IRIS
Brunetti Pierri, Raffaella
 Distribuzione geografica
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Continente #
EU - Europa 408
NA - Nord America 313
AS - Asia 83
OC - Oceania 1
SA - Sud America 1
Totale 806
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Nazione #
US - Stati Uniti d'America 313
IE - Irlanda 153
IT - Italia 109
CN - Cina 63
GB - Regno Unito 36
DE - Germania 27
UA - Ucraina 23
FR - Francia 17
SG - Singapore 17
GR - Grecia 12
CZ - Repubblica Ceca 9
SE - Svezia 8
CH - Svizzera 5
FI - Finlandia 4
RU - Federazione Russa 3
BE - Belgio 2
TR - Turchia 2
AU - Australia 1
BR - Brasile 1
PK - Pakistan 1
Totale 806
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Città #
Dublin 153
Chandler 69
Jacksonville 43
Boardman 21
Princeton 16
Roxbury 14
Ann Arbor 13
Bremen 13
Medford 11
Salerno 11
Singapore 10
Brno 9
Caserta 8
Woodbridge 8
Beijing 7
Nanjing 7
Wilmington 7
Castelfranco Emilia 6
Des Moines 6
Taiyuan 6
Cambridge 5
Jinan 5
Naples 5
Hebei 4
Munich 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
Bresso 2
Brussels 2
Collegeville 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
Fontanarosa 1
Giugliano in Campania 1
Gold Coast 1
Guangzhou 1
Hangzhou 1
Hanover 1
Helsinki 1
Hongtong 1
Houston 1
Karachi 1
Maletto 1
Milan 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
Yicheng 1
Yuanping 1
Zhengzhou 1
Totale 548
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Nome #
Mutations in the PCYT1A gene are responsible for isolated forms of retinal dystrophy 82
Post-operative results of corneal collagen cross-linking for progressive keratoconus 81
The role of optical coherence tomography in an atypical case of oculocutaneous albinism: A case report 70
A child with Myhre syndrome presenting with corectopia and tetralogy of Fallot 67
Clinical and Genetic Evaluation of a Cohort of Pediatric Patients with Severe Inherited Retinal Dystrophies 64
Clinical and genetic analysis of a european cohort with pericentral retinitis pigmentosa 60
Prevalence of macular abnormalities assessed by optical coherence tomography in patients with Usher syndrome 47
Prevalence of macular abnormalities assessed by Optical Coherence Tomography in patients with Usher Syndrome 47
Chlamydia trachomatis induces an upregulation of molecular biomarkers podoplanin, Wilms' tumour gene 1, osteopontin and inflammatory cytokines in human mesothelial cells. 46
Retinal dystrophy in an individual carrying a de novo missense variant of SMARCA4 46
Applications of Optical Coherence Tomography in the Ocular Diagnosis: From the Tear Film to the Sclera 46
Clinical and molecular characterization of achromatopsia patients: A longitudinal study 43
A novel mutation in the N-terminal region of the CYP17A1 gene in a patient with 17α-hydroxylase/17,20-lyase deficiency 35
Voretigene neparvovec gene therapy in clinical practice: treatment of the first two italian pediatric patients 33
Spectrum of Disease Severity in Patients With X-Linked Retinitis Pigmentosa Due to RPGR Mutations 32
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy 27
Infiltrating giant cell tumor in a case of Paget's disease of bone 27
Totale 853
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Categoria #
all - tutte 3.491
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 3.491
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202085 0 12 6 2 16 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
Totale 853