IRIS
TESTA, Francesco
 Distribuzione geografica
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Continente #
EU - Europa 9.467
NA - Nord America 6.450
AS - Asia 4.862
SA - Sud America 851
AF - Africa 59
OC - Oceania 15
Continente sconosciuto - Info sul continente non disponibili 13
AN - Antartide 1
Totale 21.718
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Nazione #
US - Stati Uniti d'America 6.361
RU - Federazione Russa 3.488
SG - Singapore 1.739
IE - Irlanda 1.632
CN - Cina 1.278
IT - Italia 1.089
UA - Ucraina 807
HK - Hong Kong 716
BR - Brasile 707
GB - Regno Unito 670
DE - Germania 449
FR - Francia 394
SE - Svezia 325
VN - Vietnam 285
FI - Finlandia 232
TR - Turchia 188
KR - Corea 181
IN - India 177
GR - Grecia 161
JP - Giappone 140
AR - Argentina 53
BE - Belgio 46
CA - Canada 40
AT - Austria 31
CZ - Repubblica Ceca 30
BD - Bangladesh 27
EC - Ecuador 26
MX - Messico 24
ES - Italia 23
ID - Indonesia 23
IQ - Iraq 18
NL - Olanda 17
PK - Pakistan 17
PL - Polonia 16
AU - Australia 15
CL - Cile 14
CH - Svizzera 13
PY - Paraguay 13
VE - Venezuela 13
EU - Europa 12
KE - Kenya 12
ZA - Sudafrica 12
AE - Emirati Arabi Uniti 11
SC - Seychelles 11
UZ - Uzbekistan 11
PE - Perù 10
SA - Arabia Saudita 10
MA - Marocco 9
RO - Romania 9
CO - Colombia 8
GT - Guatemala 7
KZ - Kazakistan 7
LT - Lituania 7
BY - Bielorussia 5
DZ - Algeria 5
UY - Uruguay 5
AL - Albania 4
AZ - Azerbaigian 4
MD - Moldavia 4
NP - Nepal 4
BN - Brunei Darussalam 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
EE - Estonia 3
EG - Egitto 3
HN - Honduras 3
HU - Ungheria 3
JM - Giamaica 3
JO - Giordania 3
PA - Panama 3
BH - Bahrain 2
CR - Costa Rica 2
CU - Cuba 2
IL - Israele 2
IR - Iran 2
KG - Kirghizistan 2
MY - Malesia 2
NG - Nigeria 2
PH - Filippine 2
PT - Portogallo 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
TN - Tunisia 2
AO - Angola 1
AQ - Antartide 1
BO - Bolivia 1
CY - Cipro 1
DM - Dominica 1
ET - Etiopia 1
GE - Georgia 1
GY - Guiana 1
LB - Libano 1
LV - Lettonia 1
MN - Mongolia 1
NO - Norvegia 1
OM - Oman 1
QA - Qatar 1
SN - Senegal 1
SV - El Salvador 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 21.718
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Città #
Dublin 1.618
Jacksonville 1.198
Moscow 1.112
Chandler 960
Santa Clara 910
Hong Kong 715
Singapore 711
Princeton 230
Boardman 208
Seoul 181
Roxbury 177
Ann Arbor 175
Hefei 160
Ashburn 145
Beijing 140
Woodbridge 140
Bengaluru 139
Bremen 128
Cambridge 120
Medford 119
Dallas 104
The Dalles 101
Wilmington 101
Ho Chi Minh City 86
Rome 75
Nanjing 66
San Mateo 64
Hanoi 61
Caserta 60
Naples 59
Munich 58
Jinan 57
Des Moines 52
New York 51
São Paulo 49
Los Angeles 48
Istanbul 47
Brussels 44
Dong Ket 42
Mountain View 40
Shenyang 37
Nuremberg 34
Taiyuan 34
Tianjin 32
Brno 30
Rio de Janeiro 30
Bologna 27
Guangzhou 23
Haikou 23
Turku 23
Düsseldorf 22
Nanchang 22
Norwalk 21
Milan 20
Casoria 19
Changsha 19
Council Bluffs 19
Lanzhou 19
Belo Horizonte 18
Hebei 18
Taizhou 18
Redwood City 17
Auburn Hills 16
Chicago 16
Ningbo 16
Aversa 15
Brasília 15
Helsinki 15
London 15
Napoli 15
Reggio Nell'emilia 15
San Francisco 15
Castelfranco Emilia 14
Vienna 14
Brooklyn 13
Toronto 13
Zhengzhou 13
Hangzhou 12
Houston 12
Perth 12
Tokyo 12
Kunming 11
Padova 11
Biên Hòa 10
Florence 10
Goiânia 10
Guayaquil 10
Nairobi 10
Tashkent 10
Atlanta 9
Jakarta 9
Quito 9
Baghdad 8
Bauru 8
Boston 8
Columbus 8
Da Nang 8
Dubai 8
Haiphong 8
Mumbai 8
Totale 11.517
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Nome #
Caratteristiche cliniche e diagnosi della retinite pigmentosa monolaterale 195
An Alu-mediated duplication in NMNAT1, involved in NAD biosynthesis, causes a novel syndrome, SHILCA, affecting multiple tissues and organs 188
Analisi di correlazione genotipo fenotipo in una famiglia con retinite pigmentosa autosomica dominante associata ad una nuova mutazione nel gene PRPF8 178
Analisi del gene della periferina/rds in famiglie con distrofia a pattern dell’epitelio pigmentato retinico 171
Caratterizzazione clinico-genetica di pazienti italiani con Distrofia Cristallina di Bietti 169
Mutations in the PCYT1A gene are responsible for isolated forms of retinal dystrophy 143
Emeralopia stazionaria congenita. Caratteristiche cliniche e diagnosi differenziale 142
