristics of patients with Usher Syndrome due to MYO7A mutations enrolled in a prospective natural history study 142
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity 141
Analisi dei polimorfismi del gene paraoxonasi in pazienti affetti da degenerazione maculare senile 141
Clinical expression of cone dystrophy associated with a novel deleterious ABCR (ABCA4) mutation in an italian family 140
Spectrum of Disease Severity in Patients With X-Linked Retinitis Pigmentosa Due to RPGR Mutations 140
Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy. 139
Molecular and clinical characterization of albinism in a large cohort of Italian patients 138
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients 138
Pericentral Retinitis Pigmentosa is associated with a high prevalence of USH2A pathogenic variants in an Italian cohort of patients 138
Molecular epidemiology of Usher syndrome in Italy 137
Clinical case of retinitis pigmentosa and drusen of the head of the optical nerve 136
Decorso clinico della Retinite Pigmentosa nelle varie forme genetiche 136
Interplay between Intravitreal RvD1 and Local Endogenous Sirtuin-1 in the Protection from Endotoxin-Induced Uveitis in Rats. 136
A multidisciplinary approach to inherited retinal dystrophies from diagnosis to initial care: a narrative review with inputs from clinical practice 135
Autosomal recessive retinitis pigmentosa gene analysis in Italian patients 134
An Italian family affected by autosomal dominant microcephaly with chorioretinal degeneration 134
XXIII International Congress of Ophthalmology 133
Totale 16.299
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Categoria #
all - tutte 107.786
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 107.786
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.414 0 0 0 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
2025/202615.409 569 761 664 669 1.214 8.525 989 601 533 356 296 232
2026/20272.239 189 494 972 584 0 0 0 0 0 0 0 0
Totale 32.887