IRIS
TESTA, Francesco
 Distribuzione geografica
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Continente #
NA - Nord America 5.840
EU - Europa 5.715
AS - Asia 2.302
SA - Sud America 324
AF - Africa 34
OC - Oceania 14
Continente sconosciuto - Info sul continente non disponibili 12
Totale 14.241
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Nazione #
US - Stati Uniti d'America 5.802
IE - Irlanda 1.630
IT - Italia 999
UA - Ucraina 799
SG - Singapore 753
HK - Hong Kong 669
GB - Regno Unito 633
CN - Cina 552
DE - Germania 395
FR - Francia 377
SE - Svezia 320
BR - Brasile 300
FI - Finlandia 208
TR - Turchia 181
GR - Grecia 161
BE - Belgio 45
VN - Vietnam 42
CZ - Repubblica Ceca 30
RU - Federazione Russa 28
KR - Corea 23
AT - Austria 20
CA - Canada 18
IN - India 15
AU - Australia 14
EU - Europa 12
NL - Olanda 12
CH - Svizzera 11
SC - Seychelles 11
AE - Emirati Arabi Uniti 10
ID - Indonesia 9
MX - Messico 8
PL - Polonia 8
RO - Romania 8
AR - Argentina 7
ES - Italia 7
PK - Pakistan 7
CL - Cile 6
GT - Guatemala 6
MA - Marocco 6
BD - Bangladesh 5
IQ - Iraq 5
KZ - Kazakistan 5
ZA - Sudafrica 5
AZ - Azerbaigian 4
BY - Bielorussia 4
DZ - Algeria 4
KE - Kenya 4
MD - Moldavia 4
VE - Venezuela 4
EC - Ecuador 3
EE - Estonia 3
HU - Ungheria 3
JP - Giappone 3
LT - Lituania 3
NP - Nepal 3
PY - Paraguay 3
UZ - Uzbekistan 3
AL - Albania 2
CU - Cuba 2
IL - Israele 2
KG - Kirghizistan 2
NG - Nigeria 2
PA - Panama 2
PH - Filippine 2
SA - Arabia Saudita 2
SK - Slovacchia (Repubblica Slovacca) 2
BN - Brunei Darussalam 1
CY - Cipro 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EG - Egitto 1
GE - Georgia 1
IR - Iran 1
JM - Giamaica 1
JO - Giordania 1
NO - Norvegia 1
PE - Perù 1
PT - Portogallo 1
SN - Senegal 1
Totale 14.241
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Città #
Dublin 1.618
Jacksonville 1.197
Chandler 960
Santa Clara 895
Hong Kong 668
Princeton 230
Singapore 212
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 56
The Dalles 56
Jinan 53
Des Moines 52
Istanbul 47
Brussels 44
Dong Ket 42
Mountain View 40
Naples 37
Shenyang 34
Taiyuan 34
New York 33
Brno 30
Tianjin 25
Los Angeles 24
Seoul 23
Düsseldorf 22
Haikou 22
Munich 22
Nanchang 22
Bologna 21
Norwalk 21
São Paulo 21
Nuremberg 20
Lanzhou 19
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
Perth 12
Rio de Janeiro 12
Zhengzhou 12
Houston 11
Kunming 11
Padova 11
Belo Horizonte 10
Florence 10
Toronto 9
Vienna 9
Hangzhou 8
London 8
Brasília 7
Dubai 7
Falkenstein 7
Jakarta 7
Jiaxing 7
Maletto 7
Portici 7
Washington 7
Collegeville 6
Fuzhou 6
Guatemala City 6
Nizhniy Novgorod 6
Salerno 6
Seattle 6
St Petersburg 6
Torre del Greco 6
Council Bluffs 5
Fairfield 5
Falls Church 5
Gatchina 5
Palermo 5
Teramo 5
Almaty 4
Avella 4
Avellino 4
Baku 4
Bari 4
Baselicaduce 4
Brescia 4
Campinas 4
Totale 8.583
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Nome #
Caratteristiche cliniche e diagnosi della retinite pigmentosa monolaterale 161
An Alu-mediated duplication in NMNAT1, involved in NAD biosynthesis, causes a novel syndrome, SHILCA, affecting multiple tissues and organs 145
Analisi di correlazione genotipo fenotipo in una famiglia con retinite pigmentosa autosomica dominante associata ad una nuova mutazione nel gene PRPF8 141
Analisi del gene della periferina/rds in famiglie con distrofia a pattern dell’epitelio pigmentato retinico 137
Caratterizzazione clinico-genetica di pazienti italiani con Distrofia Cristallina di Bietti 126
Sicurezza ed efficacia della terapia genica nell'Amaurosi Congenita di Leber: un anno di followup. 107
Emeralopia stazionaria congenita. Caratteristiche cliniche e diagnosi differenziale 105
Diagnosi differenziale nelle forme atipiche di retinite pigmentosa 105
Activation of Melanocortin Receptors MC1 and MC5 Attenuates Retinal Damage in Experimental Diabetic Retinopathy 101
Mutations in the PCYT1A gene are responsible for isolated forms of retinal dystrophy 101
