IRIS
TESTA, Francesco
 Distribuzione geografica
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Continente #
EU - Europa 15.329
NA - Nord America 8.270
AS - Asia 6.060
SA - Sud America 886
Continente sconosciuto - Info sul continente non disponibili 432
AF - Africa 66
OC - Oceania 19
AN - Antartide 1
Totale 31.063
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Nazione #
RU - Federazione Russa 9.114
US - Stati Uniti d'America 8.123
SG - Singapore 2.059
IE - Irlanda 1.633
CN - Cina 1.391
IT - Italia 1.203
VN - Vietnam 876
HK - Hong Kong 816
UA - Ucraina 811
BR - Brasile 729
GB - Regno Unito 707
DE - Germania 459
FR - Francia 420
SE - Svezia 328
FI - Finlandia 235
IN - India 204
TR - Turchia 189
KR - Corea 186
GR - Grecia 161
JP - Giappone 147
CA - Canada 69
AR - Argentina 55
BE - Belgio 47
MX - Messico 35
AT - Austria 31
BD - Bangladesh 30
CZ - Repubblica Ceca 30
ES - Italia 29
EC - Ecuador 28
NL - Olanda 27
IQ - Iraq 24
PL - Polonia 24
ID - Indonesia 23
PK - Pakistan 19
AU - Australia 18
CH - Svizzera 17
CL - Cile 15
VE - Venezuela 15
UZ - Uzbekistan 14
CO - Colombia 13
PY - Paraguay 13
ZA - Sudafrica 13
AE - Emirati Arabi Uniti 12
EU - Europa 12
KE - Kenya 12
PE - Perù 11
RO - Romania 11
SC - Seychelles 11
MA - Marocco 10
SA - Arabia Saudita 10
GT - Guatemala 9
LT - Lituania 8
KZ - Kazakistan 7
CR - Costa Rica 6
DZ - Algeria 6
PH - Filippine 6
TH - Thailandia 6
AZ - Azerbaigian 5
BY - Bielorussia 5
JM - Giamaica 5
JO - Giordania 5
MD - Moldavia 5
NP - Nepal 5
UY - Uruguay 5
AL - Albania 4
EG - Egitto 4
HN - Honduras 4
HR - Croazia 4
BN - Brunei Darussalam 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
EE - Estonia 3
HU - Ungheria 3
KG - Kirghizistan 3
MY - Malesia 3
PA - Panama 3
BB - Barbados 2
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
TT - Trinidad e Tobago 2
TW - Taiwan 2
VI - Stati Uniti Isole Vergini 2
AO - Angola 1
AQ - Antartide 1
BO - Bolivia 1
CG - Congo 1
CI - Costa d'Avorio 1
CY - Cipro 1
DM - Dominica 1
ET - Etiopia 1
GE - Georgia 1
Totale 30.631
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Città #
Moscow 3.227
Dublin 1.620
Jacksonville 1.203
Santa Clara 964
Chandler 960
Singapore 915
Hong Kong 792
San Jose 775
Ashburn 346
Ho Chi Minh City 272
Princeton 230
Boardman 208
Hanoi 206
Seoul 184
Roxbury 177
Ann Arbor 175
Beijing 169
Hefei 160
Woodbridge 140
Bengaluru 139
Bremen 128
Cambridge 120
Medford 119
Dallas 118
Los Angeles 112
Wilmington 102
The Dalles 101
Council Bluffs 97
Rome 86
New York 85
Nanjing 66
San Mateo 64
Da Nang 62
Caserta 60
Naples 60
Munich 58
Jinan 57
Des Moines 54
São Paulo 53
Memphis 51
Istanbul 47
Brussels 45
Dong Ket 42
Mountain View 40
Shenyang 37
Haiphong 36
Nuremberg 34
Taiyuan 34
Tianjin 32
Milan 31
Brno 30
Rio de Janeiro 30
Bologna 28
Chicago 28
Orem 27
Guangzhou 23
Haikou 23
Turku 23
Düsseldorf 22
London 22
Nanchang 22
San Francisco 22
Atlanta 21
Norwalk 21
Biên Hòa 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
Houston 14
Manchester 14
Mumbai 14
Vienna 14
Warsaw 14
Tashkent 13
Zhengzhou 13
Bến Tre 12
Florence 12
Guayaquil 12
Hangzhou 12
Perth 12
Buffalo 11
Kunming 11
Totale 15.783
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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 243
Analisi di correlazione genotipo fenotipo in una famiglia con retinite pigmentosa autosomica dominante associata ad una nuova mutazione nel gene PRPF8 241
Caratteristiche cliniche e diagnosi della retinite pigmentosa monolaterale 231
Caratterizzazione clinico-genetica di pazienti italiani con Distrofia Cristallina di Bietti 224
Analisi del gene della periferina/rds in famiglie con distrofia a pattern dell’epitelio pigmentato retinico 216
Iatrogenic ophthalmic artery occlusion after platelet-rich plasma dermal filler documented with ultra-widefield imaging 215
Post-operative results of corneal collagen cross-linking for progressive keratoconus 205
Activation of Melanocortin Receptors MC1 and MC5 Attenuates Retinal Damage in Experimental Diabetic Retinopathy 202
A pilot study for development of a novel tool for clinical decision making to identify fallers among ophthalmic patients 201
Mutations in the PCYT1A gene are responsible for isolated forms of retinal dystrophy 197
