TESTA, Francesco
 Distribuzione geografica
Continente #
EU - Europa 5.429
NA - Nord America 4.714
AS - Asia 689
AF - Africa 17
SA - Sud America 16
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 12
Totale 10.890
Nazione #
US - Stati Uniti d'America 4.701
IE - Irlanda 1.628
IT - Italia 877
UA - Ucraina 793
GB - Regno Unito 626
CN - Cina 488
FR - Francia 375
DE - Germania 347
SE - Svezia 319
FI - Finlandia 200
GR - Grecia 160
TR - Turchia 132
BE - Belgio 42
VN - Vietnam 42
AU - Australia 13
EU - Europa 12
IN - India 12
SC - Seychelles 11
BR - Brasile 10
CH - Svizzera 10
RU - Federazione Russa 10
CA - Canada 8
PL - Polonia 8
ES - Italia 7
RO - Romania 7
AT - Austria 5
NL - Olanda 5
MD - Moldavia 4
SG - Singapore 4
AE - Emirati Arabi Uniti 3
CL - Cile 3
HU - Ungheria 3
MX - Messico 3
CU - Cuba 2
JP - Giappone 2
NG - Nigeria 2
ZA - Sudafrica 2
AR - Argentina 1
DK - Danimarca 1
DZ - Algeria 1
EC - Ecuador 1
EE - Estonia 1
IL - Israele 1
IR - Iran 1
KE - Kenya 1
KR - Corea 1
KZ - Kazakistan 1
NO - Norvegia 1
PE - Perù 1
PH - Filippine 1
PK - Pakistan 1
Totale 10.890
Città #
Dublin 1.616
Jacksonville 1.197
Chandler 960
Princeton 231
Roxbury 178
Ann Arbor 175
Boardman 138
Woodbridge 138
Bremen 129
Cambridge 121
Medford 119
Wilmington 101
Beijing 67
Nanjing 65
San Mateo 64
Caserta 59
Rome 56
Ashburn 53
Jinan 53
Des Moines 52
Dong Ket 42
Brussels 41
Mountain View 40
Shenyang 34
Taiyuan 34
New York 33
Tianjin 25
Düsseldorf 22
Haikou 22
Nanchang 22
Norwalk 21
Lanzhou 19
Hebei 18
Naples 18
Bologna 17
Redwood City 17
Taizhou 17
Auburn Hills 16
Guangzhou 16
Ningbo 16
Changsha 15
Napoli 15
Reggio Nell'emilia 15
Castelfranco Emilia 14
Zhengzhou 12
Houston 11
Kunming 11
Los Angeles 11
Perth 11
Milan 10
Florence 8
Hangzhou 8
Helsinki 8
Padova 8
Jiaxing 7
Maletto 7
Portici 7
Washington 7
Collegeville 6
London 6
Salerno 6
Seattle 6
Torre del Greco 6
Fairfield 5
Falls Church 5
Fuzhou 5
Palermo 5
Teramo 5
Avella 4
Avellino 4
Aversa 4
Bari 4
Baselicaduce 4
Brescia 4
Catania 4
Changchun 4
Edinburgh 4
Mumbai 4
Peschiera Del Garda 4
Pozzuoli 4
Radomsko 4
Vienna 4
Atella 3
Atlanta 3
Brampton 3
Budapest 3
Chicago 3
Dubai 3
Fiumefreddo Bruzio 3
Forlì 3
Gunzenhausen 3
Hanover 3
Menlo Park 3
Montereale Valcellina 3
Nocera Inferiore 3
Parma 3
Pune 3
Puxian 3
Sarno 3
Spinea 3
Totale 6.412
Nome #
Caratteristiche cliniche e diagnosi della retinite pigmentosa monolaterale 145
An Alu-mediated duplication in NMNAT1, involved in NAD biosynthesis, causes a novel syndrome, SHILCA, affecting multiple tissues and organs 128
Analisi di correlazione genotipo fenotipo in una famiglia con retinite pigmentosa autosomica dominante associata ad una nuova mutazione nel gene PRPF8 125
Analisi del gene della periferina/rds in famiglie con distrofia a pattern dell’epitelio pigmentato retinico 119
Caratterizzazione clinico-genetica di pazienti italiani con Distrofia Cristallina di Bietti 107
Emeralopia stazionaria congenita. Caratteristiche cliniche e diagnosi differenziale 94
Diagnosi differenziale nelle forme atipiche di retinite pigmentosa 94
Sicurezza ed efficacia della terapia genica nell'Amaurosi Congenita di Leber: un anno di followup. 91
Studio clinico sulla retinite pigmentosa pericentrale: confronto tra forme ereditarie e sporadiche 80
Post-operative results of corneal collagen cross-linking for progressive keratoconus 79
Mutations in the PCYT1A gene are responsible for isolated forms of retinal dystrophy 79
Activation of Melanocortin Receptors MC1 and MC5 Attenuates Retinal Damage in Experimental Diabetic Retinopathy 78
Union Makes Strength: A Worldwide Collaborative Genetic and Clinical Study to Provide a Comprehensive Survey of RD3 Mutations and Delineate the Associated Phenotype 77
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina. 76
Studio di correlazione genotipo fenotipo in sindrome di Stargardt 73