Studio clinico sulla retinite pigmentosa pericentrale: confronto tra forme ereditarie e sporadiche 95
Post-operative results of corneal collagen cross-linking for progressive keratoconus 93
Union Makes Strength: A Worldwide Collaborative Genetic and Clinical Study to Provide a Comprehensive Survey of RD3 Mutations and Delineate the Associated Phenotype 92
AAV-mediated photoreceptor transduction of the pig cone-enriched retina 92
Valutazione della Progressione della Atrofia Corioretinica Pigmentata Paravenosa (PPRCA): Case Report 89
Studio clinico genetico di pazienti con amaurosi congenita di Leber 88
A pilot study for development of a novel tool for clinical decision making to identify fallers among ophthalmic patients 88
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina. 87
Identifying fallers among ophthalmic patients using classification tree methodology 87
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial 85
Wearable Improved Vision System for Color Vision Deficiency Correction 84
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 83
Biofeedback Rehabilitation in Patients with Stargardt disease: a randomized controlled trial 83
Evaluation of Italian Patients with Leber Congenital Amaurosis due to AIPL1 Mutations Highlights the Potential Applicability of Gene Therapy 82
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation 82
Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with leber congenital amaurosis type 2 81
Trattamento con acetazolamide dell’edema maculare cistoide in pazienti affetti da retinite pigmentosa. 81
Clinical and genetic analysis of a european cohort with pericentral retinitis pigmentosa 81
The role of optical coherence tomography in an atypical case of oculocutaneous albinism: A case report 80
Strategie chirurgiche nella terapia genica 80
Studio di correlazione genotipo fenotipo in sindrome di Stargardt 80
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy 79
Trattamento dell'edema maculare cistoide in pazienti con retinite pigmentosa 79
Aspetti clinici dell’albinismo oculo-cutaneo correlato a mutazioninei geni TYR e MATP 79
Analisi molecolare del gene ABCR in famiglie con Sindrome di Stargardt 79
Clinical and Genetic Evaluation of a Cohort of Pediatric Patients with Severe Inherited Retinal Dystrophies 79
Incidence of high myopia in italian patients with retinitis pigmentosa 78
Pupillometric analysis for assessment of gene therapy in Leber Congenital Amaurosis patients 78
Efficacia della terapia genica per l’Amaurosi Congenita di Leber fino a tre anni dopo la somministrazione del vettore virale 78
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene. 77
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 77
Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian population 77
Apolipoprotein E polymorphisms in age-related macular degeneration in an Italian population 77
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 77
Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family 76
Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration 75
Nuova mutazione del gene ABCR associata a distrofia dei coni 75
Studio clinico-genetico di una famiglia con retinite pigmentosa autosomica dominante associata ad una nuova mutazione nel gene PRPF8. 75
Evaluation of ocular gene therapy in an italian patient affected by congenital leber amaurosis type 2 treated in both eyes 75
Aspetti clinici e genetici nella malattia di Best 74
Differente espressione clinica in una famiglia italiana con mutazione nel gene RDS-periferina e distrofia dell'epitelio pigmentato retinico 74
Intrafamilial heterogeneity of congenital optic disc pit maculopathy 74
Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease 73
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene 72
Photorefractive Keratectomy on Purely Refractive Accommodative Esotropia. 72
An Atypical Form of Bietti Crystalline Dystrophy 72
Caso clinico di retinite pigmentosa e drusen della testa del nervo ottico 72