AAV-mediated photoreceptor transduction of the pig cone-enriched retina 188
Carbonic anhydrase inhibitors in patients with X-linked retinoschisis: effects on macular morphology and function 185
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial 184
Emeralopia stazionaria congenita. Caratteristiche cliniche e diagnosi differenziale 180
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy 177
Clinical and Genetic Evaluation of a Cohort of Pediatric Patients with Severe Inherited Retinal Dystrophies 177
Clinical and genetic analysis of a european cohort with pericentral retinitis pigmentosa 177
Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease 175
Prevalence of macular abnormalities assessed by Optical Coherence Tomography in patients with Usher Syndrome 175
Identifying fallers among ophthalmic patients using classification tree methodology 173
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene 170
Aspetti clinici dell’albinismo oculo-cutaneo correlato a mutazioninei geni TYR e MATP 170
Biofeedback Rehabilitation in Patients with Stargardt disease: a randomized controlled trial 170
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation 170
An Atypical Form of Bietti Crystalline Dystrophy 167
Association between genotype and disease progression in Italian stargardt patients: A retrospective natural history study 167
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 165
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 164
Evaluation of ocular gene therapy in an italian patient affected by congenital leber amaurosis type 2 treated in both eyes 164
High levels of serum ubiquitin and proteasome in a case of HLA-B27 uveitis 164
A novel mutation in the RDS gene in an Italian family with pattern dystrophy 162
Photorefractive Keratectomy on Purely Refractive Accommodative Esotropia. 159
Sicurezza ed efficacia della terapia genica nell'Amaurosi Congenita di Leber: un anno di followup. 159
CHM/REP1 transcript expression and loss of visual function in patients affected by choroideremia 159
Union Makes Strength: A Worldwide Collaborative Genetic and Clinical Study to Provide a Comprehensive Survey of RD3 Mutations and Delineate the Associated Phenotype 158
Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family 156
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene. 155
Diagnosi differenziale nelle forme atipiche di retinite pigmentosa 155
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 154
The role of optical coherence tomography in an atypical case of oculocutaneous albinism: A case report 153
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 153
Clinical presentation and disease course in Choroideremia patients 153
Caso clinico di retinite pigmentosa e drusen della testa del nervo ottico 152
Mild clinical presentation of joubert syndrome in a male adult carrying biallelic mks1 truncating variants 152
Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with leber congenital amaurosis type 2 151
Aspetti clinici delle carriers di coroideremia 151
Intrafamilial heterogeneity of congenital optic disc pit maculopathy 151
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy 149
Studio clinico sulla retinite pigmentosa pericentrale: confronto tra forme ereditarie e sporadiche 149
Clinical and genetic features in Italian Bietti crystalline dystrophy patients 149
Analisi di mutazione del gene REP1 in famiglie Italiane affette da coroideremia 149
Valutazione della Progressione della Atrofia Corioretinica Pigmentata Paravenosa (PPRCA): Case Report 148
Incidence of high myopia in italian patients with retinitis pigmentosa 146
Age related macular degeneration 146
A Novel Variant in TUBB4B Causes Progressive Cone‐Rod Dystrophy and Early Onset Sensorineural Hearing Loss 144
Prevalence of macular abnormalities assessed by optical coherence tomography in patients with Usher syndrome 144
Efficacia della terapia genica per l’Amaurosi Congenita di Leber fino a tre anni dopo la somministrazione del vettore virale 144
Wearable Improved Vision System for Color Vision Deficiency Correction 144
Pupillometric analysis for assessment of gene therapy in Leber Congenital Amaurosis patients 143
Studio clinico genetico di pazienti con amaurosi congenita di Leber 143