Identifying fallers among ophthalmic patients using classification tree methodology 73
Evaluation of Italian Patients with Leber Congenital Amaurosis due to AIPL1 Mutations Highlights the Potential Applicability of Gene Therapy 72
Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with leber congenital amaurosis type 2 71
AAV-mediated photoreceptor transduction of the pig cone-enriched retina 71
Studio clinico genetico di pazienti con amaurosi congenita di Leber 71
Wearable Improved Vision System for Color Vision Deficiency Correction 71
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial 70
Biofeedback Rehabilitation in Patients with Stargardt disease: a randomized controlled trial 69
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene. 68
The role of optical coherence tomography in an atypical case of oculocutaneous albinism: A case report 68
Trattamento con acetazolamide dell’edema maculare cistoide in pazienti affetti da retinite pigmentosa. 68
Analisi molecolare del gene ABCR in famiglie con Sindrome di Stargardt 68
Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian population 66
A pilot study for development of a novel tool for clinical decision making to identify fallers among ophthalmic patients 65
Valutazione della Progressione della Atrofia Corioretinica Pigmentata Paravenosa (PPRCA): Case Report 64
Studio clinico-genetico di una famiglia con retinite pigmentosa autosomica dominante associata ad una nuova mutazione nel gene PRPF8. 64
Efficacia della terapia genica per l’Amaurosi Congenita di Leber fino a tre anni dopo la somministrazione del vettore virale 64
Incidence of high myopia in italian patients with retinitis pigmentosa 63
Nuova mutazione del gene ABCR associata a distrofia dei coni 63
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 63
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families 62
Trattamento dell'edema maculare cistoide in pazienti con retinite pigmentosa 62
XXIII International Congress of Ophthalmology 62
Molecular epidemiology of Usher syndrome in Italy 61
Strategie chirurgiche nella terapia genica 61
Photorefractive Keratectomy on Purely Refractive Accommodative Esotropia. 60
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy 60
Apolipoprotein E polymorphisms in age-related macular degeneration in an Italian population 60
Aspetti clinici dell’albinismo oculo-cutaneo correlato a mutazioninei geni TYR e MATP 60
Analisi di mutazione del gene REP1 in famiglie Italiane affette da coroideremia 60
Cone-rod dystrophy phenotype associated with ABCA4 (ABCR) gene mutation 60
Evaluation of ocular gene therapy in an italian patient affected by congenital leber amaurosis type 2 treated in both eyes 60
Clinical and Genetic Evaluation of a Cohort of Pediatric Patients with Severe Inherited Retinal Dystrophies 60
Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration 59
A novel mutation in the RDS gene in an Italian family with pattern dystrophy 59
X-lnked retinitis pigmentosa (RP3): screening for new mutations and promoter analysis of RPGR gene 59
Intrafamilial heterogeneity of congenital optic disc pit maculopathy 59
Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy. 58
Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa 58
Aspetti clinici e genetici nella malattia di Best 58
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation 58
Association of a homozygous nonsense mutation in the ABCA4 (ABCR) gene with cone-rod dystrophy phenotype in an Italian family 57
Malattia di Coats e retinite pigmentosa. Un caso clinico 57
Pupillometric analysis for assessment of gene therapy in Leber Congenital Amaurosis patients 57
Studio clinico in una carrier di coroideremia con una manifestazione completa della malattia 57
Age related macular degeneration 57
Decorso clinico della Retinite Pigmentosa nelle varie forme genetiche 57