Studio clinico in una carrier di coroideremia con una manifestazione completa della malattia 72
XXIII International Congress of Ophthalmology 72
Analisi di mutazione del gene REP1 in famiglie Italiane affette da coroideremia 72
Cone-rod dystrophy phenotype associated with ABCA4 (ABCR) gene mutation 72
A novel mutation in the RDS gene in an Italian family with pattern dystrophy 71
Aspetti clinici delle carriers di coroideremia 71
Retinite pigmentosa autosomica dominante: correlazione genotipo fenotipo in una famiglia italiana con mutazione nel gene NRL 71
Association between genotype and disease progression in Italian stargardt patients: A retrospective natural history study 71
Molecular epidemiology of Usher syndrome in Italy 70
Carbonic anhydrase inhibitors in patients with X-linked retinoschisis: effects on macular morphology and function 70
Age related macular degeneration 69
X-lnked retinitis pigmentosa (RP3): screening for new mutations and promoter analysis of RPGR gene 69
Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa 68
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina 68
Analisi molecolare del gene ABCR in famiglie con Sindrome di Stargardt 68
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 67
Malattia di Coats e retinite pigmentosa. Un caso clinico 66
Sindrome di Usher: una valutazione clinica 66
A novel mutation in the VMD2 gene in an Italian family with Best maculopathy 66
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 66
Decorso clinico della Retinite Pigmentosa nelle varie forme genetiche 66
Analisi di mutazione del gene XLRS1 in famiglie Italiane affette da retinoschisi X-linked congenita 66
X-lnked retinitis pigmentosa (RP3): screening for new mutations and promoter analysis of RPGR gene 66
High levels of serum ubiquitin and proteasome in a case of HLA-B27 uveitis 66
Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy. 65
Analisi molecolare del gene RPGR in pazienti affetti da retinite pigmentosa X-linked 65
Mutation analysis of RPGR gene in patients with X-linked Retinitis Pigmentosa (RP3) 65
Aspetti ecografici della retinoschisi X-linked congenita 65
Severo fenotipo clinico in carriers di coroideremia associato ad una nuova mutazione del gene CHM 65
Studio dei polimorfismi del gene paraoxonasi nella degenerazione maculare senile 65
Analisi molecolare di mutazioni in pazienti affettti da retinite pigmentosa associata al cromosoma X 65
Clinical expression of cone dystrophy associated with a novel deleterious ABCR (ABCA4) mutation in an italian family 64
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 64
Correlazione tra spessore maculare ed acutezza visiva centrale in pazienti affetti da retinite pigmentosa. 64
Retinite pigmentosa X-linked (RP3): ricerca di nuove mutazioni ed analisi del promotore del gene RPGR 64
Melanocortin receptor agonists MCR1-5 protect photoreceptors from high-glucose damage and restore antioxidant enzymes in primary retinal cell culture 64
Clinical presentation and disease course in Choroideremia patients 64
Genotyping microarray (gene chip) for the ABCR (ABCA4) gene 63
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity 62
Prevalence of macular abnormalities assessed by optical coherence tomography in patients with Usher syndrome 62
Clinical expression of juvenile x-linked retinoschisis in Italian families with mutations in the XLRS1 gene 62
Analisi dei polimorfismi del gene paraoxonasi in pazienti affetti da degenerazione maculare senile 62
Studio multicentrico nell’amaurosi congenita di leber: aspetti clinici e genetici 62
Totale 7.856
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Categoria #
all - tutte 60.618
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 60.618
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202093 0 0 0 0 0 0 0 0 0 0 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
2024/20253.022 20 54 45 125 549 506 445 370 434 450 24 0
Totale 14.651