Melanocortin receptor agonists MCR1-5 protect photoreceptors from high-glucose damage and restore antioxidant enzymes in primary retinal cell culture 143
Biofeedback rehabilitation and visual cortex response in stargardt’s disease: A randomized controlled trial 143
Visual function and retinal changes after voretigene neparvovec treatment in children with biallelic RPE65-related inherited retinal dystrophy 142
Aspetti clinici e genetici nella malattia di Best 142
X-lnked retinitis pigmentosa (RP3): screening for new mutations and promoter analysis of RPGR gene 142
Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration 141
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina. 141
Choroidal vascularity features in patients with choroideremia and cystoid spaces 141
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) 140
Trattamento con acetazolamide dell’edema maculare cistoide in pazienti affetti da retinite pigmentosa. 139
A novel mutation in the VMD2 gene in an Italian family with Best maculopathy 138
X-lnked retinitis pigmentosa (RP3): screening for new mutations and promoter analysis of RPGR gene 138
Clinical and molecular characterization of achromatopsia patients: A longitudinal study 138
Characterization of Italian Bietti Crystalline Dystrophy Patients with CYP4V2 Mutations 137
Clinical expression of juvenile x-linked retinoschisis in Italian families with mutations in the XLRS1 gene 137
Voretigene neparvovec gene therapy in clinical practice: treatment of the first two italian pediatric patients 137
Baseline characteristics of patients with Usher Syndrome due to MYO7A mutations enrolled in a prospective natural history study 137
Whole genome sequencing identifies elusive variants in genetically unsolved Italian inherited retinal disease patients 136
Evaluation of Italian Patients with Leber Congenital Amaurosis due to AIPL1 Mutations Highlights the Potential Applicability of Gene Therapy 136
Clinical expression of cone dystrophy associated with a novel deleterious ABCR (ABCA4) mutation in an italian family 135
Trattamento dell'edema maculare cistoide in pazienti con retinite pigmentosa 135
Analisi di mutazione del gene XLRS1 in famiglie Italiane affette da retinoschisi X-linked congenita 135
Analisi molecolare del gene ABCR in famiglie con Sindrome di Stargardt 135
Spectrum of Disease Severity in Patients With X-Linked Retinitis Pigmentosa Due to RPGR Mutations 135
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients 134
Pericentral Retinitis Pigmentosa is associated with a high prevalence of USH2A pathogenic variants in an Italian cohort of patients 134
Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian population 132
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity 131
Analisi dei polimorfismi del gene paraoxonasi in pazienti affetti da degenerazione maculare senile 131
Interplay between Intravitreal RvD1 and Local Endogenous Sirtuin-1 in the Protection from Endotoxin-Induced Uveitis in Rats. 131
An Italian family affected by autosomal dominant microcephaly with chorioretinal degeneration 131
Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy. 130
Decorso clinico della Retinite Pigmentosa nelle varie forme genetiche 130
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 129
Molecular epidemiology of Usher syndrome in Italy 129
A multidisciplinary approach to inherited retinal dystrophies from diagnosis to initial care: a narrative review with inputs from clinical practice 128
Autosomal recessive retinitis pigmentosa gene analysis in Italian patients 128
Studio clinico-genetico di una famiglia con retinite pigmentosa autosomica dominante associata ad una nuova mutazione nel gene PRPF8. 128
XXIII International Congress of Ophthalmology 128
Macular Function and Morphologic Features in Juvenile Stargardt Disease Longitudinal Study 128
Totale 15.573
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Categoria #
all - tutte 102.469
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 102.469
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.461 0 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
2025/202615.409 569 761 664 669 1.214 8.525 989 601 533 356 296 232
2026/2027415 189 226 0 0 0 0 0 0 0 0 0 0
Totale 31.063