Activation of Melanocortin Receptors MC1 and MC5 Attenuates Retinal Damage in Experimental Diabetic Retinopathy 142
Post-operative results of corneal collagen cross-linking for progressive keratoconus 141
AAV-mediated photoreceptor transduction of the pig cone-enriched retina 138
A pilot study for development of a novel tool for clinical decision making to identify fallers among ophthalmic patients 137
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial 136
Identifying fallers among ophthalmic patients using classification tree methodology 131
Diagnosi differenziale nelle forme atipiche di retinite pigmentosa 129
Sicurezza ed efficacia della terapia genica nell'Amaurosi Congenita di Leber: un anno di followup. 128
Biofeedback Rehabilitation in Patients with Stargardt disease: a randomized controlled trial 128
Clinical and genetic analysis of a european cohort with pericentral retinitis pigmentosa 127
Evaluation of ocular gene therapy in an italian patient affected by congenital leber amaurosis type 2 treated in both eyes 126
Clinical and Genetic Evaluation of a Cohort of Pediatric Patients with Severe Inherited Retinal Dystrophies 125
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation 125
Association between genotype and disease progression in Italian stargardt patients: A retrospective natural history study 124
Carbonic anhydrase inhibitors in patients with X-linked retinoschisis: effects on macular morphology and function 123
Union Makes Strength: A Worldwide Collaborative Genetic and Clinical Study to Provide a Comprehensive Survey of RD3 Mutations and Delineate the Associated Phenotype 122
Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family 121
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 121
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene 120
Aspetti clinici dell’albinismo oculo-cutaneo correlato a mutazioninei geni TYR e MATP 120
Studio clinico sulla retinite pigmentosa pericentrale: confronto tra forme ereditarie e sporadiche 119
An Atypical Form of Bietti Crystalline Dystrophy 119
Valutazione della Progressione della Atrofia Corioretinica Pigmentata Paravenosa (PPRCA): Case Report 117
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 117
The role of optical coherence tomography in an atypical case of oculocutaneous albinism: A case report 116
A novel mutation in the RDS gene in an Italian family with pattern dystrophy 116
Wearable Improved Vision System for Color Vision Deficiency Correction 115
Clinical presentation and disease course in Choroideremia patients 115
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene. 113
Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease 113
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy 112
Pupillometric analysis for assessment of gene therapy in Leber Congenital Amaurosis patients 112
Studio clinico genetico di pazienti con amaurosi congenita di Leber 112
Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with leber congenital amaurosis type 2 111
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy 111
CHM/REP1 transcript expression and loss of visual function in patients affected by choroideremia 111
Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration 110
Photorefractive Keratectomy on Purely Refractive Accommodative Esotropia. 110
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina. 110
Aspetti clinici delle carriers di coroideremia 109
Trattamento con acetazolamide dell’edema maculare cistoide in pazienti affetti da retinite pigmentosa. 109
High levels of serum ubiquitin and proteasome in a case of HLA-B27 uveitis 109
Evaluation of Italian Patients with Leber Congenital Amaurosis due to AIPL1 Mutations Highlights the Potential Applicability of Gene Therapy 108
Incidence of high myopia in italian patients with retinitis pigmentosa 108
Analisi molecolare del gene ABCR in famiglie con Sindrome di Stargardt 108
Caso clinico di retinite pigmentosa e drusen della testa del nervo ottico 107
Age related macular degeneration 107
Efficacia della terapia genica per l’Amaurosi Congenita di Leber fino a tre anni dopo la somministrazione del vettore virale 107
Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian population 106
