Brunetti Pierri, Raffaella
 Distribuzione geografica
Continente #
EU - Europa 428
NA - Nord America 379
AS - Asia 102
OC - Oceania 1
SA - Sud America 1
Totale 911
Nazione #
US - Stati Uniti d'America 378
IE - Irlanda 153
IT - Italia 114
CN - Cina 66
GB - Regno Unito 39
DE - Germania 31
UA - Ucraina 23
SG - Singapore 20
FR - Francia 17
GR - Grecia 12
CZ - Repubblica Ceca 9
TR - Turchia 9
SE - Svezia 8
BE - Belgio 5
CH - Svizzera 5
FI - Finlandia 5
KR - Corea 5
LT - Lituania 4
RU - Federazione Russa 3
AU - Australia 1
BR - Brasile 1
CA - Canada 1
HK - Hong Kong 1
PK - Pakistan 1
Totale 911
Città #
Dublin 153
Chandler 69
Santa Clara 62
Jacksonville 43
Boardman 21
Princeton 16
Roxbury 14
Ann Arbor 13
Bremen 13
Singapore 13
Medford 11
Salerno 11
Brno 9
Caserta 8
Woodbridge 8
Beijing 7
Istanbul 7
Munich 7
Nanjing 7
Wilmington 7
Castelfranco Emilia 6
Des Moines 6
Taiyuan 6
Brussels 5
Cambridge 5
Jinan 5
Naples 5
Seoul 5
Hebei 4
Tianjin 4
Washington 4
Haikou 3
Nanchang 3
Napoli 3
Ningbo 3
Peschiera Del Garda 3
Rome 3
San Mateo 3
Taizhou 3
Arzano 2
Ashburn 2
Atella 2
Avellino 2
Aversa 2
Bresso 2
Collegeville 2
Helsinki 2
Kunming 2
Lanzhou 2
New York 2
Torre Del Greco 2
Auburn Hills 1
Bologna 1
Boydton 1
Brasília 1
Calvizzano 1
Cedar Knolls 1
Cervignano d'Adda 1
Changchun 1
Cimitile 1
Fontanarosa 1
Frankfurt am Main 1
Giugliano in Campania 1
Gold Coast 1
Guangzhou 1
Hangzhou 1
Hanover 1
Hong Kong 1
Hongtong 1
Houston 1
Karachi 1
London 1
Los Angeles 1
Maletto 1
Milan 1
Ottawa 1
Redwood City 1
Seattle 1
Seregno 1
Sesto San Giovanni 1
Shenyang 1
St Petersburg 1
Torre del Greco 1
Trieste 1
Volgograd 1
Voronezh 1
Wuxi 1
Yicheng 1
Yuanping 1
Zhengzhou 1
Totale 641
Nome #
Post-operative results of corneal collagen cross-linking for progressive keratoconus 86
Mutations in the PCYT1A gene are responsible for isolated forms of retinal dystrophy 85
A child with Myhre syndrome presenting with corectopia and tetralogy of Fallot 75
The role of optical coherence tomography in an atypical case of oculocutaneous albinism: A case report 73
Clinical and genetic analysis of a european cohort with pericentral retinitis pigmentosa 70
Clinical and Genetic Evaluation of a Cohort of Pediatric Patients with Severe Inherited Retinal Dystrophies 69
Prevalence of macular abnormalities assessed by Optical Coherence Tomography in patients with Usher Syndrome 54
Applications of Optical Coherence Tomography in the Ocular Diagnosis: From the Tear Film to the Sclera 54
Prevalence of macular abnormalities assessed by optical coherence tomography in patients with Usher syndrome 53
null 52
Retinal dystrophy in an individual carrying a de novo missense variant of SMARCA4 51
Chlamydia trachomatis induces an upregulation of molecular biomarkers podoplanin, Wilms' tumour gene 1, osteopontin and inflammatory cytokines in human mesothelial cells. 50
A novel mutation in the N-terminal region of the CYP17A1 gene in a patient with 17α-hydroxylase/17,20-lyase deficiency 39
Spectrum of Disease Severity in Patients With X-Linked Retinitis Pigmentosa Due to RPGR Mutations 39
Voretigene neparvovec gene therapy in clinical practice: treatment of the first two italian pediatric patients 39
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy 38
Infiltrating giant cell tumor in a case of Paget's disease of bone 33
Totale 960
Categoria #
all - tutte 4.507
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 4.507


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202049 0 0 0 0 0 11 13 3 5 7 3 7
2020/2021133 4 2 5 29 27 1 18 9 3 9 21 5
2021/2022120 5 1 2 3 30 1 3 5 4 19 7 40
2022/2023287 19 10 13 12 33 28 1 13 142 9 5 2
2023/2024131 9 6 9 5 40 2 3 0 1 2 6 48
2024/2025107 0 7 0 14 54 32 0 0 0 0 0 0
Totale 960