Retinite pigmentosa X-linked (RP3): ricerca di nuove mutazioni ed analisi del promotore del gene RPGR 57
Analisi molecolare del gene RPGR in pazienti affetti da retinite pigmentosa X-linked 57
Retinite pigmentosa autosomica dominante: correlazione genotipo fenotipo in una famiglia italiana con mutazione nel gene NRL 57
Analisi molecolare del gene ABCR in famiglie con Sindrome di Stargardt 57
Clinical and genetic analysis of a european cohort with pericentral retinitis pigmentosa 57
Aspetti clinici delle carriers di coroideremia 56
Differente espressione clinica in una famiglia italiana con mutazione nel gene RDS-periferina e distrofia dell'epitelio pigmentato retinico 56
Aspetti ecografici della retinoschisi X-linked congenita 56
Severo fenotipo clinico in carriers di coroideremia associato ad una nuova mutazione del gene CHM 56
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 56
Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease 55
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene 54
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity 54
A Normal EOG in Best Macular Dystrophy Associated to a Novel Novo de Novo Mutation in VMD2 Gene 54
X-lnked retinitis pigmentosa (RP3): screening for new mutations and promoter analysis of RPGR gene 54
Mutation analysis of RPGR gene in patients with X-linked Retinitis Pigmentosa (RP3) 54
Studio dei polimorfismi del gene paraoxonasi nella degenerazione maculare senile 54
Analisi molecolare di mutazioni in pazienti affettti da retinite pigmentosa associata al cromosoma X 54
New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease 53
Caso clinico di retinite pigmentosa e drusen della testa del nervo ottico 53
Carbonic anhydrase inhibitors in patients with X-linked retinoschisis: effects on macular morphology and function 53
Sindrome di Usher: una valutazione clinica 52
Analisi dei polimorfismi del gene paraoxonasi in pazienti affetti da degenerazione maculare senile 52
Analisi di mutazione del gene XLRS1 in famiglie Italiane affette da retinoschisi X-linked congenita 52
Correlazione genotipo fenotipo in famiglie con coroideremia 52
Molecular and clinical characterization of albinism in a large cohort of Italian patients 51
An Atypical Form of Bietti Crystalline Dystrophy 51
Analisi molecolare del gene RP2 in famiglie affette da retinite pigmentosa associata al cromosoma X 51
Association between genotype and disease progression in Italian stargardt patients: A retrospective natural history study 51
A novel mutation in the VMD2 gene in an Italian family with Best maculopathy 50
Genotyping microarray (gene chip) for the ABCR (ABCA4) gene 50
Clinical and genetic features in Italian Bietti crystalline dystrophy patients 50
Nuova mutazione nel gene RDS/periferina in una famiglia italiana affetta da distrofia a pattern della retina 50
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 50
CLINICAL PRESENTATION and DISEASE COURSE of USHER SYNDROME because of MUTATIONS in MYO7A or USH2A 50
High levels of serum ubiquitin and proteasome in a case of HLA-B27 uveitis 50
Identification and characterization of C1orf36, a transcript highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa 49
Intrafamilial clinical heterogeneity associated with a novel mutation of the retinal degeneration slow/peripherin gene 49
Totale 6.412
Categoria #
all - tutte 36.363
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 36.363


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201973 0 0 0 0 0 0 0 0 0 24 12 37
2019/20201.472 251 249 61 28 221 54 247 82 100 86 57 36
2020/20212.114 136 10 211 318 325 13 238 202 32 267 241 121
2021/20221.551 87 8 39 29 467 16 28 99 62 141 110 465
2022/20233.312 274 117 38 273 389 304 2 191 1.559 28 67 70
2023/2024865 114 44 44 106 407 52 14 55 2 27 0 0
Totale 11.260