Intrafamilial heterogeneity of congenital optic disc pit maculopathy 106
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 105
Studio di correlazione genotipo fenotipo in sindrome di Stargardt 105
Analisi di mutazione del gene REP1 in famiglie Italiane affette da coroideremia 105
Prevalence of macular abnormalities assessed by Optical Coherence Tomography in patients with Usher Syndrome 105
Clinical and genetic features in Italian Bietti crystalline dystrophy patients 104
Apolipoprotein E polymorphisms in age-related macular degeneration in an Italian population 104
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 104
A novel mutation in the VMD2 gene in an Italian family with Best maculopathy 103
Aspetti clinici e genetici nella malattia di Best 103
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 102
Analisi di mutazione del gene XLRS1 in famiglie Italiane affette da retinoschisi X-linked congenita 102
Mild clinical presentation of joubert syndrome in a male adult carrying biallelic mks1 truncating variants 102
Baseline characteristics of patients with Usher Syndrome due to MYO7A mutations enrolled in a prospective natural history study 102
Prevalence of macular abnormalities assessed by optical coherence tomography in patients with Usher syndrome 101
Strategie chirurgiche nella terapia genica 101
X-lnked retinitis pigmentosa (RP3): screening for new mutations and promoter analysis of RPGR gene 100
X-lnked retinitis pigmentosa (RP3): screening for new mutations and promoter analysis of RPGR gene 100
Molecular epidemiology of Usher syndrome in Italy 99
Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy. 98
Sindrome di Usher: una valutazione clinica 98
Clinical expression of cone dystrophy associated with a novel deleterious ABCR (ABCA4) mutation in an italian family 98
Trattamento dell'edema maculare cistoide in pazienti con retinite pigmentosa 98
XXIII International Congress of Ophthalmology 97
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) 97
Analisi dei polimorfismi del gene paraoxonasi in pazienti affetti da degenerazione maculare senile 96
Studio clinico-genetico di una famiglia con retinite pigmentosa autosomica dominante associata ad una nuova mutazione nel gene PRPF8. 96
Studio clinico in una carrier di coroideremia con una manifestazione completa della malattia 95
Malattia di Coats e retinite pigmentosa. Un caso clinico 94
Differente espressione clinica in una famiglia italiana con mutazione nel gene RDS-periferina e distrofia dell'epitelio pigmentato retinico 94
An Italian family affected by autosomal dominant microcephaly with chorioretinal degeneration 94
Biofeedback rehabilitation and visual cortex response in stargardt’s disease: A randomized controlled trial 94
Choroidal vascularity features in patients with choroideremia and cystoid spaces 94
Genotyping microarray (gene chip) for the ABCR (ABCA4) gene 93
Characterization of Italian Bietti Crystalline Dystrophy Patients with CYP4V2 Mutations 93
Clinical expression of juvenile x-linked retinoschisis in Italian families with mutations in the XLRS1 gene 93
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina 93
Molecular and clinical characterization of albinism in a large cohort of Italian patients 92
Autosomal recessive retinitis pigmentosa gene analysis in Italian patients 92
Nuova mutazione del gene ABCR associata a distrofia dei coni 92
Reproducibility of en-face Optical Coherence Tomography Imaging for Macular Atrophy Area Evaluation in Juvenile Macular Degeneration 92
Analysis of the ABCA4 genomic locus in Stargardt disease 92
Toward a novel medical device based on chromatic pupillometry for screening and monitoring of inherited ocular disease: A pilot study 92
Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa 91
Totale 11.298
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Categoria #
all - tutte 81.159
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 81.159
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.114 0 0 0 0 0 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
2024/20253.610 20 54 45 125 549 506 443 366 431 448 333 290
2025/20266.896 569 761 664 669 1.214 3.019 0 0 0 0 0 0
Totale 22.135